阅读说明：本技术 一种血液样本类型识别检测系统 (Blood sample type identification and detection system ) 是由 胡飞 黄莎 邱笑违 董飒英 于 2019-11-28 设计创作，主要内容包括：本发明公开一种血液样本类型识别检测系统,样本载体上形成有样本通道,样本通道于全血识别单元的末端连接血浆识别单元,样本通道于血浆识别单元的末端连接血清识别单元；全血识别单元包括全血识别传感器和全血信号采集线路,全血识别传感器置于样本通道内部,全血信号采集线路连接全血识别传感器；血浆识别单元包括血浆识别传感器和血浆信号采集线路,血浆识别传感器置于样本通道内部,血浆信号采集线路连接血浆识别传感器；血清识别单元包括血清识别传感器和血清信号采集线路,血清识别传感器置于样本通道内部,血清信号采集线路连接血清识别传感器。可用于免疫检测系统工作前对血液样本类型进行判断,以满足不同项目检测的判断需求。(The invention discloses a blood sample type identification and detection system.A sample channel is formed on a sample carrier, the tail end of a whole blood identification unit of the sample channel is connected with a plasma identification unit, and the tail end of the plasma identification unit of the sample channel is connected with a serum identification unit; the whole blood identification unit comprises a whole blood identification sensor and a whole blood signal acquisition circuit, the whole blood identification sensor is arranged in the sample channel, and the whole blood signal acquisition circuit is connected with the whole blood identification sensor; the plasma identification unit comprises a plasma identification sensor and a plasma signal acquisition circuit, the plasma identification sensor is arranged in the sample channel, and the plasma signal acquisition circuit is connected with the plasma identification sensor; the serum identification unit comprises a serum identification sensor and a serum signal acquisition circuit, the serum identification sensor is arranged in the sample channel, and the serum signal acquisition circuit is connected with the serum identification sensor. The method can be used for judging the type of the blood sample before the immune detection system works so as to meet the judgment requirements of different project detection.)

1. A blood sample type identification and detection system is characterized by comprising a sample carrier, a whole blood identification unit, a plasma identification unit and a serum identification unit, wherein a sample channel is formed on the sample carrier;

when the whole blood identification unit, the plasma identification unit and the serum identification unit exist simultaneously, the sample introduction end of the sample channel is connected with the whole blood identification unit, the tail end of the sample channel is connected with the plasma identification unit, and the tail end of the sample channel is connected with the serum identification unit;

the whole blood identification unit comprises a whole blood identification sensor and a whole blood signal acquisition circuit, the whole blood identification sensor is arranged in the sample channel, and the whole blood signal acquisition circuit is connected with the whole blood identification sensor;

the plasma identification unit comprises a plasma identification sensor and a plasma signal acquisition circuit, the plasma identification sensor is arranged in the sample channel, and the plasma signal acquisition circuit is connected with the plasma identification sensor;

the serum identification unit comprises a serum identification sensor and a serum signal acquisition circuit, the serum identification sensor is arranged in the sample channel, and the serum signal acquisition circuit is connected with the serum identification sensor.

2. The blood sample type identification and detection system of claim 1, wherein the whole blood identification sensor is an electrochemical sensor, the whole blood identification sensor is fitted by identifying the impedance in the whole blood sample and substituting a standard impedance curve to obtain the hematocrit, and the whole blood identification sensor reflects the existence and the quantity of red blood cells in the whole blood sample according to the hematocrit, and adopts one of a screen-printed carbon electrode, a silver-evaporated electrode or a gold-sputtered electrode.

3. The blood sample type identification and detection system of claim 1, wherein the whole blood identification sensor is an optical sensor, and the whole blood identification sensor obtains hematocrit by identifying light transmittance or red spectrum light absorption of the whole blood sample, and the presence and quantity of red blood cells in the whole blood sample are reflected according to the hematocrit.

4. The blood sample type identification and detection system according to claim 1, wherein the serum identification sensor is an electrochemical sensor, thrombin is provided in the serum identification sensor, whether the serum is serum or not is determined according to whether fibrinogen activating the thrombin is contained, the enzyme activity unit of the thrombin is 10-1000U, the serum identification sensor is one of a screen-printed carbon electrode, a vapor-deposited silver electrode or a sputtered gold electrode, and the thrombin is collected on the surface of the electrode in a polymer grafting, macromolecule embedding or chemical bond adsorption manner.

