阅读说明：本技术 便携式诊断设备及其方法 (Portable diagnostic apparatus and method thereof ) 是由 赵弘 严惠霖 伊萨贝莉·塞西尔·安吉拉·杜缇 于 2019-08-23 设计创作，主要内容包括：一种用于使用微流体盒(22)来检测来自样品的至少一种分析物的方法和便携式诊断设备(20)。所述便携式诊断设备(20)包括盒容纳单元、盒驱动器单元(30)和光学单元(32)。一种获得患病率信息的方法和设备,其包括至少一个所述便携式诊断设备(20)。一种用于管理便携式诊断设备的网络并获得患病率信息的方法和系统,其包括至少一个所述便携式诊断设备(20)。一种具有多个自动化特征的诊断系统,其能够为近患者临床评估和诊断提供一步解决方案。(A method and portable diagnostic device (20) for detecting at least one analyte from a sample using a microfluidic cartridge (22). The portable diagnostic apparatus (20) includes a cartridge accommodating unit, a cartridge driver unit (30), and an optical unit (32). A method and apparatus for obtaining prevalence information, comprising at least one of said portable diagnostic devices (20). A method and system for managing a network of portable diagnostic devices and obtaining prevalence information, comprising at least one of the portable diagnostic devices (20). A diagnostic system with multiple automated features that can provide a one-step solution for near-patient clinical assessment and diagnosis.)

1. A portable diagnostic apparatus for detecting at least one analyte from a sample using a microfluidic cartridge having a plurality of micropumps, a plurality of reservoirs connected to at least one diagnostic portion via microchannels, and a plurality of microvalves for sealing fluid in the reservoirs from flowing into the reaction sites, the portable diagnostic apparatus comprising a cartridge housing unit, a cartridge driver unit, and an optical unit,

the cartridge housing unit is configured to house the microfluidic cartridge;

the cartridge driver unit includes

a) A microvalve controller configured to control the microvalve, and

b) a micro pump controller configured to actuate the micro pump,

wherein the micro-pump controller and the micro-valve controller are cooperatively operable to actuate fluid flow from the reservoir to the diagnostic portion in a predetermined sequence when the microfluidic cartridge is placed in the cartridge receiving unit; and is

The optical unit is aligned with the diagnostic portion when the microfluidic cartridge is placed in the cartridge receiving unit;

thereby, the portable diagnostic device is able to control and monitor reactions within the microfluidic cartridge.

2. The portable diagnostic apparatus of claim 1, wherein the microvalve controller includes at least one heating element configured to apply thermal energy to a thermally deformable surface of the at least one microvalve to cause the microvalve to open.

3. The portable diagnostic device of claim 2, wherein the at least one heating element is juxtaposed to the at least one microvalve of the microfluidic cartridge when the cartridge is placed in the cartridge receiving unit.

4. The portable diagnostic device of claim 3, wherein the heating element is an infrared emitter.

5. The portable diagnostic device of claim 1, wherein the micropump controller comprises at least one electrical connector for electrically connecting with the at least one micropump of the microfluidic cartridge and is configured to provide an electrical current to the at least one micropump.

6. The portable diagnostic device of claim 1, wherein

The optical unit comprises an illumination assembly and a sensor assembly, wherein

a. The illumination assembly is configured to transmit light to a diagnostic portion of the microfluidic cartridge, and

b. the sensor assembly is configured to detect at least one signal generated by the diagnostic portion due to the presence of an analyte when the microfluidic cartridge is inserted and operated at a predetermined condition.

7. The portable diagnostic device of claim 6, wherein the illumination assembly comprises a light source having a wavelength in the range of 600nm to 650nm, and the at least one data signal is a fluorescence signal.

8. The portable diagnostic device of claim 1, further comprising a control unit configured to perform one or more of:

a. providing a predetermined sequence to the cartridge driver unit to direct at least one fluid within the microfluidic cartridge to move;

b. providing predetermined conditions to the optical unit for performing a quantitative and/or qualitative analysis of the analyte;

c. storing a data signal obtained from the optical unit; and

d. controlling and monitoring the operation of the device.

9. The portable diagnostic device of claim 8, wherein the control unit is configured to provide a predetermined sequence to the cartridge driver unit and a predetermined condition to the optical unit based on the identity of the microfluidic cartridge.

10. The portable diagnostic apparatus of claim 1, further comprising a housing for anchoring the cartridge housing unit, the cartridge driver unit, and the optical unit therein,

the cartridge accommodating unit further comprises a rail assembly and a tray, wherein

The track assembly includes a pair of slidable tracks,

the tray is configured to house the microfluidic cartridge and is anchored on the pair of rails,

wherein the track is capable of sliding the tray into and out of the housing such that the microfluidic cartridge can be inserted into the housing.

11. The portable diagnostic apparatus of claim 10, wherein the track assembly of the cartridge-containing unit, the cartridge driver unit, and the optical unit are mounted within the housing in a configuration such that

When the microfluidic cartridge is inserted into the portable diagnostic device, there is a space for receiving the microfluidic cartridge, the space comprising one or more microvalve positions, one or more micropump positions, and reaction positions corresponding to the positions of the one or more microvalves, the one or more micropumps, and the reaction sites, respectively, when the microfluidic cartridge is inserted into the space;

the heating element of the microvalve controller is mounted proximate to the microvalve position, wherein heat can be directed to the microvalve on the microfluidic cartridge when the microfluidic cartridge is inserted; and

the one or more electrical connectors of the micropump controller are mounted side-by-side with the one or more micropumps to electrically connect with the at least one micropump when the microfluidic cartridge is inserted into the portable diagnostic device.

12. The portable diagnostic device of claim 1, wherein the optical unit comprises an illumination assembly comprising a light source and a sensor assembly comprising a light sensor, wherein the light source and the light sensor are mounted to be directed toward the diagnostic portion of the microfluidic cartridge.

13. The portable diagnostic apparatus of claim 1, further comprising a built-in or removable rechargeable battery.

14. The portable diagnostic apparatus of claim 8, further comprising an identification unit to read an identification of the microfluidic cartridge and transmit a corresponding identification signal to the control unit.

15. The portable diagnostic apparatus of claim 14, further comprising a switch to trigger the identification unit to read the identification of the microfluidic cartridge when the microfluidic cartridge is positioned in a designated area.

16. The portable diagnostic apparatus of claim 1, wherein the portable diagnostic apparatus does not comprise any means for actuating a fluid external to the microfluidic cartridge, and wherein the portable diagnostic apparatus does not provide any reagents.

17. The portable diagnostic device of claim 8, further comprising a user interface unit configured to display the quantitative and/or qualitative analysis of the analyte, wherein the user interface unit is connected to the control unit.

18. The portable diagnostic device of claim 1, wherein

The cartridge receiving unit and the cartridge driver unit are configured to connect with the microfluidic cartridge when the microfluidic cartridge is secured at a designated area;

the cartridge housing unit houses and fixes the microfluidic cartridge at the designated region;

the microvalve controller is in juxtaposition with at least one microvalve; and is

The micro-pump controller is electrically connected to at least one micro-pump;

thereby, fluid actuation and analyte detection are performed within the designated area during operation.

19. The portable diagnostic apparatus of claim 18, wherein the cartridge receiving unit comprises a track assembly and a tray, wherein

The track assembly includes a cavity for slidably receiving the tray,

the tray includes a cartridge chamber for housing the microfluidic cartridge such that the microfluidic cartridge is positioned at the designated area.

20. The portable diagnostic apparatus of claim 1, further comprising a smart device, wherein the smart device comprises

a. An environmental measurement module for obtaining environmental data, wherein the environmental data comprises at least one environmental parameter at the location;

b. a data storage module for storing raw data, wherein the raw data comprises one or more of environmental data and diagnostic data; and

c. a transmitter for transmitting the raw data to a remote server.

21. The portable diagnostic device of claim 20, wherein the environmental data is selected from the group consisting of positioning data, humidity, temperature, and time.

22. The portable diagnostic apparatus of claim 20, wherein the smart device can optionally connect to and communicate with the portable diagnostic apparatus and the remote server.

23. The portable diagnostic apparatus of claim 20, wherein the smart device further comprises a battery, wherein the battery is rechargeable and capable of operating without recharging for 30 days.

24. A method of detecting at least one analyte from a sample using the portable diagnostic device of claim 1 or claim 2, wherein the sample is loaded into a microfluidic cartridge having

A diagnostic portion comprising at least one pre-supplied reactant; and

a microfluidic portion comprising a plurality of microvalves, a plurality of micropumps, and a plurality of reservoirs comprising at least one pre-supplied reagent; and wherein

The microfluidic cartridge is located at a diagnostically designated region of the cartridge receiving unit;

wherein the method comprises the steps of:

a) directing the sample and at least one reagent from the microfluidic portion to the diagnostic portion in a predetermined sequence within the microfluidic cartridge by opening at least one microvalve sealing at least one reservoir of the microfluidic cartridge and actuating at least one micropump in the microfluidic cartridge;

b) providing a predetermined condition to the diagnostic portion of the microfluidic cartridge to generate at least one signal;

c) detecting the at least one data signal using an optical sensor and collecting diagnostic data; and

d) analyzing the diagnostic data to quantitatively and/or qualitatively determine the presence of the analyte.

25. The method of claim 24, further comprising the step of:

a) reading the identity of the microfluidic cartridge;

b) providing a predetermined order to the cartridge driver unit based on the identification of the microfluidic cartridge and providing a predetermined condition to the optical unit.

26. A method of obtaining prevalence information comprising

a. Obtaining diagnostic data or a sample at a location using the portable diagnostic device of claim 20, wherein the diagnostic data comprises at least one biochemical or pathological measurement of the subject;

b. obtaining environmental data at the location;

c. transmitting the diagnostic data and the environmental data to a server;

d. collecting and storing, in the server, the diagnostic data and the environmental data for a plurality of subjects in a plurality of locations to form a database; and

e. analyzing prevalence information for the subject at the plurality of locations in the database.

27. A system for managing a network of portable diagnostic devices, comprising

At least one portable diagnostic device according to claim 20,

at least one user terminal, and

a server, which comprises

A data module for collecting and storing raw data, wherein the raw data comprises one or more of:

(a) diagnostic data obtained at a location using a portable diagnostic device, wherein the diagnostic data comprises at least one biochemical or pathological measurement of the subject,

(b) environmental data obtained at the location using an environmental measurement module, wherein the environmental data comprises at least one environmental parameter,

(c) device data obtained from the portable diagnostic device, an

(d) Data module for analyzing said raw data

Wherein the server is connected to the user terminal and the portable diagnostic device.

28. The system of claim 27, comprising a plurality of portable diagnostic devices, wherein the server is a cloud-based platform wirelessly connected to the user terminal and the portable diagnostic devices.

29. The system of claim 27, wherein the data module performs one or more of the following steps:

1. collecting raw data;

2. analyzing the raw data to provide a result; and

3. transmitting the result to the user terminal;

and provide one or more of the following results:

1. prevalence at different locations displayed on a map;

2. prevalence over time;

3. the severity of the disease in a particular location; and

4. correlation between environmental conditions and device status.

30. The system of claim 27, wherein the data module further comprises one or more access controls to the raw data and the results.

31. A method of using the system of claim 27, comprising the steps of:

i. obtaining and storing raw data at the location on a data storage module;

transmitting the raw data from the data storage module to a server;

collecting and storing, in the server, a plurality of raw data from a plurality of portable diagnostic devices to form a database;

analyzing the database to provide results; (ii) a

Wherein the raw data comprises one or more of:

i. diagnostic data obtained at a location using a portable diagnostic device, wherein the diagnostic data comprises at least one biochemical or pathological measurement of a subject;

environmental data obtained at the location using an environmental measurement module, wherein the environmental data comprises at least one environmental parameter;

device data obtained from the portable diagnostic device.

32. The method of claim 31, wherein the raw data is transmitted to the server once per hour even when the portable diagnostic device is not connected to an external power source.

33. The method of claim 31, wherein the raw data is diagnostic data obtained at a location using a portable diagnostic device, wherein the diagnostic data comprises at least one biochemical or pathological measurement and location data of a subject; and the results provide prevalence information.

34. The method of claim 31, wherein the raw data is one or more of temperature, humidity, time, positioning data, and device data; and the results provide information associated with the performance of the portable diagnostic device.

Technical Field

The present invention relates to a system for detecting an analyte and a method of using the same. More particularly, the present invention relates to a microfluidic cartridge, an apparatus for such a microfluidic cartridge.

Background

Traditional diagnosis, screening, staging, veterinary, pharmaceutical testing, etc. are often performed in the laboratory, and testing is often time consuming, expensive, and requires many resources, supplies, and support. Current systems require multiple steps between initial sample collection and diagnostic result receipt. They require a high degree of human involvement and are therefore prone to human error. In some models, reagents are added manually by the user, which means that potential reagent spills may pose health and safety risks to the user. In some models, diagnostic testing involves multiple manual steps, such as loading reagents. Finally, in some models, the results are interpreted by the user, which may lead to discrepancies and even potential misunderstandings.

Disclosure of Invention

In view of the foregoing background, it is an object of the present invention to provide an improved diagnostic system for detecting one or more analytes.

According to one aspect, a diagnostic system includes two parts: an apparatus and a microfluidic cartridge for detecting at least one or more analytes.

In some embodiments, the diagnostic system is a portable, self-contained system for detecting an analyte. In some embodiments, the diagnostic system performs at least one immunoassay. In some embodiments, the diagnostic system performs at least one immunofluorescence assay. In some embodiments, the apparatus includes a microfluidic cartridge driver unit, an optical inspection unit, and a control unit and power supply unit. In some embodiments, the device can perform binding and detection of analytes without any fluid interface with the instrument. In some embodiments, a microfluidic cartridge housing unit houses a microfluidic cartridge holding a microarray and an integrated microfluidic chip. In some embodiments, the microfluidic cartridge contains a sample containing an analyte and performs different process steps in the detection of the analyte. In some embodiments, all process steps, including the reaction of analytes on the microarray, detection of signals, analysis of data, and display of results, are performed automatically by the apparatus on a single tray without any user intervention. The complete detection of an analyte using the present invention requires only a few minutes.

In one aspect, a portable diagnostic device is provided for detecting at least one analyte from a sample using a microfluidic cartridge. The microfluidic cartridge has a plurality of micropumps, a plurality of reservoirs connected to at least one diagnostic moiety via microchannels, and a plurality of microvalves for sealing fluid in the reservoirs from flowing into the reaction sites. The portable diagnostic apparatus includes a cartridge accommodating unit, a cartridge driver unit, and an optical unit. The cartridge-receiving unit is configured to receive a microfluidic cartridge. The cartridge driver unit includes: a) a microvalve controller configured to control the microvalve, and b) a micropump controller configured to actuate the micropump. The micro-pump controller and the micro-valve controller are configured to cooperate to actuate fluid flow from the reservoirs to the diagnostic portion in a predetermined sequence when the microfluidic cartridge is placed in the cartridge receiving unit. The optical unit is aligned with the diagnostic portion when the microfluidic cartridge is placed in the cartridge receiving unit. The portable diagnostic device can control and monitor reactions within the microfluidic cartridge.

In some embodiments, the microvalve controller includes at least one heating element configured to apply thermal energy to a thermally deformable surface of the at least one microvalve to cause the microvalve to open.

In some embodiments, the at least one heating element is juxtaposed to the at least one microvalve of the microfluidic cartridge when the cartridge is placed in the cartridge receiving unit.

In some embodiments, the heating element is an infrared emitter.

In some embodiments, the micropump controller comprises at least one electrical connector for electrically connecting with the at least one micropump of the microfluidic cartridge and is configured to provide an electrical current to the at least one micropump.

In some embodiments, the optical unit includes an illumination assembly and a sensor assembly. The illumination assembly is configured to transmit light to a diagnostic portion of the microfluidic cartridge. The sensor assembly is configured to detect at least one signal generated by the diagnostic portion due to the presence of the analyte when the microfluidic cartridge is inserted and operated at a predetermined condition.

In some embodiments, the illumination assembly includes a light source having a wavelength in the range of 600nm to 650nm, and the at least one data signal is a fluorescent signal.

In some embodiments, the portable diagnostic device further comprises a control unit configured to perform one or more of the following: a. providing a predetermined sequence to a cartridge driver unit to direct at least one fluid within the microfluidic cartridge to move; b. providing predetermined conditions to the optical unit for performing a quantitative and/or qualitative analysis of the analyte; c. storing a data signal obtained from the optical unit; controlling and monitoring operation of the portable diagnostic device.

In some embodiments, the control unit is configured to provide a predetermined order to the cartridge driver unit and a predetermined condition to the optical unit in dependence on the identity of the microfluidic cartridge.

In some embodiments, the portable diagnostic apparatus further comprises a housing for anchoring the cartridge accommodating unit, the cartridge driver unit and the optical unit therein.

The cartridge accommodating unit further includes a rail assembly and a tray. The track assembly includes a pair of slidable tracks. The tray is configured to receive the microfluidic cartridge and is anchored to the pair of rails. The track can slide the tray into and out of the housing so that the microfluidic cartridge can be inserted into the housing.

In some embodiments, the track assembly of the cartridge-receiving unit, the cartridge driver unit, and the optical unit are mounted within the housing in a configuration such that when the microfluidic cartridge is inserted into the portable diagnostic device, there is a space for receiving the microfluidic cartridge that includes one or more microvalve positions, one or more micropump positions, and reaction positions that correspond to the positions of the one or more microvalves, the one or more micropumps, and the reaction sites, respectively, when the microfluidic cartridge is inserted into the space. The heating element of the microvalve controller is mounted near the microvalve position, wherein heat can be directed to the microvalve on the microfluidic cartridge when the microfluidic cartridge is inserted. The one or more electrical connectors of the micropump controller are mounted side-by-side with the one or more micropumps to electrically connect with the at least one micropump when the microfluidic cartridge is inserted into the portable diagnostic device.

In some embodiments, the optical unit comprises an illumination assembly comprising a light source and a sensor assembly comprising a light sensor. The light source and the light sensor are mounted to be directed toward a diagnostic portion of the microfluidic cartridge.

In some embodiments, the portable diagnostic device further comprises a built-in or detachable rechargeable battery.

In some embodiments, the portable diagnostic device further comprises a switch to trigger the identification unit to read the identification of the microfluidic cartridge when the microfluidic cartridge is positioned in the designated area.

In some embodiments, the portable diagnostic apparatus does not include any means for actuating a fluid external to the microfluidic cartridge, and wherein the portable diagnostic apparatus does not provide any reagents.

In some embodiments, the portable diagnostic device further comprises a user interface unit configured to display a quantitative and/or qualitative analysis of the analyte, wherein the user interface unit is connected to the control unit.

In some embodiments, the cartridge receiving unit and the cartridge driver unit are configured to connect with the microfluidic cartridge when the microfluidic cartridge is secured at the designated area. The cartridge housing unit houses and fixes the microfluidic cartridge at a designated region. The microvalve controller is juxtaposed to the at least one microvalve. The micro-pump controller is electrically connected to the at least one micro-pump. Fluid actuation and analyte detection are performed within the designated area during operation.

In some embodiments, the cartridge receiving unit includes a rail assembly and a tray. The track assembly includes a cavity for slidably receiving the tray. The tray includes a cartridge chamber for receiving the microfluidic cartridge such that the microfluidic cartridge is positioned at the designated area.

In some embodiments, the portable diagnostic device further comprises at least one of the following sensors controlled by the controller: a. a humidity sensor; b. a temperature sensor; such that one or more environmental data can be collected at about the time the microfluidic cartridge is used in the device.

In some embodiments, the portable diagnostic device further comprises a data storage module for storing one or more of environmental data and diagnostic data; and a transmitter for transmitting the environmental data and the diagnostic data to a remote server.

In some embodiments, the portable diagnostic apparatus further comprises an intelligent device, wherein the intelligent device comprises: a. an environmental measurement module for obtaining environmental data, wherein the environmental data comprises at least one environmental parameter at the location; b. a data storage module for storing raw data, wherein the raw data comprises one or more of environmental data and diagnostic data; a transmitter for transmitting the raw data to a remote server.

In some embodiments, the environmental data is selected from the group consisting of positioning data, humidity, temperature, and time.

In some embodiments, the smart device may optionally be connected to and communicate with a portable diagnostic apparatus and a remote server.

In some embodiments, the smart device further comprises a battery, wherein the battery is rechargeable and can operate without charging for 30 days.

According to another aspect, a microfluidic cartridge is provided that includes a microfluidic portion and a diagnostic portion. The microfluidic part comprises: i. a plurality of reservoirs capable of holding fluid therein; connecting one or more reservoirs to a plurality of microchannels of a diagnostic moiety; a plurality of microvalves operable between a closed state and an open state to respectively seal and open the microchannel connections; a plurality of micropumps coupled to the one or more reservoirs. The microvalve in the closed state allows fluid to be stored and sealed within the reservoir, while the microvalve in the open state allows fluid to flow between the reservoir and the diagnostic portion. The micropump can be actuated to move fluid from the reservoir to the diagnostic portion so that multiple reagents can be preloaded in a sealed manner and stored in the microfluidic cartridge until use.

In some embodiments, the diagnostic portion comprises a diagnostic chamber for receiving at least one fluid from the microfluidic portion.

In some embodiments, the microfluidic cartridge further comprises a waste reservoir connected to the diagnostic portion via an outlet to contain waste fluid ejected from the diagnostic chamber.

In some embodiments, the diagnostic portion is at least partially transparent to optical detection.

