Airflow management for evaporator devices
阅读说明:本技术 用于蒸发器装置的气流管理 (Airflow management for evaporator devices ) 是由 A·阿特金斯 A·鲍恩 S·克里斯滕森 N·J·哈顿 E·利昂迪盖 J·蒙西斯 C·J· 于 2019-07-23 设计创作,主要内容包括:本申请公开了一种蒸发装置,包括具有容纳可蒸发材料的贮器、加热元件和芯吸元件的料盒,所述芯吸元件能够将可蒸发材料吸到加热元件以被蒸发。芯吸元件可包括与贮器接触的两个端部。料盒可包括用于控制料盒中气流的气流控制特征。(An evaporation device includes a cartridge having a reservoir containing an evaporable material, a heating element, and a wicking element capable of drawing the evaporable material to the heating element to be evaporated. The wicking element may include two ends in contact with the reservoir. The cartridge may comprise an air flow control feature for controlling the air flow in the cartridge.)
1. A cartridge for an evaporator device, the cartridge comprising:
a receptacle chamber defined by a receptacle barrier, the receptacle chamber configured to hold a liquid vaporizable material;
an evaporation chamber in fluid communication with the pocket chamber and comprising a wicking element configured to draw the liquid vaporizable material from the pocket chamber to the evaporation chamber to be evaporated by a heating element;
an air flow passage extending through the evaporation chamber;
an air flow control feature for controlling a storage pressure in the reservoir chamber.
2. The cartridge of claim 1, wherein the airflow control feature comprises a fluid passage extending between the reservoir chamber and the airflow passage.
3. The cartridge of claim 2, wherein the diameter of the fluid channel is sized to allow surface tension of the liquid vaporizable material to prevent the liquid vaporizable material from passing through the fluid channel when the reservoir pressure is about the same as the second pressure along the air flow channel.
4. The cartridge of claim 3, wherein the diameter is sized to allow the surface tension of the liquid vaporizable material to be broken when the storage pressure is less than the second pressure along the airflow passage, thereby allowing a volume of air to pass through the airflow control feature and into the reservoir chamber.
5. The cartridge of claim 1, wherein the airflow control feature comprises a check valve or a duckbill valve.
6. The cartridge of claim 2, wherein the airflow control feature comprises a coating comprising a venting material extending over the opening of the fluid channel.
7. The cartridge of claim 6, wherein the coating comprises a Polytetrafluoroethylene (PTFE) material.
8. The cartridge of claim 1, wherein the airflow control feature comprises one or more of a diaphragm, a valve, and a pump.
9. The cartridge of claim 1, wherein the airflow control feature comprises a vent channel extending along at least one side of a wicking housing containing the evaporation chamber, wherein the vent channel extends between the reservoir chamber and the evaporation chamber.
10. The cartridge of claim 1, wherein the airflow control feature comprises a vent channel extending through a wicking housing containing the evaporation chamber, wherein the vent channel extends between the reservoir chamber and the evaporation chamber.
11. The cartridge of claim 1, further comprising a pressure sensor configured to detect a pressure along the airflow channel.
12. The cartridge of claim 1, further comprising a secondary channel configured to draw air through a portion of the cartridge, the secondary channel configured to merge with the airflow channel downstream of the evaporation chamber.
13. The cartridge of claim 1, further comprising a pressure sensing channel extending between the cartridge outlet and the pressure sensor, the pressure sensing channel being separate from the air flow channel.
14. The cartridge according to claim 1, further comprising an inlet located along a first side of the cartridge and an outlet located along a second side of the cartridge, the air flow channel extending between the inlet and the outlet, the inlet and the outlet being located along the first side and the second side, respectively, such that the inlet and the outlet are open when the cartridge is inserted into the evaporator device body in the first position and closed when the cartridge is inserted into the evaporator device body in the second position.
15. The cartridge of claim 1, wherein the wicking element comprises a flat configuration including at least one pair of opposing sides extending parallel to each other.
16. A method, comprising:
allowing the airflow to pass through an evaporation chamber of the evaporator device, thereby combining the airflow with an aerosol formed in the evaporation chamber by evaporating liquid vaporizable material drawn from a porous wick extending between the evaporation chamber and a reservoir chamber containing the liquid vaporizable material;
drawing the liquid vaporizable material from the reservoir chamber to the vaporization chamber along the porous wick, thereby creating a first pressure within the reservoir chamber that is less than a second pressure in an area outside the reservoir chamber;
breaking the surface tension of the liquid vaporizable material along a vent passage extending between the receptacle chamber and an area outside the receptacle chamber, thereby allowing a volume of air to enter the receptacle chamber from the vent passage; and
the first pressure in the reservoir chamber is increased such that the first pressure is substantially equal to the second pressure.
17. The method of claim 16, further comprising preventing passage of fluid along the vent passage due to the first pressure being substantially equal to the second pressure.
18. The method of claim 17, wherein the preventing is controlled by a fluid tension of the vaporizable fluid.
19. The method of claim 18, wherein the vaporizable fluid comprises at least one of a liquid vaporizable material and air.
20. The method of claim 17, wherein the airflow control feature comprises a vent channel extending through a wicking housing containing the evaporation chamber.
21. The method of claim 20, wherein the airflow control feature comprises a fluid passage extending between the reservoir chamber and the airflow passage.
Technical Field
The subject matter described herein relates to vaporizer devices, including portable vaporizer devices for generating an inhalable aerosol from one or more vaporizable materials.
Background
A vaporizer device, which may also be referred to as a vaporizer, an electronic vaporizer device, or an E-vaporizer device, may be used to deliver an aerosol (or "vapor") containing one or more active ingredients by inhalation of the aerosol by a user of the vaporizer device. For example, Electronic Nicotine Delivery Systems (ENDS) include a class of vaporizer devices that are battery powered and can be used to simulate the experience of smoking tobacco, but do not burn tobacco or other substances.
In use of the vaporizer device, the user inhales an aerosol, commonly referred to as a vapor, which may be generated by a heating element that vaporizes (e.g., at least partially converts a liquid or solid to a vapor phase) a vaporizable material, which may be a liquid, a solution, a solid, a wax, or any other form, so long as it is compatible with the use of the particular vaporizer device. The vaporizable material used with the vaporizer can be disposed within a cartridge (e.g., a detachable portion of the vaporizer that contains the vaporizable material in a reservoir) that includes a mouthpiece (e.g., for inhalation by a user).
To receive the inhalable aerosol generated by the vaporizer device, in some examples, the user may activate the vaporizer device by applying a puff, by pressing a button, or by some other method. As the term is commonly used (and is also used herein), inhalation refers to the user inhaling in a manner that causes a volume of air to be drawn into the vaporizer device, thereby creating an inhalable aerosol by the combination of vaporized vaporizable material and air.
A typical method of a vaporizer device for generating an inhalable aerosol from a vaporizable material includes heating the vaporizable material in a vaporization chamber (or heater chamber) to convert the vaporizable material into a vapor (or vapor) phase. A vaporization chamber generally refers to an area or volume in a vaporization apparatus in which a heat source (e.g., conductive, convective, and/or radiant) causes heating of a vaporizable material to produce a mixture of air and vaporized vaporizable material to form a vapor for inhalation by a user of the vaporization apparatus.
In some vaporizer device embodiments, the vaporizable material can be withdrawn from the reservoir or reservoir chamber and enter the vaporization chamber through a wicking element (wick). This process of drawing the vaporizable material into the vaporization chamber can be due, at least in part, to the capillary action provided by the wick, which pulls the vaporizable material along the wick in the direction of the vaporization chamber. However, as the vaporizable material is drawn out of the reservoir, the pressure within the reservoir decreases, thereby creating a vacuum and resisting capillary action. This can reduce the efficiency with which the wick draws the vaporizable material into the vaporization chamber, for example, when a user draws on the vaporization device, thereby reducing the efficiency with which the vaporization device vaporizes a desired amount of vaporizable material. Furthermore, the vacuum created in the reservoir eventually results in the inability to draw all of the vaporizable material into the vaporization chamber, thereby wasting the vaporizable material. Accordingly, there is a need for an improved evaporation device and/or evaporation cartridge that ameliorates or overcomes these problems.
The term "vaporizer apparatus" as used herein in accordance with the present subject matter generally refers to a portable, self-contained apparatus that is convenient for personal use. Typically, such devices are controlled by one or more switches, buttons, touch-sensitive devices or other user input functions or the like (which may be generally referred to as controls) on the vaporizer, although a number of devices (e.g., smartphones, smartwatches, other wearable electronic devices, etc.) that can wirelessly communicate with external controllers have recently become available. In this context, control generally refers to the ability to affect one or more of various operating parameters, which may include, but is not limited to, any of turning a heater on and/or off, adjusting a minimum and/or maximum temperature to which the heater is heated during operation, various game or other interactive features of a user accessible device, and/or other operations.
Disclosure of Invention
In certain aspects of the present subject matter, challenges associated with the presence of liquid vaporizable material in or near certain susceptible components of an electronic vaporizer device may be addressed by including one or more of the features described herein or equivalent/equivalent methods as will be understood by those of ordinary skill in the art. Aspects of the present subject matter relate to methods and systems for managing airflow in an evaporator unit.
In one aspect, embodiments of a cartridge for an evaporator device are described. The cartridge may comprise a pocket chamber defined by a pocket barrier. The receptacle chamber may be configured to hold a liquid vaporizable material. The cartridge may further include an evaporation chamber in fluid communication with the reservoir chamber, and include a wicking element configured to draw liquid vaporizable material from the reservoir chamber to the evaporation chamber for evaporation by the heating element. The cartridge may further comprise an air flow channel extending through the evaporation chamber and an air flow control feature for controlling the storage pressure in the reservoir chamber.
In some variations, one or more of the following features may optionally be included in any feasible combination. The air flow control feature may include a fluid passage extending between the reservoir chamber and the air flow passage. The diameter of the fluid channel is sized to allow a surface tension of the liquid vaporizable material to prevent the liquid vaporizable material from passing through the fluid channel when the reservoir pressure is about the same as the second pressure along the air flow channel. The diameter may be sized to allow the surface tension of the liquid vaporizable material to be broken when the storage pressure is less than the second pressure along the airflow passageway, thereby allowing a volume of air to pass through the airflow control feature and into the reservoir chamber.
In some embodiments, the air flow control feature may comprise a check valve or a duckbill valve. The airflow control feature may include a coating including a venting material attached to extend over the opening of the fluid passage. The coating may include a Polytetrafluoroethylene (PTFE) material. The airflow control features may include one or more of a diaphragm, a valve, and a pump. The air flow control feature may include a vent channel extending along at least one side of the wicking housing containing the evaporation chamber, and the vent channel may extend between the reservoir chamber and the evaporation chamber. The air flow control feature may include a vent channel extending through a wicking housing containing the evaporation chamber, and the vent channel may extend between the reservoir chamber and the evaporation chamber.
In some embodiments, the cartridge may further comprise a pressure sensor configured to sense pressure along the air flow channel. The cartridge may further comprise an auxiliary channel configured to draw air through a portion of the cartridge, and the auxiliary channel may be configured to merge with the airflow channel downstream of the evaporation chamber. The cartridge may further comprise a pressure sensing channel extending between the outlet of the cartridge and the pressure sensor, and the pressure sensing channel may be separate from the air flow channel.
The cartridge may further comprise an inlet located along a first side of the cartridge and an outlet located along a second side of the cartridge. The air flow path may extend between the inlet and the outlet, and the inlet and the outlet may be located along the first side and the second side, respectively, such that the inlet and the outlet are open when the cartridge is inserted into the evaporator device body in the first position and closed when the cartridge is inserted into the evaporator device body in the second position. The wicking element may comprise a flat configuration including at least one pair of opposing sides extending parallel to one another.
In another related aspect of the present subject matter, a method includes allowing an airflow to pass through an evaporation chamber of an evaporator device, thereby combining the airflow with an aerosol formed in the evaporation chamber. The aerosol may be formed by evaporating a liquid vaporizable material drawn from a porous wick extending between an evaporation chamber and a reservoir chamber containing the liquid vaporizable material. The method may further include drawing the liquid vaporizable material from the reservoir chamber to the vaporization chamber along the porous wick, thereby creating a first pressure within the reservoir chamber that is less than a second pressure in an area outside the reservoir chamber. Further, the method may include breaking the surface tension of the liquid vaporizable material along a vent passage extending between the receptacle chamber and an area outside the receptacle chamber, thereby allowing a volume of air to enter the receptacle chamber from the vent passage. Additionally, the method may include increasing the first pressure in the reservoir chamber such that the first pressure is approximately equal to the second pressure.
In some embodiments, the method may further include preventing passage of fluid along the vent passage due to the first pressure being substantially equal to the second pressure. This prevention may be controlled by the fluid tension of the vaporizable fluid. The vaporizable fluid can include at least one of a liquid vaporizable material and air. The airflow control feature may include a vent channel extending through a wicking housing containing the evaporation chamber. The air flow control feature may include a fluid passage extending between the reservoir chamber and the air flow passage.
The details of one or more variations of the subject matter described herein are set forth in the accompanying drawings and the description below. Other features and advantages of the subject matter described herein will be apparent from the description and drawings, and from the claims.