5. The blood sample type identification and detection system according to claim 1, wherein the serum identification sensor is an optical sensor, thrombin is provided in the serum identification sensor, whether the serum is contained or not is determined according to whether fibrinogen activating the thrombin, the enzyme activity unit of the thrombin is 100U-1000U, the thrombin is solidified in the detection window of the serum identification sensor, and the thrombin solidification area is greater than or equal to the detection window area of the serum identification sensor.

6. The blood sample type identification and detection system according to claim 1, wherein the plasma identification sensor is an electrochemical sensor attached with an ion selective membrane, the plasma identification sensor is one of a screen-printed carbon electrode, an evaporated silver electrode or a sputtered gold electrode, the ion selective membrane is covered on the surface of the electrode in a spot membrane drying manner, and the ion intensity in the blood sample is measured by a cyclic voltammetry method in an electrochemical method;

the ion selective membrane is selectively permeable to ions of valence 1 and is used to determine the ionic strength of monovalent cations in a blood sample.

7. The blood sample type identification and detection system of claim 6, wherein when the valence ion is higher than 1 in the blood sample, the ion passage is realized by changing the size of the air gap of the ion selective membrane and the valence group of the electrostatic exchange.

8. The blood sample type identification and detection system according to claim 1, wherein the blood sample type identification sensor is an optical sensor, thrombin is provided in the blood sample identification sensor, whether the blood sample is plasma or not is determined according to whether fibrinogen activating the thrombin is contained, the enzyme activity unit of the thrombin is 100U-1000U, the thrombin is solidified in a detection window of the blood sample identification sensor, and the thrombin solidification area is larger than or equal to the detection window area of the blood sample identification sensor.

9. The blood sample type identification and detection system according to claim 1, wherein the signals collected by the whole blood signal collection circuit, the serum signal collection circuit and the plasma signal collection circuit are one or two of optical signals or electrical signals; the blood sample type is identified as whole blood, serum or plasma from the collected signals.

10. The blood sample type identification and detection system of any one of claims 1 to 9, integrated into an immuno lateral flow assay system or a microfluidic immuno assay system.

Technical Field

The invention relates to a blood sample type identification and detection system, and belongs to the technical field of medical in-vitro diagnosis.

Background

Clinically, sample preservation means such as anticoagulation, procoagulant and the like are widely applied. Different sample processing methods have different degrees of influence on clinical detection results, wherein the influence on sample matrix effect and instrument signal acquisition is reflected. In an immunoassay system, an antigen-antibody immune reaction is susceptible to conditions such as ion concentration, pH, hematocrit and the like, and therefore, the response of the immune reaction to a sample type is particularly obvious.

The collection and separation of blood samples is of great importance in clinical testing, and is one of the key links in quality control before diagnostic analysis. The type of a sample needs to be specified before the traditional immunodiagnosis, so that the sample collection cost before the diagnosis and analysis is improved invisibly, and the application range of a diagnosis method is easy to limit.

Disclosure of Invention

Aiming at the defects in the prior art, the invention provides a blood sample type identification and detection system which can be used for judging the type of a blood sample before an immunodetection system works so as to meet the judgment requirements of detection of different items.

The technical scheme for solving the technical problems is as follows: a blood sample type identification and detection system comprises a sample carrier, a whole blood identification unit, a plasma identification unit and a serum identification unit, wherein a sample channel is formed on the sample carrier;

when the whole blood identification unit, the plasma identification unit and the serum identification unit exist simultaneously, the sample introduction end of the sample channel is connected with the whole blood identification unit, the tail end of the sample channel is connected with the plasma identification unit, and the tail end of the sample channel is connected with the serum identification unit;

the whole blood identification unit comprises a whole blood identification sensor and a whole blood signal acquisition circuit, the whole blood identification sensor is arranged in the sample channel, and the whole blood signal acquisition circuit is connected with the whole blood identification sensor;

the plasma identification unit comprises a plasma identification sensor and a plasma signal acquisition circuit, the plasma identification sensor is arranged in the sample channel, and the plasma signal acquisition circuit is connected with the plasma identification sensor;

the serum identification unit comprises a serum identification sensor and a serum signal acquisition circuit, the serum identification sensor is arranged in the sample channel, and the serum signal acquisition circuit is connected with the serum identification sensor.