In some embodiments, the microfluidic cartridge further comprises a microporous membrane configured to remove gas from the sample and/or the reagent.

In some embodiments, a waste reservoir is connected to the microporous membrane to remove gases from the waste.

In some embodiments, at least one reservoir is filled with at least one fluid, wherein the fluid is a reagent and is sealed closed with a microvalve.

In some embodiments, the microfluidic cartridge further comprises a plurality of reagents that are individually preloaded, sealed, and stored in reservoirs; and at least one reactant pre-supplied at the diagnostic portion.

In some embodiments, the at least one reservoir for holding at least one sample further comprises a sample inlet with a removable lid.

According to another aspect, a portable diagnostic system is provided comprising a portable diagnostic device as described herein and optionally a microfluidic cartridge as described herein.

According to another aspect, there is provided a method of detecting at least one analyte from a sample using a portable diagnostic device as described above. Loading a sample onto a microfluidic cartridge having a diagnostic portion and a microfluidic portion, the diagnostic portion including at least one pre-supplied reagent, and the microfluidic portion including a plurality of microvalves, a plurality of micropumps, and a plurality of reservoirs including at least one pre-supplied reagent. The microfluidic cartridge is positioned at a diagnostically designated region of the cartridge-receiving unit. The method comprises the steps of a) directing the sample and at least one reagent from the microfluidic portion to the diagnostic portion in a predetermined sequence within the microfluidic cartridge by opening at least one microvalve sealing at least one reservoir of the microfluidic cartridge and actuating at least one micropump in the microfluidic cartridge; b) providing a predetermined condition to a diagnostic portion of the microfluidic cartridge to generate at least one signal; c) detecting the at least one data signal using an optical sensor and collecting diagnostic data; and d) analyzing the diagnostic data to quantitatively and/or qualitatively determine the presence of the analyte.

In some embodiments, further comprising the steps of: a) reading an identification of the microfluidic cartridge; b) the cartridge driver unit is provided with a predetermined sequence based on the identification of the microfluidic cartridge and with predetermined conditions to the optical unit.

According to another aspect, there is provided a method of obtaining prevalence information, comprising: a. obtaining diagnostic data or a sample at a location using the portable diagnostic device of claim 20, wherein the diagnostic data comprises at least one biochemical or pathological measurement of the subject; b. obtaining environmental data at the location; c. transmitting the diagnostic data and the environmental data to a server; d. collecting and storing, in a server, diagnostic data and environmental data for a plurality of subjects in a plurality of locations to form a database; analyzing prevalence information for the subject at a plurality of locations in the database.

According to another aspect, a system for managing a network of portable diagnostic devices comprises at least one portable diagnostic device as described herein, at least one user terminal, and a server. The server includes a data module for collecting and storing raw data, wherein the raw data includes one or more of: (1) diagnostic data obtained at a location using a portable diagnostic device, wherein the diagnostic data comprises at least one biochemical or pathological measurement of the subject, (2) environmental data obtained at the location using an environmental measurement module, wherein the environmental data comprises at least one environmental parameter, and (3) device data obtained from the portable diagnostic device, and (4) a data module for analyzing the raw data. The server is connected to the user terminal and the portable diagnostic device.

In some embodiments, the system further comprises a plurality of portable diagnostic devices, wherein the server is a cloud-based platform wirelessly connected to the user terminal and the portable diagnostic devices.

In some embodiments, the data module performs one or more of the following steps: (1) collecting raw data; (2) analyzing the raw data to provide results; and (3) transmitting the result to the user terminal. The data module also provides one or more of the following results: (1) prevalence at different locations displayed on a map; (2) prevalence over time; and (3) the severity of the disease in a particular location; and (4) correlation between environmental conditions and device status.

In some embodiments, the data module further includes one or more access controls to the raw data and results.

In some embodiments, the server remotely provides technical support or one or more software updates. For example, the server may transmit an updated version of the device software via a network. The server may also provide information about how to resolve a particular machine error of the device. In some embodiments, the data module may evaluate information about the environmental parameters of the device, such as temperature, humidity, time, and location data (e.g., location), and compare it to the error code received by the device to determine if one or more environmental parameters caused the error code. The data module may provide remote technical support for the user, instructions on how to solve the problem, or other forms of technical support in solution. The data module may also remotely transmit the software update to the smart device.

In some embodiments, the data module further provides a correlation between the environmental condition and the prevalence. In some embodiments, the environmental condition comprises temperature, humidity, or time. In some embodiments, the environmental condition is determined by a third party source rather than by the portable diagnostic device.

In some embodiments, the data module further includes one or more access controls to the raw data and results.

According to another aspect, there is provided a method of using the system described herein, comprising the steps of: (1) obtaining and storing raw data at the location on a data storage module; (2) transmitting the raw data from the data storage module to the server; (3) collecting and storing, in a server, a plurality of raw data from a plurality of portable diagnostic devices to form a database; (4) the database is analyzed to provide results. The raw data includes one or more of: (1) diagnostic data obtained at a location using a portable diagnostic device, wherein the diagnostic data comprises at least one biochemical or pathological measurement of the subject; (2) environmental data obtained at the location using an environmental measurement module, wherein the environmental data includes at least one environmental parameter; (3) device data obtained from a portable diagnostic device.

In some embodiments, the raw data is transmitted to the server once per hour even when the portable diagnostic device is not connected to an external power source.

In some embodiments, the raw data is diagnostic data obtained at a location using a portable diagnostic device, wherein the diagnostic data comprises at least one biochemical or pathological measurement and location data of the subject; and the results provide prevalence information.

In some embodiments, the raw data is one or more of temperature, humidity, time, positioning data, and device data; and as a result provides information associated with the performance of the portable diagnostic device. In some embodiments, the performance of the portable diagnostic device is indicated by operating conditions, such as error codes, system voltage, total operating hours, and total number of tests for the machine. The results include, but are not limited to, error codes, the manner in which the error codes are repaired, and the correlation between the error codes and one or more of temperature, humidity, positioning data, and time.

Various embodiments of the present disclosure have many advantages, such as providing a "one-step" solution for detecting analytes in situ. For example, some embodiments provide a diagnostic system with a plurality of automated features that can provide a one-step solution for near-patient clinical assessment and diagnosis.

In some embodiments, the diagnostic system is portable and requires minimal user intervention. Near patient testing may be performed by medical professionals (e.g., physicians and nurses) or trained non-professionals (e.g., clinic staff and caregivers).

Exemplary devices for detecting analytes involve relatively small amounts or volumes of sample (in some embodiments, a few microliters (μ Ι) to hundreds of μ Ι) while using an integrated reaction to a detection instrument/method. Therefore, it is a genuine "field test device" which will provide real convenience to field personnel. Thus, the special handling and transport of the analyte to the laboratory and the excessive transport time that may affect the quality of the analyte are greatly reduced.

Another advantage is that the apparatus of some embodiments requires little or no sample preparation compared to conventional diagnostic methods or systems, thereby reducing processing time.

Another advantage of some embodiments is that it can be applied in various fields of diagnostics and food safety analysis. For example, a method of detecting one or more analytes associated with the presence of a disease in a subject. Such applications include, but are not limited to, animal immunodiagnosis (e.g., swine influenza virus (e.g., H1N1) infection, Porcine Reproductive and Respiratory Syndrome (PRRS), bovine Foot and Mouth Disease (FMD), Classical Swine Fever (CSFV) infection, and Bovine Spongiform Encephalopathy (BSE) infection), food safety testing (e.g., detection of food allergens (e.g., peanut, seafood), aflatoxins, and melamine), clinical testing in human subjects (e.g., infectious diseases (e.g., Sexually Transmitted Disease (STD), middle east respiratory syndrome coronavirus (MERS-CoV), and influenza virus infection), tropical diseases (e.g., dengue virus and japanese encephalitis virus infection), and emerging infectious diseases that are antigen/antibody immune mechanisms in their pathological pathways), influenza a, influenza b, RSV, HPIV, adenovirus, dengue, chikungunya, influenza b, Detection of Zika, malaria, leptospirosis, toxoplasmosis, canine distemper virus Ab, canine parvovirus Ab or heartworm. Some embodiments may be adapted to analyze multiple analytes in the same sample and in the same process, thereby significantly reducing the cost and processing time involved in examining multiple diseases/analytes.

The exemplary embodiments are particularly configured to enable all required steps to be performed on a single tray without user intervention. These steps include (1) reactions in the microfluidic cartridge, (2) detection of signals from the microfluidic cartridge, and (3) analysis and display of the results to a user. They provide an automated rapid diagnostic device that minimizes the possibility of human interaction and human error. It provides a one-step foolproof solution for near patient rapid diagnosis that can be used by minimally trained laymen.

In some exemplary embodiments (e.g., microvalve controllers), the actuation assembly provides a sealed compartment for storing at least one reagent within a reservoir and actively and precisely actuating at least one fluid within the microfluidic cartridge.

The reaction and detection of some exemplary embodiments (e.g., single tray systems) can be performed in the same cartridge without the need to separate the diagnostic portion from the detection portion. Microfluidic cartridges (e.g., for preloaded chip embodiments) are self-contained, i.e., all reagents required for reactions during the manufacturing process are pre-supplied (or preloaded) within the microfluidic cartridge, such that no reagents are required in the field.

In summary, the various embodiments provide advantages such as low cost, time and space savings, portability, minimal resources required, and a low degree of skill and technician to perform a complete analyte test quickly, on a large scale, and efficiently in the field.

Drawings

FIG. 1 is a block diagram illustrating a diagnostic system according to one embodiment of the present invention.

FIG. 2 is a schematic diagram of a diagnostic system according to an exemplary embodiment of the present invention.

Fig. 3 is a schematic bottom view of a tray of a diagnostic system with a diagnostic chip (right) and without a diagnostic chip (left) according to an exemplary embodiment of the present invention.

Fig. 4 is a schematic diagram of a fluid control assembly of a microfluidic cartridge handling unit of an apparatus according to an exemplary embodiment of the present invention.

Fig. 5 is a schematic view of an optical inspection unit of a diagnostic system according to an exemplary embodiment of the present invention.

Fig. 6A is a schematic top (left), side (middle) and bottom (right) view of a microfluidic cartridge according to an exemplary embodiment of the present invention.

Fig. 6B is a schematic exploded view of a microfluidic cartridge according to an exemplary embodiment of the present invention; fig. 6C is a schematic exploded view of a microfluidic cartridge according to another exemplary embodiment of the present invention.

Fig. 7 is a flow chart of a production sequence of a microfluidic cartridge according to another exemplary embodiment of the present invention.

Fig. 8 is a flowchart of a coating process and deposition of a detection spot on a diagnostic chip according to an embodiment of the present invention, according to another exemplary embodiment of the present invention.

FIG. 9 depicts detection of fluorescent antigen (FluA) according to an exemplary embodiment of the invention.

Fig. 10A is a block diagram of a portable diagnostic device according to an exemplary embodiment of the present invention.

Fig. 10B is a block diagram of a portable diagnostic device according to another exemplary embodiment of the present invention.

Fig. 11A is a schematic top (left), side (middle) and bottom (right) view of a microfluidic cartridge according to an exemplary embodiment of the present invention.

Fig. 11B is a schematic exploded view of a microvalve membrane and a top portion of a microfluidic cartridge according to the same exemplary embodiment of the present invention as shown in fig. 11A.

Fig. 11C is a schematic exploded view of a microfluidic cartridge according to the same exemplary embodiment of the present invention as shown in fig. 11A.

Fig. 12A is a schematic exploded view of a microfluidic cartridge according to another exemplary embodiment of the present invention.

Fig. 12B is a schematic top view of a microvalve membrane of a microfluidic cartridge according to the same exemplary embodiment of the present invention as shown in fig. 12A.

Fig. 12C is a schematic top view of a top portion of a microfluidic cartridge according to the same exemplary embodiment of the present invention as shown in fig. 12A.

Fig. 12D is a schematic bottom view of a top portion of a microfluidic cartridge according to the same exemplary embodiment of the present invention as shown in fig. 12A.

Fig. 12E is a schematic top view of a bottom portion of a microfluidic cartridge according to the same exemplary embodiment of the present invention as shown in fig. 12A.

Fig. 12F is a schematic bottom view of a bottom portion of a microfluidic cartridge according to the same exemplary embodiment of the present invention as shown in fig. 12A.

Fig. 13A and 13B are schematic diagrams of fluid movement within a microfluidic cartridge driven by a cartridge driver unit, according to an example embodiment.

Fig. 14A is a schematic exploded view of a portable diagnostic device according to an exemplary embodiment of the present invention.

Fig. 14B is a schematic exploded view of another example of a portable diagnostic device.

FIG. 15A is a top perspective view of a microvalve controller of a microfluidic cartridge driver unit according to one exemplary embodiment of the present invention.

Figure 15B is a bottom perspective view of the same microvalve controller shown in figure 15A.

Fig. 16A and 16B are schematic views of a microfluidic cartridge-containing unit according to an exemplary embodiment of the present invention.

Fig. 16C is a schematic view of the tray of the same microfluidic cartridge housing unit as shown in fig. 16A.

Fig. 16D is a schematic view of the same tray as shown in fig. 16C but with a microfluidic cartridge inserted therein.

Fig. 17 is an exploded view of an optical unit and an identification unit of a diagnostic apparatus according to one embodiment of the present invention.

Fig. 18 is a schematic diagram of an assembly of an optical unit, an identification unit, a cartridge driving unit, and a cartridge accommodating unit of a diagnostic apparatus according to an exemplary embodiment of the present invention.

Fig. 19 is a flowchart of the operation of a diagnostic device according to an exemplary embodiment of the present invention.

FIG. 20 is a schematic diagram of a system for managing a network of field diagnostic devices and obtaining prevalence or other information, according to an embodiment of the invention.

FIG. 21 is a flow diagram of a method of obtaining prevalence or environmental information, according to an embodiment of the invention.

FIG. 22 is a flow diagram of the operation of the system of FIG. 20 according to one embodiment of the invention.

FIG. 23 is a flow diagram illustrating the flow of information and data for various components of a system according to one embodiment of the invention.

FIG. 24 is a schematic diagram of an assembly of a smart device and a unit interacting therewith, according to one embodiment of the invention.

Detailed Description

As used herein and in the claims, "comprising" means including, but not excluding, the following elements.

As used herein and in the claims, "coupled" or "connected" refers to a connection, either directly or indirectly, through one or more physical means, unless otherwise indicated.

As used herein and in the claims, "microfluidic" refers to the precise control and manipulation of fluids or liquids that are geometrically constrained to a small sub-millimeter scale at which capillary penetration controls mass transport to less than 0.01 ml. The microfluidic systems disclosed herein do not include paper-based microfluidic systems. "microfluidic cartridge" refers to a cartridge having a microfluidic structure that includes various components, modules, chambers, etc. that are fluidically connected and configured to process a fluid sample. The microfluidic cartridges disclosed herein perform biological or biochemical assays, such as immunoassays. The microfluidic cartridges disclosed herein do not include applications for Polymerase Chain Reaction (PCR) or nucleic acid sequencing. "immunoassay" refers to an assay that involves the coupling of an antibody or antigen to a molecule to detect an analyte. The molecule may be one that can generate a fluorescent signal or other detectable signal.

"sample" refers to the substance to be tested and includes, but is not limited to, a blood sample, a serum sample, a urine sample, a sweat sample, a saliva sample, a tear drop sample, a nasal swab, a nasopharyngeal swab, or a sample including other bodily fluids or other non-human sample. In some embodiments, the sample is processed such that testing can be performed by a microfluidic system. For example, a solid sample may be treated with a buffer or other reagent to isolate or extract the analyte of interest.

As used herein and in the claims, "analyte" refers to, but is not limited to, pathogens and biomolecules present in, for example, a bodily fluid, nasal swab, or serum sample from a target individual (including, but not limited to, for example, an animal or human subject). It is to be understood that when the term "analyte" is used, it can refer to one or more analytes.

As used herein and in the claims, "reactant" refers to, but is not limited to, a substance of interest that reacts with one or more analytes (e.g., antibodies or antigens). The substance may be immobilized for use on a diagnostic chip. It is to be understood that when the term "reactant" is used, it can refer to one or more reactants.

As used herein and in the claims, "fluid" refers to any liquid, including but not limited to liquid samples, reagents, buffers.

As used herein and in the claims, "diagnosis" refers to the detection of an analyte (not limited to only one or more disease-related analytes). However, the diagnostic systems described herein do not involve amplification of nucleic acids, such as Polymerase Chain Reaction (PCR) or nucleic acid sequencing.

As used herein and in the claims, "pre-supplied" or "pre-loaded" refers to a fluid (e.g., reagents and/or reactants) that is supplied or loaded during the manufacturing process of a microfluidic cartridge such that a user does not need to supply or load the liquid.

As used herein and in the claims, "micropump" refers to a fluid actuator that actuates at least one fluid.

As used herein and in the claims, "microvalves" refer to barriers between channels and/or reservoirs. In some exemplary embodiments, the microvalve is a closed valve in a resting position and can be opened under active operation so that fluids or reagents can be pre-sealed within the reservoir for long term storage.

It will be understood that, although the terms first, second, third, etc. may be used herein to describe various limitations, elements, components, regions, layers and/or sections, these limitations, elements, components, regions, layers and/or sections should not be limited by these terms. These terms are only used to distinguish one limitation, element, component, region, layer or section from another limitation, element, component, region, layer or section. Thus, a first limitation, element, component, region, layer or section discussed below could be termed a second limitation, element, component, region, layer or section without departing from the teachings of the present application.

It will be further understood that when an element is referred to as being "on" or "connected" or "coupled" to another element, it can be directly on or on the other element or connected or coupled to the other element or intervening elements may be present. In contrast, when an element is referred to as being "directly on" or "directly connected" or "directly coupled" to another element, there are no intervening elements present. Other words used to describe the relationship between elements (e.g., "between … …" and "directly between … …", "adjacent" and "directly adjacent", etc.) should be interpreted in a similar manner. When an element is referred to herein as being "over" another element, it can be over or under the other element, and can be directly coupled to the other element, or intervening elements may be present, or the elements may be separated by a void or gap.

It will be further understood that when elements are referred to as being "top" or "bottom," these terms are used to describe relative positions between the elements. Thus, a "top" portion, element, component, region, layer or section discussed below could be termed a "bottom" portion, element, component, region, layer or section without departing from the teachings of the present application.

Example 1

1. Device

Fig. 1 and 2 show a diagnostic system that includes (1) a diagnostic device 20 and (2) a microfluidic cartridge 22 that operates with the diagnostic device 20. The microfluidic cartridge 22, which includes a microfluidic chip 24 and a diagnostic chip 26, is configured to collect and manipulate at least one sample, which may include at least one analyte. The microfluidic cartridge 22 also contains and/or holds at least one reagent. The diagnostic apparatus 20 is a portable, hand-held and compact device comprising a control unit 28, a microfluidic cartridge driver unit 30, an optical inspection unit 32 and a display unit 34. The control unit 28 controls and is connected to a microfluidic cartridge driver unit 30, an optical inspection unit 32 and a display unit 34. The microfluidic cartridge driver unit 30 is configured to receive and drive the microfluidic cartridge 22 such that the collected sample and reagents pass through the microfluidic chip 24 and the diagnostic chip 26 in a predetermined sequence. The microfluidic cartridge driver unit 30 also allows the inspection or analysis of the diagnostic chip to be performed at the same location (location/position) on the same microfluidic cartridge after the reactions are performed in a predetermined order. The optical inspection unit 32 is configured to inspect the diagnostic chip 26 at the same location on the same microfluidic cartridge where the reaction is also performed to analyze for the presence of the analyte. The display unit 34 is configured to display relevant information containing the analysis/diagnosis result to the user. Fig. 2 shows that the control unit 28, the microfluidic cartridge driver unit 30, the optical inspection unit 32, the display unit 34 and the power supply unit 65 are enclosed in a stand-alone diagnostic device. In one exemplary embodiment, the device includes a microfluidic cartridge receiving aperture on its front panel for receiving the microfluidic cartridge 22.

1.1 microfluidic Cartridge driver Unit

1.1.1 trays and Cartridge compartments

The microfluidic cartridge driver unit includes a tray 52 and a cartridge chamber 42 (see fig. 3).

The cartridge chamber 42 is configured to receive the microfluidic cartridge 22. The tray 52 includes a cartridge chamber 42 that houses the microfluidic cartridge 22. The tray 52 serves as the same location for performing the following operations: (1) reactions to be run in a predetermined sequence and (2) inspection and analysis of the diagnostic chip. In another exemplary embodiment, the electrical connector 44 is located underneath the microfluidic cartridge 22 and serves as an interface for the microfluidic cartridge 22 to drive/control and provide power/current to the microfluidic cartridge 22.

The single tray system eliminates the possibility of human error by design. Fig. 3 shows an empty tray (left) and a tray equipped with microfluidic cartridges 22 (right).

The microfluidic cartridge 22 and the cartridge chamber 42 are configured such that there is only one possible way in which the microfluidic cartridge 22 can fit into the cartridge chamber 42 and the tray 52, and thus the possibility of placing the diagnostic chip 26 of the microfluidic cartridge 22 in an undesirable orientation or position is eliminated.