Drawings
The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate certain aspects of the subject matter disclosed herein and together with the description, help explain some of the principles associated with the disclosed implementations. In the drawings:
FIG. 1A shows a first embodiment of an evaporator system including an evaporator apparatus having a cartridge and an evaporator apparatus body in accordance with embodiments of the present subject matter;
FIG. 1B is a top view of an embodiment of the evaporator device shown in FIG. 1A, showing the cartridge separated from the evaporator device body;
FIG. 1C is a top view of the evaporator device of FIG. 1B with the cartridge inserted into the cartridge receptacle of the evaporator device body;
FIG. 1D shows a perspective view of the evaporator apparatus of FIG. 1B;
FIG. 1E shows a perspective view of a cartridge of the evaporator device of FIG. 1B;
FIG. 1F shows another perspective view of the cartridge of FIG. 1E;
FIG. 2A shows a schematic view of a first embodiment of a reservoir system configured for an evaporator pod and/or an evaporator apparatus to improve airflow within the evaporator apparatus;
FIG. 2B shows a schematic view of a second embodiment of a reservoir system configured for an evaporator cartridge and/or an evaporator device to improve airflow within the evaporator device;
FIG. 3A shows a front view of an embodiment of a vented evaporation chamber element including a conduit vent coupled to a wicking housing;
FIG. 3B shows a front cross-sectional view of the vented evaporation chamber element of FIG. 3A;
FIG. 4A shows a front view of another embodiment of a vented evaporation chamber element comprising a channel extending through a wicking housing;
FIG. 4B shows a front cross-sectional view of the vented evaporation chamber element of FIG. 4A;
FIG. 5A shows a front view of yet another embodiment of a vented evaporation chamber element comprising a channel extending through a wicking housing;
FIG. 5B shows a front cross-sectional view of the vented evaporation chamber element of FIG. 5A;
FIG. 6A shows a top perspective view of another embodiment of a vented evaporation chamber element comprising two vent channels, each partially defined by a channel extending along the front side of the wicking housing;
FIG. 6B shows a partial view of the cartridge of FIG. 6A, showing the wicking shell and the vent;
FIG. 7A shows a top perspective view of another embodiment of a vented evaporation chamber element comprising two vent channels, each partially defined by a channel extending along one side of a wicking housing;
FIG. 7B shows a partial view of the cartridge of FIG. 7A, showing the wicking shell and the vent;
FIG. 8A shows a top perspective view of another embodiment of a vented evaporation chamber element including a vent channel defined in part by a chamfer of a wicking housing;
FIG. 8B shows a partial view of the cartridge of FIG. 8A, showing the wicking shell and the vent;
FIG. 9A shows a top perspective view of another embodiment of a vented evaporation chamber element comprising two vent channels, each partially defined by a chamfered portion of a wicking housing;
FIG. 9B shows a partial view of the cartridge of FIG. 9A, showing the wicking shell and the vent;
FIG. 10 illustrates another embodiment of a vented evaporation chamber element comprising at least one molded vent connected to and extending parallel to an airflow channel;
FIG. 11 illustrates another embodiment of a vented evaporation chamber element comprising at least one molded vent connected to and extending parallel to a wicking channel;
FIG. 12A shows a schematic of features of an evaporator cartridge with a flat wick;
FIG. 12B shows a top perspective view of the flat wick of FIG. 12A;
FIG. 13A illustrates another embodiment of an evaporator cartridge consistent with an embodiment of the present subject matter;
FIG. 13B shows a partial front view of the evaporator cartridge of FIG. 13A;
FIG. 14A shows another embodiment of an evaporator cartridge inserted into another embodiment of an evaporator device body including a pressure sensor;
FIG. 14B shows a front view of an evaporator cartridge inserted into the evaporator apparatus body of FIG. 14A;
FIG. 14C shows an exemplary schematic of a pressure sensor in the evaporator apparatus body of FIG. 14A at various locations along the air path;
FIG. 14D illustrates an exemplary coupling of the evaporator cartridge and evaporator apparatus body of FIG. 14A; and
FIG. 14E illustrates an exemplary quench air flow channel of the evaporator cartridge and evaporator apparatus body of FIG. 14A.
When used in practice, like reference numerals refer to like structures, features or elements.
Detailed Description
Embodiments of the present subject matter include devices that involve evaporating one or more materials for inhalation by a user. The term "evaporator" is used generically in the following description to refer to an evaporator device. Examples of vaporizers consistent with embodiments of the present subject matter include electronic vaporizers and the like. Such vaporizers are typically portable, hand-held devices that heat a vaporizable material to provide an inhalable dose of the material.
The vaporizable material used with the vaporizer can optionally be disposed within a cartridge (e.g., a portion of the vaporizer that contains the vaporizable material in a reservoir or other receptacle and can be refilled when empty, or disposable to facilitate a new cartridge containing additional vaporizable material of the same or a different type). The evaporator may be an evaporator using the cartridge, an evaporator without the cartridge, or a multi-purpose evaporator that can be used with or without the cartridge. For example, the multi-purpose vaporizer may include a heating chamber (e.g., an oven) configured to receive vaporizable material directly within the heating chamber, and also to receive a cartridge or other replaceable device having a reservoir, volume, or the like for at least partially containing a usable amount of vaporizable material.
In various embodiments, the vaporizer may be configured to be used with liquid vaporizable materials (e.g., carrier solutions in which active and/or inactive ingredients are suspended or held in solution or pure liquid form in the vaporizable material itself) or solid vaporizable materials. The solid vaporizable material may include plant material that emits some portion of the plant material as vaporizable material (e.g., such that some portion of the plant material remains as waste after the vaporizable material is emitted for inhalation by a user), or alternatively may be in a solid form of the vaporizable material itself (e.g., "wax") such that all solid material may ultimately be vaporized for inhalation. The liquid vaporizable material can also be completely vaporized or can include some portion of the liquid material remaining after all of the material suitable for inhalation has been consumed.
Fig. 1A-1F illustrate an
After the vaporizable material is converted to the vapor phase, and depending on the type of vaporizer, the physical and chemical properties of the vaporizable material, and/or other factors, at least some of the vapor phase vaporizable material may condense to form particulate matter that is at least partially in partial equilibrium with the vapor phase as part of an aerosol, which may form some or all of the inhalable dose provided by
Vaporizers for use with liquid vaporizable materials (e.g., pure liquids, suspensions, solutions, mixtures, etc.) typically include an atomizer 141 in which a wicking element (also referred to herein as a wick (not shown in fig. 1A), which may include any material capable of causing fluid movement by capillary pressure) delivers a quantity of liquid vaporizable material to a portion of the atomizer that includes a heating element (also not shown in fig. 1A). The wicking element is generally configured to draw liquid vaporizable material from a reservoir configured to hold (and in use can hold) the liquid vaporizable material such that the liquid vaporizable material can be vaporized by heat transferred from the heating element. The wicking element may also optionally allow air to enter the reservoir to replace the volume of liquid removed. In other words, capillary action pulls the liquid vaporizable material into the wick for vaporization by the heating element (as described below), and in some embodiments of the present subject matter, air can be returned to the reservoir through the wick to at least partially equalize the pressure in the reservoir. Other methods of allowing air back into the reservoir to equalize pressure are also within the scope of the present subject matter.
The heating element may be or include one or more of a conduction heater, a radiant heater, and a convection heater. One type of heating element is a resistive heating element, which may be constructed of or at least include a material (e.g., a metal or alloy, such as nichrome, or non-metallic resistor) configured to dissipate electrical power in the form of heat when an electrical current is passed through one or more resistive segments of the heating element. In some embodiments of the present subject matter, the atomizer may include a heating element comprising a resistive coil or other heating element wound, positioned within, integrated into the overall shape of, pressed into thermal contact with, or otherwise arranged to transfer heat to the wicking element to vaporize liquid vaporizable material drawn from the reservoir by the wicking element for subsequent inhalation by a user in a gas phase and/or a condensed phase (e.g., aerosol particles or droplets). Other wicking element, heating element, and/or atomizer assembly configurations are also possible, as discussed further below.
Certain vaporizers may also or alternatively be configured to generate an inhalable dose of a vapor-phase and/or aerosol-phase vaporizable material by heating a non-liquid vaporizable material, such as, for example, a solid-phase vaporizable material (e.g., wax, etc.) or a plant material (e.g., tobacco leaf and/or tobacco leaf portion) that contains a vaporizable material. In such vaporizers, the resistive heating element can be part of, incorporated into, or otherwise in thermal contact with, an oven or other heating chamber wall in which the non-liquid vaporizable material is placed. Alternatively, one or more resistive heating elements may be used to heat air passing through or over the non-liquid vaporizable material to cause convective heating of the non-liquid vaporizable material. In other embodiments, one or more resistive heating elements may be disposed in intimate contact with the plant material such that direct conductive heating of the plant material occurs from the bulk of the plant material (e.g., as opposed to merely by conduction inwardly from the oven walls).
The heating element may be activated (e.g., a controller, which is optionally part of an evaporator body as described below) in association with a user drawing on (e.g., drawing, inhaling, etc.) the
Activation of the heating element may be caused by automatic detection of suction based on one or more signals generated by one or more sensors 113, such as one or more pressure sensors arranged to detect pressure (or optionally measure changes in absolute pressure) along the airflow path relative to ambient pressure, one or more motion sensors of the evaporator, one or more flow sensors of the evaporator, a capacitive lip sensor of the evaporator; in response to detecting user interaction with one or more input devices 116 (e.g., buttons or other tactile control devices of the vaporizer 100), receiving a signal from a computing device in communication with the vaporizer; and/or by other methods for determining that aspiration is occurring or about to occur.
As mentioned in the preceding paragraph, a vaporizer consistent with embodiments of the present subject matter may be configured to connect (e.g., wirelessly or via a wired connection) to a computing device (or optionally two or more devices) in communication with the vaporizer. To this end, the controller 104 may include
The computing device that is part of the vaporizer system as defined above may be used for any of one or more functions, such as controlling dosage (e.g., dose monitoring, dose setting, dose limiting, user tracking, etc.), controlling sessions (e.g., session monitoring, session setting, session limiting, user tracking, etc.), controlling nicotine delivery (e.g., switching between nicotine and non-nicotine vaporizable material, adjusting the amount of nicotine delivered, etc.), obtaining location information (e.g., location of other users, retailer/commercial site location, e-cig location, relative or absolute location of the vaporizer itself, etc.), vaporizer personalization (e.g., naming the vaporizer, locking/password protecting the vaporizer, adjusting one or more parental controls, associating the vaporizer with a user group, registering the vaporizer with a manufacturer or warranty organization, etc.), or the like, Engaging in social activities with other users (e.g., games, social media communications, interacting with one or more groups, etc.), and so forth. The terms "session," "vaporizer session," or "vapor session" are generally used to refer to a period of time dedicated to the use of a vaporizer. The period may include a time period, a number of doses, an amount of vaporizable material, and the like.
In examples where the computing device provides a signal associated with activation of the resistive heating element, or in other examples where the computing device is coupled with a vaporizer to implement various controls or other functions, the computing device executes one or more sets of computer instructions to provide a user interface and underlying data processing. In one example, detection by the computing device of user interaction with one or more user interface elements may cause the computing device to send a signal to
The temperature of the resistive heating element of the evaporator may depend on a number of factors, including the amount of electrical power delivered to the resistive heating element and/or the duty cycle of the delivered electrical power, conductive heat transfer to other portions of the electronic evaporator and/or to the environment, latent heat loss due to evaporation of the vaporizable material from the wicking element and/or the atomizer as a whole, and convective heat loss due to airflow (e.g., air moving through the heating element or atomizer as a whole when a user inhales on the electronic evaporator). As described above, to reliably activate or heat the heating element to a desired temperature, in some embodiments of the present subject matter, the vaporizer may utilize a signal from a pressure sensor to determine when the user is inhaling. The pressure sensor may be located in the airflow path and/or may be connected (e.g., by a channel or other path) to the airflow path that connects the inlet for air to the device and the outlet through which the user inhales the generated vapour and/or aerosol, such that the pressure sensor experiences a change in pressure simultaneously with air passing through the evaporator device from the air inlet to the air outlet. In some embodiments of the present subject matter, the heating element may be activated in association with a user's puff, e.g., by automatic detection of the puff, e.g., by a pressure sensor that detects a pressure change in the airflow path.
In general, the pressure sensor (as well as any other sensors 113) may be located on the controller 104 (e.g., a printed circuit board assembly or other type of circuit board) or coupled (e.g., electrically or electronically connected, either physically or via a wireless connection) to the controller 104. In order to accurately make measurements and maintain the durability of the evaporator, it is beneficial to provide a resilient seal 127 to separate the airflow path from the rest of the evaporator. The seal 127, which may be a gasket, may be configured to at least partially surround the pressure sensor such that the connection of the pressure sensor to the internal circuitry of the evaporator is separate from the portion of the pressure sensor exposed to the airflow path. In the case of a cartridge-based evaporator, the seal 127 may also separate one or more electrically connected components between the
A general type of vaporizer that has gained popularity recently includes a
Cartridge-based configurations for vaporizers that generate an inhalable dose of a non-liquid vaporizable material by heating the non-liquid vaporizable material are also within the scope of the present subject matter. For example, a vaporizer cartridge may include a quantity of plant material treated and formed in direct contact with portions of one or more resistive heating elements, and such a vaporizer cartridge may be configured to be mechanically and electrically coupled to a vaporizer body that includes a processor, a power source, and electrical contacts for connecting to respective cartridge contacts to complete a circuit with the one or more resistive heating elements.
In evaporators in which the power source 112 is part of the
In some embodiments of the present subject matter, the at least two cartridge contacts and the at least two receptacle contacts may be configured to electrically connect in any of at least two orientations. In other words, by inserting the
In one example of an attachment structure for coupling the
Further to the discussion above regarding the electrical connection between the evaporator cartridge and the evaporator body, which is reversible, such that at least two rotational orientations of the evaporator cartridge in the cartridge socket are possible, in some evaporators the shape of the evaporator cartridge, or at least the shape of the end of the evaporator cartridge configured to be inserted into the cartridge socket, may have a rotational symmetry of at least 2 steps. In other words, the evaporator cartridge, or at least the insertion end of the evaporator cartridge, may be 180 ° rotationally symmetric about an axis along which the evaporator cartridge is inserted into the cartridge socket. In this configuration, the circuitry of the evaporator can support the same operation regardless of what symmetrical orientation of the evaporator cartridge occurs.