As a preferable scheme of the blood sample type identification detection system, the whole blood identification sensor adopts an electrochemical sensor, the whole blood identification sensor identifies the impedance in the whole blood sample and substitutes a standard impedance curve for fitting to obtain the hematocrit, the existence and the quantity of red blood cells in the whole blood sample are reflected according to the hematocrit, and the whole blood identification sensor adopts one of a screen printing carbon electrode, a vapor deposition silver electrode or a sputtering gold electrode.

As a preferable scheme of the blood sample type identification detection system, the whole blood identification sensor adopts an optical sensor, obtains the hematocrit by identifying the light transmittance or red spectrum light absorption rate of the whole blood sample, and reflects the existence and the quantity of red blood cells in the whole blood sample according to the hematocrit.

The serum identification sensor adopts an electrochemical sensor, thrombin is arranged in the serum identification sensor, whether the serum identification sensor is serum or not is judged according to whether fibrinogen activating the thrombin is contained or not, the enzyme activity unit of the thrombin is 10U-1000U, the serum identification sensor adopts one of a screen printing carbon electrode, a vapor deposition silver electrode or a sputtering gold electrode, and the thrombin is integrated on the surface of the electrode in a polymer grafting, macromolecule embedding or chemical bond adsorption mode.

The preferable scheme of the blood sample type identification and detection system is that the serum identification sensor adopts an optical sensor, thrombin is arranged in the serum identification sensor, whether the serum is serum or not is judged according to whether fibrinogen activating the thrombin is contained, the enzyme activity unit of the thrombin is 100U-1000U, the thrombin is solidified in a detection window of the serum identification sensor, and the solidification area of the thrombin is larger than or equal to the area of the detection window of the serum identification sensor.

As a preferred scheme of the blood sample type identification and detection system, the plasma identification sensor adopts an electrochemical sensor attached with an ion selective membrane, the plasma identification sensor adopts one of a screen printing carbon electrode, a vapor deposition silver electrode or a sputtering gold electrode, the ion selective membrane covers the surface of the electrode in a spot membrane drying mode, and the ion intensity in the blood sample is measured by adopting a cyclic voltammetry method in an electrochemical method;

the ion selective membrane is selectively permeable to ions of valence 1 and is used to determine the ionic strength of monovalent cations in a blood sample.

As a preferable aspect of the blood sample type identification detection system, when a valence ion higher than 1 is present in the blood sample, the ion passage is achieved by changing the void size of the ion selective membrane and the valence group of the electrostatic exchange.

The blood sample type identification detection system preferably adopts an optical sensor, thrombin is arranged in the plasma identification sensor, whether the plasma is blood plasma or not is judged according to whether fibrinogen activating the thrombin is contained or not, the enzyme activity unit of the thrombin is 100U-1000U, the thrombin is solidified in a detection window of the plasma identification sensor, and the solidification area of the thrombin is larger than or equal to the area of the detection window of the plasma identification sensor.

As a preferred scheme of the blood sample type identification and detection system, the signals collected by the whole blood signal collection circuit, the serum signal collection circuit and the plasma signal collection circuit are one or two of optical signals or electric signals; the blood sample type is identified as whole blood, serum or plasma from the collected signals.

As a preferable scheme of the blood sample type identification detection system, the system is integrated into an immune lateral chromatography test system or a microfluidic immune test system.

The invention has wide application capability, can meet the requirements of judging the types of blood samples detected by different items, can be realized by only replacing the width of a sample channel when immunodetection needs different fluxes, and does not need to change three test units of an identification system. After the different sample identification units are adopted, manufacturers can produce the sample identification system according to different requirements, the sample types do not need to be selected according to different projects, and the use cost can be greatly reduced.

Drawings

In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings used in the description of the embodiments or the prior art will be briefly described below. It should be apparent that the drawings in the following description are merely exemplary, and that other embodiments can be derived from the drawings provided by those of ordinary skill in the art without inventive effort.