In one exemplary embodiment, the tray has no anchoring system and has>A tolerance of 0.5 mm. The microarray is physically small and the camera captures a small area (about 2x3 mm)²)。

In one exemplary embodiment, an anchoring system is added to the tray 52 to ensure that the diagnostic chip is secured in the tray 52. In another exemplary embodiment, the anchoring system consists of two anchoring clips positioned orthogonally to each other. Once the diagnostic chip is placed in the tray, the two anchoring clips working together will greatly restrict the movement of the diagnostic chip. Less movement means less variation in the possible position of the biological assay, thus increasing detection accuracy and precision. The addition of an additional anchoring clip reduces the tolerance to 0.1mm and allows for more accurate detection since variations in the position of the biometric are minimized.

In one exemplary embodiment, the microfluidic cartridge driver unit 30 contains a track system that includes at least one tray track that guides the tray and ensures that the bioassay is placed directly under the light source 51 and camera 62. The track system is configured to receive at least two edges of the tray and is capable of expanding in a length direction while maintaining the tray and the microfluidic cartridge 22 above a mounting structure to which the track system is configured to be secured.

1.1.2 microfluidic Cartridge manipulation Unit

The microfluidic cartridge driver unit 30 includes a microfluidic cartridge manipulation unit 41 that controls fluid movement of the microfluidic cartridge 22 (see fig. 2). The microfluidic cartridge manipulation unit 41 contains electrical connectors 44 that serve as an interface for the microfluidic cartridge 22 to drive/control and provide electrical power/current to the microfluidic cartridge 22 to perform a predetermined sequence to drive reagents and samples from the microfluidic chip 24 to the diagnostic chip 26 for reaction.

Fig. 4 shows the fluid control assembly 45 on the microfluidic cartridge handling unit 41. More specifically, the figure shows a cross-sectional view of two reservoirs on a microfluidic cartridge handling unit. In some exemplary embodiments, the microfluidic cartridge handling unit 41 further comprises at least one fluid control assembly 45 configured to control at least one fluid movement within the microfluidic cartridge. The fluid control assembly 45 is positioned immediately adjacent to the cartridge chamber. In one exemplary embodiment, the fluid control assembly 45 is located less than 10cm from the cartridge chamber. The fluid control assembly 45 changes the viscosity of at least one particular portion of the microfluidic cartridge by controlling the illumination light that provides the heat load on the particular portion of the microfluidic chip and opening the valve that facilitates fluid movement. The gas generated by electrolysis of the hydrogel helps to push the reagent through the opening. In one exemplary embodiment, the specific portion is a plastic film sealing the microfluidic cartridge. The predetermined sequence is discussed in detail herein and is also shown in fig. 4. Irradiating the plastic film covering the different reservoirs in a specific order causes the reagents to leave the reservoirs and start the reaction in a specific order, for example first with a wash buffer, then with a blocking buffer, then with the antibody, and then with a wash buffer. The control signal and power are provided to the fluid control assembly 45.

1.2 optical inspection Unit

The optical inspection unit 32 as shown in fig. 5 weighs less than a few kilograms (kg) and may be used for in-situ analyte analysis/detection. The optical inspection unit 32 comprises an optical sensor 48 and an illumination system 50. In some embodiments, optical inspection unit 32 further includes one or more filters 56. In some embodiments, optical inspection unit 32 further includes a reader 58 and a switch 60. The tray of the microfluidic cartridge driver unit 30 is below the optical inspection unit 32. The microfluidic cartridge driver unit 30 is configured such that when the microfluidic cartridge is assembled or secured in the microfluidic cartridge driver unit 30, the diagnostic chip of the microfluidic cartridge is directly beneath the optical inspection unit 32 for inspection. The illumination system 50 comprises at least one light source 51. In some embodiments, the illumination system 50 comprises at least one light source 51 and/or at least one condenser lens 54. In one exemplary embodiment, the light source 51 may be a monochromatic or polychromatic laser or LED. The light source 51 should be strong enough to excite the fluorophore. In one exemplary embodiment, the light source 51 may be a high intensity LED spotlight having a blue LED color, such as the TMS lite high intensity LED spotlight HBF-00-08-1-B-5V. The specification of the TMS lite high brightness LED spot lamp HBF-00-08-1-B-5V is shown in the following tables 1 and 2.

Table 1.

Mechanical information
		Shell material	Aluminium
Storage temperature range	The temperature is 0-45 ℃ and the humidity is 20-85%
		Weight (D)	-
Outer diameter	30
		Inner diameter	6
Thickness of	69

Table 2.

In another exemplary embodiment, the illumination system 50 includes a diode laser that radiates at least one laser beam having at least one predetermined wavelength on the diagnostic chip 26 to generate at least one signal. The predetermined wavelength of the laser beam is selected such that at least one signal detectable by the optical sensor 48 can be generated. The intensity and wavelength of the laser beam can be selected/controlled by the user via the control unit 28 to detect a particular analyte. The laser beam is turned at an angle to the diagnostic chip 26 to avoid reflections and generate a higher quality signal. The predetermined wavelength is, for example, in the range of 465 to 500nm, 400 to 700nm, 430 to 465nm, 500 to 550nm, 550 to 580nm, 580 to 620nm, or 620 to 700 nm.

In one exemplary embodiment, the light source 51 includes a light pipe 53 that uniformly discharges light. The light pipe 53 is configured such that it directs light to a condenser lens 54 or other optical component and helps focus the light beam onto the biological assay on the diagnostic chip. The light pipe 53 is aligned with the bioassay on the diagnostic chip at a specific location on the microfluidic cartridge, and the position of the microfluidic cartridge is determined by the tray and tray track.

In an exemplary embodiment, the illumination system 50 comprises at least one condenser lens 54 such that the focusing of the light from the light source 51 is optimized. In some embodiments, a condenser lens 54 is located on the end of the light pipe 53 opposite the light source 51. In some embodiments, a condenser lens 54 is positioned in front of the light source 51. The focusing lens 54 and camera 62 may each be independently mounted or fixed on one or more frames to prevent any undesired movement during optical setup. In one exemplary embodiment, the condenser lens 54 may be a convex lens having a focal length of 25.4mm, such as a LB1761-N-BK7 biconvex lens from Thorlabs inc,in and f are 25.4mm, and the film is not coated. The specification of the condenser lens 54 is as follows:

designing a wavelength: 587.6nm

Focal length: f is 25.3 plus or minus 1 percent

Back focal length (REF): bf 22.2mm

Clear aperture: > 90%

Surface quality: 40-20 scratches and pits

Centering and deviating: <3 minutes of arc

Diameter tolerance: +0.0/-0.1mm

Thickness tolerance: plus or minus 0.1mm

When the tray 52 is in its docked position, the microfluidic chamber is located below the optical sensor 48 and the illumination system 50. The optical sensor 48 includes a camera 62 and at least one objective lens 64. In some embodiments, the optical sensor 48 further includes at least one camera lens 55. The optical sensor 48 receives a signal from the diagnostic chip 26, which is generated by the illumination system 50 irradiating laser light on the diagnostic chip 26 of the microfluidic cartridge 22 held on the tray of the cartridge chamber. The received signal is then sent to the control unit 28 for analysis. The optical sensor 48 may have a high quantum efficiency in the wavelength range it detects. In an exemplary embodiment, the camera 62 of the optical sensor 48 may be a Charge Coupled Device (CCD) or any other suitable camera. In one exemplary embodiment, the camera 62 is a near infrared optimized camera with an 2/3-type (11.0 mm diagonal) CCD sensor.

The camera lens 55 of the optical sensor 48 may be any suitable camera lens or higher quality lens, such as a microscope grade lens, depending on the type of immunoassay used. In one exemplary embodiment, the camera lens 55 is responsible for assisting the camera in focusing on the biological assay, since the biological assay is physically small. In one exemplary embodiment, the camera lens 55 is a C-bayonet lens. In some embodiments, a C-bayonet lens is located between the camera and the objective lens. In some exemplary embodiments, the C-bayonet lens is securely attached to the camera. In one exemplary embodiment, the focal length of the C-bayonet lens is 16 mm. In one exemplary embodiment, objective 64 of optical sensor 48 is a planar achromatic objective, 4X magnification, 0.1 numerical aperture, working distance of 18.5mm, such as RMS4X-4X Olympus flat field achromatic objective, 0.10NA, 18.5mm WD, by Thorlabs, Inc.

In one exemplary embodiment, the optical inspection unit 32 further includes one or more filters 56. One or more filters 56 may be used to filter out any light generated from the light source having undesired wavelengths and any undesired noise in the signal picked up by the camera. Depending on the light source and fluorophore used, one or more filters 56 may be used. The illumination system 50 is connected to the filter. In one exemplary embodiment, one or more filters 56 are mounted and aligned between the camera lens 55 and the objective lens 64. This allows any light having an undesired wavelength to be filtered out and only light having a particular wavelength or range of wavelengths to pass through to the biological assay. The camera 62 is connected to the camera lens 55 and the two components are connected to one or more filters 56. This connection to the one or more filters 56 allows any undesired signals (e.g., noise, which typically has a different wavelength, resulting from the biological assay or any undesired reaction) to be filtered and thus minimizes undesired interference with the true signal. One or more filters 56 are coupled to the light pipe, which help focus the filtered light beam onto the biological assay. In one exemplary embodiment, a fluorescence filter set for FITC fluorescein (emission wavelength of 513-556nm and excitation wavelength of 467-498nm) such as, for example, a 67-004 fluorescence filter set for FITC fluorescein at Techspc is used. The specification for the 67-004 fluorescence filter set for FITC fluorescein is shown below:

compatible fluorophores: FITC

Film coating: hard coating film

Dichroic cut wavelength (nm): 506.00

Dichroic filters:#67-080

an emission filter:#67-031

emission wavelength (nm): 513-556

Excitation filter:#67-028

excitation wavelength (nm): 467-498

The manufacturer: EO (ethylene oxide)

Substrate: fused quartz

Type (2): fluorescent filter external member

Wavelength range (nm): 467-556

RoHS: conform to

In some exemplary embodiments, the optical inspection unit 32 further includes a switch 60. In another exemplary embodiment, the switch 60 is a micro-switch. The micro switch is attached to the rear of the tray rail and is electrically connected to the power supply unit 65. The microswitch is automatically activated when the tray 52 is pushed into the docked position by the tray track. After activation, the micro-switch may turn on the reader to read the identity of the microfluidic cartridge.

In some exemplary embodiments, the optical inspection unit 32 further comprises a reader 58 to read the identity of the microfluidic cartridge. In one exemplary embodiment, the reader 58 is a bar code reader. The barcode reader can read a 2D barcode attached or affixed to the microfluidic cartridge.

In one exemplary embodiment, the user manually selects the appropriate program to run the diagnostic chip or microfluidic cartridge. In some embodiments, the program uses a specific predetermined sequence of electrical pulses to drive the appropriate reaction, analyze and calculate the results using a microarray of the appropriate size.

In some exemplary embodiments, an internal barcode reader is incorporated into the system, wherein the barcode reader is located above the location where the microfluidic cartridge is to be placed. In one exemplary embodiment, the barcode is attached or affixed to the microfluidic cartridge (fig. 5). In another exemplary embodiment, a two-dimensional (2D) code is attached or affixed to the microfluidic cartridge. A 2D code incorporating the identity of the microfluidic cartridge, the analyte or disease to be tested, the expiration date of the chip is placed on the microfluidic cartridge during the manufacturing process. After the microfluidic cartridge is inserted into the tray, the barcode reader is activated and the barcode reader automatically scans the 2D code. The software can automatically select the correct program to use based on the 2D code. This feature eliminates the need to manually select the pulse program, making the design more user friendly and less prone to human error. In one exemplary embodiment, the software may also identify microfluidic cartridges that have been previously used or are defective. The software displays a warning message on the screen and does not continue to execute the program.

The components in the optical inspection unit 32 are arranged such that a compact integrated optical inspection unit is formed. This compact design results in a smaller, lighter diagnostic system. Diagnosis ofThe system should be small enough and light enough to be moved between clinics when needed. In one exemplary embodiment, the present invention is small enough and light enough to be carried around to a domestic flight. In one exemplary embodiment, the device has dimensions of about 30x30x30cm³The weight is about 5-6 kg.

The following describes events associated with the optical inspection unit 32:

s1, a user places the microfluidic cartridge into a tray or microfluidic chamber.

S2, the user pushes the tray into the equipment under the guidance of the tray track.

S3, when the tray is pushed in, the switch is activated.

S4, the switch starts the bar code reader.

S5, the reader reads the code printed on the microfluid box.

S6. the code contains the identification of the microfluidic cartridge, which prompts the software of the control unit to automatically select the program associated with the microfluidic cartridge.

S7. once the software selects the correct program, a specific sequence of electrical pulses is generated and passed through the microfluidic cartridge via an electrical connector located at the bottom of the tray. The present electrical pulses sequentially drive the reagents in the microfluidic chip out of their reservoirs and into the reaction chambers in a predetermined sequence. The electrical pulses may also drive the fluid control assembly 45 to facilitate fluid movement within the microfluidic cartridge.

S8. once the reaction is completed in the reaction chamber, the illumination system is activated and the biological assay is excited by the light beam.

S9, capturing an optical image by the optical sensor, and analyzing the image through software.

And S10, displaying the result on a screen for a user to check. No manual interpretation is required.

1.3 control Unit

The control unit 28 typically includes a microprocessor (CPU), memory, and input/output (I/O) interfaces. The control unit 28 controls the quantitative and qualitative analysis, interfacing and storage of the signals obtained from the optical examination unit 32 and controls and monitors all operations of the diagnostic device 20.

The control unit 28 further includes a non-transitory computer readable medium for storing computer readable code such that when the code is executed by the microprocessor, it instructs all parts of the diagnostic device 20 to perform and operate the steps as described above and herein. A non-transitory computer-readable medium may include any known type of data storage and/or transmission media, including magnetic media, optical media, Random Access Memory (RAM), Read Only Memory (ROM), a data cache, a data object, and so forth. Further, memory may reside at a single physical location (comprising one or more types of data storage), or be distributed across multiple physical systems in various forms.

In one embodiment, the control unit 28 includes software modules that may be required for system operation. These modules include an operating system, an application module, an image processing module, a microfluidic cartridge driver software module for controlling fluid flow in the microfluidic chip 24 as previously described, and a user interface software module. The operating system manages computer hardware resources and provides general-purpose services to all computer software modules. The operating system may be Apple iOS, Android, Microsoft Windows, or Linux. The operating system also incorporates various communication protocols, either wired or wireless, such as Local Area Network (LAN), USB, Wi-fi, Bluetooth, etc. An application module is a set of programs designed to perform operations on a device. It manages device data as well as job data, program data, client data, microfluidic cartridge data, pump settings, optical sensor settings, and data collected from optical inspection unit 32. The image processing module optical inspection unit 32 collects data. The image processing module selects a target region of the diagnostic chip 26 and controls the acquisition of images therefrom. The image processing module also corrects the brightness and contrast of the acquired image. When receiving these images from the image processing module, the control unit 28 measures and compares the images of the diagnostic chip 26 according to the settings of the optical sensor 48. The image processing module then counts and calculates according to the set limits and sends the analysis results to the user interface software module. The microfluidic cartridge driver software module is designed to instruct the microfluidic cartridge driver unit 30 to control the current and the time at which this current is delivered to the microfluidic pump at the microfluidic chip 24. The higher the current and/or the longer the time this current is delivered, the more fluid can then be pumped from the reservoir 80. The user interface software module is an interface that allows a user to interact with the device through graphical icons, visual indicators (e.g., symbols and commands). The user interface software module makes the device very user-friendly to non-technical personnel by allowing users to easily obtain, understand, add, edit and delete information without any special skills. It also allows the user to feel that they are in close connection with the optical examination unit 32, with the help of graphical, acoustic interaction and the transmission of notifications and commands given by the user interface software module.

1.4 Power supply Unit

In the apparatus, a power supply unit 65 is provided. The power supply unit 65 contains at least one rechargeable battery pack, a battery charger port, a power switch and power management electronics. Conventional rechargeable batteries may be made of lithium-ion, lithium polymer, or other high capacity batteries. The rechargeable battery pack in the power supply unit 65 may support several hours of operation of the device without a common power source (e.g., in remote areas). The power supply unit 65 is equipped with battery protection circuitry that can protect the rechargeable battery pack from overcharge, overcurrent, and overtemperature, thereby ensuring safety of the device and the user. The power supply unit 65 is also provided with battery connectors so that the user can replace a fully discharged battery with a fully charged backup battery for prolonged use. Power management electronics are used to convert the voltage of the rechargeable battery pack to different voltages required by different system units. The power management electronics are connected to the control unit 28, the rechargeable battery pack, the microfluidic cartridge driver unit 30 and the optical inspection module. The power management electronics can start, terminate and modify the voltage whenever needed to save power consumption of the device. These command signals are given by the control unit 28. Further, the battery charger provides Direct Current (DC) via a battery charger port at the back panel of the device to charge the rechargeable battery pack in the system. The device may operate even if the rechargeable battery pack runs out, with a common or external power source being provided. The battery charger port may be removed after the rechargeable battery pack is charged. In an exemplary embodiment, the diagnostic platform may operate using a plug-in power supply or battery only. The use of rechargeable batteries allows the device to be taken outdoors and used in rural areas where the power supply may be scarce.

In one exemplary embodiment, the specifications of the battery are as follows:

type (2): RRC2024

Voltage: 14.40V

Capacity: 6.60Ah

Maximum charging current: 4.62A

Maximum charging voltage: 16.80V

Maximum discharge current: 10.00A

Size: (L x W x H)167.7mm x107.6mm x21.8mm (maximum)

Weight: 590g

In one exemplary embodiment, the battery may be carried around to a domestic flight and shipped internationally when installed on a diagnostic platform.

In one exemplary embodiment, a fully charged battery supports operation of the device for at least about 5 hours.

In one exemplary embodiment, the battery is rechargeable and replaceable by the user. The battery allows the device to operate in areas without electrical or temperature control.

Example 2

2. Microfluidic cartridge

The microfluidic cartridge 22 as shown in fig. 6A, 6B and 6C contains a diagnostic chip 26 secured to a microfluidic chip 24. In the embodiment shown, it is smaller than a credit card and has a thickness of 1-10 mm. The microfluidic chip 24 includes an electrical connection interface 78 for receiving control signals and power provided through the electrical connectors 44 of the cartridge chamber 42, a top portion 68, and a bottom portion 70 attached to the top portion 68. In this example, the top portion 68 and the bottom portion 70 are assembled together by an adhesive material or by a welding process. The bottom portion 70 may be made of an electrically insulating material (e.g., plastic and resin materials). As shown in fig. 6A, the top portion 68 has a plurality of micro-grooves 66, channel openings in fluid connection with the microfluidic chip 24, and an adhesive 74 for attaching the microfluidic chip 24 at the channel openings. As shown in fig. 6C, the bottom portion 70 of the microfluidic cartridge has a groove in which a microporous membrane 76 is to be placed. In one exemplary embodiment, the top portion 68 comprises a plastic film that seals the microfluidic cartridge. The plastic film receives the light control signal provided by the fluid control assembly 45 of the microfluidic cartridge driver unit. When sufficient light control signals are received at a particular valve position on the microfluidic chip 24, the plastic film covering the valve changes viscosity. The change in viscosity causes the shape of the valve to change from a planar shape to a dome shape, allowing the valve to open. The light control signal may be sent at different valve positions at different times to control the sequence of agent release (see fig. 4).

Referring now to fig. 6A and 6C, the top portion 68 may be made of acrylic, polycarbonate, or similar types of plastics. It may be transparent to allow a user to observe the fluid state inside the microfluidic chip 24. The plastic part may be manufactured by a plastic injection molding process in association with other processes, such as hot embossing and micro-machining methods. The top portion 68 contains a plurality of micro-grooves 66 in a corresponding plurality of reservoirs 80, wherein at least one reservoir is configured to receive a sample from the top and at least one reservoir is configured to hold at least one reagent to facilitate a reaction or interaction between the analyte interacting molecules and the analyte. Thus, detection of the analyte may be facilitated. The reagent held in the at least one reservoir is selected from the group consisting of: wash buffer and blocking buffer. In one embodiment, the wash buffer is Phosphate Buffered Saline (PBS) and the blocking buffer is PBS and Bovine Serum Albumin (BSA). The sample is driven from the microfluidic chip 24 to the diagnostic chip 26 for analyte reaction/interaction on the diagnostic chip 26. In each reservoir 80, at least one microfluidic channel 86 is located below the micro-groove 66 at the interface between the top portion 68 and the bottom portion 70, as shown in fig. 6A and 6C. Reagents and samples are driven from the microfluidic chip 24 to the diagnostic chip 26 through the microfluidic channel 86 and then to the channel opening.

Each reservoir 80 is integrated with a micropump configured with a small amount of hydrogel 82 placed therein (see fig. 6C). Hydrogel 82 contacts conductive circuit traces 84 on the build material that are bonded to bottom portion 70. These micropumps are operated by electrical current supplied through conductive circuit trace 84. These micropumps transport the sample and reagents to the channel openings by pushing the sample and reagents through the microfluidic channel 86 by expanding and contracting the hydrogel 82. The expansion and contraction of the hydrogel 82 is controlled by the microfluidic cartridge manipulation unit 41 of the microfluidic cartridge driver unit 30 of the diagnostic device 20 by sending signals and power through the connection between the electrical connector 44 and an electrical connection interface that is also electrically connected to the electrically conductive circuit trace 84. These pumps are packaged so that this avoids contamination and cross-contamination problems. In one exemplary embodiment, the volume of each reservoir 80 is in the range of 20-150 μ l. In one exemplary embodiment, the number of reservoirs in one microfluidic cartridge is 5-12. For clarity, "mixed sample and reagent" is synonymous with "mixture of sample and reagent" and refers to the mixture of sample and reagent formed by the above steps.