In some examples, the evaporator cartridge or at least one end of the evaporator cartridge configured to be inserted into the cartridge socket may have a non-circular cross-section transverse to an axis along which the evaporator cartridge is inserted into the cartridge socket. For example, the non-circular cross-section may be generally rectangular, generally elliptical (e.g., having a generally oval shape), non-rectangular but have two sets of parallel or generally parallel opposing sides (e.g., having a parallelogram shape), or other shapes having at least 2-order rotational symmetry. In this context, substantially having a shape indicates that substantial similarity to the described shape is apparent, but the sides of the shape in question need not be perfectly linear and the vertices need not be perfectly sharp. In the description of any non-circular cross-section referred to herein, it is contemplated that either or both of the edges or the vertices of the cross-sectional shape may be rounded.
The at least two cartridge contacts and the at least two receptacle contacts may take various forms. For example, one or both sets of contacts may include conductive pins, tabs, posts, receiving holes for pins or posts, and the like. Some types of contacts may include springs or other urging features to create better physical and electrical contact between the contacts on the vaporizer cartridge and the vaporizer body. The electrical contacts may optionally be gold plated, and/or may comprise other materials.
1B-1D illustrate an embodiment of a
Fig. 1E illustrates an
Fig. 1F shows other features that may be included in an
As shown in FIG. 1E, this configuration allows air to flow down into the
As described above, withdrawing the vaporizable material from the reservoir can create a vacuum in the reservoir, and this vacuum can reduce or prevent the capillary action provided by the wick. This can reduce the efficiency with which the wick draws vaporizable material into the vaporization chamber, thereby reducing the efficiency with which the vaporization device vaporizes a desired amount of vaporizable material, such as when a user draws on the vaporization device. Furthermore, the vacuum created in the reservoir eventually results in the inability to draw all of the vaporizable material into the vaporization chamber, thereby wasting the vaporizable material. Various features and devices are described below that ameliorate or overcome these problems. For example, various features are described herein for controlling air flow in an evaporator apparatus that may provide advantages and improvements over existing methods while also introducing additional benefits as described herein.
The vaporizer devices and/or cartridges described herein include one or more features that control and improve the airflow in the vaporizer device and/or cartridge, thereby improving the efficiency and effectiveness of the vaporizer device in vaporizing vaporizable material.
Fig. 2A and 2B show schematic views of first and second embodiments of reservoir systems 200a, 200B, respectively, configured for use with an evaporator cartridge (e.g., evaporator cartridge 120) and/or an evaporator device (e.g., evaporator 100) to improve airflow within the evaporator device. More specifically, the reservoir systems 200a, 200B shown in fig. 2A and 2B improve the regulation of pressure within the
As shown in fig. 2A and 2B, the reservoir systems 200a, 200B include a
The reservoir systems 200a, 200b also include an
As shown in fig. 2A and 2B, each reservoir system 200a, 200B may further include a
For example, embodiments of
The positioning of the vent 246 (e.g., passive vent) and the
As shown in fig. 2A, an
In another embodiment, as shown in FIG. 2B, the
The
Fig. 3A and 3B illustrate an embodiment of a vented
Wicking
The
Fig. 4A and 4B illustrate another embodiment of a vented
Fig. 5A and 5B illustrate yet another embodiment of a vented
After aspiration, when the wicking action of the wick draws vaporizable material from the reservoir to the
Fig. 6A and 6B show an embodiment of a
Similar to that discussed above, when a user draws on the vaporizer apparatus, the airflow flows along the
Fig. 8A and 8B illustrate another embodiment of a vented
Similar to that discussed above, when a user draws on the vaporizer apparatus, the airflow passes along the
Fig. 10 shows another embodiment of a vented evaporation chamber element 1070 that includes a wicking housing 1060 and another embodiment of a vent 1046. The vent 1046 shown in fig. 10 includes two vent channels 1076 molded into wicking housing 1060. Additionally, the vent passage 1076 extends parallel to and merges with the airflow coupling element 1072, the airflow coupling element 1072 configured to connect (e.g., by press-fitting, etc.) a cannula thereto to form another portion of the airflow passage 1038. As such, when the sleeve is connected with the airflow coupling element 1072, the vent passage 1076 may extend along the side of the sleeve and between the reservoir and the evaporation chamber 1042.
Fig. 11 shows another embodiment of a vented
In some embodiments, a flat wick design may be used. The planar surface side may have an increased surface area over conventional cylindrical wicks, providing increased vapor transport from the reservoir to the evaporation chamber. The flat wick design may have advantageous wicking properties based on geometry, and may also improve manufacturing (e.g., based on ease of insertion, ability to be used for secondary cutting, etc.). In some embodiments, a heating element, such as a coil or wire, may be placed along one or more sides of the wick. In some embodiments, the heating element may be wrapped around the wick. The wick may be formed from one or more materials, such as silica, cotton, fiberglass, and the like. In some aspects, the wick may provide a higher capillarity than a wick made of other materials, thereby helping to provide increased vapor transport from the reservoir to the evaporation chamber.
Fig. 12A shows a
Controlling and/or promoting air flow through the air flow channels of the cartridge and/or controlling air pressure in certain portions of the cartridge may help draw vaporizable material into the vaporization chamber, thereby ensuring that the vaporizer device produces a desired amount of aerosol. Some embodiments of the present subject matter described herein include one or more air control features that passively and/or actively allow air to enter the reservoir to displace the vaporizable material exiting the reservoir. This configuration may be activated and/or assisted by the negative pressure created by the user drawing on the evaporator device, as will be explained in more detail below.
In some embodiments, one or more portions of the cartridge (e.g., the reservoir) may include one or more airflow control features, which may include one or more of the various vent embodiments described herein. The airflow control features may facilitate controlling airflow using various mechanisms, such as through passive systems, passively powered but actively controlled systems, and/or active systems, among others. Embodiments of various airflow control features are described in more detail below.
Fig. 13A shows a
Due at least in part to the material of the
A
Wicking consistent with embodiments of the present invention may have orientations other than that shown in the illustrations of the exemplary cartridges of fig. 13A and 13B. For example, the
Passive systems for controlling air flow through the air
In some embodiments, positioning the airflow control features 1344 at certain locations along the cartridge may improve and/or otherwise enhance the vaporization efficiency and/or effectiveness of the vaporizable material. For example, placing apertures away from the ends of the
Positioning the
As described above, the arrangement of the airflow control features 1344 may improve and/or increase the evaporation rate of the vaporizable material at least during and/or after pumping. In some embodiments, the airflow control features 1344 may be placed near the ends of the
In some embodiments, the air flow control features 1344 may comprise valves, such as duckbill or check valves, among others. The airflow control features 1344 comprising valves may desirably be positioned in the same and/or similar locations as described above. The valve may allow air to enter the
The valve of the
In some embodiments, the airflow control features 1344 may comprise a venting material or membrane. The venting material or membrane may be positioned over an opening in the wick, such as the outer surface of a hole. The venting material may include an expanded Polytetrafluoroethylene (PTFE) surface or other material. The venting material or membrane may allow air to enter the reservoir and/or may help restrict or prevent the vaporizable material from exiting the reservoir. The venting material may be positioned in the same and/or similar locations as described above, as desired. For example, in some embodiments, a venting material or membrane may be used as a heat seal over the aperture.
Passively driven but actively controlled systems that control airflow through the
In some embodiments, the passive septum system may include a septum, such as a resealable pierceable elastomeric septum. The membrane may be located in a lower portion, such as the bottom side of the evaporator cartridge. In such a configuration, the evaporator device may include a needle that pierces the membrane when the evaporator cartridge is inserted into the evaporator device. The passive diaphragm system may include a vent, among other components. When assembled, the vent may be located below the needle. The vent may desirably direct the airflow into the environment. This configuration allows direct venting to the environment even when the air pressure outside the evaporator cartridge is low.
In some embodiments, the passive diaphragm system may include a valve. The valve desirably controls the flow of air into the reservoir. For example, the valve may be mechanically and/or electronically controlled. In some embodiments, the passive diaphragm system comprises a microprocessor. The microprocessor may open and/or close the valves as desired. By controlling the operation of the valves, the microprocessor can control the flow rate of air and/or liquid into or out of the reservoir, such as the average flow rate of air and/or liquid. Such a configuration may allow for easier estimation of the evaporation rate, for example by using power and/or temperature measurements from a heating element using one or more sensors. Such a configuration may desirably allow the valve to be closed when the vaporizer apparatus is not in use, thereby minimizing oxygen and/or moisture exchange with the environment. Such a configuration may ideally extend the life of the cartridge.
Active systems that control airflow via air control features may include active diaphragm systems, among other configurations. The active septum system may include a septum, such as a resealable pierceable elastomeric septum. The membrane may be located in a lower portion of the box, such as the bottom side of the evaporator box. In such a configuration, the evaporator device may include a needle that pierces the membrane when the evaporator cartridge is inserted into the evaporator device.
In some embodiments, the active membrane system may include a pump. The pump may desirably control the flow of air into the reservoir. For example, the pump may be mechanically and/or electronically controlled. In some embodiments, the active membrane system comprises a microprocessor. The microprocessor may activate and/or activate the pump as desired. The microcontroller may determine the appropriate amount of air to pump into the reservoir to achieve the desired evaporation rate. In such a configuration, the flow rate of air through the system may ideally be independent of, or may be minimally dependent on, the negative pressure applied by the user during suction. Indeed, the pump may directly control the air flow and, for example, allow more or less air flow than is passively driven by the user's suction and open valve. In some embodiments, the pump may reduce the mechanical complexity of the airflow control features and/or may allow for high frequency and/or low stroke pumps, such as PCB-scale piezoelectric pumps. Piezoelectric pumps can produce high flow rates and/or can maximize air pressure to desirably control the flow of air and/or liquid throughout the system.
Separated vapor path
It may be desirable to prevent leakage from the reservoir to the environment and/or to other portions of the evaporator box. The evaporator pod may be pressurized by an air seal located at an end of the evaporator pod opposite the heater. The air seal may create an inverse vacuum to help limit or prevent leakage and to retain the vaporizable material within the receptacle. In some embodiments, the evaporator device includes a pressure sensor. The pressure sensor may determine whether the evaporator means, e.g. the heater, should be activated, e.g. by determining whether a user's suction is being applied. The pressure sensor may be dependent on a pressure signal caused by air flow in communication with the pressure sensor. When the liquid travels along the same path, the pressure signal may fail, for example, by damaging and/or desensitizing the pressure sensor.
Some evaporator cartridges include a single airflow passage that extends across the evaporation chamber and directly outward to the user, such as through the center of the reservoir. The air path may communicate pressure signals caused by the user's breath to the pressure sensor, communicate vapor from the heater to the user, mix the vapor with cold air to condense the vapor into an aerosol, and/or provide air to be discharged back into the reservoir during or after an inhalation. Some of the vaporizable material exiting the reservoir may not be vaporized, and the vaporizable material recondensed in the airflow passageway may flow freely back to the pressure sensor, which may damage the pressure sensor. Surface tension of the vaporizable material clogging the pressure sensor can undesirably reduce the pressure signal and/or reduce the likelihood that the vaporizer device will actuate properly. The following disclosure includes evaporator embodiments that include a separate pressure sensing passageway that overcomes the problems described above.
Fig. 14A shows a schematic view of a
Fig. 14B shows an exemplary airflow through the
Fig. 14C shows an exemplary schematic of
In some embodiments, it may be desirable to
For example, fig. 14D shows
Fig. 14D schematically shows an example of an assembly of a
Fig. 14E shows an exemplary air flow through the
The quench
Separating the quench air from the gas stream traveling over the heater may desirably provide design flexibility. In some embodiments, the quench air may be separately directed to allow the flow of air past the heater to be directed through one or more valves, such as check valves (not shown). This may allow the vaporizable material in the reservoir to be sealed except during suction, allowing the vaporizer apparatus to have a high moisture and/or oxygen barrier between uses. This configuration may adjust the air pressure at the heater as desired, such as through a valve. Such a configuration may desirably limit the amount of vaporizable material withdrawn from the reservoir such that the amount of vaporizable material withdrawn is less than or equal to the amount of vaporizable material vaporizable by the heater.
Exemplary Nicotine liquid formulations
Included herein, among other things, are nicotine liquid formulations for use in electronic vaporizers (e.g., devices provided herein). In embodiments, the nicotine liquid formulation comprises nicotine and an acid, such as an organic acid. In embodiments, the nicotine liquid formulation includes a liquid carrier.
Nicotine is a chemical irritant and when provided to an animal, e.g. a mammal such as a human, nicotine increases e.g. heart rate and blood pressure. The stimulating effect of nicotine may be referred to herein as nicotine stimulation. In various embodiments, the stimulatory effect is correlated with nicotine serum levels. In various embodiments, the transfer of nicotine to the subject is associated with physical and/or emotional satisfaction. In various embodiments, the devices and formulations provided herein are useful for reducing a user's craving for a traditional cigarette.