FIG. 1 is a schematic diagram of a blood sample type identification and detection system according to an embodiment of the present invention;

FIG. 2 is a schematic diagram of a whole blood identification unit in the blood sample type identification and detection system provided by the embodiment of the invention;

FIG. 3 is a schematic diagram of a serum identification unit in the blood sample type identification and detection system according to an embodiment of the present invention;

fig. 4 is a schematic diagram of a plasma identification unit in the blood sample type identification and detection system according to the embodiment of the present invention.

In the figure, 1, sample carrier; 2. a sample channel; 3. a whole blood discrimination unit; 4. a serum identification unit; 5. a plasma identification unit; 6. a whole blood identification sensor; 7. a whole blood signal collection circuit; 8. a serum identification sensor; 9. a serum signal acquisition circuit; 10. a plasma recognition sensor; 11. a plasma signal collection circuit; 12. thrombin; 13. an ion selective membrane.

Detailed Description

In order to make the aforementioned objects, features and advantages of the present invention comprehensible, embodiments accompanied with figures are described in detail below. In the following description, numerous specific details are set forth in order to provide a thorough understanding of the present invention. This invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein.

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. The terminology used herein in the description of the invention is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. As used herein, the term "and/or" includes any and all combinations of one or more of the associated listed items.

Referring to fig. 1, fig. 2, fig. 3 and fig. 4, a blood sample type identification and detection system is provided, which includes a sample carrier 1, a sample channel 2 formed on the sample carrier 1, a whole blood identification unit 3, a serum identification unit 4 and a plasma identification unit 5, wherein a sample introduction end of the sample channel 2 is connected to the whole blood identification unit 3, the sample channel 2 is connected to the plasma identification unit 5 at a terminal of the whole blood identification unit 3, and the sample channel 2 is connected to the serum identification unit 4 at a terminal of the plasma identification unit 5; the whole blood identification unit 3 comprises a whole blood identification sensor 6 and a whole blood signal collection circuit 7, the whole blood identification sensor 6 is arranged in the sample channel 2, and the whole blood signal collection circuit 7 is connected with the whole blood identification sensor 6; the serum identification unit 4 comprises a serum identification sensor 8 and a serum signal acquisition circuit 9, the serum identification sensor 8 is arranged in the sample channel 2, and the serum signal acquisition circuit 9 is connected with the serum identification sensor 8; the plasma identification unit 5 comprises a plasma identification sensor 10 and a plasma signal acquisition circuit 11, wherein the plasma identification sensor 10 is arranged in the sample channel 2, and the plasma signal acquisition circuit 11 is connected with the plasma identification sensor 10.

In one embodiment of the blood sample type identification and detection system, the whole blood identification sensor 6 is an electrochemical sensor, the whole blood identification sensor 6 obtains the hematocrit by identifying the impedance of the whole blood sample and fitting the impedance into a standard impedance curve, the presence and the number of red blood cells in the whole blood sample are reflected according to the hematocrit, and the whole blood identification sensor 6 is one of a screen-printed carbon electrode, a silver-evaporated electrode or a gold-sputtered electrode.

Specifically, the main difference between whole blood, plasma and serum is represented by the presence of hematocrit, which can generate a background signal and reduce the sample volume, and the influence of the presence of erythrocytes on the detection signal of the immunoassay system can be effectively calibrated by identifying the hematocrit.

In one embodiment of the blood sample type identification detection system, the whole blood identification sensor 6 is an optical sensor, and the whole blood identification sensor 6 obtains the hematocrit by identifying the light transmittance or red spectrum light absorption of the whole blood sample, and reflects the presence and quantity of red blood cells in the whole blood sample according to the hematocrit.

Specifically, the hematocrit can be measured independently by an electrochemical sensor or an optical sensor or in a cooperative measurement manner. The electrochemical sensor substitutes a standard impedance curve by identifying the impedance in the blood sample, and the hematocrit is obtained by fitting. The optical sensor obtains the hematocrit by recognizing the light transmittance or red spectrum light absorption of the blood sample. The effective correction range of the hematocrit sensor is 10% -80%.