In one exemplary embodiment, a removable cover is provided at the opening for sample introduction to prevent leakage or evaporation of the sample (see fig. 6B).

In one exemplary embodiment, the expansion and contraction of the hydrogel 82 is further controlled by a fluid control assembly 45 that receives signals from the control unit and power from the power source (see fig. 4). Upon receiving the signal, the fluid control assembly 45 irradiates light onto a specific area of a plastic film on the microfluidic chip. The irradiating light may change the viscosity of the hydrogel, thereby facilitating the pushing of the sample and reagents through the microfluidic channel by the micropump.

Each electrical connector 44 on the bottom of the microfluidic cartridge 22 is associated with a particular reservoir. When connected, an electrical pulse is passed through the electrical connector 44 and electrolyzes the hydrogel in the particular reservoir. The electrolysis process produces oxygen and hydrogen gas, and these gases expand to push the fluid inside the reservoir out of the reservoir. The valve at the reservoir outlet is sealed by a plastic film but on irradiation the valve will open and allow the reagent in the reservoir to be pushed through the channel/next reservoir (depending on the location of the outlet connection). The flow rate of the reagents is controlled by the sequence of electrical pulses, which are delivered to the electrical connector 44 at the bottom of the chip.

The diagnostic chip 26 may be made of glass, silicon or plastic and is fixed to the microfluidic chip 24. The bottom surface of the diagnostic chip 26 (i.e., the surface facing the channel opening) that is pre-coated with an array of detection spots that can react/interact with the analytes present in the sample to generate at least one signal under certain conditions (e.g., one or more fluorescent signals when irradiated by a laser of a certain wavelength) is disposed toward and in fluid communication with the channel opening. In one embodiment, each of these detection spots comprises at least one analyte interacting molecule that reacts/interacts with at least one analyte. In a particular embodiment, the analyte-interacting molecule is a specific protein or peptide that binds to at least one specific virus/bacterium (e.g., antigen) in its intact state or in part suitable for detection. The array of test spots is located within 1-15 millimeters (mm) of the circumference of the channel opening so that the mixed sample and reagent can be spread across the array as it is pumped out of the channel opening. The bottom surface of the diagnostic chip 26 facing the microfluidic chip 24 is first coated with a first coating for immobilizing the subsequently coated detection spots without changing the configuration of the detection spots (e.g., keeping the binding sites of the analyte-interacting molecules contained in the detection spots accessible for one or more analytes). The first coating should also create a hydrophilic environment for the analyte to react/interact with. It is optimized to minimize non-specific reactions/interactions and thereby reduce the background noise signal in the present device. Once the first coating is complete, the detection spots are deposited in a predetermined pattern (e.g., an array) on the bottom surface of the diagnostic chip 26. The drop-on-demand method is selected to disperse them onto the diagnostic chip 26. In one embodiment, the drop on demand method may be performed by a microarray printer. The diagnostic chip 26 with the mixed reagents and sample (which may contain the analyte) reacted/interacted thereon may be detached from the microfluidic chip 24 and placed on the diagnostic chip holder 58 for further analysis by the optical inspection unit 32. The mixed sample and reagent on the diagnostic chip 26 may be dried before or after detaching the diagnostic chip 26 from the microfluidic chip 24.

In one exemplary embodiment, the microfluidic cartridge 22 (test cartridge) is comprised of (1) a biological assay printed on a diagnostic chip 26 and (2) a microfluidic chip 24 preloaded with reagents required for proper operation of the microfluidic cartridge 22. The production sequence of the microfluidic cartridge 22 is shown in fig. 7. First, the bioassay material is fixed to the diagnostic chip 26. Next, the diagnostic chip 26 is attached or secured to the microfluidic chip 24 to form the microfluidic cartridge 22. One or more reagents are then preloaded into one or more reservoirs of the microfluidic cartridge 22. Finally, the reagent chamber is sealed with, for example, a plastic film.

In an exemplary embodiment, the biological assay may be based on an immunoassay or any other type of biological detection system. The bioassay consists of one or more positive and negative controls. Each bioassay may detect one disease at a time or may detect multiple diseases simultaneously. Unlike most near-patient tests, no external positive or negative control runs are required prior to running the microfluidic cartridge 22.

In one exemplary embodiment, the diagnostic chip 26 and the microfluidic chip 24 are pre-fixed during the manufacturing process and are not separated during the reaction and detection steps. The diagnostic chip 26 is pre-attached to the microfluidic chip 24. The present exemplary embodiment eliminates errors or any other induced inaccuracies caused when a user attaches the diagnostic chip 26 to the microfluidic chip 24. The present exemplary embodiment eliminates the disassembly step, thereby eliminating or at least significantly reducing the risk of (1) reagent leakage (resulting in contamination) or (2) diagnostic chip jamming and nicking the user.

In one exemplary embodiment, all reagents are preloaded into the microfluidic chip 24 and sealed during the manufacturing process. Given that near-patient testing is typically performed by trained non-professionals, preloading reagents eliminates the possibility of human error (e.g., loading reagents into the wrong slots, improperly using pipettes, adding the wrong volume of reagent, and spilling reagent during the loading process). Preloading the reagents may also minimize user contact with the chemicals. The user-friendly microfluidic cartridge eliminates all preparation processes associated with reagent loading, thus minimizing the possibility of human error and reducing preparation time by five minutes.

In one exemplary embodiment, the shape of the microfluidic cartridge is configured such that there is only one possible way to fit or insert the microfluidic cartridge 22 (and thus, the diagnostic chip 26) into the microfluidic chamber 42 of the tray 52. The microfluidic cartridge 22 is fixed in a desired position and orientation.

In an exemplary embodiment, the steps of coating and depositing the detection spots (containing antigens such as H7N9 influenza virus) on the surface of the diagnostic chip 26 are shown in FIG. 8 and described in detail below:

for the cleaning step 88: the diagnostic chip 26 of glass material is partially immersed in a 250 milliliter (ml) beaker containing acetone. Then, ultrasonic treatment is performed for 5 minutes (min) to clean the immersed portion of the diagnostic chip 26. Then, the diagnostic chip 26 was transferred to another 250ml beaker containing ethanol with tweezers. Then, sonication was performed again for 5 minutes.

For the hydroxylation step 90: seventy-five (75) ml of 95% sulfuric acid was transferred to a 250ml beaker. Twenty-five (25) ml of 34.5% volume (v/v) hydrogen peroxide was then pipetted into the same beaker so that the final concentration of hydrogen peroxide was 8.63% and the resulting volume ratio of concentrated sulfuric acid and 34.5% hydrogen peroxide (piranha solution) was 1:3 v/v. Thus, the diagnostic chip 26 from cleaning step 88 is then partially immersed in the above solution at room temperature for 2 hours (hr). Then, the treated diagnostic chip 26 was picked up from the piranha solution with tweezers, and rinsed with ultrapure water for 5 minutes using a washing bottle. The piranha solution was discarded into a waste bottle. Next, the treated diagnostic chip 26 was transferred to a 250ml beaker containing 95% absolute ethanol with tweezers. Then, sonication was performed for 5 minutes. This step for the treated diagnostic chip 26 is then repeated once again in another 250ml beaker containing purified water.

For the acidification step 92: twenty-five (25) ml of hydrochloric acid was transferred to a 50ml reaction tube. Twenty-five (25) ml of ethanol was then added to the same tube. Then, the diagnostic chip 26 from the hydroxylation step 90 was transferred to the above solution with tweezers and reacted at 37 degrees Celsius (. degree. C.) for 3 hours. Then, the treated diagnostic chip 26 was picked up from the solution with tweezers, and rinsed with ultrapure water for 5 minutes using a washing bottle. The solution was discarded into a waste bottle. Thus, the washed diagnostic chip 26 is then transferred with tweezers into a 250ml beaker containing 95% absolute ethanol. Then, sonication was performed for 5 minutes.

Then, the diagnostic chip 26 was transferred to another 250ml beaker containing purified water with tweezers. Then, sonication was performed again for 5 minutes. Thereafter, the treated diagnostic chip 26 is then transferred with tweezers into a 250ml beaker and incubated in an oven to dry at 60 ℃ for 30 minutes, followed by an amination step 94 as described below.

For the amination step 94: six o' clock sixty four one (6.641) grams (g) (3-aminopropyl) triethoxysilane (APTES) (moisture sensitive) was pipetted into a 50ml reaction tube (first use) at room temperature. Then, forty-three (43) ml of ethanol was pipetted into the same tube. Next, 0.1ml of acetic acid was added to the same tube. Then, the treated diagnostic chip 26 from the acidification step 92 is transferred to the above solution with tweezers and reacted at 50 ℃ for 24 hours. Therefore, the diagnostic chip 26 was then transferred with tweezers into a 250ml beaker containing 95% absolute ethanol. Then, sonication was performed for 5 minutes. Then, the diagnostic chip 26 was transferred to another 250ml beaker containing purified water with tweezers, and then sonicated again for 5 minutes. Thereafter, the treated diagnostic chip 26 was transferred to a 250ml beaker with tweezers and incubated in an oven to dry at 120 ℃ for 30 minutes.

For addition step 96-addition of aldehyde groups: twenty-five percent glutaraldehyde was prepared separately in 50ml reaction tubes. Then, the treated diagnostic chip 26 from the amination step 94 is transferred into the above solution with tweezers and reacted at room temperature for 24 hours. As a result, the diagnostic chip 26 was then transferred with tweezers into a 250ml beaker containing 95% absolute ethanol. Then, sonication was performed for 5 minutes. Then, the diagnostic chip 26 was transferred to another 250ml beaker containing purified water with tweezers, and then sonicated again for 5 minutes. This step was then repeated once more in another 250ml beaker containing purified water. Next, the treated diagnostic chip 26 was transferred to a 250ml beaker with tweezers and incubated in an oven to dry at 60 ℃ for 30 minutes.

In an alternative embodiment, the diagnostic chip 26 is rinsed with deionized water and then sonicated in a 1:3 volume ratio (v/v) cleaning detergent to deionized water mixture for 5 minutes. The cleaned diagnostic chip 26 is then immersed in deionized water for 5 minutes (after decantation) and finally in acetone for 5 minutes. Then, the cleaned diagnostic chip 26 is dried with compressed air. Next, 3-glycidoxypropyltrimethoxysilane was dissolved in acetone and mixed with collodion solution (10% from Wako) using a pipette. The diagnostic chip 26 is dipped into the present mixture and slowly removed from the mixture. Then, the diagnostic chip 26 is dried in air and turned into a white film. The coated diagnostic chip 26 was further incubated at 80 ℃ for 1 hour. Then, after equilibration at room temperature, the diagnostic chip 26 was immersed in 20ml of ethanol for 5 minutes. The diagnostic chip 26 is then rinsed thoroughly with water, followed by acetone and water. The diagnostic chip 26 becomes transparent and may be stored at room temperature prior to use (e.g., printing step 98 described below).

For the printing step 98-printing of PBS buffer, H7N9 antigen, or BSA on the diagnostic chip 26 coated with aldehyde groups as described in step 96 or on the transparent diagnostic chip 26 obtained from the acidification step 92: for printing with PBS buffer, an ink preparation agent of 4ml of PBS solution of 40% glycerol was prepared and filled into a printer box. For printing the H7N9 antigen, an ink formulation of 0.1ml of H7N9 antigen (available from SinoBiological, 1 milligram (mg)/ml) and 40% glycerol in 1.5ml of PBS solution was prepared and the mixture was filled into a printer box. For printing with BSA, an ink formulation was prepared with 1ml of 1000 milligrams (μ g)/ml BSA (ex Thermo, product No. 23208) solution and 4ml of PBS solution of 40% glycerol and the mixture was filled into a printer box. Next, a FUJTFILM Dimatrix material printer (model DMP-2831) was set up. The prepared cartridge is then mounted on the printhead (care is taken to ensure that no bubbles are observed in the solution, especially those trapped in the inlet flow channels. otherwise, the cartridge is gently pressed with a finger until the bubbles are removed from the channel). Then, the solution drop stability of 16 nozzles was verified. At least one well-conditioned nozzle is also selected for dot printing onto the processed diagnostic chip 26 from the joining step 96. Then, 200 μm dots of H7N9 antigen or BSA were printed on the treated diagnostic chip 26. The printed diagnostic chip 26 is then transferred to a petri dish with a lid and then incubated in a drying oven for 2 hours at 37 ℃ in a drying step 100.

The printed side of the treated diagnostic chip 26 of glass material from the drying step 100 is then attached to the top portion 68 of the microfluidic chip 24 loaded with the test sample as previously described using adhesive 74, and the microfluidic cartridge 22 will be optically inspected by the optical inspection unit 32 after reaction/interaction with the analyte-containing sample.

Example 3

Test method

Another exemplary embodiment provides operation of a diagnostic system and a method of on-site diagnostics. Reagents for facilitating analyte detection are preloaded into the separate reservoirs 80 and sealed during the manufacturing process. The reagent held in the at least one reservoir is selected from the group consisting of: wash buffer (e.g., PBS), blocking buffer (e.g., Bovine Serum Albumin (BSA)), lysis buffer (e.g., PBS), antigen, antibody, and fluorophore (e.g., fluorescein in PBS). In one embodiment, the wash buffer is PBS and the blocking buffer is PBS and BSA. In one exemplary embodiment, the microfluidic cartridge contains 5-12 reservoirs for holding reagents or samples. In some embodiments, the reagent volume is between 20-200 ul. In some embodiments, the reagent volume is 50 uL. The reagents may be stored in one or more reservoirs. For example, if the capacity of one reservoir is insufficient to hold all of the required volume of a particular reagent, additional reservoirs may be used for the same reagent.

During the manufacturing process, the diagnostic chip 26 is pre-fixed to the microfluidic chip 24. By dispensing the sample into the reservoir 80 in the loading step, the microfluidic chip 24 is first loaded with an appropriate amount of sample (e.g., a serum sample, nasal swab, or nasopharyngeal swab), which may contain an analyte. In one exemplary embodiment, the sample volume is between 20-200 ul. The surface of the diagnostic chip 26 with the array of detection spots and the first coating faces the channel opening and the microfluidic chip 24. The array of detection spots and the first coating will be located within 1-15mm from the opening of the channel. The microfluidic cartridge 22 is then docked to the cartridge chamber 42 of the microfluidic cartridge driver unit 30 in a docking step by pushing the electrical connection interface through the microfluidic cartridge receiving aperture such that the electrical connection interface will contact the electrical connector 44. In one exemplary embodiment, the microfluidic chip of the microfluidic cartridge will be directly underneath the fluid control assembly 45. The identification of the microfluidic cartridge is then read by the reader when a signal is received from the switch, where the signal is sent when the tray is inserted into the docking position along the tray track. In one exemplary embodiment, the microfluidic cartridge is identified by a 2D code and read by a barcode reader. The microfluidic cartridges are identified by the control unit and the desired predetermined sequence is automatically selected. In the spreading analyte step, the mixed sample and reagent are spread across an array of detection spots. This is accomplished by flowing the sample and reagents from the reservoir 80 through the microfluidic channel 86 of the microfluidic chip 24 to the channel opening. When current and signals are received from the microfluidic cartridge chambers through the electrical connection interface via electrical connector 44, the micropump drives the sample through the microfluidic channel 86 at the time, speed, and sequence indicated by the microprocessor of the control unit 28. The mixed sample and reagent exiting the channel opening (the sample mixing with the reagent as it flows through microfluidic channel 86 of microfluidic chip 24 as previously described) spreads across the bottom surface of diagnostic chip 26. As the sample passes through it from the microfluidic channel 86, any air bubbles in the reservoir 80 will be removed through the microporous membrane 76 located at the bottom portion 70 of the microfluidic chip 24. The area over which the mixed sample and reagent are spread covers the location where the array of test spots is located so that the analyte can react/interact with the analyte interacting molecules in the test spots. In one embodiment, the analyte spreading step may further comprise the steps of: the microfluidic chip 24 is further driven to dispense a second ancillary reagent located at one reservoir 80 by flowing through microfluidic channel 86 of the microfluidic chip 24 to the diagnostic chip 26, thereby attaching a second molecule to facilitate detection of the reacted or interacted analyte after the mixed sample and reagent are dispensed on the detection array. When pumping and analyte reaction/interaction ceases, the microfluidic cartridge 22 remains in the same position in the cartridge chamber 42 of the microfluidic cartridge driver unit 30. In one exemplary embodiment, the analyte spreading step may further comprise the steps of: actuating the fluid control assembly 45 changes the viscosity of at least one particular portion of the microfluidic cartridge by controlling the illumination light on a particular portion of the microfluidic chip and opening a valve that facilitates fluid movement. The mixed sample and reagent on the diagnostic chip 26 may be dried. Thereafter, the analyzing step may be started. The diagnostic chip 26 of the microfluidic cartridge is located below the optical sensor 48 and is not separated from the microfluidic cartridge after the analyte spreading step. After receiving the activation signal from the microprocessor, a light beam (e.g., a laser beam) from the illumination system 50 is then directed onto the diagnostic chip 26 to generate at least one signal that can be detected by the optical sensor 48 (if the mixed sample and reagent contains an analyte). In one embodiment, the at least one signal comprises a fluorescent signal that is generated when the diagnostic chip 26 is illuminated with appropriate light of an appropriate wavelength (e.g., 488 nm). The collected signals will be converted to digital data which will then be transferred to and analyzed in the microprocessor of the control unit 28 to determine the presence of the analyte either quantitatively or qualitatively. The result will be displayed on the display unit 34 of the device in a relatively short time (fast), for example in the range of 10-25 minutes.

In one exemplary embodiment, there are many steps that require manual assembly and disassembly of the microfluidic cartridge, as well as manual selection of the testing procedure.

In one exemplary embodiment, the present invention has been designed with minimal human involvement, which minimizes the possibility of human error. After all reagents are preloaded into the microfluidic cartridge and sealed, only the sample chamber inlet is exposed and is the only apparent inlet where the sample should be loaded. This design minimizes the possibility of a user loading a sample into the wrong chamber. When the microfluidic cartridge is inserted into the device, the barcode reader scans the data matrix on the microfluidic cartridge and either rejects the cartridge (if it is already in use) or accepts the microfluidic cartridge and automatically selects the correct test procedure. This feature prevents any used microfluidic cartridge from being accidentally reused and prevents the user from making mistakes when selecting a test procedure on the diagnostic platform. The software embedded in the diagnostic platform analyzes the test results and displays them on the screen, which eliminates any possibility of human misinterpretation when reading the results. FIG. 9 shows exemplary report details for displaying test results on a screen. The report details show that direct interpretation of the results, i.e. both positive and negative controls were effective, and the target influenza a was detected.

Accordingly, the exemplary embodiments of the present invention have been fully described. Although the description refers to particular embodiments, it will be apparent to those skilled in the art that the present invention may be practiced with modification of these specific details. Accordingly, the present invention should not be construed as limited to the embodiments set forth herein.

For example, the apparatus may further comprise at least one USB port or any other data communication means to allow operation of the general data transfer communication protocol. A display unit is provided in the device for a human-machine interface. The display unit 34 is a high resolution color display, which may be a Liquid Crystal Display (LCD), an Organic Light Emitting Diode (OLED), or other kind of display. The display unit may be integrated with the touch screen panel; thus, it can receive commands from a human finger touch. The display unit is connected to the control unit 28. However, the way it displays the displayed content is through a graphical user interface.

Exemplary microfluidic chips that can be used may be the microfluidic chips disclosed in german patent application nos. DE102010061910.8, DE102010061909.4 and DE 502007004366.4.

In yet another alternative embodiment, instead of using at least one laser beam, at least one beam may be used to generate at least one signal for analysis. In this alternative embodiment, the illumination system 50 emits at least one light beam having at least one predetermined wavelength on the diagnostic chip 26. The illumination system 50 comprises a Light Emitting Diode (LED), at least one optical filter and at least one dichroic mirror.

In another embodiment, the illumination system 50 may have more than one diode laser or more than one LED.

In yet another embodiment, the camera 62 of the inspection unit 32 may be a digital high resolution camera 62, wherein the sensor is selected from the group of: complementary Metal Oxide Semiconductor (CMOS) sensors and Charge Coupled Device (CCD) sensors. The image sensor of the digital high resolution camera 62 has a megapixel number in the range of 1.0 megapixels to 30 megapixels.

In yet another embodiment, the diagnostic device 20 may contain multiple microfluidic cartridge driver units 30 and multiple optical inspection units 32, such that multiple analyses/diagnostics may be run simultaneously. While we have described several embodiments of our invention, it is to be understood that these examples can be varied to provide other embodiments of our invention. Accordingly, the scope of the invention should be determined by the following claims and not by the specific examples provided herein.

Numbering example

The invention is further described with reference to the following numbered examples.

1. An apparatus for detecting at least one analyte from a sample, comprising:

a microfluidic cartridge driver unit comprising:

a tray comprising a cartridge chamber configured to receive a microfluidic cartridge configured for a reaction, wherein the reaction comprises an interaction or reaction with the analyte; and

a microfluidic cartridge handling unit comprising at least one electrical connector configured to connect with the microfluidic cartridge for electrical connection therewith;

an optical inspection unit configured for analyte detection, wherein the analyte detection comprises detecting at least one signal generated by the microfluidic cartridge due to the presence of the analyte in a predetermined condition, the optical inspection unit comprising:

an illumination system configured to communicate light to the microfluidic cartridge, thereby providing the predetermined condition;

an optical sensor configured to detect the at least one signal;

at least one optical filter configured to filter out any undesired wavelengths or noise from the light generated by the illumination system; and

a control unit configured to control the quantitative and qualitative analysis, interfacing and storage of the at least one signal obtained from the optical inspection unit, and to control and monitor the operation of the apparatus;

wherein the tray is configured such that the reaction and the analyte detection are performed at the same location on the same microfluidic cartridge.