Aspects of the present disclosure relate to methods for navigating among usersFormulations and devices that exhibit nicotine-related biological effects (e.g., nicotine stimulating effects). In embodiments, the nicotine-related biological effect (e.g., nicotine stimulating effect) is associated with a conventional cigarette, such as Pall
Or NewportThe biological effect of the cigarette is equivalent. In embodiments, a conventional cigarette is the user preferred cigarette type. A "nicotine-related biological effect" is an effect detectable by a user (e.g., a subject) and includes, but is not limited to, a stimulating effect (also referred to herein as a nicotine stimulating effect) or a relaxing effect (e.g., reducing anxiety or irritability). In embodiments, the nicotine-related biological effect is a stimulatory effect (also referred to herein as a nicotine stimulatory effect). In embodiments, the nicotine-related biological effect is an increased concentration. In an embodiment, the nicotine-related biological effect is increased alertness. The nicotine stimulating effect may be manifested, for example, as an increase in heart rate, an increase in blood pressure, and/or a sense of satisfaction (e.g., physical or emotional satisfaction) of the user. In embodiments, increased nicotine-related biological effects (e.g., nicotine stimulating effects such as faster elevation of heart rate) may be achieved within, for example, about 10 seconds, about 20 seconds, about 40 seconds, about 60 seconds, about 80 seconds, about 100 seconds, about 120 seconds, about 140 seconds, about 160 seconds, about 180 seconds, about 200 seconds, about 220 seconds, about 240 seconds, about 260 seconds, about 280 seconds, about 300 seconds, about 320 seconds, about 340 seconds, about 360 seconds, about 7 minutes, about 8 minutes, about 9 minutes, or about 10 minutes after delivery of nicotine or protonated nicotine in accordance with the teachings of the present disclosure. In an embodiment, the nicotine stimulating effect is an increase in heart rate. According to teachings of the present disclosure, the nicotine or protonated nicotine may be delivered within, for example, about 10 seconds, about 20 seconds, about 40 seconds, about 60 seconds, about 80 seconds, about 100 seconds, about 120 seconds, about 140 seconds, about 160 seconds, about 180 seconds, about 200 seconds, about 220 seconds, about 240 seconds, about 260 seconds, about 280 seconds, about 300 seconds, about 320 seconds, about 340 seconds, about 360 seconds, about 7 minutes, about 8 minutes, about 9 minutes, or about 10 minutesAn increase in heart rate is achieved. In embodiments, an effective amount of nicotine (e.g., protonated nicotine) increases the user's heart rate by about 10%, or about 15%, or about 20%, or about 25%, or about 30%, or about 35%, or about 40%, or about 45%, or about 50%, or about 55%, or about 60% relative to the user's heart rate prior to nicotine (e.g., protonated nicotine) delivery in accordance with the teachings of the present disclosure. In embodiments, an effective amount of protonated nicotine increases the heart rate of a user by about 10%, or about 15%, or about 20%, or about 25%, or about 30%, or about 35%, or about 40%, or about 45%, or about 50%, or about 55%, or about 60% relative to the heart rate of a corresponding user receiving the same amount of nicotine in free base form. In an embodiment, the heart rate is a resting heart rate. In an embodiment, the nicotine-related biological effect is a reduction in craving for cigarettes. In embodiments, the reduced craving is experienced within about 10 seconds, about 20 seconds, about 40 seconds, about 60 seconds, about 80 seconds, about 100 seconds, about 120 seconds, about 140 seconds, about 160 seconds, about 180 seconds, about 200 seconds, about 220 seconds, about 240 seconds, about 260 seconds, about 280 seconds, about 300 seconds, about 320 seconds, about 340 seconds, about 360 seconds, about 7 minutes, about 8 minutes, about 9 minutes, or about 10 minutes after nicotine or protonated nicotine delivery in accordance with the teachings of the present disclosure. In embodiments, the nicotine-related biological effect is a pleasant sensation in the throat or chest. In embodiments, the nicotine-related biological effect is any combination of 2,3, 4, 5 or more effects associated with nicotine disclosed herein or known in the art. Such effects are not limited to what the user may perceive, and thus may include objective and subjective effects.In embodiments, the use of a nicotine liquid formulation provided herein simulates the nicotine delivery peak of a conventional cigarette. In embodiments, the Cmax and/or Tmax values of the user's plasma nicotine levels are comparable to (or close to, e.g., 90-100% or at least about 80%, 85%, 90% or 95% of) those of a conventional cigarette. In embodiments, the rate of nicotine absorption in the user's plasma is the same as that of a conventional cigarette (e.g., the Cmax and Tmax values are at least about 90% of the conventional cigarette Cmax and Tmax values). In embodiments, the rate of absorption of nicotine from the user's plasma or blood is lower than in conventional cigarettes, but sufficient to, for example, reduce cravings for conventional cigarettes. In embodiments, formulations that exhibit the fastest nicotine absorption rate in plasma (e.g., nicotine-organic acid formulations) are more preferred in the satisfaction assessment and are evaluated to be more equivalent to cigarette satisfaction as compared to formulations that exhibit a slower rate of nicotine rise in plasma. In an embodiment, the user rates his or her satisfaction rating as at least 3 on a scale ranging from 1 to 7, where 1 is none at all, 2 is little, 3 is little, 4 is moderate, 5 is some, 6 is more, and 7 is extreme. In an embodiment, the user rates his or her satisfaction rating on a scale of 4. In an embodiment, the user rates his or her satisfaction rating on a scale of 5. In an embodiment, the user rates his or her satisfaction rating on a scale of 6. In an embodiment, the user rates his or her satisfaction rating on a scale of 7.
In one aspect, a nicotine liquid formulation is provided that includes nicotine, an acid (e.g., an organic acid), and a liquid carrier. In embodiments, upon heating the formulation, an inhalable aerosol comprising an effective amount of nicotine and/or protonated nicotine is formed. In embodiments, upon heating the formulation, an inhalable aerosol comprising an effective amount of protonated nicotine is formed. In embodiments, the formulation is located in a cartridge. In embodiments, the cartridge is in an electronic nicotine delivery system. An "effective amount" of a compound (e.g., nicotine) is an amount sufficient to cause the compound to achieve the stated purpose (e.g., to achieve the effect of its administration) relative to the absence of the compound. The term "effective amount" also includes an amount more than sufficient to achieve the stated purpose, provided that the purpose is achieved without undue adverse side effects (such as toxicity or irritation) commensurate with a reasonable benefit/risk ratio when used in the manner of this disclosure. In embodiments, an effective amount of nicotine (e.g., protonated nicotine, free-base nicotine, or a combination thereof) is an amount of nicotine sufficient to produce a nicotine-related biological effect (e.g., nicotine stimulating effect) in a user.
In one aspect, a method of providing nicotine to a user (also referred to herein as a subject) of an electronic nicotine delivery system is provided. "providing" nicotine to a user includes making the nicotine available (e.g., via an electronic nicotine delivery system) or administering the nicotine to the user (e.g., via an electronic nicotine delivery system). In embodiments, the administration is self-administration. In embodiments, "providing" nicotine to a user may include making a device designed to be operated by the user available, sold, and/or delivered to the user for a user desiring to self-administer nicotine. In embodiments, the nicotine is self-administered by inhalation of an aerosol comprising nicotine, wherein the nicotine is produced by the device upon operation of the device.
In embodiments, the method comprises (a) heating a nicotine liquid formulation in an electronic nicotine delivery system to produce an inhalable aerosol, wherein the formulation comprises nicotine and an organic acid in a liquid carrier; and (b) the user inhales the aerosol, wherein the aerosol comprises an amount of protonated nicotine that causes the user to experience a nicotine-related biological effect.
In embodiments, the method comprises (a) heating a nicotine liquid formulation in an electronic nicotine delivery system to produce an inhalable aerosol, wherein the formulation comprises nicotine and an organic acid in a liquid carrier; and (b) the user inhales the aerosol, wherein the aerosol comprises an amount of the organic acid that causes the user to experience a nicotine-related biological effect.
In embodiments, the method comprises (a) heating a nicotine liquid formulation in an electronic nicotine delivery system to produce an inhalable aerosol, wherein the formulation comprises nicotine and an organic acid in a liquid carrier; and (b) inhaling an aerosol by the user, wherein the aerosol comprises nicotine and an amount of an organic acid sufficient to cause an increased nicotine-related biological effect in the user relative to the absence of the organic acid after inhalation by the user.
In embodiments, the method comprises (a) operating (a) (a user) an electronic nicotine delivery system comprising a nicotine liquid formulation as disclosed herein, the formulation comprising nicotine, an organic acid, and a liquid carrier, wherein the electronic nicotine delivery system heats the formulation to an operating temperature, thereby producing an inhalable aerosol comprising an effective amount of protonated nicotine; and (b) (the user) inhaling the inhalable aerosol. Operating the electronic nicotine delivery system includes activating basic electronic components of the electronic nicotine delivery system to allow heating and inhalation. In embodiments, operating the electronic nicotine delivery system comprises, consists essentially of, or consists of a user holding and drawing from a mouthpiece of the electronic nicotine delivery system. In embodiments, an effective amount is an amount that a user experiences a nicotine-related biological effect upon inhalation.
In embodiments, the effective amount of nicotine is effective to reduce a user's craving for a traditional cigarette. In embodiments, cravings are reduced altogether such that the user is not craving for traditional cigarettes. In embodiments, the nicotine-related biological effect is a physiological response similar or equivalent to the response to nicotine provided by smoking a conventional cigarette. In embodiments, the nicotine-related biological effect is a nicotine stimulation that mimics (e.g., is equivalent to) a traditional cigarette. In an embodiment, the nicotine-related biological effect is an increase in heart rate that simulates an increase in heart rate for a user smoking a conventional cigarette. The heart rate of a user smoking a conventional cigarette may be referred to herein as the "heart rate of the conventional cigarette". If the heart rate is about the same as, of about the same order of magnitude as, or of about the same rate of increase as that of a conventional cigarette, the increased heart rate "mimics" the heart rate of a conventional cigarette.
In embodiments, the method comprises (a) heating a nicotine liquid formulation in an electronic nicotine delivery system to produce an inhalable aerosol, wherein the formulation comprises nicotine and an organic acid in a liquid carrier; and (b) inhalation by the user of the aerosol, wherein the organic acid is present in an amount such that the user's craving for a conventional cigarette is reduced or absent.
In embodiments, the method comprises (a) heating a nicotine liquid formulation in an electronic nicotine delivery system to produce an inhalable aerosol, wherein the formulation comprises nicotine and an organic acid in a liquid carrier; and (b) the user inhales the aerosol, wherein the organic acid is present in an amount such that the user has a physiological response similar or equivalent to that of nicotine provided by smoking a conventional cigarette.
In embodiments, the method comprises (a) heating a nicotine liquid formulation in an electronic nicotine delivery system to produce an inhalable aerosol, wherein the formulation comprises nicotine and an organic acid in a liquid carrier; and (b) the user inhales the aerosol, wherein the organic acid is present in an amount such that the user experiences an increased nicotine-related biological effect (e.g., a faster rise in heart rate) that mimics a traditional cigarette.
In embodiments, the method comprises (a) heating a nicotine liquid formulation in an electronic nicotine delivery system to produce an inhalable aerosol, wherein the formulation comprises nicotine and an organic acid in a liquid carrier; and (b) the user inhales the aerosol, wherein the organic acid is present in an amount sufficient to provide nicotine stimulation that mimics nicotine stimulation of a conventional cigarette.
In embodiments, the aerosol comprises protonated nicotine sufficient to cause an increase in plasma nicotine levels in a user's body after inhalation by the user, simulating a conventional cigarette.
In embodiments, the method comprises (a) heating a nicotine liquid formulation in an electronic nicotine delivery system to produce an inhalable aerosol, wherein the formulation comprises nicotine and benzoic acid in a liquid carrier, wherein the formulation comprises a protonated nicotine amount of about 0.5% to about 5% or about 1.5% to about 2.5%; and (b) inhalation of the aerosol by the user. In embodiments, most or all of the nicotine is protonated in the formulation. In embodiments, at least 85-95%, 85-90%, 85-99%, 90-95%, 90-99%, or 95-99% of the nicotine in the formulation is protonated. In embodiments, at least about 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% of the nicotine is protonated. In embodiments, from about 85%, 86%, 87%, 88%, 89% or 90% to about 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% of the nicotine is protonated. In embodiments, 100% of the nicotine is protonated. In embodiments, at least 85% of the nicotine is protonated. In embodiments, at least 90% of the nicotine is protonated. In an embodiment, at least 91% of the nicotine is protonated. In embodiments, at least 92% of the nicotine is protonated. In embodiments, at least 93% of the nicotine is protonated. In embodiments, at least 94% of the nicotine is protonated. In embodiments, at least 95% of the nicotine is protonated. In embodiments, at least 96% of the nicotine is protonated. In embodiments, at least 97% of the nicotine is protonated. In embodiments, at least 98% of the nicotine is protonated. In embodiments, at least 99% of the nicotine is protonated.
In embodiments, more or all of the nicotine in the aerosol to be produced (e.g., in the device, or according to the methods provided herein) is protonated. In embodiments, at least 85-95%, 85-90%, 85-99%, 90-95%, 90-99%, or 95-99% of the nicotine in the aerosol is protonated. In embodiments, at least about 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% of the nicotine is protonated. In embodiments, from about 85%, 86%, 87%, 88%, 89% or 90% to about 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% of the nicotine is protonated. In embodiments, 100% of the nicotine is protonated. In embodiments, at least 85% of the nicotine is protonated. In embodiments, at least 90% of the nicotine is protonated. In an embodiment, at least 91% of the nicotine is protonated. In embodiments, at least 92% of the nicotine is protonated. In embodiments, at least 93% of the nicotine is protonated. In embodiments, at least 94% of the nicotine is protonated. In embodiments, at least 95% of the nicotine is protonated. In embodiments, at least 96% of the nicotine is protonated. In embodiments, at least 97% of the nicotine is protonated. In embodiments, at least 98% of the nicotine is protonated. In embodiments, at least 99% of the nicotine is protonated.
In embodiments, the method comprises (a) heating a nicotine liquid formulation in an electronic nicotine delivery system to produce an inhalable aerosol, wherein the formulation comprises nicotine and benzoic acid in a liquid carrier; and (b) inhalation of the aerosol by the user.
In embodiments, the method comprises (a) heating a nicotine liquid formulation in an electronic nicotine delivery system to produce an inhalable aerosol, wherein the formulation comprises nicotine and lactic acid in a liquid carrier; and (b) inhalation of the aerosol by the user.
In embodiments, the method comprises (a) heating a nicotine liquid formulation in an electronic nicotine delivery system to produce an inhalable aerosol, wherein the formulation comprises nicotine, benzoic acid, and lactic acid in a liquid carrier; and (b) inhalation of the aerosol by the user.