In an embodiment of the blood sample type identification and detection system, the serum identification sensor 8 is an electrochemical sensor, thrombin 12 is arranged in the serum identification sensor 8, whether the serum is serum or not is determined according to whether fibrinogen activating the thrombin 12 is contained or not, the enzyme activity unit of the thrombin 12 is 10U-1000U, the serum identification sensor 8 adopts one of a screen printing carbon electrode, a vapor deposition silver electrode or a sputtering gold electrode, and the thrombin 12 is collected on the surface of the electrode in a polymer grafting, macromolecule embedding or chemical bond adsorption mode.

In an embodiment of the blood sample type identification and detection system, the serum identification sensor 8 is an optical sensor, thrombin 12 is disposed in the serum identification sensor 8, whether the serum is serum or not is determined according to whether fibrinogen activating the thrombin 12 is included, the enzyme activity unit of the thrombin 12 is 100U-1000U, the thrombin 12 is solidified in a detection window of the serum identification sensor 8, and the solidification area of the thrombin 12 is greater than or equal to the detection window area of the serum identification sensor 8.

One difference between serum and plasma, whole blood, is the absence of fibrinogen. It is well known that the presence of thrombin 12 converts fibrinogen into a fibrin clot. In the differentiation of whole blood, plasma and serum, only when the serum sample fails to activate the thrombin 12 in the serum recognition sensor 8, both the plasma and the whole blood activate the thrombin 12 system due to the presence of fibrinogen, and a fibrin clot is formed. Due to the fibrin clot, the current intensity and light transmittance of the blood sample will change. During the process of thrombin 12 catalyzing fibrinogen coagulation, the sample has an index change tendency that impedance is increased and then decreased due to clot formation, and the light transmittance is gradually increased along with the formation of fibrin clot.

Specifically, the thrombin 12 needs to be collected on the electrode surface by polymer grafting, macromolecule embedding and chemical bond adsorption, and similarly, the thrombin 12 should be solidified in the detection window of the optical sensor. The area covered by the thrombin 12 should be less than or equal to the area covered by the electrochemical sensor, except that the area of the thrombin 12 cured should be greater than or equal to the area within the optical sensor window. The whole blood sample and the plasma sample have obvious difference in the electrochemical sensor and the optical sensor due to the existence of blood cells and the clot generated by the fibrinogen under the catalysis of the thrombin 12, and the electrochemical curve and the light transmittance can be obviously distinguished.

In one embodiment of the blood sample type identification and detection system, the plasma identification sensor 10 is an electrochemical sensor attached with an ion selective membrane 13, the plasma identification sensor 10 is one of a screen-printed carbon electrode, a vapor-deposited silver electrode or a sputtered gold electrode, the ion selective membrane 13 is covered on the surface of the electrode in a spot membrane drying manner, and the ion intensity in the blood sample is measured by adopting a cyclic voltammetry method in an electrochemical method; the ion selective membrane 13 is selectively permeable to 1 valent ions and is used to determine the ionic strength of monovalent cations in a blood sample.

Plasma is an extracellular matrix of blood, and whole blood after anticoagulation treatment is whole blood, and a yellowish liquid obtained after centrifugation to remove blood cells is plasma. The common anticoagulant comprises ethylene diamine tetraacetic acid, sodium oxalate, heparin and sodium citrate, the ion strength of the anticoagulant in blood is 1.0 mg/ml-200 mg/ml, the original ionic environment of a blood sample mainly comprises potassium, sodium, calcium and the like, and the ionic environment of potassium: 3.5-5.5 mmol/L; sodium: 135-150 mmol/L; calcium: 2.25-2.75 mmol/L, namely the ionic strength of the blood sample is about 5mg/ml, so the influence of the anticoagulant on the ionic strength of the blood sample is obvious.

Specifically, the ion selective membrane 13 is a membrane that selectively transmits 1-valent ions, and the strength of monovalent cation ions in a blood sample can be measured. Sodium ions and lithium ions carried by anticoagulant in blood are selectively measured through the functions of void, electrostatic exchange and diffusion, the electronic strength in the blood is judged, the electronic strength is transmitted to a calibration system through signal acquisition line conduction, and the detection result is corrected properly through a preset calibration scheme.