2. The apparatus of embodiment 1, wherein the tray is configured such that the tray is slidably removable to accommodate the microfluidic cartridge in a docked position.

3. The apparatus of embodiment 2, wherein the tray further comprises an anchoring system to secure the microfluidic cartridge.

4. The apparatus of embodiment 3, wherein the anchoring system comprises two anchoring clips positioned orthogonal to each other.

5. The apparatus of embodiment 3 or embodiment 4, wherein the anchoring system is configured such that a tolerance of a position of the microfluidic cartridge is less than 0.1 mm.

6. The apparatus of any of embodiments 1-5, wherein the optical inspection unit further comprises a reader to identify the identity of the microfluidic cartridge and the desired predetermined order.

7. The apparatus of embodiment 6, further comprising a switch.

8. The apparatus of any of claims 1 to 7, wherein the optical inspection unit further comprises at least one lens for focusing an image.

9. The apparatus of any of embodiments 1-8, wherein the microfluidic cartridge manipulation unit further comprises at least one fluid control component configured to facilitate at least one fluid movement within the microfluidic cartridge.

10. The apparatus of any of embodiments 1-9, wherein the optical sensor comprises a camera and at least one objective lens.

11. The apparatus of claim 9, wherein the optical sensor is selected from the group consisting of: complementary Metal Oxide Semiconductor (CMOS) sensors and Charge Coupled Device (CCD) sensors.

12. The apparatus of any of embodiments 1-11, wherein the illumination system comprises at least one light source and optionally at least one condenser lens.

13. The apparatus of any of embodiments 12, wherein the light source comprises at least one light pipe.

14. The apparatus of any of embodiments 1-13, wherein the analyte is an influenza virus antigen and the wavelength of the diode laser is 488 nm.

15. The apparatus of any of embodiments 1-14, wherein the control unit is capable of controlling the microfluidic cartridge driver unit.

16. The apparatus of any of embodiments 1-15, wherein the apparatus comprises a power source comprising a built-in rechargeable battery.

Example 4

For the following examples, the term "microfluidic portion" refers to the "microfluidic chip" used in the previous examples; the term "microvalve" refers to the "valve" used in the previous example; the term "diagnostic portion" refers to the "diagnostic chip" used in the previous examples; the term "track assembly" refers to the "track system" used in the previous examples; the term "optical unit" refers to the "optical inspection unit" used in the previous examples; the term "lighting assembly" refers to the "lighting system" used in the previous examples; the term "sensor component" refers to the "optical sensor" used in the previous examples; the term "cartridge driver unit" refers to the "fluid control assembly" used in the previous examples; the term "tray cover" refers to the "tray plate" used in the previous examples; the term "microchannel" refers to the "microfluidic channel" used in the previous examples.

Referring now to fig. 10A, a diagnostic system 101 is shown that includes a portable diagnostic device 300 and a microfluidic cartridge 200 that operates with the portable diagnostic device 300. The microfluidic cartridge 200, which includes a microfluidic portion 210 and a diagnostic portion 220, is configured to collect and manipulate at least one sample, which may include at least one analyte. The microfluidic cartridge 200 also contains and/or holds at least one reagent. The portable diagnostic apparatus 300 is a portable, hand-held, and compact device that includes a microfluidic cartridge driver unit 320, an optical unit 330, and an optional control unit 340. In this example, the optical unit 330 is an optical inspection unit. In some embodiments, the portable diagnostic device 300 optionally includes a user interface unit 350 for interfacing with a user. In this example, the user interface unit 350 is a display unit. The control unit 340 controls and interfaces with the microfluidic cartridge driver unit 320, the optical unit 330, and the user interface unit 350. The microfluidic cartridge driver unit 320 is configured to receive and drive the microfluidic cartridge 200 such that the collected sample and reagents travel through the microfluidic portion 210 and the diagnostic portion 220 in a predetermined sequence. The microfluidic cartridge driver unit 320 also allows the inspection or analysis of the diagnostic portion 220 to be performed at the same location on the same microfluidic cartridge after the reactions are completed in a predetermined sequence. The optical unit 330 is configured to examine the diagnostic portion 220 at the same location on the same microfluidic cartridge 200 where the reaction is also performed to analyze for the presence of the analyte. The user interface unit 350 is configured to display relevant information including analysis/diagnosis results to a user.

Example 5

Referring now to fig. 10B, another exemplary embodiment of the diagnostic system 101 is shown that includes (1) a portable diagnostic device 300 and (2) a microfluidic cartridge 200 that operates with the portable diagnostic device 300. In this example, microfluidic cartridge 200 includes a microfluidic portion 210 and a diagnostic portion 220. Microfluidic portion 210 further includes at least one microvalve 216 and at least one micropump 215. The portable diagnostic apparatus 300 is a portable, hand-held, and compact device that includes a control unit 340, a microfluidic cartridge driver unit 320, an optical unit 330, and a cartridge receiving unit 310. In this example, the portable diagnostic device 300 further comprises an identification unit 370 to identify the identity of the microfluidic cartridge 200. Fig. 10B shows that the control unit 340, the microfluidic cartridge driver unit 320, the optical unit 330, the user interface unit 350, the cartridge housing unit 310, and the power supply unit 360 (not shown) are enclosed in a stand-alone diagnostic device. In this example, the control unit 340 is electrically connected with the cartridge housing unit 310, the microfluidic cartridge driver unit 320, the optical unit 330, and the user interface unit 350 to ensure that the microfluidic cartridge 200 is in a desired designated area for analysis, to control fluid flow in the microfluidic cartridge 200, to control quantitative and qualitative analysis, interfacing, and storage of the at least one signal obtained from the optical inspection unit, and to control and monitor operation of the apparatus. In some exemplary embodiments, the cartridge accommodating unit 310 includes a tray 311 and a rail assembly 312. In this example, the tray 311 is slidable from the cartridge receiving unit 310 and includes a cartridge chamber for receiving the microfluidic cartridge 200 such that a user can pull at least a portion of the tray 311 from the portable diagnostic device 300, mount the microfluidic cartridge 200 onto the cartridge chamber of the tray 311 and insert the tray 311 into the track assembly 312 to ensure that the microfluidic cartridge is positioned at a desired designated area of the portable diagnostic device 300. In another exemplary embodiment, the tray 311 may be slidably detachable from the cartridge accommodating unit 310 so that the user may completely remove the tray 311 from the apparatus. The track assembly 312 is fixedly attached to the portable diagnostic device 300 and is configured to receive the tray 311 into which the microfluidic cartridge 200 is inserted. In one exemplary embodiment, the portable diagnostic device 300 includes a microfluidic cartridge receiving cavity (not shown) on its front panel for receiving the microfluidic cartridge 200. The portable diagnostic device 300 may also be enclosed in a freestanding housing.

Example 6

Microfluidic cartridge

Referring now to fig. 11A, one exemplary embodiment of a front (left), side (middle), and back (right) view of a microfluidic cartridge 200 is shown. The microfluidic cartridge 200, which includes a microfluidic portion 210 and a diagnostic portion 220, is configured to collect and manipulate at least one sample, which may include at least one analyte. In this example, diagnostic portion 220 contains a diagnostic chip (not shown) and adhesive tape 224. The microfluidic cartridge 200 may also contain at least one reactant disposed on a diagnostic chip (not shown). In this example, tape 224 fixedly attaches the diagnostic chip to diagnostic portion 220. The adhesive tape 224 has a certain thickness and is made of a plastic material (e.g., polycarbonate) coated with an adhesive material on opposite sides. The adhesive tape 224 has an enclosed area therein forming a diagnostic chamber for the preloaded reactants and a reaction chamber for fluid communication between the diagnostic portion 220 and the microfluidic portion 210. In this example, an inlet 226 for fluids (e.g., fluids and reagents from the microfluidic portion) and a reservoir outlet 228 for waste are disposed within the enclosed area of the adhesive tape 224. In some embodiments, the at least one reactant is pre-supplied on the diagnostic chip 220, that is, the reactant is pre-loaded during the manufacturing process, thereby saving the user the effort, resources, and time to prepare the diagnostic chip. Microfluidic cartridges may contain a combination of microvalves, microchannels, reservoirs, inlets and outlets, etc., positioned in various configurations to allow for various geometries of fluid transfer. In some embodiments, the microfluidic cartridge may include at least one sample reservoir and at least one reagent reservoir. In addition, microfluidic cartridges may be made with built-in waste reservoirs to handle fluids, such as biohazardous materials, after analysis. In the illustrated embodiment, it is smaller in size than a credit card, 1-10mm thick, and about 30-60mm x 50-80mm in size. In another exemplary embodiment, the microfluidic cartridge may be about 5mm thick and may be about 40mm x 60mm in size. The inlet of the sample reservoir is covered by a sample cover 212, allowing the user to open the sample cover 212 and hold the sample reservoir closed while applying the sample to avoid potential contamination. The cover layer (i.e., microvalve membrane 240) has been removed to show the inlet and outlet ports 218a, 218b, 218c, 218d, 218e and 218 f. In this example, 219a, 219b, 219c, and 219d are inlets for reagents, respectively, which allows different reagents to be introduced into each corresponding reagent reservoir 213 (not shown) during the manufacturing process, thereby saving the user the effort, resources, and time to apply the appropriate reagents. 218a, 218b, 218c, 218d, 218e and 218f are inlet/outlet node pairs of respective reagent reservoirs (not shown). The microfluidic cartridge 200 may also include an indicator showing the cartridge identification 230 of the microfluidic cartridge 200. In one exemplary embodiment, the cartridge identifier 230 may be fixedly attached to the top portion. In another exemplary embodiment, the cartridge flag 230 may be fixedly attached to the microvalve membrane 240. In this example, the cartridge identification 230 is shown as a unique serial number and a two-dimensional (2D) barcode that can be identified by an identification unit 370 (not shown). The microfluidic cartridge 200 includes an electrical connection interface 2151 for receiving control signals and power provided through electrical connectors provided on a cartridge chamber of a cartridge housing unit (not shown).

Fig. 11A (right) shows the opposite side (bottom side) of the microfluidic cartridge 200. Microfluidic chip 210 includes an electrical connection interface 2151 for receiving control signals from a device to provide power or current to microfluidic cartridge 200. Fig. 11A also shows that the diagnostic portion 220 is at least partially transparent to the sample detection. The microfluidic cartridge 200 also contains a microporous membrane cavity 291.

Referring now to fig. 11B, the microvalve film 240, the sample lid 212, the diagnostic chip 222, and the adhesive tape 224 are blown (blob out) out of the microfluidic cartridge 200 for better illustration. In this example, microvalve membrane 240 is a membrane having microvalves 216a, 216b, 216c, 216d, 216e and 216 f. The microvalve membrane 240 may be attached to the top portion of the microfluidic cartridge 200 by adhesive means known in the art. The microvalve membrane 240 covers and seals the microfluidic portion 210 of the microfluidic cartridge 200. In some embodiments, microvalve membrane 240 (and microvalve 216) is made of a material that expands and changes its shape in response to a stimulus (e.g., temperature). In some embodiments, only the microvalve 216 portion is made of a material that expands and changes its shape in response to a stimulus (e.g., temperature), and other suitable materials are used for the remainder of that portion of the microvalve membrane 240. In this example, the entire micro-valve membrane 240 is made of parafilm. In still other embodiments, the microvalve membrane may be made of polyurethane and/or nylon. Microvalves 216a, 216b, 216c, 216d, 216e and 216f are planar and normally close to seal inlet/outlet nodes 218a (not shown), 218b, 218c, 218d, 218e and 218f, respectively, of corresponding reagent reservoirs (not shown). When the microvalve is exposed to heat, the material of the microvalve expands and changes to a dome shape (i.e., an open state), thereby allowing fluid communication between inlet/outlet nodes 218a (not shown), 218b, 218c, 218d, 218e, and 218f, respectively. In some exemplary embodiments, the opening of the microvalve is irreversible, that is, the microvalve is disposable and cannot be closed again after opening. In yet another exemplary embodiment, the opening of the microvalve is reversible. In some exemplary embodiments, the microvalve membrane may be transparent or translucent, allowing a user to observe the flow of fluid in the microfluidic cartridge 200. In another exemplary embodiment, the microvalve regions may be dark (e.g., black) to better absorb light energy (and thus thermal energy). In this example, the microvalves are represented as black dots on the microvalve membrane. In this example, the removable sample cover 212 is shaped to match the diameter of the inlet of the sample reservoir 211. The diagnostic portion 220 is in fluid communication with the microfluidic portion 210 through an opening, an inlet 226, and an outlet 228, respectively. In this example, the reactant can be disposed on the diagnostic chip 222 within the enclosed region of the diagnostic chamber.

In some embodiments, the microfluidic cartridge 200 may include a microvalve membrane, a top portion, at least one adhesive layer, a plurality of micropumps, a microporous membrane, and a bottom portion. Referring now to FIG. 11C, an exploded view of the same exemplary embodiment of FIG. 11A is shown. For clarity, some identical or similar elements are present in the present microfluidic cartridge, but only one of them is annotated as an example. In this example, the microfluidic cartridge 200 includes a microvalve membrane 240 having a plurality of microvalves (e.g., 216b), a top portion 250, an adhesive layer 270, a plurality of micropumps (not shown), a microporous membrane 260, and a bottom portion 290, which are assembled together as a single unit with an adhesive material or by a welding process. The micro-valve film 240 may be a thin film made of parafilm. In still other embodiments, the microvalve membrane 240 may be made of polyurethane and/or nylon. The microvalve membrane 240 receives thermal energy as a control signal provided by a microvalve controller of a microfluidic cartridge driver unit (not shown; to be described later) to control the opening of the microvalve when in use. When sufficient light control signals are received at a particular microvalve location on the microvalve membrane 240, the microvalve changes viscosity. The change in viscosity causes the shape of the microvalve to change from a planar shape to a dome shape, allowing the microvalve to open. The light control signal may be sent at different valve positions at different times to control the sequence of agent release. Top portion 250 includes one sample inlet 212, multiple reagent inlets (e.g., 219b), multiple pairs of inlet/outlet junctions (e.g., 218b), and adhesive tape 224. The tape 224 may be made of plastic (e.g., acrylic, polycarbonate) and it defines a diagnostic chamber within the diagnostic portion 220. The reagent inlet 219b forms a fluid introduction port in fluid communication with a reservoir (not shown) disposed on an opposite side of the top portion 250. Adhesive layer 270 is a plastic film having a thickness that is made of a plastic material (e.g., polycarbonate) that is coated with an adhesive material on both opposing sides to provide an adhesive force to join top portion 250 and bottom portion 290 together. Adhesive layer 270 has a thickness and contains a plurality of grooves (e.g., 271b) that are cavities of the space for the reservoirs containing reagents and samples. Each recess (e.g., 271b) has a position corresponding to a respective position of the reservoir, thereby allowing the reservoir to be in direct contact with the next layer (i.e., bottom portion 290). The base plate of the bottom portion 290 may be made of an electrically insulating material, such as plastic and resin materials. The bottom portion 290 has a groove 291 for placing the microporous membrane 260 therein. The bottom portion 290 also contains a plurality of electrical connection interfaces (not shown) for electrically connecting to the device and a plurality of conductive traces (e.g., 294 b). The space formed between each conductive trace (e.g., 294b) and each corresponding recess (e.g., 271b) allows for placement of a hydrogel therein. The electrical connection interface is electrically connected to the conductive traces. The conductive traces (e.g., 294b) may be in direct or indirect contact with the hydrogel (not shown).

Still referring to fig. 11C, the top portion 240 may be made of acrylic, polycarbonate, or similar types of plastic materials. It may be transparent or partially transparent to allow a user to observe the state of the fluid inside the microfluidic portion 210. The plastic part may be manufactured by a plastic injection molding process in association with other processes, such as hot embossing and micro-machining methods. The top portion 250 contains a plurality of cavities (e.g., 271b) corresponding to a plurality of reservoirs (not shown), wherein at least one reservoir is configured to hold a sample from the top portion and at least one reservoir is configured to hold at least one reagent to facilitate a reaction or interaction between the analyte interacting molecule and the analyte. Thus, detection of the analyte may be facilitated. The reagent held in the at least one reservoir may be a wash buffer or a blocking buffer. The sample is driven from microfluidic portion 210 to diagnostic portion 220 for analyte reaction/interaction on diagnostic chip 222. Reagents and samples are driven from microfluidic portion 210 to diagnostic portion 220 through microfluidic channels (not shown) and then to inlet 226.

Each reservoir (not shown) is integrated with a micropump configured with a small amount of hydrogel (not shown) placed therein. The hydrogel contacts conductive traces (e.g., 294b) on the build material that are bonded to the bottom portion 290. These micropumps are operated by an electrical current supplied through a conductive trace (e.g., 294 b). These micropumps push the sample and reagents through the microfluidic channel by expanding and contracting the hydrogel, thereby driving the sample and reagents to the channel opening. The expansion and contraction of the hydrogel is controlled by the microfluidic cartridge driver unit 320 of the diagnostic device by sending signals and power through the connections between the electrical connection interface (not shown, on the bottom opposite side of the bottom portion) and the conductive traces (e.g., 294 b). In some embodiments, the hydrogel of the micropump is encapsulated so that contamination and cross-contamination problems can be avoided. In still other embodiments, the hydrogel of the micropump may be in direct contact with a fluid (e.g., a reagent or a sample) within the reservoir. In some embodiments, the microfluidic cartridge further comprises a micropump membrane for sealing the hydrogel. The microvalve membrane also covers all reservoirs to prevent fluid leakage. The micro-pump membrane also helps to push fluid out of the reservoir by the micro-pump action of the microfluidic cartridge. The micropump membrane may contain grooves of the microporous membrane, allowing the microporous membrane to be in direct contact with the surrounding environment. In one exemplary embodiment, the volume of each reservoir (not shown) is in the range of 20-150 μ l. In another exemplary embodiment, the volume of each reservoir (not shown) is in the range of 20-200. mu.l. In one exemplary embodiment, the number of reservoirs in one microfluidic cartridge is 5-12. In an exemplary embodiment, a detachable sample cover 212 is provided at the opening for sample introduction to prevent leakage or evaporation of the sample (see fig. 11C).

Each conductive trace (e.g., 294b) of the microfluidic cartridge 200 is associated with a particular reservoir. When connected, an electrical pulse from the electrical connection interface passes through the conductive trace and electrolyzes the hydrogel in the particular reservoir. The electrolysis process produces oxygen and hydrogen gas, and these gases expand to push the fluid inside the reservoir out of the reservoir. The valve at the reservoir outlet is sealed with a plastic film, but upon irradiation, the valve will open and allow the reagent in the reservoir to be pushed through the microchannel/next reservoir (depending on the location of the outlet connection). The flow rate of the reagents is controlled by the sequence of electrical pulses that are delivered to the electrically conductive traces of the bottom portion 290 of the microfluidic cartridge 200.

The diagnostic chip 222 may be made of glass, silicon or plastic and fixed to the diagnostic portion. The bottom surface of the diagnostic chip 222 (i.e., the surface facing the channel opening) that is pre-coated with an array of detection spots that can react/interact with the analyte present in the sample to generate at least one signal under certain conditions (e.g., one or more fluorescent signals when irradiated by a laser of a certain wavelength) is disposed toward and in fluid communication with the channel opening. In one embodiment, each of these detection spots comprises at least one analyte interacting molecule that reacts/interacts with at least one analyte. In a particular embodiment, the analyte-interacting molecule is a specific protein or peptide that binds to at least one specific virus/bacterium (e.g., antigen) in its intact state or in part suitable for detection. The array of detection spots is located at the diagnostic chip 222 of the diagnostic portion so that when the sample and reagents are pumped out of the inlet 226 (FIG. 11B), they can be spread across the array. The bottom surface of the diagnostic chip 222 is first coated with a first coating that serves to immobilize the subsequently coated detection spots without changing the configuration of the detection spots (e.g., keeping the binding sites of the analyte-interacting molecules contained in the detection spots accessible for one or more analytes). The first coating should also create a hydrophilic environment for the analyte to react/interact with. It is optimized to minimize non-specific reactions/interactions and thereby reduce the background noise signal in the present device. Once the first coating is complete, the detection spots are deposited in a predetermined pattern (e.g., an array) on the bottom surface of the diagnostic chip 222. The drop-on-demand method is selected to disperse them onto the diagnostic chip 222. In one embodiment, the drop on demand method may be performed by a microarray printer. In some embodiments, the microfluidic cartridge is pre-supplied with at least one reagent and/or at least one reactant, and it is disposable. In some embodiments, the microfluidic cartridge includes a plurality of reservoirs for storing reagents, samples, and waste. The reservoir may be in fluid communication with the microchannel.