In one aspect, a method of preparing an inhalable aerosol comprising nicotine and benzoic acid is provided. In embodiments, the method comprises heating nicotine and benzoic acid in an electronic inhaler to produce an aerosol, wherein the aerosol comprises nicotine and an amount of benzoic acid sufficient to cause an increased nicotine-related biological effect (e.g., a faster rise in heart rate) in the user relative to the absence of benzoic acid after inhalation by the user. In one aspect, a method of preparing an inhalable aerosol comprising nicotine and lactic acid is provided. In embodiments, the method comprises heating nicotine and lactic acid in an electronic inhaler to produce an aerosol, wherein the aerosol comprises nicotine and lactic acid in an amount sufficient to cause an increased nicotine-related biological effect (e.g., a faster rise in heart rate) relative to the absence of lactic acid after inhalation by a user. In one aspect, a method of preparing an inhalable aerosol comprising nicotine, benzoic acid, and lactic acid is provided. In embodiments, the method comprises heating nicotine and benzoic acid and lactic acid in an electronic inhaler to produce an aerosol, wherein the aerosol comprises nicotine and an amount of benzoic acid and lactic acid sufficient to cause an increased nicotine-related biological effect (e.g., a faster rise in heart rate) in the user relative to the absence of benzoic acid and lactic acid after inhalation by the user.
In embodiments, the method comprises heating a nicotine liquid formulation in an electronic nicotine delivery system to produce an inhalable aerosol, the formulation comprising nicotine and one or more organic acids in a liquid carrier, wherein the one or more organic acids comprise a keto acid, an aliphatic monocarboxylic acid, an aliphatic dicarboxylic acid, an aromatic acid, and/or a hydroxy acid.
In embodiments, the formulation comprises an amount of a carboxylic acid sufficient to cause an increased nicotine-related biological effect (e.g., a faster rise in heart rate) in the user after inhalation relative to the absence of the carboxylic acid.
In embodiments, the method comprises heating a nicotine liquid formulation in an electronic nicotine delivery system to produce an inhalable aerosol, the formulation comprising nicotine and an organic acid in a liquid carrier, wherein (a) the formulation comprises the organic acid in an amount sufficient to cause an increased nicotine-related biological effect (e.g., a faster rise in heart rate) in the user after inhalation relative to the absence of the organic acid; and (b) the electronic nicotine delivery system includes a cartridge, wherein the cartridge functions as a reservoir for holding the formulation and as a mouthpiece for the electronic nicotine delivery system.
In embodiments, the method comprises heating a nicotine liquid formulation comprising nicotine and an organic acid in a liquid carrier in an electronic nicotine delivery system to produce an inhalable aerosol, wherein (a) the pH of the liquid formulation is sufficiently acidic to cause an increased nicotine-related biological effect (e.g., a faster rise in heart rate) in the user after inhalation relative to the absence of the organic acid; and (b) the electronic nicotine delivery system includes a cartridge, wherein the cartridge functions as a reservoir for holding the formulation and as a mouthpiece for the electronic nicotine delivery system. In embodiments, the pH of the formulation is less than 7.0. In embodiments, the pH of the formulation is from about 2.5 to about 6.5. In embodiments, the pH of the formulation is from about 3 to about 6.5. In embodiments, the pH of the formulation is from about 4 to about 6.5. In embodiments, the pH of the formulation is from about 5 to about 6.5. In embodiments, the pH of the formulation is from about 6 to about 6.5. In embodiments, the pH of the formulation is from about 3 to about 5.5. In embodiments, the pH of the formulation is from about 3.5 to about 5.5. In embodiments, the pH of the formulation is about 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, or 6.5.
In embodiments, the aerosol comprises protonated nicotine at a level such that the user has a plasma Cmax value of nicotine of about 80-100% or at least about 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% of a conventional cigarette. In embodiments, the aerosol comprises protonated nicotine at a level such that the user has a plasma nicotine Tmax value of about 80-100% or at least about 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% of a conventional cigarette.
In embodiments, the aerosol comprises nicotine in combination with an organic acid in an amount such that the user has a plasma Cmax value of nicotine of about 80-100% or at least about 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% of a conventional cigarette. In embodiments, the aerosol comprises nicotine in combination with an organic acid in an amount such that the user has a plasma nicotine Tmax value of about 80-100% or at least about 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% of a conventional cigarette.
In one aspect, provided herein is a device (e.g., an electronic nicotine delivery system as disclosed herein) comprising a nicotine liquid formulation disclosed herein.
In one aspect, provided herein is an electronic nicotine delivery system cartridge comprising a nicotine liquid formulation disclosed herein. In an embodiment, the cartridge is in a package, for example a blister package. In embodiments, the cartridge is located in an electronic nicotine delivery system. In embodiments, the cartridge serves as a reservoir for the mouthpiece and formulation. In an embodiment, the cartridge is an atomizer.
In embodiments, the aerosol generated by the electronic nicotine delivery system is generated from a single nicotine liquid formulation in a single reservoir contained within the electronic nicotine delivery system or cartridge thereof.
Non-limiting examples of nicotine liquid formulations comprising one or more organic acids are disclosed in U.S. patent nos. 9,215,895; U.S. patent application publication numbers 2016/0302471; and PCT international application publication No. WO2018/031600, the entire contents of each of which are incorporated herein by reference.
Unless specified otherwise and depending on the context, the term "nicotine" means "free base nicotine and/or protonated nicotine" (without taking counter-ions into account). In embodiments, the nicotine in the nicotine liquid formulations provided herein is naturally occurring nicotine (e.g., an extract from a nicotine species such as tobacco) or synthetic nicotine. In embodiments, the nicotine is (-) -nicotine, (+) -nicotine or mixtures thereof. In embodiments, the nicotine is used in a relatively pure form (e.g., greater than about 80%, 85%, 90%, 95%, 99%, 99.5%, or 99.9% purity by weight prior to combining with one or more other ingredients of the formulation). In embodiments, the nicotine of the formulations provided herein is "clear" in appearance to avoid or minimize the formation of tar-like residues in subsequent formulation steps. In embodiments, 90-100% or at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99.1%, 99.2%, 99.3%, 99.4%, 99.5%, 99.6%, 99.7%, 99.8%, or 99.9% of the nicotine in the formulation is (-) -nicotine.
In embodiments, the nicotine liquid formulation comprises an organic acid.
The term "organic acid" refers to an organic compound having acidic properties (e.g., according to
Definitions, or Lewis definitions) the common organic acids are carboxylic acids, the acidity of which is related to their carboxyl group (-COOH) the dicarboxylic acids have two carboxylic acid groups the relative acidity of the organic acids is measured by their pKa values, and one skilled in the art knows how to determine the acidity of the organic acids based on their given pKa values the term "keto acid" as used herein refers to organic compounds containing a carboxylic acid group and a keto group the common types of keto acids include α -keto acids or 2-oxo acids, such as pyruvic acid or oxaloacetic acid, the keto group of which is adjacent to the carboxylic acid, β -keto acids or 3-oxo acids, such as acetoacetic acid, having a keto group at the second carbon atom of the carboxylic acid, and γ -keto acids or 4-oxo acids, such as levulinic acid, having a keto group at the third carbon atom of the carboxylic acid.In embodiments, the organic acid is a carboxylic acid. In embodiments, the carboxylic acid is an aliphatic acid. In embodiments, the aliphatic acid is a straight chain aliphatic acid. In embodiments, the aliphatic acid is a branched aliphatic acid. In embodiments, the aliphatic acid is an aliphatic monocarboxylic acid. In embodiments, the aliphatic acid is an aliphatic dicarboxylic acid. In embodiments, the aliphatic dicarboxylic acid is malonic acid or succinic acid. In embodiments, the carboxylic acid is an aromatic acid. In embodiments, the aromatic acid is benzoic acid or phenylacetic acid.
In embodiments, the carboxylic acid is a hydroxy acid. In embodiments, the hydroxy acid is lactic acid.
In embodiments, the organic acid is a keto acid, in embodiments, α -keto acid, in embodiments, α -keto acid is pyruvic acid or oxaloacetic acid in embodiments, β -keto acid, in embodiments, β -keto acid is acetoacetic acid.
In embodiments, the organic acid is any one or more of 2-furoic acid, acetic acid, acetoacetic acid, α -methylbutyric acid, ascorbic acid, benzoic acid, β -methylvaleric acid, butyric acid, caproic acid, citric acid, formic acid, fumaric acid, glycolic acid, heptanoic acid, isobutyric acid, isovaleric acid, lactic acid, levulinic acid, malic acid, malonic acid, myristic acid, pelargonic acid, caprylic acid, oxalic acid, oxaloacetic acid, phenylacetic acid, propionic acid, pyruvic acid, succinic acid, and tartaric acid.
Non-limiting examples of organic acids include aromatic acids, such as optionally substituted benzoic acids, hydroxy acids, heterocyclic acids, terpenic acids, sugar acids, such as pectic acids, amino acids, cycloaliphatic acids, dicarboxylic acids, aliphatic acids, keto acids, and the like.
In embodiments, the formulation includes one or more carboxylic acids. Non-limiting examples of carboxylic acids include monocarboxylic acids, dicarboxylic acids (organic acids containing two carboxylic acid groups), and carboxylic acids containing aromatic groups, such as benzoic acid, hydroxycarboxylic acids, heterocyclic carboxylic acids, terpenic acids, and sugar acids; such as pectic acids, amino acids, cycloaliphatic acids, aliphatic carboxylic acids, ketocarboxylic acids, and the like. In embodiments, the formulation comprises one or more of formic acid, acetic acid, propionic acid, butyric acid, valeric acid, caproic acid, caprylic acid, capric acid, citric acid, lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, linoleic acid, linolenic acid, phenylacetic acid, benzoic acid, pyruvic acid, levulinic acid, tartaric acid, lactic acid, malonic acid, succinic acid, fumaric acid, gluconic acid, sugar acids, salicylic acid, sorbic acid, malonic acid, and malic acid. In embodiments, the formulation comprises one or more of benzoic acid, pyruvic acid, salicylic acid, levulinic acid, malic acid, succinic acid, and citric acid. In embodiments, the formulation comprises one or more of benzoic acid, pyruvic acid, and salicylic acid. In an embodiment, the formulation comprises benzoic acid. In embodiments, the formulation comprises lactic acid. In embodiments, the formulation comprises benzoic acid and lactic acid. In an embodiment, the formulation comprises at least one of benzoic acid, oxalic acid, salicylic acid, succinic acid, sorbic acid, pyruvic acid, levulinic acid, or lactic acid.
In embodiments, the organic acid used in the nicotine liquid formulation does not decompose at the operating temperature of the electronic nicotine delivery system.
In embodiments, the formulation does not include citric acid. In embodiments, the formulation does not include pyruvic acid. In embodiments, the formulation does not include malic acid. In embodiments, the formulation includes no more than 10, 9, 8, 7, 6, 5, 4, 3, 2, or 1 acid. In embodiments, the formulation includes no more than 10, 9, 8, 7, 6, 5, 4, 3, 2, or 1 organic acid. In embodiments, the formulation includes no more than 10 organic acids. In embodiments, the formulation includes no more than 9 organic acids. In embodiments, the formulation includes no more than 8 organic acids. In embodiments, the formulation includes no more than 7 organic acids. In embodiments, the formulation includes no more than 6 organic acids. In embodiments, the formulation includes no more than 5 organic acids. In embodiments, the formulation includes no more than 4 organic acids. In embodiments, the formulation includes no more than 3 organic acids. In embodiments, the formulation includes no more than 2 organic acids. In embodiments, the formulation contains only 1 organic acid. In embodiments, the formulation includes no more than 10 carboxylic acids. In embodiments, the formulation includes no more than 9 carboxylic acids. In embodiments, the formulation includes no more than 8 carboxylic acids. In embodiments, the formulation includes no more than 7 carboxylic acids. In embodiments, the formulation includes no more than 6 carboxylic acids. In embodiments, the formulation includes no more than 5 carboxylic acids. In embodiments, the formulation includes no more than 4 carboxylic acids. In embodiments, the formulation includes no more than 3 carboxylic acids. In embodiments, the formulation includes no more than 2 carboxylic acids. In embodiments, the formulation comprises only 1 carboxylic acid.
In embodiments, the formulation includes an organic compound that exhibits acidic characteristics and is capable of forming a counterion with nicotine when in the form of a conjugate base. Exemplary compounds include phenols such as guaiacol, vanillin, protocatechuic aldehyde, and the like.
In embodiments, the concentration of nicotine in the nicotine liquid formulation is from about 0.5% to about 25%, wherein the concentration is the ratio of the weight of nicotine to the total weight of the solution, i.e. (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 1% (w/w) to about 20% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 1% (w/w) to about 18% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 1% (w/w) to about 15% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 4% (w/w) to about 12% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 1% (w/w) to about 18% (w/w), about 3% (w/w) to about 15% (w/w), or about 4% (w/w) to about 12% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 0.5% (w/w) to about 10% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 0.5% (w/w) to about 5% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 0.5% (w/w) to about 4% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 0.5% (w/w) to about 3% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 0.5% (w/w) to about 2% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 0.5% (w/w) to about 1% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 1% (w/w) to about 10% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 1% (w/w) to about 5% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 1% (w/w) to about 4% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 1% (w/w) to about 3% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 1% (w/w) to about 2% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 2% (w/w) to about 10% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 2% (w/w) to about 5% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 2% (w/w) to about 4% (w/w). In embodiments, the nicotine liquid formulation has a concentration of about 0.5%, 0.6%, 0.7%, 0.8%, 0.9%, 1.0%, 1.1%, 1.2%, 1.3%, 1.4%, 1.5%, 1.6%, 1.7%, 1.8%, 1.9%, 2.0%, 2.1%, 2.2%, 2.3%, 2.4%, 2.5%, 2.6%, 2.7%, 2.8%, 2.9%, 3.0%, 3.1%, 3.2%, 3.3%, 3.4%, 3.5%, 3.6%, 3.7%, 3.8%, 3.9%, 4.0%, 4.5%, 5.0%, 5.5%, 6.0%, 6.5%, 7.0%, 7.5%, 8.0%, 8.5%, 9.0%, 9.5%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19% or more (w/w% or more increments therein. In an embodiment, the nicotine liquid formulation has a nicotine concentration of about 5% (w/w) of the nicotine liquid formulation. In an embodiment, the nicotine liquid formulation has a nicotine concentration of about 4% (w/w). In an embodiment, the nicotine liquid formulation has a nicotine concentration of about 3% (w/w). In an embodiment, the nicotine liquid formulation has a nicotine concentration of about 2% (w/w). In an embodiment, the nicotine liquid formulation has a nicotine concentration of about 1% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 0.5% (w/w).