In one embodiment of the blood sample type identification detection system, when a valence ion higher than 1 is present in the blood sample, the ion passage is achieved by changing the void size of the ion selective membrane 13 and the electrostatically exchanged valence groups. The electrochemical sensor ion selective membrane 13 for plasma sample identification preferentially passes 1 valent cations, such as ions exhibiting other valences, by altering the void size and the valency groups electrostatically exchanged. Since the ionic strength of whole blood interferes with the results, the correction factor for hematocrit needs to be considered.

In an embodiment of the blood sample type identification and detection system, the plasma identification sensor 10 is an optical sensor, the plasma identification sensor 10 is provided with thrombin 12, whether the plasma is plasma or not is determined according to whether fibrinogen activating the thrombin 12 is contained or not, the enzyme activity unit of the thrombin 12 is 100U-1000U, the thrombin 12 is solidified in a detection window of the plasma identification sensor 10, and the solidification area of the thrombin 12 is greater than or equal to the area of the detection window of the plasma identification sensor 10.

In one embodiment of the blood sample type identification and detection system, the signals collected by the whole blood signal collection circuit 7, the serum signal collection circuit 9 and the plasma signal collection circuit 11 are one or two of optical signals or electrical signals; the blood sample type is identified as whole blood, serum or plasma from the collected signals.

Specifically, when whole blood, plasma and serum are identified, the same signal of optical signals and electric signals or a combination of multiple signals can be used, for example, the electric signals are used by the whole blood identification unit 3, the serum identification unit 4 and the plasma identification unit 5, wherein the whole blood identification unit 3 determines the hematocrit according to the impedance, the plasma identification unit 5 determines the ionic strength of the blood sample through the ion selective membrane 13, and the plasma identification unit 5 determines whether fibrinogen exists in the sample through an electrochemical sensor. In addition, the whole blood discrimination unit 3, the serum discrimination unit 4, and the plasma discrimination unit 5 may all use optical signals, wherein the whole blood discrimination unit 3 determines the ion intensity in the blood sample through the light transmittance or the red spectrum light absorption rate, the plasma discrimination unit 5 determines the ion intensity in the blood sample through the ion selective membrane 13, and the serum discrimination unit 4 determines the light transmittance of the fibrin clot through the optical sensor.

Specifically, the whole blood discrimination unit 3, the serum discrimination unit 4, and the plasma discrimination unit 5 may all be used to determine whole blood, serum, and plasma, respectively. The whole blood recognition unit 3 and the plasma recognition unit 5 can be used in combination, and the hematocrit of 0% and the blood sample having an ionic strength of 4.0 to 6.0mg/ml are serum samples, which can be estimated from the hematocrit size and the sample ionic strength.

Specifically, the serum discrimination unit 4 and the plasma discrimination unit 5 may be used in combination, and the type of the sample of plasma and serum may be determined by measurement of fibrinogen and determination of ionic strength, and whether the type of the sample is whole blood may be determined by formation of fibrin clot into an electrochemical curve.

In the first application of the technical scheme, the whole blood identification unit 3, the serum identification unit 4 and the plasma identification unit 5 are all used, the whole blood identification sensor 6, the serum identification sensor 8 and the plasma identification sensor 10 respectively adopt electrochemical sensors, the electrochemical sensors respectively adopt three conditions of screen printing carbon electrodes, evaporation silver electrodes and sputtering gold electrodes, and the thrombin 12 in the serum identification sensor 8 is integrated on the surface of the electrodes in a polymer grafting, macromolecule embedding or chemical bond adsorption mode. In the plasma identification sensor 10, the ion selective membrane 13 is solidified through membrane spotting, drying and electrochemical sensors, and the prepared blood sample type identification and detection system is integrated into an immune lateral chromatography test system and a microfluidic immune test system, and 120 samples, 39 whole blood samples, 39 plasma samples and 42 serum samples are selected. The test results are as follows:

screen printing carbon electrode	Whole blood sample	Plasma sample	Serum sample
				Number of test cases	39	39	42
Rate of agreement	100％	100％	100％
				Number of packed red blood cellsMeasurement of	39	0	0
Silver evaporation plated electrode	Whole blood sample	Plasma sample	Serum sample
				Number of test cases	39	39	42
Rate of agreement	100％	100％	100％
				Hematocrit count	39	0	0
Sputtering gold electrode	Whole blood sample	Plasma sample	Serum sample
				Number of test cases	39	39	42
Rate of agreement	100％	100％	100％
				Hematocrit count	39	0	0

It can be seen that the whole blood identification sensor 6, the serum identification sensor 8 and the plasma identification sensor 10 adopt electrochemical sensors and any one of screen printing carbon electrodes, evaporation silver electrodes and sputtering gold electrodes, the accuracy of the type identification detection result of the blood sample of a previously known type is 100%, and in addition, the hematocrit can be accurately measured.