Example 7

Referring now to fig. 12A-12F, another exemplary embodiment of a microfluidic cartridge 200 is shown. Fig. 12A shows an exploded view of an exemplary embodiment of a microfluidic cartridge 200. The figure shows how the microfluidic cartridge is assembled using different layers of materials. In the present exemplary embodiment, the microfluidic cartridge 200 is assembled with the micro-valve film 240 on the top, followed by the top portion 250, the first adhesive layer 270a, the microporous membrane 260, the micro-pump membrane 280, the second adhesive layer 270b, and the bottom layer 290 in this order. The top layer 250 further comprises a microfluidic portion with a sample cover 212 and a diagnostic portion with an adhesive tape 224 and a diagnostic chip 222. The adhesive tape 224 is configured to form a diagnostic chamber (not shown) in the diagnostic portion 220 with the diagnostic chip 222. In some exemplary embodiments, the microfluidic cartridge 200 comprises a microfluidic portion 210 and a diagnostic portion 220, wherein the microfluidic portion 210 comprises a plurality of reservoirs (not shown) capable of holding fluid therein, a plurality of microchannels (not shown) for fluidic connection from the reservoirs to the diagnostic portion 220, a plurality of microvalves 216 operable between a closed state and an open state to seal and open the microchannel connections, respectively, and at least one micropump coupled to at least one of the reservoirs; wherein the microvalve 216 in the closed state allows fluid to be stored and sealed within the reservoir and the microvalve 216 in the open state allows fluid to flow between the reservoir and the diagnostic portion 220; and wherein the micropump can be actuated to move fluid from the reservoir to the diagnostic portion such that multiple reagents can be preloaded and stored in a sealed manner in the microfluidic cartridge 200 until use. A notch is provided in one corner in each layer.

FIG. 12B shows a detailed view of the microvalve membrane of the same exemplary embodiment of FIG. 12A. In this example, microvalve membrane 240 is a membrane having six microvalves 216g, 216h, 216i, 216j, 216k and 216 l. The microvalve membrane 240 can be made at least partially of parafilm and attached to the top portion 250 of the microfluidic cartridge 200 by any adhesive means known in the art (as shown in fig. 12C). In still other embodiments, the microvalve membrane may be made of polyurethane and/or nylon. After reagent is loaded or supplied through an inlet (not shown), the microvalve membrane 240 may be fixedly attached to the top to seal the reagent during the manufacturing process for storage until use. The membrane covers and seals the microfluidic portion 210 of the microfluidic cartridge 200. In some embodiments, the microvalve membrane 240 (and microvalve 216) is made of a material that expands and changes its shape in response to a stimulus (e.g., temperature), as described in the previous examples. Microvalves 216g, 216h, 216i, 216j, 216k and 216l are planar and seal in a normally closed state corresponding inlet/outlet junctions 218g, 218h, 218i, 218j, 218k and 218l, respectively, of corresponding reagent reservoirs (as shown in fig. 12D). In the present exemplary embodiment, when microvalves 216g, 216h, 216i, 216j, 216k and 216l are exposed to heat, the material of microvalves 216g, 216h, 216i, 216j, 216k and 216l expands and changes to a dome shape (i.e., an open state), thereby allowing fluid communication between inlet/outlet nodes 218. In some exemplary embodiments, the opening of the microvalve is irreversible, that is, the microvalve is single use and cannot be closed again after opening, thereby avoiding user reuse of the microfluidic cartridge. In yet another exemplary embodiment, the opening of the microvalve is reversible. In some exemplary embodiments, the microvalve membrane may be transparent or translucent, allowing a user to observe the flow of fluid in the microfluidic cartridge 200. In another exemplary embodiment, the microvalve regions may be dark (e.g., black) to better absorb light energy (and thus thermal energy). In this example, microvalves 216g, 216h, 216i, 216j, 216k and 216l are represented as black dots on the microvalve membrane.

Fig. 12C and 12D show detailed structures of two opposite sides of the top portion 250 of the sample exemplary embodiment of fig. 12A, respectively. In the same exemplary embodiment, the top portion 250 contains the microfluidic portion 210 and the diagnostic portion 220 in one corner near the recess. In some exemplary embodiments, at least one reservoir is filled with at least one fluid, wherein the fluid is a reagent and is sealed with a microvalve. In some exemplary embodiments, the at least one reservoir for holding at least one sample further comprises a sample inlet 217 having a removable lid. In some exemplary embodiments, the microfluidic cartridge further comprises a plurality of reagents preloaded, sealed, and stored in a plurality of reservoirs, respectively; and at least one reactant pre-supplied at the diagnostic portion. Each reservoir has an inlet and an outlet, which may be connected by a fluid passageway. The microfluidic portion 210 includes a sample inlet 217 (as shown in fig. 12A) that can be sealed by a sample lid 212 and a microchannel (as shown in fig. 12D) extending from the sample inlet 217. In this example, the microfluidic portion 210 further comprises a reservoir 213n (or sample reservoir) for holding the introduced sample, six reservoirs 213g, 213h, 213i, 213j, 213k and 213l (or reagent reservoirs) for storing reagents, and a reservoir 213m (or waste reservoir) for holding waste. The reservoir may be in the form of a tube of any desired shape, for example S-shaped as shown in fig. 12D. At one end of sample reservoir 213n there is one microchannel (after passage through the microporous membrane) in fluid communication with sample inlet 217, and at the other end of sample reservoir 213n there is another microchannel connected from the other (reagent) reservoir to the other microchannel. The reagent reservoirs 213g, 213h, 213i, 213j, 213k and 213l comprise inlets 219g, 219h, 219i, 219j, 219k and 219l, respectively, at one end, which are capable of introducing at least one reagent into the corresponding reservoirs. At the other end of the reagent reservoir, there are inlet/outlet nodes 218g, 218h, 218i, 218j, 218k, 218l, which are sealed by corresponding microvalves 216g, 216h, 216i, 216j, 216k and 216l, respectively (as shown in fig. 12B). Each pair of inlet/outlet junctions 218 includes an outlet for a reagent reservoir and an inlet for a microchannel connected to the other portion of the microfluidic section. The microchannel connects the sample reservoir and/or the reagent reservoir to the diagnostic portion. These reservoirs may be interconnected by microchannels. In this example, the microfluidic portion 210 further comprises a sample reservoir 213n, and the removable sample cap 212 is shaped to match the diameter of the inlet of the sample reservoir 213 n. The diagnostic portion 220 is in fluid communication with the microfluidic portion 210 through an inlet 226 and an outlet 228. In some embodiments, the microfluidic cartridge further comprises at least one reservoir for holding waste. In some embodiments, the microfluidic portion further comprises a waste reservoir 213m, wherein the waste reservoir 213m is connected to the diagnostic portion via an outlet to contain waste fluid expelled from the diagnostic chamber. Fig. 12D shows opposite sides of the top portion of the same exemplary embodiment of fig. 12C. In this example, the fluidic channel is a microchannel. In some embodiments, the reservoir may be configured to form a chamber for holding fluid and may have any desired shape and form. In this example, the reservoirs are designed in an S-shape to save space so that the microfluidic cartridge can be compact and small in size. In some embodiments, the diagnostic portion includes a diagnostic chamber to receive at least one fluid from the microfluidic portion. In some embodiments, the diagnostic portion is at least partially transparent to optical detection.

Referring now back to fig. 12A of the same exemplary embodiment of microfluidic cartridge 200, a first adhesive layer 270a is shown. In this example, a first adhesive layer 270a attaches the bottom (opposite) side of the top portion 250 to the top sides of the microporous membrane 260 and the micro-pump membrane 280. The first adhesive layer 270a may be made using any suitable plastic material (e.g., polycarbonate) having a coating of adhesive material on two opposing sides. In the present exemplary embodiment, the first adhesive layer 270a has a certain thickness and includes seven grooves 271a, which are cavities of spaces for reservoirs containing reagents and samples. The thickness of the adhesive layer 270a may correspond to the thickness of the reservoir in the top portion. The location of the groove 271a corresponds to the corresponding location of the reservoir, allowing the reservoir to be in direct contact with the next layer (i.e., the micro-pump membrane 280). In some embodiments, the microfluidic cartridge 200 further comprises a microporous membrane configured to remove gas from a fluid (e.g., sample and/or one or more reagents). The first adhesive layer 270a also includes a plurality of microchannel openings 272 (five microchannel openings, as shown in fig. 12A). The microchannel openings 272 serve as connecting channels for transporting fluid between discrete microchannels in the top portion 250. The microchannel openings 272 form a fluid channel to connect between the microchannels in the top portion 250 and the microporous membrane 260, allowing fluids (e.g., sample, reagents, and waste) to pass through the microporous membrane 260, thereby removing any air bubbles in the fluid. The microporous membrane 260 may be made of any hydrophobic material that is permeable to gas but impermeable to liquid (e.g., PTFE).

Fig. 12A also shows a micro-pump film 280 disposed between the first adhesive layer 270a and the second adhesive layer 270b, allowing for direct attachment between the top and bottom portions. The micro-pump membrane 280 acts as a separator between the reservoir and the micro-pump, thereby avoiding direct contact of the hydrogel in the micro-pump with fluids (e.g., sample and reagents). The micro-pump membrane 280 also contains a groove 283, which is a cavity of space for accommodating the microporous membrane 260, allowing the microporous membrane 260 to be in direct contact with the surrounding environment. The micro-pump membrane 280 may be made of a paraffin membrane or plastic (e.g., polyurethane and/or nylon). The micro-pump membrane 280 covers all reservoirs to prevent fluid leakage. They work in conjunction with a micro-pump to push fluid out of the reservoir by the micro-pump action of the cassette.

Fig. 12A also shows a second adhesive layer 270 b. In this example, the second adhesive layer 270b attaches the opposite side of the micro-pump membrane 280 to the bottom portion 290. Any suitable adhesive material may be used to fabricate the second adhesive layer 270 b. In the present exemplary embodiment, the second adhesive layer 270b has a certain thickness and includes seven grooves 271b, which are cavities of a space for accommodating the micro pump. The thickness of the adhesive layer 270b may correspond to the thickness of the micro-pump. In this example, a hydrogel (not shown) acts as a micro-pump and is disposed within the recess 271b of the second adhesive layer 270 b. The location of the recess 273 corresponds to the corresponding location of the reservoir, allowing the reservoir to be in direct contact with the next layer (i.e., the micropump membrane 280) so that the micropump of the microfluidic cartridge 200 can act on the reservoir to push fluids (e.g., sample and reagents) out of the reservoir.

Reference is now made to fig. 12E and 12F, which illustrate two opposing sides of the bottom portion 290 of the same exemplary embodiment of the microfluidic cartridge of fig. 12A. The bottom portion 290 may be made of an electrically insulating material (e.g., plastic and resin materials). The bottom portion 290 of the microfluidic cartridge has a groove 291 in which the microporous membrane 260 is placed. The bottom portion 290 also includes a plurality of conductive circuit traces 294g, 294h, 294i, 294j, 294k, and 294l (FIG. 12E) that are electrically connected with the electrical connection interfaces 293 on opposite sides of the bottom portion 290. The electrical connection interface 293 transmits electricity from the device to the microfluidic cartridge 200 to activate the micropump. A micro-pump (not shown) constructed with a small amount of hydrogel was juxtaposed to the corresponding reservoir (see fig. 12D). The hydrogel of the micro-pump 215 is in contact with their corresponding conductive circuit traces 294g, 294h, 294i, 294j, 294k, and 294l, respectively, which are bonded to the build material of the bottom section 290. These micropumps are operated by electrical current supplied through conductive circuit trace 294. When receiving current, the conductive traces 294g, 294h, 294i, 294j, 294k, and 294l transmit electricity to electrolyze the hydrogel, thereby generating gases that push the micro-pump membrane 280 upward, thereby pushing fluid out of the reservoir. These micropumps push the sample and reagent through the microchannel, thereby mixing the sample and reagent into the microchannel by expanding and contracting the hydrogel. The expansion and contraction of the hydrogel is controlled by the cartridge driver unit of the portable diagnostic device 300 by sending signals and power through the connection between the electrical connectors of the cartridge-receiving unit 310 and the electrical connection interface 293 of the bottom portion 290, which is also electrically connected with the conductive circuit traces 294g, 294h, 294i, 294j, 294k, and 294l of the bottom portion 290. In some embodiments, the micropump is packaged such that contamination and cross-contamination issues may be avoided. In some embodiments, the pumps are in direct contact with the fluid (e.g., reagent or sample) within the reservoir. In some embodiments, the microfluidic cartridge further comprises a micropump membrane for sealing the hydrogel. In this example, the microfluidic cartridge 200 contains a micro-pump membrane 280 that covers the entire area of the reservoir to prevent any fluid leakage and direct contact of the hydrogel with the fluid within the reservoir. The bottom portion 290 also contains an electrical sensing element 292 (fig. 12E) alongside the area of the waste reservoir to detect the presence and amount of fluid flowing into the waste reservoir using volume sensing technology.

Example 8

Reference is now made to fig. 13A and 13B, which illustrate how the exemplary microfluidic cartridge 200 operates during use. For clarity and simplicity, only one set of reagent reservoirs, microvalves, hydrogel or micropumps and inlet/outlet nodes are shown. During the manufacturing process, each reagent is first loaded or supplied to the reagent reservoir 213 through the reagent inlet 219. The surface of the top portion 250 having the reagent inlet 219 is then sealed by the microvalve membrane 240 to prevent fluid leakage from the reagent inlet 219 and outlet 218' of the reservoir 213. Valve seat 252 may be configured to support microvalve 216 so that it does not collapse in the resting state. Valve seat 252 is located between reservoir 213 and fluid microchannel 214 to separate the two compartments so that fluid in reservoir 213 cannot flow through fluid microchannel 214 when microvalve 216 is in the closed state. The outlet 218' and inlet 218 "form an inlet/outlet junction that is sealed by the microvalve 216. The microvalves 216 on the present microvalve membrane 240 are arranged side-by-side with each pair of fluid inlet and outlet nodes (218' and 218") of the top portion 250. A reactant (e.g., an antibody) may be pre-coated on the diagnostic chip 222 within the enclosed region of the diagnostic chamber 221 formed with the adhesive tape 224. The different parts (i.e., the microvalve membrane 240, the top part 250, the adhesive layers 270a, 270b, the micropump membrane 280, the microporous membrane 260 and the bottom part 290 of the microfluidic cartridge 200) are assembled together by an adhesive means or a welding process. The microfluidic cartridge 200 may be sealed and packaged for shipping.

When in use, a fluid-containing sample is introduced into the microfluidic cartridge 200 by opening the sample lid and introducing the sample through a sample inlet (not shown). Suitable sample preparation may be performed prior to sample introduction. The sample flows into the microchannel and reaches the microchannel opening. At the microchannel opening, the sample contacts the microporous membrane to remove any air bubbles in the fluid. The sample then enters the microchannel and flows into the diagnostic chamber 221.

At this point, the sample and reagent reservoirs will be filled with all necessary samples and reagents, respectively. Then, current from the microvalve controller and the micropump controller is applied to the microfluidic cartridge 200 to activate the microvalve 216 of the microfluidic cartridge 200 and the hydrogel 2152 of the micropump. Referring now to fig. 13B, a heating element of a microvalve controller (not shown) disposed on the microvalve 216 emits energy (e.g., infrared light) to the microvalve 216 to open the microvalve 216. This event places fluid microchannel 214 in fluid communication with reservoir 213 and diagnostic chamber 221. The micropump contains a hydrogel 2152 that is in direct or indirect contact with conductive traces 294. The conductive traces 294 receive electrical current from the device through an electrical connection interface (not shown) to the hydrogel 2152 in a predetermined sequence. An electrical pulse is passed through the conductive trace 294 and electrolyzes the hydrogel 2152 in the particular reservoir 213. Oxygen and hydrogen are generated by the electrolysis process and these gases expand, causing the chamber holding the hydrogel 2152 to expand, causing the micro-pump membrane 280 to push the fluid (sample and/or reagents) within the reservoir 213 out of the reservoir 213 in a controlled and precise manner. The fluid is pushed out of reservoir 213 and into microchannel 214 through the junction of fluid outlet 218' and inlet 218 ". The arrows in fig. 13B show the fluid flow direction. The fluid then reaches another microchannel opening 272 a. At the microchannel opening 272a, the fluid contacts the microporous membrane 260 to remove any air bubbles. The fluid then enters another microchannel and flows into the diagnostic chamber 221, which is the detection zone.

At the detection zone, the sample reacts with the pre-coated reactants on the diagnostic chip 222. After the reaction is complete, the waste flows to the waste reservoir through a waste reservoir inlet (not shown).

Then, the diagnostic portion is ready for optical inspection.

Example 9

Portable diagnostic device

Referring now to fig. 14A, an exemplary embodiment of a diagnostic system 101 includes a portable diagnostic device 300 and a microfluidic cartridge 200 operating with the portable diagnostic device 300. In this example, the diagnostic apparatus 300 includes a control unit 340, a microfluidic cartridge driver unit 320, an optical unit 330, a user interface unit 350, a cartridge housing unit 310, and a power supply unit 360. Portable diagnostic device 300 is enclosed in a housing 301, wherein housing 301 comprises top cover 351, side covers 352 and 353, back cover 354, front panel 355, and base 356. In some exemplary embodiments, the optical unit 330 includes an illumination component 331 and a sensor component 332. The illumination assembly includes a light source 331A, a light pipe 331B, and a filter 331C. The sensor assembly includes a camera 332A, a camera lens 332B, and an objective lens 332C.

Referring now to fig. 14B, another exemplary embodiment of the diagnostic system 101 includes a portable diagnostic device 400 and a microfluidic cartridge (not shown) that operates with the portable diagnostic device 400. In some exemplary embodiments, the portable diagnostic device 400 may contain all of the units in the portable diagnostic device 300. In some exemplary embodiments, the portable diagnostic apparatus 400 includes a cartridge driver unit 420, an optical unit 430, a display unit 450, a cartridge accommodating unit 410, a power supply unit 460, and an identification unit 470. In an exemplary embodiment, the portable diagnostic device 400 optionally contains a control unit 440. The control unit 440 controls and is operatively connected to the cartridge driver unit 420, the optical unit 430, and the display unit 450. In some other exemplary embodiments, each unit may have its own control unit, and no single control unit is present in the portable diagnostic device. In one exemplary embodiment, the microfluidic cartridge driver unit contains a microvalve controller 421 and a microvalve controller 422. When the microfluidic cartridge is placed in the cartridge-receiving unit 410, the microvalve controller 421 and the micropump controller 422 can cooperate to actuate the flow of fluid from the reservoirs to the diagnostic portion in a predetermined sequence. In one exemplary embodiment, the cartridge accommodating unit 410 includes a tray 411 and a rail assembly 412. In this example, the tray 411 is slidably detachable from the cartridge accommodating unit 410. The rail assembly 412 is fixedly attached to the portable diagnostic device 400 and is configured to receive the tray 411. In this example, an assembly 480 of the cartridge-receiving unit 410, the optical unit 430, and the identification unit 470 is shown in fig. 14B to illustrate the configuration and spatial relationship between these units. A detailed description of assembly 480 is disclosed in fig. 18.

In one exemplary embodiment, portable diagnostic device 400 is enclosed in housing 401, wherein housing 401 comprises top cover 451, side covers 452 and 453, back cover 454, front panel 455, and base 456. In the present exemplary embodiment, the track assembly 412, the microfluidic cartridge driver unit 420, the optical unit 430, and the identification unit 470 of the cartridge accommodation unit 410 are mounted within the housing in a configuration such that when a microfluidic cartridge is inserted into the device, there is a space (not shown) for accommodating the microfluidic cartridge. The space includes one or more micro valve positions and one or more micro pump positions. The space also contains reaction sites corresponding to the positions of the one or more microvalves, the one or more micropumps, and the reaction sites, respectively, when the microfluidic cartridge is inserted into the space. A more detailed description of this space is provided in fig. 18. In one exemplary embodiment, the front panel 455 of the housing contains a microfluidic cartridge receiving chamber 455A. The microfluidic cartridge is inserted into the space by passing through the receiving chamber 455A.

In some exemplary embodiments, the control unit 440 may have the same configuration as the control unit described in the previous example. The control unit 440 controls the quantitative and qualitative analysis, interfacing and storing of the signals obtained from the optical unit 430, and controls and monitors all operations of the portable diagnostic apparatus 400.

In some exemplary embodiments, the power supply unit 460 may have the same configuration as the power supply unit described in the previous example. In some exemplary embodiments, the power supply unit 460 may contain a built-in or removable rechargeable battery.

In an exemplary embodiment, the portable diagnostic device 400 may further include at least one USB port or any other data communication means in the data communication port 455B to allow operation of a universal data transfer communication protocol. In still another exemplary embodiment, the display unit 450 is provided in the portable diagnostic apparatus 400 for a human-machine interface. The display unit 450 is a high resolution color display, which may be a Liquid Crystal Display (LCD), an Organic Light Emitting Diode (OLED), or other kind of display. The display unit 450 may be integrated with a touch screen panel; thus, it can receive commands from a human finger touch. The display unit 450 is connected to the control unit 440. However, the way it displays the displayed content is through a graphical user interface.

Referring now to fig. 15A, the microvalve controller 421 of the cartridge driver unit 420 as shown in fig. 14B includes a substrate 530 having a flat surface cut to a shape suitable for the cartridge chamber (not shown in this figure). And a plurality of nuts 510 and sockets 520 are provided thereon. In the present exemplary embodiment, screws (not shown) within nuts 510 are used to securely mount microvalve controller 421 to rail assembly 412 of cartridge receiving unit 410 in fig. 14B. The socket 520 is configured to provide an electrical connection between the microfluidic cartridge driver unit 420 and a control unit (not shown in this figure), and to provide power or current to the microvalve controller 421.