In embodiments, the nicotine concentration of the nicotine liquid formulation is about 0.5% (w/w), 1% (w/w), about 2% (w/w), about 3% (w/w), about 4% (w/w), about 5% (w/w), about 6% (w/w), about 7% (w/w), about 8% (w/w), about 9% (w/w), about 10% (w/w), about 11% (w/w), about 12% (w/w), about 13% (w/w), about 14% (w/w), about 15% (w/w), about 16% (w/w), about 17% (w/w), about 18% (w/w), about 19% (w/w) or about 20% (w/w). In embodiments, the nicotine concentration of the nicotine liquid formulation is from about 0.5% (w/w) to about 20% (w/w), from about 0.5% (w/w) to about 18% (w/w), from about 0.5% (w/w) to about 15% (w/w), from about 0.5% (w/w) to about 12% (w/w), from about 0.5% (w/w) to about 10% (w/w), from about 0.5% (w/w) to about 8% (w/w), about 0.5% (w/w) to about 7% (w/w), about 0.5% (w/w) to about 6% (w/w), about 0.5% (w/w) to about 5% (w/w), about 0.5% (w/w) to about 4% (w/w), about 0.5% (w/w) to about 3% (w/w), or about 0.5% (w/w) to about 2% (w/w). In embodiments, the nicotine concentration of the nicotine liquid formulation is from about 1% (w/w) to about 20% (w/w), from about 1% (w/w) to about 18% (w/w), from about 1% (w/w) to about 15% (w/w), from about 1% (w/w) to about 12% (w/w), from about 1% (w/w) to about 10% (w/w), from about 1% (w/w) to about 8% (w/w), about 1% (w/w) to about 7% (w/w), about 1% (w/w) to about 6% (w/w), about 1% (w/w) to about 5% (w/w), about 1% (w/w) to about 4% (w), about 1% (w/w) to about 3% (w/w), or about 1% (w/w) to about 2% (w/w). In embodiments, the nicotine concentration of the nicotine liquid formulation is from about 2% (w/w) to about 20% (w/w), from about 2% (w/w) to about 18% (w/w), from about 2% (w/w) to about 15% (w/w), from about 2% (w/w) to about 12% (w/w), from about 2% (w/w) to about 10% (w/w), about 2% (w/w) to about 8% (w/w), about 2% (w/w) to about 7% (w/w), about 2% (w/w) to about 6% (w/w), about 2% (w/w) to about 5% (w/w), about 2% (w/w) to about 4% (w/w), or about 2% (w/w) to about 3% (w/w). In embodiments, the nicotine concentration of the nicotine liquid formulation is from about 3% (w/w) to about 20% (w/w), from about 3% (w/w) to about 18% (w/w), from about 3% (w/w) to about 15% (w/w), from about 3% (w/w) to about 12% (w/w), from about 3% (w/w) to about 10% (w/w), from about 3% (w/w) to about 8% (w/w), from about 3% (w/w) to about 7% (w/w), from about 3% (w/w) to about 6% (w/w), from about 3% (w/w) to about 5% (w/w), or from about 3% (w/w) to about 4% (w/w). In embodiments, the nicotine concentration of the nicotine liquid formulation is from about 4% (w/w) to about 20% (w/w), from about 4% (w/w) to about 18% (w/w), from about 4% (w/w) to about 15% (w/w), from about 4% (w/w) to about 12% (w/w), from about 4% (w/w) to about 10% (w/w), from about 4% (w/w) to about 8% (w/w), from about 4% (w/w) to about 7% (w/w), from about 4% (w/w) to about 6% (w/w), or from about 4% (w/w) to about 5% (w/w). In embodiments, the nicotine concentration of the nicotine liquid formulation is from about 5% (w/w) to about 20% (w/w), from about 5% (w/w) to about 18% (w/w), from about 5% (w/w) to about 15% (w/w), from about 5% (w/w) to about 12% (w/w), from about 5% (w/w) to about 10% (w/w), from about 5% (w/w) to about 8% (w/w), from about 5% (w/w) to about 7% (w/w), or from about 5% (w/w) to about 6% (w/w). In embodiments, the nicotine concentration of the nicotine liquid formulation is from about 6% (w/w) to about 20% (w/w), from about 6% (w/w) to about 18% (w/w), from about 6% (w/w) to about 15% (w/w), from about 6% (w/w) to about 12% (w/w), from about 6% (w/w) to about 10% (w/w), from about 6% (w/w) to about 8% (w/w), or from about 6% (w/w) to about 7% (w/w). In embodiments, the nicotine liquid formulation has a nicotine concentration of about 2% (w/w) to about 6% (w/w). In an embodiment, the nicotine liquid formulation has a nicotine concentration of about 5% (w/w).
In embodiments, the concentration of nicotine in the nicotine liquid formulation is from about 1%, 1.1%, 1.2%, 1.3%, 1.4%, 1.5%, 1.6% or 1.7% to about 2.5%, 2.4%, 2.3%, 2.2%, 2.1%, 2.0%, 1.9% or 1.8% (w/w). In embodiments, the nicotine concentration in the nicotine liquid formulation is about 1%, 1.1%, 1.2%, 1.3%, 1.4%, 1.5%, 1.6%, 1.7%, 1.8%, 1.9%, 2.0%, 2.1%, 2.2%, 2.3%, 2.4% or 2.5% (w/w).
In embodiments, the concentration of protonated nicotine in the nicotine liquid formulation is from about 0.5% (w/w) to about 25% (w/w). In embodiments, the concentration of protonated nicotine in the nicotine liquid formulation is from about 1% (w/w) to about 20% (w/w). In embodiments, the concentration of protonated nicotine in the nicotine liquid formulation is from about 1% (w/w) to about 18% (w/w). In embodiments, the concentration of protonated nicotine in the nicotine liquid formulation is from about 1% (w/w) to about 15% (w/w). In embodiments, the concentration of protonated nicotine in the nicotine liquid formulation is from about 4% (w/w) to about 12% (w/w). In embodiments, the concentration of protonated nicotine in the nicotine liquid formulation is from about 2% (w/w) to about 6% (w/w). In embodiments, the concentration of protonated nicotine in the nicotine liquid formulation is about 5% (w/w). In embodiments, the concentration of protonated nicotine in the nicotine liquid formulation is about 4% (w/w). In embodiments, the concentration of protonated nicotine in the nicotine liquid formulation is about 3% (w/w). In embodiments, the concentration of protonated nicotine in the nicotine liquid formulation is about 2% (w/w). In embodiments, the concentration of protonated nicotine in the nicotine liquid formulation is about 1% (w/w).
In embodiments, the concentration of protonated nicotine in the nicotine liquid formulation is from about 1%, 1.1%, 1.2%, 1.3%, 1.4%, 1.5%, 1.6%, or 1.7% to about 2.5%, 2.4%, 2.3%, 2.2%, 2.1%, 2.0%, 1.9%, or 1.8% (w/w). In embodiments, the concentration of protonated nicotine in the nicotine liquid formulation is about 1%, 1.1%, 1.2%, 1.3%, 1.4%, 1.5%, 1.6%, 1.7%, 1.8%, 1.9%, 2.0%, 2.1%, 2.2%, 2.3%, 2.4% or 2.5% (w/w).
In embodiments, the concentration of the organic acid in the nicotine liquid formulation is from about 0.5% to about 25%, wherein the concentration is the weight of the organic acid to the weight of the total solution, i.e. (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 1% (w/w) to about 20% (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 1% (w/w) to about 18% (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 1% (w/w) to about 15% (w/w). In an embodiment, the nicotine liquid formulation has an organic acid concentration of about 4% (w/w) to about 12% (w/w). In embodiments, the nicotine liquid formulation has a concentration of organic acid from about 1% (w/w) to about 18% (w/w), from about 3% (w/w) to about 15% (w/w), or from about 4% (w/w) to about 12% (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 0.5% (w/w) to about 10% (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 0.5% (w/w) to about 5% (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 0.5% (w/w) to about 4% (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 0.5% (w/w) to about 3% (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 0.5% (w/w) to about 2% (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 0.5% (w/w) to about 1% (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 1% (w/w) to about 10% (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 1% (w/w) to about 5% (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 1% (w/w) to about 4% (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 1% (w/w) to about 3% (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 1% (w/w) to about 2% (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 2% (w/w) to about 10% (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 2% (w/w) to about 5% (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 2% (w/w) to about 4% (w/w). In embodiments, the nicotine liquid formulation has a concentration of about 0.5%, 0.6%, 0.7%, 0.8%, 0.9%, 1.0%, 1.1%, 1.2%, 1.3%, 1.4%, 1.5%, 1.6%, 1.7%, 1.8%, 1.9%, 2.0%, 2.1%, 2.2%, 2.3%, 2.4%, 2.5%, 2.6%, 2.7%, 2.8%, 2.9%, 3.0%, 3.1%, 3.2%, 3.3%, 3.4%, 3.5%, 3.6%, 3.7%, 3.8%, 3.9%, 4.0%, 4.5%, 5.0%, 5.5%, 6.0%, 6.5%, 7.0%, 7.5%, 8.0%, 8.5%, 9.0%, 9.5%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19% or more (including any increment of w/w of organic acid therein). In an embodiment, the nicotine liquid formulation has a nicotine liquid formulation with an organic acid concentration of about 5% (w/w). In an embodiment, the nicotine liquid formulation has an organic acid concentration of about 4% (w/w). In an embodiment, the nicotine liquid formulation has an organic acid concentration of about 3% (w/w). In an embodiment, the nicotine liquid formulation has an organic acid concentration of about 2% (w/w). In an embodiment, the nicotine liquid formulation has an organic acid concentration of about 1% (w/w). In an embodiment, the nicotine liquid formulation has an organic acid concentration of about 0.5% (w/w).
In embodiments, the nicotine liquid formulation has an organic acid concentration of about 0.5% (w/w), 1% (w/w), about 2% (w/w), about 3% (w/w), about 4% (w/w), about 5% (w/w), about 6% (w/w), about 7% (w/w), about 8% (w/w), about 9% (w/w), about 10% (w/w), about 11% (w/w), about 12% (w/w), about 13% (w/w), about 14% (w/w), about 15% (w/w), about 16% (w/w), about 17% (w/w), about 18% (w/w), about 19% (w/w) or about 20% (w/w). In embodiments, the nicotine liquid formulation has from about 0.5% (w/w) to about 20% (w/w), from about 0.5% (w/w) to about 18% (w/w), from about 0.5% (w/w) to about 15% (w/w), from about 0.5% (w/w) to about 12% (w/w), from about 0.5% (w/w) to about 10% (w/w), from about 0.5% (w/w) to about 8% (w/w), from about 0.5% (w/w) to about 7% (w/w), from about 0.5% (w/w) to about 6% (w/w), from about 0.5% (w/w) to about 5% (w/w), from about 0.5% (w/w) to about 4% (w/w), from about 0.5% (w/w) to about 3% (w/w), or from about 0.5% (w/w) to about 2% (w/w) ) The organic acid concentration of (c). In embodiments, the nicotine liquid formulation has from about 1% (w/w) to about 20% (w/w), from about 1% (w/w) to about 18% (w/w), from about 1% (w/w) to about 15% (w/w), from about 1% (w/w) to about 12% (w/w), from about 1% (w/w) to about 10% (w/w), from about 1% (w/w) to about 8% (w/w), from about 1% (w/w) to about 7% (w/w), from about 1% (w/w) to about 6% (w/w), from about 1% (w/w) to about 5% (w/w), from about 1% (w/w) to about 4% (w/w), from about 1% (w/w) to about 3% (w/w), or from about 1% (w/w) to about 2% (w/w) ) The organic acid concentration of (c). In embodiments, the nicotine liquid formulation has from about 2% (w/w) to about 20% (w/w), from about 2% (w/w) to about 18% (w/w), from about 2% (w/w) to about 15% (w/w), from about 2% (w/w) to about 12% (w/w), from about 2% (w/w) to about 10% (w/w), an organic acid concentration from about 2% (w/w) to about 8% (w/w), from about 2% (w/w) to about 7% (w/w), from about 2% (w/w) to about 6% (w/w), from about 2% (w/w) to about 5% (w/w), from about 2% (w/w) to about 4% (w/w), or from about 2% (w/w) to about 3% (w/w). In embodiments, the nicotine liquid formulation has an organic acid concentration from about 3% (w/w) to about 20% (w/w), from about 3% (w/w) to about 18% (w/w), from about 3% (w/w) to about 15% (w/w), from about 3% (w/w) to about 12% (w/w), from about 3% (w/w) to about 10% (w/w), from about 3% (w/w) to about 8% (w/w), from about 3% (w/w) to about 7% (w/w), from about 3% (w/w) to about 6% (w/w), from about 3% (w/w) to about 5% (w/w), or from about 3% (w/w) to about 4% (w/w). In embodiments, the nicotine liquid formulation has an organic acid concentration from about 4% (w/w) to about 20% (w/w), from about 4% (w/w) to about 18% (w/w), from about 4% (w/w) to about 15% (w/w), from about 4% (w/w) to about 12% (w/w), from about 4% (w/w) to about 10% (w/w), from about 4% (w/w) to about 8% (w/w), from about 4% (w/w) to about 7% (w/w), from about 4% (w/w) to about 6% (w/w), or from about 4% (w/w) to about 5% (w/w). In embodiments, the nicotine liquid formulation has an organic acid concentration from about 5% (w/w) to about 20% (w/w), from about 5% (w/w) to about 18% (w/w), from about 5% (w/w) to about 15% (w/w), from about 5% (w/w) to about 12% (w/w), from about 5% (w/w) to about 10% (w/w), from about 5% (w/w) to about 8% (w/w), from about 5% (w/w) to about 7% (w/w), or from about 5% (w/w) to about 6% (w/w). In embodiments, the nicotine liquid formulation has an organic acid concentration from about 6% (w/w) to about 20% (w/w), from about 6% (w/w) to about 18% (w/w), from about 6% (w/w) to about 15% (w/w), from about 6% (w/w) to about 12% (w/w), from about 6% (w/w) to about 10% (w/w), from about 6% (w/w) to about 8% (w/w), or from about 6% (w/w) to about 7% (w/w). In an embodiment, the nicotine liquid formulation has a concentration of organic acid from about 2% (w/w) to about 6% (w/w). In an embodiment, the nicotine liquid formulation has an organic acid concentration of about 5% (w/w).