In the second application of the technical scheme, the whole blood identification unit 3, the serum identification unit 4 and the plasma identification unit 5 are all used, the whole blood identification sensor 6, the serum identification sensor 8 and the plasma identification sensor 10 adopt optical sensors, the optical sensors are made of high-light-transmittance glass, quartz and PC materials to prepare light-transmitting windows, and the prepared blood sample type identification and detection system is integrated into an immune lateral chromatography test system and a microfluidic immune test system, and 120 samples, 39 samples of the whole blood sample, 39 samples of the plasma sample and 42 samples of the serum sample are selected. The test results are as follows:

optical sensor	Whole blood sample	Plasma sample	Serum sample
				Number of test cases	39	39	42
Rate of agreement	100％	100％	100％
				Hematocrit count	39	0	0

As can be seen, the whole blood recognition sensor 6, the serum recognition sensor 8, and the plasma recognition sensor 10 employ optical sensors, and the accuracy of the type recognition detection result of a blood sample of a previously known type is 100%, and in addition, the hematocrit can be accurately measured.

In the third application of the technical scheme, only the whole blood identification unit 3 and the plasma identification unit 5 are used, the whole blood identification sensor 6 adopts an optical sensor, the plasma identification sensor 10 adopts an electrochemical sensor, the electrochemical sensor adopts three conditions of a screen printing carbon electrode, a silver evaporation electrode and a gold sputtering electrode, the optical sensor prepares a light-transmitting window by using high-light-transmittance glass, quartz and PC materials, and the prepared blood sample type identification and detection system is integrated into an immune lateral chromatography test system and a microfluidic immune test system, and 120 samples, 39 whole blood samples, 39 plasma samples and 42 serum samples are selected. The test results are as follows:

it can be seen that the whole blood identification sensor 6 adopts an optical sensor, the plasma identification sensor 10 adopts an electrochemical sensor, and the electrochemical sensor respectively adopts three situations of a screen printing carbon electrode, a vapor deposition silver electrode and a sputtering gold electrode, so that the accuracy of the type identification detection result of the blood sample of a known type in advance is 100%, and in addition, the hematocrit can be accurately measured.

In the fourth application of the technical scheme of the invention, only the serum identification unit 4 and the plasma identification unit 5 are used, the serum identification sensor 8 and the plasma identification sensor 10 respectively adopt electrochemical sensors, the electrochemical sensors respectively adopt three conditions of screen printing carbon electrodes, evaporation silver electrodes and sputtering gold electrodes, the prepared blood sample type identification and detection system is integrated into an immune lateral chromatography test system and a microfluidic immune test system, and 120 samples, 39 whole blood samples, 39 plasma samples and 42 serum samples are selected. The test results are as follows:

it can be seen that the serum identification sensor 8 and the plasma identification sensor 10 respectively adopt electrochemical sensors, the electrochemical sensors adopt any one of screen printing carbon electrodes, evaporation silver electrodes and sputtering gold electrodes, the accuracy rate of the type identification detection result of the blood sample of a known type in advance is 100%, and in addition, the hematocrit can be accurately measured.

The technical features of the embodiments described above may be arbitrarily combined, and for the sake of brevity, all possible combinations of the technical features in the embodiments described above are not described, but should be considered as being within the scope of the present specification as long as there is no contradiction between the combinations of the technical features.

The above-mentioned embodiments only express several embodiments of the present invention, and the description thereof is more specific and detailed, but not construed as limiting the scope of the invention. It should be noted that, for a person skilled in the art, several variations and modifications can be made without departing from the inventive concept, which falls within the scope of the present invention. Therefore, the protection scope of the present patent shall be subject to the appended claims.