Referring now to fig. 15B, microvalve controller 421 includes a plurality of heating elements 541 (6 in this example) disposed on and extending outwardly from the bottom surface of substrate 530. The heating element 541 is located on the substrate to coincide with the microvalves of the cartridge (not shown in this figure) on which the device is designed to operate. When the substrate 530 is fixed in place, it is directly above the cartridge chamber (not shown in this figure), and when the cartridge is properly inserted into the device and positioned in the designated area, each heating element 541 will be directly above each microvalve. The heating element 541 is configured to apply thermal energy to a thermally deformable surface of the microvalve to cause the microvalve to open. In some embodiments, the heating element 541 is an electromagnetic radiation emitter configured to emit electromagnetic radiation as an energy source. In some further exemplary embodiments, the heating element 541 is an Infrared (IR) emitter configured to emit IR light as a source of thermal energy.

Referring now to fig. 16A, the cartridge accommodating unit 410 includes a tray 411 and a rail assembly 412. In the exemplary embodiment shown, the track assembly 412 includes a flat tray cover 1520 (also referred to as a tray plate in some embodiments) and 2 sides 1521 that define a partially enclosed compartment. The rail assembly 412 contains a space having a volume greater than that of the tray 411 for slidably receiving the tray such that when the tray 411 with the microfluidic cartridge inserted therein is slid to the docking position, the microfluidic cartridge is located at a designated area to perform reaction and detection. In some embodiments, the rail assembly 412 is fixedly attached to the portable diagnostic device 400 and is configured to receive at least two edges of the tray 411.

In the present exemplary embodiment shown, a pair of slidable rails 1510 are provided on the inside of the side surfaces 1521 opposite to each other. Only one track 1510 is shown in fig. 16A, but it should be understood that there is another track on the opposite side of the interior of side 1521. The tray 411 may be anchored to the pair of rails 1510. The pair of rails 1510 slide the tray 411 in and out of the space as previously described.

In an exemplary embodiment, the track assembly 412 further includes a microvalve controller cover 1522 fixedly attached to a top surface of the tray cover 1520 to hold the microvalve controller 421 of fig. 15A and 15B. In some exemplary embodiments, the microvalve controller cover 1522 may be an integral part of the tray cover 1520, rather than a separate part. Microvalve controller cover 1522 provides a means for supporting microvalve controller 421. In the present exemplary embodiment, three screws 1523 are used to securely mount microvalve controller 421 beneath microvalve controller cover 1522 by fastening screws 1523 into nuts 510 (shown in fig. 15A) of microvalve controller 421. In one exemplary embodiment, the microvalve controller cover 1522 forms a raised platform 1525 that extends upward from the top surface of the tray cover 1520. Raised platform 1525 has a shape that includes an opening that is positioned over slot 520 of microvalve controller 421 to allow passage of one or more wires connected to the slot. The elevated platform 1525 further contains an opening that, when the cartridge is inserted into the space and positioned at a designated area in the device, is located above the 2D code attached to the microfluidic cartridge (not shown in this figure). This opening ensures that when the cartridge is positioned at a designated area in the device, an identification unit 470 (as shown in fig. 14B) located above the cartridge-receiving unit 410 can directly access and scan the 2D code attached to the microfluidic cartridge to identify the cartridge and automatically select the program to be run.

Referring now to fig. 16B, there is shown another perspective view of the same cartridge-containing unit 410 of fig. 16A. In an exemplary embodiment, the tray cover 1520 has an opening 1524 (partially shown) for receiving the microvalve controller 421 thereon. The opening 1524 is larger than or equal to the size of the microfluidic cartridge and is divided into three regions: a first region 1524A, a second region 1524B, and a third region 1524C. In another exemplary embodiment as shown in fig. 16B, the second region 1524B may be a separate opening. The microvalve controller is positioned proximate to the first region 1524A such that when the microfluidic cartridge is inserted into the tray 411 and the tray 411 is slid into the docked position, the microvalves on the microfluidic cartridge are positioned directly underneath the microvalve controller 421. As depicted in fig. 15B, each heating element 541 of the microvalve controller 421 is positioned directly above each corresponding microvalve of the microfluidic cartridge so that heat can be directed to the microvalve when the cartridge is inserted into the device and positioned at a specified portion. An optical unit (not shown in this figure) is located directly above the second region 1524B so that when the microfluidic cartridge is placed in the designated region, the diagnostic portion of the microfluidic cartridge is directly below the light source and camera of the optical unit.

In some exemplary embodiments, the cartridge-containing unit 410 further comprises a switch 1526. In another exemplary embodiment, the switch is a microswitch. The micro-switch may be attached to the back of the rail assembly 412 and electrically connected to a power supply unit (not shown). The micro-switch is automatically activated when the tray 411 with the microfluidic cartridge inserted therein is slid to the docked position by the track assembly 412. After activation, the microswitch may turn on an identification unit (not shown) to read the identification of the microfluidic cartridge and automatically select the program to be used.

Fig. 16C shows a schematic view of the tray 411 of the cartridge housing unit 410 in fig. 16A. Fig. 16D shows the same tray 411 but with the microfluidic cartridge 200 of fig. 11A inserted therein. The tray 411 includes a tray piece 1540 and a cartridge chamber 1530. In the present embodiment, the cartridge chamber 1530 is configured in the shape of a rectangular block to accommodate the microfluidic cartridge 200 such that the microfluidic cartridge 200 is located at a designated area. The rectangular block shape defines a plane and an axis somewhat perpendicular to the plane. In one embodiment, the microfluidic cartridge 200 and the cartridge chamber 1530 are configured such that there is only one possible way in which the microfluidic cartridge 200 can fit securely into the cartridge chamber 1530 and the tray 411, and thus the possibility of inserting the microfluidic cartridge 200 in an undesired orientation or position is eliminated.

The tray 411 serves as the same location for performing the following operations: (1) reactions to be run in a predetermined sequence and (2) optical analysis of the microfluidic cartridge. In one exemplary embodiment, the tray 411 includes electrical connectors 3211 disposed on a cartridge compartment 1530 of the tray. The electrical connector 3211 is configured to receive control signals and power from the micro-pump controller 422 as shown in fig. 14B to perform a predetermined sequence by providing current to the micro-pump of the microfluidic cartridge 200. In one exemplary embodiment, the electrical connectors 3211 are located below the microfluidic cartridge 200 when the cartridge is inserted into the chamber 1530. The electrical connector 3211 is electrically connected to an electrical connection interface of the cartridge 200, and serves as an interface for the cartridge driver unit 420 to drive and control the micro pump in the cartridge 200. In another exemplary embodiment, the tray 411 includes an opening 1543 on the cartridge compartment of the tray 411. Opening 1543 is configured such that it is positioned directly beneath diagnostic portion 210 of cartridge 200 when the cartridge is inserted and secured in chamber 1530 so that light passes through diagnostic portion 210 when performing an optical analysis. The single tray system eliminates the possibility of human error by design.

In one exemplary embodiment, the tray 411 further comprises an anchoring system to ensure that the microfluidic cartridge 200 is secured in the tray when inserted into the tray 411. In one exemplary embodiment, the anchoring system is comprised of at least one cartridge clip 1541 disposed on the tray sheet 1540. In another exemplary embodiment, the anchoring system consists of two cartridge clips 1541 and 1542 positioned orthogonally to each other. Once the microfluidic cartridge 200 is inserted into the tray 411, the two clips work together to restrict its movement. Less movement means less variation in the possible position of the biological assay, thus increasing detection accuracy and precision. The addition of an additional cartridge clip reduces the tolerance to 0.1mm and allows for more accurate detection since variations in the position of the bioassay are minimized. In an exemplary embodiment, the tray 411 further includes at least one tray clip 1544 disposed on the tray tab 1540 to secure the position of the tray as it slides within the cavity of the track assembly 412 (as shown in fig. 16A).

Referring now to fig. 17, the optical unit 430 includes an illumination assembly 1610 and a sensor assembly 1620. In some embodiments, the lighting assembly 1610 includes at least one light source 1611 and a light pipe 1612. In some embodiments, the optical unit 430 further includes one or more filters 1613. In some exemplary embodiments, one or more filters 1613 are contained in a filter box (cube). In one exemplary embodiment, the sensor assembly 1620 includes a camera 1621 positioned on top of the optical unit 430, a camera lens 1622 positioned below the camera 1621, and at least one objective lens 1623. In some exemplary embodiments, the optical unit 430 further includes a camera mount 1624 located between the camera 1621 and the camera lens 1622 to connect these two components. In some exemplary embodiments, the optical unit 430 further includes a filter mount 1625 configured to connect the camera lens 1622, the one or more filters 1613, and the objective lens 1623. In one exemplary embodiment, filter mount 1625 is shaped to contain a cavity to receive one or more filters 1613 such that one or more filters 1613 may be securely fit within filter mount 1625. Filter mount 1625 further includes an opening at the top to connect camera lens 1622 and one or more filters 1613, an opening at the side to connect light pipe 1612 and one or more filters 1613, and an opening at the bottom to connect objective lens 1623 and one or more filters 1613. In some exemplary embodiments, optical unit 430 further includes a box front 1614 configured to connect lighting assembly 1610 and filter mount 1625 such that light from light source 1611 may enter one or more filters 1613 at a fixed angle. In some exemplary embodiments, the optical unit 430 further includes an objective cover 1626 configured to receive and secure an objective lens 1623. In some exemplary embodiments, the apparatus further comprises one or more standoffs 1627 that serve as a stand to support the structure of the optical unit 430 when all components are assembled together. The stand 1627 also serves as a support such that the optical unit 430 and the cassette receiving unit 410 (as shown in fig. 16A) are securely mounted on the stand in the configuration further described in fig. 18.

When the tray 411 with the microfluidic cartridge 200 inserted therein as shown in fig. 16D (but not shown in this figure) is in its docked position in the device, the diagnostic portion 210 of the microfluidic cartridge 200 is located directly below the optical unit 430 for inspection. The illumination assembly 1610 and the sensor assembly 1620 are mounted to point at a diagnostic portion of the microfluidic cartridge. A further description of this arrangement is provided in fig. 18. Illumination assembly 1610 is configured to transmit light to diagnostic portion 210 of the microfluidic cartridge, and sensor assembly 1620 is configured to detect at least one signal generated by the diagnostic portion due to the presence of an analyte when the microfluidic cartridge is inserted and operated in a predetermined condition. The optical unit 430 may be used for in-situ analyte analysis/detection. In some embodiments, the apparatus may include one or more optical units 430. The optical unit 430 may acquire an image or a signal of the sample. The optical unit may send the acquired signal to the control unit to convert the acquired signal into a meaningful value.

In some exemplary embodiments, the light source 1611 may be a monochromatic or polychromatic laser or LED. The light source 1611 should be strong enough to excite the fluorophore. In one exemplary embodiment, the light source 1611 is an LED. In some exemplary embodiments, the light source 1611 may be a high brightness LED spot light having a blue or red LED color. In some exemplary embodiments, it may be advantageous to use an LED spotlight having a red LED color, as compared to using blue, green, or other colors, for example, to facilitate reducing autofluorescence of a microfluidic cartridge (not shown). Red light from the light source 1611 may be collimated with a lens and/or filter 1613 to filter appropriate wavelengths, reflected by a mirror and focused onto a diagnostic portion of the microfluidic cartridge, and imaged with a detector (e.g., a CCD camera). The red excitation light may excite a red excited fluorophore present in the reaction sample on the diagnostic moiety. In some exemplary embodiments, other red-excited fluorophores may be used.

In another exemplary embodiment, the illumination assembly 1610 includes a light source 1611, such as a diode laser, that radiates at least one laser beam having at least one predetermined wavelength on the microfluidic cartridge 200 to generate at least one signal. The predetermined wavelength of the laser beam is selected such that at least one signal detectable by the sensor assembly 1620 can be generated. In an exemplary embodiment, the intensity and wavelength of the laser beam may be selected/controlled by a user via a control unit (not shown in this figure) to detect a specific analyte. The laser beam is turned at an angle to the microfluidic cartridge to avoid reflections and generate a higher quality signal. The predetermined wavelength is, for example, in the range of 465 to 500nm, 400 to 700nm, 430 to 465nm, 500 to 550nm, 550 to 580nm, 580 to 620nm, or 620 to 700 nm.

In one exemplary embodiment, the light source 1611 includes a light pipe 1612 that uniformly releases light. The light pipe 1612 is configured such that it directs light to other optical components and helps focus the light beam onto the biological assay on the diagnostic portion of the microfluidic cartridge when the cartridge is positioned in the designated area. The light pipe 1612 aligns the biological assay on the diagnostic portion at a particular location on the microfluidic cartridge when the cartridge is positioned in the designated area for reaction and analysis. In an exemplary embodiment, the illumination assembly 430 may further comprise at least one condenser lens (not shown) as described in example 1, such that the focus of the light from the light source 1611 is optimized.

In one embodiment, optical unit 430 may include one or more light sources, one or more lenses, one or more dichroic mirrors, one or more sensors, one or more emission filters, and/or one or more excitation filters.

When the tray 411 with the microfluidic cartridge 200 inserted therein as shown in fig. 16D (but not shown in this figure) is in its docked position in the device, the microfluidic cartridge 200 is positioned underneath the sensor assembly 1620 and the illumination assembly 1610. Sensor assembly 1620 receives signals from diagnostic portions of the microfluidic cartridge that are generated by illumination of a beam of light on the diagnostic portions by illumination assembly 1610. The received signal is then sent to a control unit (not shown) for analysis.

Sensor assembly 1620 may have a high quantum efficiency in the wavelength range it detects. In an exemplary embodiment, the camera 1621 of the sensor assembly 430 may be a Charge Coupled Device (CCD) or any other suitable camera. In one exemplary embodiment, camera 1621 is a near infrared optimized camera with an 2/3-type (11.0 mm diagonal) CCD sensor.

The camera lens 1622 of the sensor assembly 1620 may be any suitable lens of the camera 1621 or a higher quality lens, such as a microscope grade lens, depending on the type of immunoassay used. In one exemplary embodiment, the camera lens 1622 is responsible for assisting the camera 1621 in focusing on the biological assay, since the biological assay is physically small. In one exemplary embodiment, camera lens 1622 is a C-bayonet lens. In some embodiments, a C-bayonet lens is located between the camera 1621 and the objective lens 1623. In some exemplary embodiments, the C-bayonet lens is securely attached to the camera 1621. In one exemplary embodiment, the effective focal length of the C-bayonet lens is 20-30 mm.

In one exemplary embodiment, the optical unit 430 includes one or more optical filters 1613. One or more filters 1613 may be used to filter out any light generated from the light source having undesired wavelengths and any undesired noise in the signal picked up by the camera.

Depending on the light source 1611 and fluorophore used, one or more filters 1613 may be used. The illumination assembly 1610 is connected to a filter 1613. In one exemplary embodiment, the camera 1621 is connected to a camera lens 1622, and both components are connected to one or more filters 1613. One or more filters 1613 are mounted and aligned between the camera lens 1622 and the objective lens 1623. This connection to the one or more filters 1613 allows any undesired signals (e.g., noise, which typically has a different wavelength, resulting from the biological assay or any undesired reaction) to be filtered and thus minimizes undesired interference with the actual signal. In one exemplary embodiment, one or more filters 1613 are also connected to the light pipe 1612 at an angle that helps focus the filtered light beam onto the biological assay. In another exemplary embodiment, the angle is 0 degrees. In yet another exemplary embodiment, the angle is between 1 degree and 50 degrees. In one exemplary embodiment, the one or more filters 1613 is a filter set containing one or more dichroic filters, one or more emission filters, and one or more excitation filters. In one exemplary embodiment, the filter set is configured to alter the optical path such that when the microfluidic cartridge is positioned in a specified region, light generated by the light source 1611 can be directed to illuminate a diagnostic portion of the microfluidic cartridge perpendicular to the axis of the cartridge chamber.

In one exemplary embodiment, a fluorescence filter set for CY5 fluorescein was used. In another exemplary embodiment, the fluorescence filter set for CY5 fluorescein has the specifications shown below:

excitation band (nm): 600-650

Emission band (nm): 670-710

Dichroic reflection band (nm): 550-650

Cross band (nm): 650-800

In some exemplary embodiments, the optical unit 430 provides a filtered light beam having a wavelength in the range of 400nm to 700 nm. In another exemplary embodiment, the optical unit 430 provides a filtered light beam having a wavelength in the range of 600nm to 650 nm.

In one exemplary embodiment, the objective lens 1623 of the sensor assembly 1620 is a planar achromatic objective lens, 4x magnification, effective focal length 45-55nm, and the coating covers wavelengths from UV to NIR.

Fig. 17 also shows an identification unit 470 of the portable diagnostic device 400 as shown in fig. 14B. The identification unit 470 is configured to read an identification of a microfluidic cartridge (not shown in this figure) and to transmit a corresponding identification signal to a control unit (not shown). In some exemplary embodiments, the identification unit 470 includes a reader 1632 configured to read an identification of the microfluidic cartridge. In some exemplary embodiments, the identification unit 470 is attached or fixed to the optical unit 430. In one exemplary embodiment as shown in fig. 17, identification unit 470 further comprises a reader mount 1631 to receive reader 1632 and attach the reader to the bracket of optical unit 430. The reader 1632 is located directly above the designated area where the microfluidic cartridge will be placed and is directed toward the microfluidic cartridge.

In one exemplary embodiment, the reader 1632 is a bar code reader. The barcode reader can read a 2D barcode attached or affixed to the microfluidic cartridge. In one exemplary embodiment, the barcode is attached or affixed to the microfluidic cartridge (see fig. 11A). In another exemplary embodiment, a two-dimensional (2D) code is attached or affixed to the microfluidic cartridge. A 2D code incorporating the identity of the microfluidic cartridge, the analyte or disease to be tested, the expiration date of the chip is placed on the microfluidic cartridge during the manufacturing process. After the microfluidic cartridge is inserted into the tray, the barcode reader is activated and the barcode reader automatically scans the 2D code. The software can automatically select the correct program to use based on the 2D code. This feature eliminates the need to manually select the pulse program, making the design more user friendly and less prone to human error. In one exemplary embodiment, the software may also identify microfluidic cartridges that have been previously used or are defective. The software displays a warning message on the screen and does not continue to execute the program.

Referring now to fig. 18, the components of the optical unit 430, the identification unit 470, the microvalve controller 421 of the cartridge drive unit 420, and the cartridge receiving unit 410 of the portable diagnostic apparatus 400 as shown in fig. 14B are arranged such that a compact integrated assembly 480 is formed. This compact design results in a smaller, lighter diagnostic system. The diagnostic system should be small enough and light enough to be moved between clinics when needed. In one exemplary embodiment, the present invention is small enough and light enough to be carried around to a domestic flight. In one exemplary embodiment, the size of the device is about 30x30x30cm³The weight is about 5-6 kg.

Fig. 18 shows the configuration and spatial relationship between the units integrated together in the assembly 480. The spatial arrangement of the components in each unit is described above. In one exemplary embodiment, the camera 1621 and camera lens 1622 mounted thereon are located on one side of a second region 1524B (not shown in this figure, but shown in fig. 16A) of the track assembly proximate the opening 1524 and are axially aligned with the plane of the cassette compartment. In this figure, it is shown at the top of assembly 480. These two components are connected to one or more filters (not shown) that fit in filter mount 1625. The filter is mounted and optically aligned between a camera lens 1622 and an objective lens 1623 positioned below a filter mount 1625. The light pipe 1612 of the illumination assembly 1610 is also attached to an opening in the side of the filter mount 1625 and is optically aligned to illuminate on the same side of the track assembly 412 as the camera lens, perpendicular to the axis of the cartridge chamber. When the light beam generated by the light source 1611 enters the one or more filters, the one or more filters allow only light having a particular wavelength or range of wavelengths to pass through to the biological assay and filter out light having undesired wavelengths. In the present embodiment, the track assembly 412 of the cartridge accommodating unit 410 is located below the objective lens 1623 of the optical unit 430. In one embodiment, the optical unit 430 and track assembly 412 are securely mounted on two brackets 1627 located on opposite sides of the assembly 480 such that they remain together as an integral part of the device. Each bracket 1627 has a section that extends from the bottom of the track assembly 412 to the camera 1621 and is shaped to fit the optical unit 430 and the cassette receiving unit 410 to support the assembly 480 when all components are assembled together. In one exemplary embodiment, the reader mount 1631 on which the identification unit 470 of the reader 1632 is mounted is attached to the bracket of the optical unit 430 by mounting on two brackets 1627 and aligning with the third region 1524C of the opening 1524. In this embodiment, the reader 1632 is located above the cartridge-receiving unit 410 and directed to a designated area where a microfluidic cartridge (not shown) will be placed to scan a code attached to the microfluidic cartridge.

In the present exemplary embodiment shown, the track assembly 412, the microfluidic cartridge driver unit 420, the optical unit 430, and the identification unit 470 of the cartridge accommodation unit 410 are mounted within the housing in a configuration such that when a microfluidic cartridge is inserted into the device, there is a space for accommodating the microfluidic cartridge. In the present exemplary embodiment, when the microfluidic cartridge is inserted into the tray 411 and the tray 411 is slid to the docking position, the microfluidic cartridge is positioned in a specified region of the space. The space includes one or more micro valve positions and one or more micro pump positions. As shown, the microvalve controller 421 is securely mounted on the track assembly 412 and positioned alongside the microvalves of the microfluidic cartridge inserted into the space such that the heating elements of the microvalve controller 421 correspond to the positions of the microvalves. The illumination assembly 1610 and the sensor assembly 1620 are axially aligned with the plane of the cartridge chamber and mounted to be directed toward the diagnostic portion of the microfluidic cartridge. The opening 1524 ensures that the diagnostic portion of the microfluidic cartridge is located directly under the camera lens 1623 of the optical unit 430 for inspection. Sensor assembly 1620 receives signals from diagnostic portions of the microfluidic cartridge that are generated by illumination of a beam of light on the diagnostic portions by illumination assembly 1610. In one embodiment, the received signal may be sent to a control unit (not shown) for analysis.