In embodiments, the concentration of the organic acid in the nicotine liquid formulation is from about 1%, 1.1%, 1.2%, 1.3%, 1.4%, 1.5%, 1.6% or 1.7% to about 2.5%, 2.4%, 2.3%, 2.2%, 2.1%, 2.0%, 1.9% or 1.8% (w/w). In embodiments, the concentration of the organic acid in the nicotine liquid formulation is about 1%, 1.1%, 1.2%, 1.3%, 1.4%, 1.5%, 1.6%, 1.7%, 1.8%, 1.9%, 2.0%, 2.1%, 2.2%, 2.3%, 2.4% or 2.5% (w/w).
The term "about" in the context of a value or range refers to ± 10% of the recited or claimed value or range of values unless the context requires a more limiting range, unless otherwise indicated with respect to the concentration of nicotine in a nicotine liquid formulation (e.g., total nicotine, free base nicotine, and/or protonated nicotine). In each instance where a value or range of values is preceded by the term "about" in this specification, the particular value or range of values without the term "about" is also disclosed. For example, a disclosure of "about 1%" is also a disclosure of "1%". Where a range of values is provided, all integers and tenths thereof within the range are also disclosed. For example, "0.5% to 5%" is a disclosure of 0.5%, 0.6%, 0.7%, 0.8%, 0.9%, 1%, 1.1%, etc. up to and including 5%.
In an embodiment, the pH of the nicotine liquid formulation is less than 7.0. In embodiments, the pH of the formulation is from about 2.5 to about 6.5. In embodiments, the pH of the formulation is from about 3 to about 6.5. In embodiments, the pH of the formulation is from about 4 to about 6.5. In embodiments, the pH of the formulation is from about 5 to about 6.5. In embodiments, the pH of the formulation is from about 6 to about 6.5. In embodiments, the pH of the formulation is from about 3 to about 5.5. In embodiments, the pH of the formulation is from about 3.5 to about 5.5. In embodiments, the pH of the formulation is about 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, or 6.5.
In embodiments, the formulation may include various stoichiometric and/or molar ratios of acid to nicotine, acid functional group to nicotine, and acid functional group hydrogen to nicotine. In embodiments, the molar ratio of nicotine to acid (nicotine: acid) is 1:1, 1:2, 1:3, 1:4, 2:3, 2:5, 2:7, 3:4, 3:5, 3:7, 3:8, 3:10, 3:11, 4:5, 4:7, 4:9, 4:10, 4:11, 4:13, 4:14, 4:15, 5:6, 5:7, 5:8, 5:9, 5:11, 5:12, 5:13, 5:14, 5:16, 5:17, 5:18, or 5: 19. In embodiments, the molar ratio of acid to nicotine (acid: nicotine) is 1:1, 1:2, 1:3, 1:4, 2:3, 2:5, 2:7, 3:4, 3:5, 3:7, 3:8, 3:10, 3:11, 4:5, 4:7, 4:9, 4:10, 4:11, 4:13, 4:14, 4:15, 5:6, 5:7, 5:8, 5:9, 5:11, 5:12, 5:13, 5:14, 5:16, 5:17, 5:18, or 5: 19. In embodiments, the ratio is the ratio of nicotine to an acid in the formulation. In embodiments, the ratio is the ratio of nicotine to all acids in the formulation. In embodiments, the ratio is the ratio of nicotine to all organic acids in the formulation. In embodiments, the molar ratio of nicotine to acid in the formulation is 1:1, 1:2, 1:3, or 1: 4. In embodiments, the molar ratio of acid to nicotine in the formulation is about 0.25:1, about 0.3:1, about 0.4:1, about 0.5:1, about 0.6:1, about 0.7:1, about 0.8:1, about 0.9:1, about 1:1, about 1.2:1, about 1.4:1, about 1.6:1, about 1.8:1, about 2:1, about 2.2:1, about 2.4:1, about 2.6:1, about 2.8:1, about 3:1, about 3.2:1, about 3.4:1, about 3.6:1, about 3.8:1, or about 4: 1. In embodiments, the molar ratio of acidic functional groups to nicotine in the formulation is about 0.25:1, about 0.3:1, about 0.4:1, about 0.5:1, about 0.6:1, about 0.7:1, about 0.8:1, about 0.9:1, about 1:1, about 1.2:1, about 1.4:1, about 1.6:1, about 1.8:1, about 2:1, about 2.2:1, about 2.4:1, about 2.6:1, about 2.8:1, about 3:1, about 3.2:1, about 3.4:1, about 3.6:1, about 3.8:1, or about 4: 1. In embodiments, the molar ratio of acidic functional group hydrogen to nicotine in the formulation is about 0.25:1, about 0.3:1, about 0.4:1, about 0.5:1, about 0.6:1, about 0.7:1, about 0.8:1, about 0.9:1, about 1:1, about 1.2:1, about 1.4:1, about 1.6:1, about 1.8:1, about 2:1, about 2.2:1, about 2.4:1, about 2.6:1, about 2.8:1, about 3:1, about 3.2:1, about 3.4:1, about 3.6:1, about 3.8:1, or about 4: 1. In embodiments, the molar ratio of acid to nicotine in the aerosol is about 0.25:1, about 0.3:1, about 0.4:1, about 0.5:1, about 0.6:1, about 0.7:1, about 0.8:1, about 0.9:1, about 1:1, about 1.2:1, about 1.4:1, about 1.6:1, about 1.8:1, about 2:1, about 2.2:1, about 2.4:1, about 2.6:1, about 2.8:1, about 3:1, about 3.2:1, about 3.4:1, about 3.6:1, about 3.8:1, or about 4: 1. In embodiments, the molar ratio of acidic functional groups to nicotine in the aerosol is about 0.25:1, about 0.3:1, about 0.4:1, about 0.5:1, about 0.6:1, about 0.7:1, about 0.8:1, about 0.9:1, about 1:1, about 1.2:1, about 1.4:1, about 1.6:1, about 1.8:1, about 2:1, about 2.2:1, about 2.4:1, about 2.6:1, about 2.8:1, about 3:1, about 3.2:1, about 3.4:1, about 3.6:1, about 3.8:1, or about 4: 1. In embodiments, the molar ratio of acid functional group hydrogen to nicotine in the aerosol is about 0.25:1, about 0.3:1, about 0.4:1, about 0.5:1, about 0.6:1, about 0.7:1, about 0.8:1, about 0.9:1, about 1:1, about 1.2:1, about 1.4:1, about 1.6:1, about 1.8:1, about 2:1, about 2.2:1, about 2.4:1, about 2.6:1, about 2.8:1, about 3:1, about 3.2:1, about 3.4:1, about 3.6:1, about 3.8:1, or about 4: 1.
In an embodiment, the nicotine is protonated. In embodiments, the number or moles of organic acid functional groups is equal to or greater than the molar amount of nicotine. In an embodiment, the number or moles of organic acid functional groups is equal to the molar amount of nicotine.
In embodiments, the number or moles of organic acid functional groups is greater than the molar amount of nicotine.
In embodiments, the number or moles of organic acid functional groups is from about 1.1 times to about 3.0 times the molar amount of nicotine. In embodiments, the number of organic acid functional groups is from about 1.5 times to about 2.2 times the molar amount of nicotine.
In embodiments, the amount or moles of excess organic acid functional groups is about 1.1 times, or about 1.2 times, or about 1.3 times, or about 1.4 times, or about 1.5 times, or about 1.6 times, or about 1.7 times, or about 1.8 times, or about 2 times, or about 2.1 times, or about 2.2 times, or about 2.3 times, or about 2.4 times, or about 2.5 times, or about 2.6 times, or about 2.7 times, or about 2.8 times, or about 2.9 times, or about 3.0 times, etc., the molar amount of nicotine present in the formulation. In embodiments, the excess amount or moles of organic acid functional groups provide a user with less irritation upon inhalation relative to a control formulation.
In an embodiment, the molar ratio of organic acid to nicotine is about 0.5: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 0.6: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 0.7: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 0.8: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 0.9: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 1.0: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 1.1: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 1.2: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 1.3: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 1.4: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 1.5: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 1.6: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 1.7: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 1.8: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 1.9: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 2.0: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 3: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 4: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 5: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 6: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 7: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 8: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 9: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 10: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 11: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 12: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 13: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 14: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 15: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 16: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 17: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 18: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 19: 1. In an embodiment, the molar ratio of organic acid to nicotine is about 20: 1.
In embodiments, the molar ratio of organic acid to nicotine is at least 0.5: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 0.6: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 0.7: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 0.8: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 0.9: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 1.0: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 1.1: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 1.2: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 1.3: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 1.4: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 1.5: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 1.6: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 1.7: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 1.8: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 1.9: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 2.0: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 3: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 4: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 5: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 6: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 7: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 8: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 9: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 10: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 11: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 12: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 13: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 14: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 15: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 16: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 17: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 18: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 19: 1. In embodiments, the molar ratio of organic acid to nicotine is at least 20: 1.
Nicotine is an alkaloid molecule with two basic nitrogens. It may occur in different protonation states. Nicotine is "protonated" if at least one of the two nitrogens is covalently bound to a proton. Protonated nicotine includes monoprotonated nicotine, biprotonated nicotine, and combinations thereof. If one nitrogen is protonated, the nicotine is "single protonated" nicotine. If both nitrogens are protonated, the nicotine is "dual protonated" nicotine. If protonation is not present, the nicotine is referred to as "free base" nicotine. In embodiments, the nicotine becomes protonated when combined with a sufficient amount of acid. After protonation, the nicotine is positively charged and the formulation may further include a counter ion. In an embodiment, the counterion is the conjugate base of the acid. For example, where the acid is benzoic acid, the counter ion may be benzoate, thereby forming nicotine benzoate.
In embodiments, different nicotine liquid formulations produce different degrees of enhancement of nicotine-related biological effects (e.g., faster heart rate rise). In embodiments, different nicotine liquid formulations produce different degrees of satisfaction, irritation, nicotine delivery, and/or heart rate acceleration in an individual. In an embodiment, the degree of nicotine protonation has an effect on satisfaction, irritation, nicotine delivery and/or heart rate such that more protonation is more satisfactory than less protonation. In embodiments, the nicotine (e.g., nicotine in a formulation) and/or aerosol is monoprotonated. In embodiments, the nicotine (e.g., nicotine in a formulation) and/or aerosol is dual protonated. In embodiments, nicotine (e.g., nicotine in a formulation) and/or aerosol is present in more than one protonated state, e.g., the equilibrium of mono-protonated and di-protonated nicotine. In embodiments, the extent of nicotine protonation depends on the nicotine used in the formulation: the ratio of the acids. In an embodiment, the degree of protonation of nicotine is solvent dependent. In an embodiment, the degree of protonation of nicotine has not been determined.
In embodiments, the liquid carrier comprises a liquid solvent or medium: the protonated nicotine may be dissolved in the liquid solvent or vehicle (e.g., at ambient conditions such as 25 ℃) such that the protonated nicotine does not form a solid precipitate. Examples include, but are not limited to, glycerol, propylene glycol, 1, 3-propanediol, water, ethanol, and the like, and combinations thereof. In an embodiment, the liquid carrier comprises a ratio of propylene glycol to vegetable glycerin. In embodiments, the liquid carrier comprises 10% to 70% propylene glycol and 90% to 30% vegetable glycerin. In embodiments, the liquid carrier comprises 20% to 50% propylene glycol and 80% to 50% vegetable glycerin. In an embodiment, the liquid carrier comprises 30% propylene glycol and 70% vegetable glycerin. In embodiments, the liquid carrier is all propylene glycol or all vegetable glycerin. In embodiments, the liquid carrier includes another aerosol former similar to propylene glycol, glycerin or other glycols, or the like, or any combination thereof.