In some exemplary embodiments, assembly 480 further includes a switch 1526 (not shown in this figure, but shown in fig. 16B). In another exemplary embodiment, switch 1526 is a micro-switch. The micro-switch may be attached to the back of the rail assembly 412 and electrically connected to a power supply unit (not shown). The micro-switch is automatically activated when the tray 411 with the microfluidic cartridge inserted therein is slid to the docked position by the track assembly 412. After activation, the micro-switch may turn on the reader 1632 to read the identification of the microfluidic cartridge 200 and automatically select the program to be used.

Events associated with the assembly 480 of devices are described below:

s1. the user places the microfluidic cartridge into the cartridge chamber of the tray 411.

S2. the user pushes the tray 411 into the device under the guidance of the track assembly 412.

S3. when the tray 411 is pushed in and secured in the docked position, the switch 1526 is activated.

S4, the switch 1526 turns on the bar code reader 1632.

S5. the reader 1632 reads the code printed or attached on the microfluidic cartridge.

S6, the code contains the identification of the microfluidic cartridge, which prompts the software of the control unit to automatically select the program associated with the microfluidic cartridge.

S7. once the software selects the correct program, the micro valve controller 421 and micro pump controller (not shown in this figure) cooperate to actuate the flow of fluid from the reservoir to the diagnostic portion in a predetermined sequence.

S8. Once the reaction is complete in the diagnostic portion, illumination assembly 1610 is activated and the biological assay is excited by the light beam generated by light source 1611.

S9. the sensor assembly 1620 captures optical images and analyzes the images by software.

And S10, displaying the result on a screen for a user to check. No manual interpretation is required.

In one exemplary embodiment, the operation of the diagnostic device when a microfluidic cartridge is inserted therein is shown in fig. 19 and described in detail below:

block 1810 indicates directing the sample and one or more reagents from the microfluidic portion to the diagnostic portion in a predetermined sequence within the microfluidic cartridge by opening a microvalve sealing a reservoir of the microfluidic cartridge and actuating a micropump in the microfluidic cartridge.

In some exemplary embodiments, the predetermined sequence comprises a step of spreading the analytes. In the spreading analyte step, fluids (e.g., sample, buffer(s), and reagent (s)) exit the channel openings in sequence, spreading across the diagnostic chamber, and these fluids are in direct contact with the diagnostic chip. The area over which the sample, buffer solution(s) and reagent(s) are spread covers the location where the array of test spots is located so that the analyte(s) can react/interact with the analyte-interacting molecules pre-coated on the test spots. In one exemplary embodiment, the analyte spreading step may further comprise the steps of: the microfluidic cartridge is further driven to dispense a second ancillary reagent located at one reservoir by flowing through the microchannel to the diagnostic portion, thereby attaching a second molecule to facilitate detection of the reacted or interacted analyte after the sample and reagent are dispensed on the detection array. In yet another exemplary embodiment, the pre-coated analyte has bound to a molecule that is used to detect the analyte without the need for a second molecule. The molecule may be one that can generate a fluorescent signal or other detectable signal for subsequent analytical steps.

In one exemplary embodiment, the micro-pump controller of the cartridge drive unit generates a specific sequence of electrical pulses, and the sequence of electrical pulses is passed through the microfluidic cartridge via an electrical connector located at the bottom of the tray. The present sequence of electrical pulses may drive a micropump to facilitate fluid movement within the microfluidic cartridge. At the same time, the microvalve controller receives a signal from the cartridge driver unit to apply thermal energy to a particular microvalve position on the microfluidic cartridge to cause the microvalve to open. The microvalve controller and the micropump controller cooperate to drive the sample or reagents in the microfluidic cartridge out of their reservoirs and into the diagnostic portion in a predetermined sequence.

In one exemplary embodiment, the control unit of the device contains a microfluidic cartridge driver software module to control the fluidic actuation. The microfluidic cartridge driver software module is designed to instruct the cartridge driver unit as to when to control the current and to deliver this current to the micropump of the microfluidic cartridge. The higher the current and/or the longer it takes to deliver this current, the more fluid can then be pumped from the reservoir.

The microfluidic cartridge driver software module is also designed to instruct the cartridge driver unit to control the current and the time to transmit this current to the microvalve controller, which controls the opening of the microvalve by emitting thermal energy onto the surface of the microvalve to expand the microvalve.

Block 1820 indicates providing a predetermined condition to a diagnostic portion of the microfluidic cartridge to generate at least one signal.

In one exemplary embodiment, the predetermined condition comprises an analysis step. The diagnostic portion of the microfluidic cartridge is located below the optical sensor and is not separated from the microfluidic cartridge after the analyte spreading step. After receiving the activation signal from the control unit, the light beam (e.g., laser beam) from the illumination assembly of the optical unit is filtered and directed onto the diagnostic portion to generate at least one signal detectable by the sensor assembly (if the sample contains an analyte). In one embodiment, the at least one signal comprises a fluorescent signal that is generated when the diagnostic portion is illuminated with an appropriate light of an appropriate wavelength. Block 1830 indicates that the at least one signal is detected and data is collected using an optical sensor.

In one exemplary embodiment, the signal (e.g., fluorescence signal) as described above is filtered by one or more filters of the optical unit and collected by a sensor assembly of the optical unit located above the diagnostic portion. One or more filters are used to filter out any unwanted noise in the signals picked up by the cameras of the sensor assembly.

Block 1840 indicates that the data is analyzed to quantitatively and/or qualitatively determine the presence of the analyte.

In one exemplary embodiment, the collected signals will be converted to digital data which will then be transferred to and analyzed by the microprocessor of the control unit to quantitatively or qualitatively determine the presence of the analyte. In an exemplary embodiment, the results will be displayed on the display unit of the device in a relatively short time. The total process time (i.e., from insertion of the microfluidic cartridge into the device to display of the results) only requires 10-25 minutes. In yet another exemplary embodiment, the entire process time only requires about 15 minutes.

In one exemplary embodiment, the present invention has been designed with minimal human involvement, which minimizes the possibility of human error. After all reagents are preloaded into the microfluidic cartridge and sealed, only the sample chamber inlet is exposed and is the only apparent inlet where the sample should be loaded. This design minimizes the possibility of a user loading a sample into the wrong chamber. When the microfluidic cartridge is inserted into the device, the barcode reader scans the data matrix on the microfluidic cartridge and either rejects the cartridge (if it is already in use) or accepts the microfluidic cartridge and automatically selects the correct test procedure. This feature prevents any used microfluidic cartridge from being accidentally reused and prevents the user from making mistakes when selecting a test procedure on the diagnostic platform. The software embedded in the diagnostic platform analyzes the test results and displays them on the screen, which eliminates any possibility of human misinterpretation when reading the results.

Example 10

Equipment with intelligent function

Referring now to fig. 20, in one aspect, there is provided a portable diagnostic device 2010 further comprising a detachable smart device 2012, optionally connected to and in communication with the portable diagnostic device 2010, to obtain prevalence information in a location (as shown in fig. 10B), wherein the smart device 2012 includes

An environmental measurement module 2013 for obtaining environmental data, wherein the environmental data includes at least one environmental parameter at the location;

a data storage module 2016 for storing raw data, wherein the raw data includes one or more of environmental data and diagnostic data;

a transmitter 2015 for transmitting the raw data to a remote server; and

a battery 2014.

The portable diagnostic device 2010 may be used to collect different types of diagnostic data. The diagnostic data may include the type of disease, severity of disease, viral load, presence or absence of pathogens or allergens, or blood cell count. Examples of diagnostic data include, but are not limited to, data associated with: (1) animal diseases such as Porcine Reproductive and Respiratory Syndrome (PRRS), bovine Foot and Mouth Disease (FMD), Classical Swine Fever (CSFV) infection, and Bovine Spongiform Encephalopathy (BSE) infectious disease), (2) food safety (e.g., detection of food allergens (e.g., peanut, seafood), aflatoxin, and melamine) and (3) human diseases such as infectious diseases (e.g., Sexually Transmitted Disease (STD), middle east respiratory syndrome coronavirus (MERS-CoV), and influenza virus infection), tropical diseases (e.g., dengue virus and japanese encephalitis virus infection), and emerging infectious diseases of antigen/antibody immune mechanisms belonging to their pathological pathways), influenza a, influenza b, RSV, HPIV, adenovirus, dengue, chikungunya, zika, malaria, leptospirosis, toxoplasmosis, distemper virus Ab, influenza a, and, Canine parvovirus Ab or heartworm.

In other embodiments, the portable diagnostic device 2010 may measure device data, where the device data is machine information or operating status. In some embodiments, the machine information is selected from the group consisting of: model number, machine identification, machine, hardware version, software version, country of original purchase, and owner. In other embodiments, the operating state is selected from the group consisting of: error code, system voltage, total operating hours, and total number of tests.

According to another embodiment, the smart device 2012 includes an environmental measurement module 2013 that is configured to obtain environmental data that includes at least one environmental parameter at the location. In some embodiments, the environmental data is selected from the group consisting of positioning data, humidity, temperature, barometric pressure, time, and air quality (AQI, pollen count, etc.). In some embodiments, the positioning data is a global position and is acquired by a Global Positioning Satellite (GPS). In some embodiments, the environmental data is selected from the group consisting of positioning data, humidity, temperature, and time.

In some embodiments, the environmental measurement module 2013, the transmitter 2015, and the data storage module 2016 together form a smart device 2012 that may optionally be connected to and in communication with a portable diagnostic device 2010 and a remote server 2020. In some embodiments, the smart device 2012 is removable. The smart device 2012 may be any size, but in some embodiments it is smaller than the device and may fit inside the device. In some embodiments, a detachable smart device may be placed into the housing.

According to other embodiments, the smart device 2012 further includes a battery 2014. In some embodiments, the battery is rechargeable and may operate without charging for 30 days. In other embodiments, the transmitter 2015 is a wireless transmitter.

Still referring to fig. 20, another aspect of the present invention provides a system 2040 for managing a network of portable diagnostic devices 2010, each connected to and in communication with a removable smart device 2012, and obtaining prevalence information, the system comprising at least one user terminal 2030 and a server 2020 comprising a data module 2021 for collecting and storing raw data, wherein the raw data comprises one or more of:

diagnostic data obtained at a location using the portable diagnostic device 2010, wherein the diagnostic data includes at least one biochemical or pathological measurement of the subject,

the environmental data is stored in a memory of the computer,

device data obtained from the portable diagnostic device 2010, and

data module for analyzing raw data

Where the server 2020 is connected to a user terminal 2030 and a removable smart device 2012.

In some embodiments, environmental data is obtained at the location using the environmental measurement module 2013, wherein the environmental data includes at least one environmental parameter. In other embodiments, the environmental data is obtained from a third party source, such as from an environmental measurement device or from a public record (e.g., a local news source, weather station report, or the internet) about the environment at the location. Examples of environmental measurement devices include, but are not limited to, devices for measuring one or more of humidity, temperature, air velocity, air pressure, light, dust, sound, and vibration.

In some embodiments, system 2040 includes a plurality of portable diagnostic devices 2010. In some embodiments, system 2040 includes at least 2, 5, 10, 100, 1000, 10,000 portable diagnostic devices 2010. In some embodiments, the system includes 2-50, 10-100, 50-500, or 100-1000 portable diagnostic devices 2010.

In some aspects, the server 2020 is a cloud-based platform. In some embodiments, the server 2020 is wirelessly connected to the user terminal 2030 and the portable diagnostic device 2010. In some embodiments, server 2020 further includes a software update module (not shown) to transmit software to portable diagnostic device 2010. This may include software containing diagnostic test protocol updates, firmware updates, and other types of software updates. In some aspects, the server 2020 may send solutions to problems faced by the user in the form of remote technical support. For example, machine operating data or environmental data received by the server 2020 indicates that there are certain problems with the device, and the server 2020 may send information or actual software updates to address these problems.

According to another embodiment, the data module 2022 for analyzing the raw data performs one or more of the following steps:

collecting raw data;

analyzing the raw data to provide results; and transmits the result to the user terminal 2030.

In some embodiments, data module 2022 resides on server 2020. In other embodiments, the data analysis may be performed on another server, computer, or in a separate system.

In some embodiments, the analysis may be creation of a database, statistical analysis, analysis of raw data (e.g., machine operational data or environmental data) to determine the cause of a machine error, creation of a mathematical model, analysis of current trends, correlation data, and mapping prevalence to specific locations.

According to another embodiment, the data module provides one or more of the following results:

prevalence at different locations displayed on a map;

prevalence over time;

the severity of the disease in a particular location;

remote technical support; and

and (4) remote software updating.

Additionally, a correlation between environmental conditions and device status may also be determined, such as analyzing whether one or more error codes occurred due to exposure of the device to abnormal ambient temperatures (e.g., high heat) or humidity levels (high humidity) as measured by the environmental measurement module 2013. In another exemplary embodiment, other types of analysis may be performed on the data, including but not limited to correlations between environmental conditions and disease outbreaks, disease associations, trends, patterns, prevalence, and migration.

According to another embodiment, the data module 2021 further includes one or more access controls to the raw data and results. In some embodiments, the access control is selected from a password or security code, where different levels of security may be implemented. Other types of access controls known to those skilled in the art may be used, including, but not limited to, incorporating the access control into another physical device (e.g., a mobile device) and incorporating the access control therein using techniques (e.g., password, facial recognition, fingerprint identification, 2-factorial authentication, numeric keypad, or physical keys). In some embodiments, the portable diagnostic device 2010 transmits raw data to the server 2020 once every hour. In some embodiments, when the portable diagnostic device 2010 is not connected to an external power source, the portable diagnostic device 2010 transmits raw data to the server 2020.

According to another embodiment, the system 2040 comprises at least one user terminal 2030 or user interface (not shown). In some embodiments, the user terminal 2030 or interface is a computer or mobile device. In some embodiments, the mobile device is wireless network enabled and wirelessly connects to the server. In some embodiments, wireless communication is by one or more of the following wireless technologies, including but not limited to satellite, bluetooth, radio, Wi-Fi, wireless broadband, or cellular (e.g., 2G, 3G, 4G, 5G). In some embodiments, the mobile device further comprises an interface for displaying the results of the data module (e.g., mobile application).

According to another embodiment, the system 2040 includes a plurality of portable diagnostic devices 2010, a plurality of user terminals 2030 and at least one server 2020.

Another aspect of the present invention provides a method of obtaining prevalence information in a location as shown in fig. 21, and is described in detail below:

block 2110 indicates that diagnostic data or samples are obtained at the location using the portable diagnostic device, wherein the diagnostic data includes at least one biochemical or pathological measurement of the subject.

Block 2120 indicates that environment data is obtained.

Block 2130 indicates transmitting the diagnostic data and the environmental data to a server.

Block 2140 indicates that diagnostic data and environmental data for a plurality of subjects in a plurality of locations are collected and stored in a server to form a database.

Block 2150 indicates that the subject or location in the database is analyzed for prevalence or environmental information.

Some embodiments further include one or more of the following steps as shown in fig. 22, and are described in detail below:

block 2210 indicates that the raw data at the location is obtained and stored on the data storage module.

Block 2220 indicates that the raw data is transmitted from the data storage module to the server.

Block 2230 indicates that, in the server, a plurality of raw data from a plurality of subjects in a plurality of locations is collected and stored to form a database.

Block 2240 indicates that the database is analyzed to provide results, where the results provide prevalence information.

The raw data includes one or more of:

diagnostic data obtained at a location using a portable diagnostic device, wherein the diagnostic data comprises at least one biochemical or pathological measurement of the subject.

Environmental data.

Device data obtained from the device.

In some embodiments, the portable diagnostic device is a device described herein. In some embodiments, environmental data is obtained at the location using an environmental measurement module, wherein the environmental data includes at least one environmental parameter. In other embodiments, the environmental data is obtained for a third party source, such as from an environmental measurement device or from public information about the environment at the location (e.g., a local news source, weather station reports, or the internet). Examples of environmental measurement devices include, but are not limited to, devices for measuring one or more of humidity, temperature, air velocity, air pressure, light, dust, sound, and vibration. In some embodiments, the environment measuring device includes a device for measuring positioning data, such as a GPS (global positioning system).

In some embodiments, the system authorizes the user's access to the raw data, database, and results based on the access rights.

Some embodiments further comprise the step of transmitting the software from the server to the device. In some embodiments, raw data is transmitted to the server once per hour, even when the device is not connected to an external power source.

FIG. 23 is a flow diagram illustrating the flow of information and data for various components of a system according to one embodiment of the invention. The system comprises a portable diagnostic device 2010, a smart device 2012, a server 2020, and one or more system users interacting with the system via a user interface or terminal.

The portable diagnostic device 2010 records raw data (e.g., machine identification, operating status, and diagnostic data) and sends the raw data to the smart device 2012. The smart device 2012 receives the raw data, records the environmental data, and transmits the raw data and the environmental data to the server 2020.

The server 2020 receives and stores raw data and environmental data received from the smart device 2012. Server 2020 may also receive and store raw data directly from portable diagnostic device 2010 if portable diagnostic device 2010 is connected to a network. The server 2020 sends the updated software to the portable diagnostic device 2010 via a network or via the smart device 2012. The server 2020 sends the updated software directly to the smart device 2012 without using a separate network (e.g., Wi-Fi or cellular connection). Server 2020 controls access to data and statistics based on the user's access rights.

The server 2020 also analyzes data from the smart device 2012, the portable diagnostic device 2010, and even third party sources to perform data analysis and create results, such as statistics, prevalence analysis, disease trends, and other reports.

Different types of users may access the server 2020. Superuser 2304 has full control and can manage software updates for multiple devices and smart appliances. It may also control access rights of individual users to server 2020. Individual users 2305 may access data and results according to their individual user rights.

Fig. 24 is a schematic diagram of the assembly of the smart device 2012 and the units interacting therewith (i.e., the portable diagnostic device 2010 and the server 2020). The smart device 2012 includes a processor 2401, a data storage module 2408, a humidity sensor 2402, a temperature sensor 2403, a GPS2404, a connection port 2405, a connection port 2406, and a wireless module 2407.

Processor 2401 is coupled to data storage module 2408, humidity sensor 2402, temperature sensor 2403, GPS2404, connection port 2405, and wireless module 2407. Processor 2401 collects data from humidity sensor 2402, temperature sensor 2403, and GPS2404, and also collects raw data and machine data from portable diagnostic device 2010 via connection port 2405. Data collected by processor 2401 is stored in data storage module 2408. Processor 2401 may send the data directly to server 2020 via wireless module 2407 for further analysis. The wireless module 2407 is composed of a Wi-Fi module and a cellular module (e.g., 4G). In another exemplary embodiment, processor 2401 may also analyze all data.

A battery 2409 is connected to the processor 2401 via a connection port 2406, and provides power to operate the processor 2401 and enable wireless transmission of data to the server 2020.

Accordingly, the exemplary embodiments of the present invention have been fully described. Although the description refers to particular embodiments, it will be apparent to those skilled in the art that the present invention may be practiced with modification of these specific details. Accordingly, the present invention should not be construed as limited to the embodiments set forth herein.

For example, the apparatus may further comprise at least one USB port or any other data communication means to allow operation of the general data transfer communication protocol. A display unit is provided in the device for a human-machine interface. The display unit 450 is a high resolution color display, which may be a Liquid Crystal Display (LCD), an Organic Light Emitting Diode (OLED), or other kind of display. The display unit may be integrated with the touch screen panel; thus, it can receive commands from a human finger touch. The display unit is optionally connected to the control unit 440. However, the way it displays the displayed content is through a graphical user interface.

Exemplary microfluidic chips that can be used may be the microfluidic chips disclosed in german patent application nos. DE102010061910.8, DE102010061909.4, DE102014117976a1 and DE 502007004366.4.

In yet another alternative embodiment, instead of using at least one beam, at least one laser beam may be used to generate at least one signal for analysis. In this alternative embodiment, illumination assembly 1610 emits at least one laser light beam having at least one predetermined wavelength on diagnostic portion 210. The illumination assembly 1610 includes a diode laser, at least one optical filter, and at least one dichroic mirror.

In another embodiment, the lighting assembly 1610 may have more than one diode laser or more than one LED.

In yet another embodiment, the camera 1621 of the optical unit 430 may be a digital high resolution camera, wherein the sensor is selected from the group of: complementary Metal Oxide Semiconductor (CMOS) sensors and Charge Coupled Device (CCD) sensors. The image sensor of a digital high resolution camera has a megapixel number in the range of 1.0 megapixels to 30 megapixels.

In yet another embodiment, the portable diagnostic apparatus 400 may contain a plurality of cartridge driver units 420, a plurality of cartridge accommodation units 410, and a plurality of optical units 430, so that a plurality of analyses/diagnoses may be simultaneously performed. While we have described several embodiments of our invention, it is to be understood that these examples can be varied to provide other embodiments of our invention. Accordingly, the scope of the invention should be determined by the following claims and not by the specific examples provided herein.