In an embodiment, heating an amount of nicotine liquid formulation produces an aerosol, wherein at least about 50% of the acid amount is present in the aerosol. In embodiments, at least about 90% of the nicotine amount is present in the aerosol. In embodiments, at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, at least 95%, or at least about 99% of the acid is present in the aerosol. In embodiments, at least about 50% to about 99% of the acid is present in the aerosol. In embodiments, at least about 50% to about 95% of the acid is present in the aerosol. In embodiments, at least about 50% to about 90% of the acid is present in the aerosol. In embodiments, at least about 50% to about 80% of the acid is present in the aerosol. In embodiments, at least about 50% to about 70% of the acid is present in the aerosol. In embodiments, at least about 50% to about 60% of the acid is present in the aerosol. In embodiments, at least about 60% to about 99% of the acid is present in the aerosol. In embodiments, at least about 60% to about 95% of the acid is present in the aerosol. In embodiments, at least about 60% to about 90% of the acid is present in the aerosol. In embodiments, at least about 60% to about 80% of the acid is present in the aerosol. In embodiments, at least about 60% to about 70% of the acid is present in the aerosol. In embodiments, at least about 70% to about 99% of the acid is present in the aerosol. In embodiments, at least about 70% to about 95% of the acid is present in the aerosol. In embodiments, at least about 70% to about 90% of the acid is present in the aerosol. In embodiments, at least about 70% to about 80% of the acid is present in the aerosol. In embodiments, at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, at least 95%, or at least about 99% of the amount of nicotine is present in the aerosol. In embodiments, at least about 50% to about 99% of the nicotine amount is present in the aerosol. In embodiments, at least about 50% to about 95% of the nicotine amount is present in the aerosol. In embodiments, at least about 50% to about 90% of the nicotine amount is present in the aerosol. In embodiments, at least about 50% to about 80% of the nicotine amount is present in the aerosol. In embodiments, at least about 50% to about 70% of the nicotine amount is present in the aerosol. In embodiments, at least about 50% to about 60% of the nicotine amount is present in the aerosol. In embodiments, at least about 60% to about 99% of the nicotine amount is present in the aerosol. In embodiments, at least about 60% to about 95% of the nicotine amount is present in the aerosol. In embodiments, at least about 60% to about 90% of the nicotine amount is present in the aerosol. In embodiments, at least about 60% to about 80% of the nicotine amount is present in the aerosol. In embodiments, at least about 60% to about 70% of the nicotine amount is present in the aerosol. In embodiments, at least about 70% to about 99% of the nicotine amount is present in the aerosol. In embodiments, at least about 70% to about 95% of the nicotine amount is present in the aerosol. In embodiments, at least about 70% to about 90% of the nicotine amount is present in the aerosol. In embodiments, at least about 70% to about 80% of the nicotine amount is present in the aerosol.
In an embodiment, the aerosol is delivered in the form of particles small enough to be delivered through the oral or nasal cavity and to the lungs of the user, e.g., the alveoli of the user's lungs. In embodiments, the aerosol particles have a size (e.g., diameter) of from about 0.1 micron to about 5 microns, from about 0.1 micron to about 4.5 microns, from about 0.1 micron to about 4 microns, from about 0.1 micron to about 3.5 microns, from about 0.1 micron to about 3 microns, from about 0.1 micron to about 2.5 microns, from about 0.1 micron to about 2 microns, from about 0.1 micron to about 1.5 microns, from about 0.1 micron to about 1 micron, from about 0.1 micron to about 0.9 micron, from about 0.1 micron to about 0.8 micron, from about 0.1 micron to about 0.7 micron, from about 0.1 micron to about 0.6 micron, from about 0.1 micron to about 0.5 micron, from about 0.1 micron to about 0.4 micron, from about 0.1 micron to about 0.3 micron, from about 0.1 micron to about 0.6 micron, from about 0.1 micron to about 2 microns, from about 0.5 micron to about 2 microns, from about 0.1 micron to about 2 microns, from about 2 microns to about 2.5 microns, from about 2 microns, about, From about 0.2 microns to about 2.5 microns, from about 0.2 microns to about 2 microns, from about 0.2 microns to about 1.5 microns, from about 0.2 microns to about 1 micron, from about 0.2 microns to about 0.9 microns, from about 0.2 microns to about 0.8 microns, from about 0.2 microns to about 0.7 microns, from about 0.2 microns to about 0.6 microns, from about 0.2 microns to about 0.5 microns, from about 0.2 microns to about 0.4 microns, from about 0.2 microns to about 0.3 microns, from about 0.3 microns to about 5 microns, from about 0.3 microns to about 4.5 microns, from about 0.3 microns to about 4 microns, from about 0.3 microns to about 3.5 microns, from about 0.3 microns to about 3 microns, from about 0.3 microns to about 2.5 microns, from about 0.3 microns to about 0.3 microns, from about 0.3 microns to about 0.9 microns, from about 0.3 microns to about 0.5 microns, from about 0.3 microns to about 0 microns, from about 0.3 microns to about 0.3 microns, from about 0.3 microns to about 0 microns, from about 0.3 microns to about 0.5 microns, from about 0 microns to about 0.3 microns, from about 0 microns to about 0.3 microns to about 0.6 microns, from about 0, From about 0.3 microns to about 0.5 microns, from about 0.3 microns to about 0.4 microns, from about 0.4 microns to about 5 microns, from about 0.4 microns to about 4.5 microns, from about 0.4 microns to about 4 microns, from about 0.4 microns to about 3.5 microns, from about 0.4 microns to about 3 microns, from about 0.4 microns to about 2.5 microns, from about 0.4 microns to about 2 microns, from about 0.4 microns to about 1.5 microns, from about 0.4 microns to about 1 micron, from about 0.4 microns to about 0.9 microns, from about 0.4 microns to about 0.8 microns, from about 0.4 microns to about 0.7 microns, from about 0.4 microns to about 0.6 microns, from about 0.4 microns to about 0.5 microns, from about 0.5 microns to about 5 microns, from about 0.5 microns to about 4.5 microns, from about 0.5 microns to about 5 microns, from about 0.5 microns to about 0.5 microns, from about 0.5 microns to about 5 microns, from about 0.5 microns, from about 0.5 microns to about 1 micron, from about 0.5 microns to about 0.9 microns, from about 0.5 microns to about 0.8 microns, from about 0.5 microns to about 0.7 microns, from about 0.5 microns to about 0.6 microns, from about 0.6 microns to about 5 microns, from about 0.6 microns to about 4.5 microns, from about 0.6 microns to about 4 microns, from about 0.6 microns to about 3.5 microns, from about 0.6 microns to about 3 microns, from about 0.6 microns to about 2.5 microns, from about 0.6 microns to about 2 microns, from about 0.6 microns to about 1.5 microns, from about 0.6 microns to about 1 micron, from about 0.6 microns to about 0.9 microns, from about 0.6 microns to about 0.8 microns, from about 0.6 microns to about 0.7 microns, from about 0.8 microns to about 5 microns, from about 0.5 microns to about 0.8 microns, from about 0.6 microns to about 0.8 microns, from about 0.8 microns to about 8 microns, from about 0.8 microns to about 2 microns, from about 8 microns, from about 0.5 microns to about 8 microns, from about 0.8 microns to about 8 microns, from about 8 microns to about 8 microns, from about 0.5 microns, from about 8 microns to about 8, From about 0.8 microns to about 1.5 microns, from about 0.8 microns to about 1 micron, from about 0.8 microns to about 0.9 microns, from about 0.9 microns to about 5 microns, from about 0.9 microns to about 4.5 microns, from about 0.9 microns to about 4 microns, from about 0.9 microns to about 3.5 microns, from about 0.9 microns to about 3 microns, from about 0.9 microns to about 2.5 microns, from about 0.9 microns to about 2 microns, from about 0.9 microns to about 1.5 microns, from about 0.9 microns to about 1 micron, from about 1 micron to about 5 microns, from about 1 micron to about 4.5 microns, from about 1 micron to about 4 microns, from about 1 micron to about 3.5 microns, from about 1 micron to about 3 microns, from about 1 micron to about 2.5 microns, from about 1 micron to about 2 microns, from about 1 micron to about 1.5 microns.
In an embodiment, the amount of nicotine liquid formulation provided to the heater comprises a volume or a mass. In embodiments, the amount is quantified "per puff". In embodiments, the amount comprises a volume of about 1 μ L, about 2 μ L, about 3 μ L, about 4 μ L, about 5 μ L, about 6 μ L, about 7 μ L, about 8 μ L, about 9 μ L, about 10 μ L, about 15 μ L, about 20 μ L, about 25 μ L, about 30 μ L, about 35 μ L, about 40 μ L, about 45 μ L, about 50 μ L, about 60 μ L, about 70 μ L, about 80 μ L, about 90 μ L, about 100 μ L, or greater than about 100 μ L. In embodiments, the amount includes a mass of about 1mg, about 2mg, about 3mg, about 4mg, about 5mg, about 6mg, about 7mg, about 8mg, about 9mg, about 10mg, about 15mg, about 20mg, about 25mg, about 30mg, about 35mg, about 40mg, about 45mg, about 50mg, about 60mg, about 70mg, about 80mg, about 90mg, about 100mg, or greater than about 100 mg.
In embodiments, nicotine in the aerosol from the devices provided herein is delivered (e.g., absorbed) faster than nicotine in the smoke from a conventional cigarette, such that less nicotine is required in the aerosol. In embodiments, a puff of the aerosol has less nicotine than a puff from a conventional cigarette. In embodiments, the "one puff of aerosol" is a first, second, third, fourth, fifth, sixth, seventh, eighth, ninth, or tenth puff from a device comprising a cartridge disclosed herein when the device is fully charged and a new cartridge is used. In embodiments, the "one puff from the conventional cigarette" is a first, second, third, fourth, fifth, sixth, seventh, eighth, ninth, or tenth puff from the conventional cigarette after the first lighting of the cigarette. In embodiments, a "puff" is an aerosol (in the case of the devices disclosed herein) or a smoke (in the case of a conventional cigarette) of about 40ml, 45ml, 50ml, 55ml, 60ml, 65ml, 70ml, 75ml, or 80ml volume. In an embodiment, the puff is drawn from a device or a conventional cigarette over a period of 1-5 seconds. In an embodiment, the puff is drawn from a device or a conventional cigarette in a period of 2-3 seconds. In an embodiment, the puff is drawn from a device or a conventional cigarette in a period of 2-3 seconds. In embodiments, the puff is drawn from a device or a conventional cigarette over a period of about 1 second, 2 seconds, 3 seconds, 4 seconds, or 5 seconds. In an embodiment, the puff is drawn from a device or a conventional cigarette within a period of about 1 second. In an embodiment, the puff is drawn from a device or a conventional cigarette within a period of about 2 seconds. In an embodiment, the puff is drawn from a device or a conventional cigarette within a period of about 3 seconds. In an embodiment, the puff is drawn from a device or a conventional cigarette within a period of about 4 seconds. In an embodiment, the puff is drawn from a device or a conventional cigarette within a period of about 5 seconds. In an embodiment, there is less nicotine in the puff from the device disclosed herein than in a conventional cigarette, wherein the puff from the device has a volume of about 70ml and is drawn from the device over a period of about 3 seconds, and wherein the puff from the conventional cigarette has a volume of about 55ml and is drawn from the conventional cigarette over a period of about 2 seconds. In embodiments, a 40-80ml puff (e.g., 40ml, 45ml, 50ml, 55ml, 60ml, 65ml, 70ml, 75ml, or 80ml) lifted from a device disclosed herein over a period of about 1-5 seconds (e.g., about 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 2-4, 2-3, or 1-3 seconds) has about 0.5-1mg nicotine. In embodiments, the puff has about 0.5, 0.55, 0.6, 0.65, 0.75, 0.80, 0.85, 0.95, or 1mg of nicotine. In embodiments, the smoking cigarette has 0.5-0.75mg nicotine. In an embodiment, the puff has about 0.75-1mg nicotine. In embodiments, the puff has 0.65-0.85mg nicotine.
In embodiments, a greater portion of nicotine in the aerosol from the devices provided herein is delivered (e.g., absorbed) by the user than nicotine in the smoke from a conventional cigarette, such that the user exhales less nicotine. As used herein, an "exhaled nicotine amount" is the amount of nicotine that leaves the airway of a user when the user exhales for the first time after inhaling a puff. In embodiments, the user exhales less nicotine when using the devices disclosed herein than when using a conventional cigarette. In embodiments, the amount of nicotine exhaled using the devices disclosed herein is at least about 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, or 95% less than when using a conventional cigarette. In embodiments, at least about 75, 80, 85, 90, 95, 96, 97, 98, or 99% of the nicotine remains in the user (i.e., is not exhaled) when the user inhales the aerosol generated by the devices provided herein. In embodiments, about 80-100%, 80-90%, 85-95%, 90-100%, 95-100%, 90-95%, 90-99%, 95-99% of the nicotine is not exhaled when a user inhales the aerosol generated by a device provided herein. In embodiments, when a user inhales an aerosol generated by a device provided herein, no nicotine is exhaled. In embodiments, the devices provided herein are more effective than conventional cigarettes in controlling nicotine dosage per puff.
In embodiments, the nicotine liquid formulation may include one or more flavors.
In the examples, the flavor of the component acid used in the formulation is a consideration in selecting the acid. In the examples, suitable acids are those which are minimally or non-toxic to humans at the concentrations employed. In embodiments, a suitable acid is compatible with the electronic nicotine delivery system component it contacts or is contactable with at the use concentration conditions. That is, such an acid does not degrade or otherwise react with the electronic nicotine delivery system component with which it is or may come into contact. In an embodiment, the odor of the component acid used to protonate nicotine is a consideration in selecting a suitable acid. In embodiments, the concentration of protonated nicotine in the carrier may affect user satisfaction. In embodiments, the flavor of the formulation is modulated by altering the acid. In an embodiment, the flavor of the formulation is modified by the addition of exogenous flavor. In the examples, the unpleasant tasting or smelling acid is used in minimal amounts to mitigate such traits. In the examples, exogenous, tasting or smelling pleasant acids are added to the formulations. Non-limiting examples of organic acids that can provide some degree of flavor and aroma to the aerosol include acetic acid, oxalic acid, malic acid, isovaleric acid, lactic acid, citric acid, phenylacetic acid, and myristic acid.
In an embodiment, the amount of inhaled nicotine aerosol (e.g., comprising protonated nicotine) may be determined by a user. In an embodiment, the user may change the amount of nicotine, for example, by adjusting his or her inhalation intensity.
In an embodiment, the electronic nicotine delivery system does not deliver an increased oxygen level to the user, for example, compared to an ambient oxygen level. In embodiments, the electronic nicotine delivery system does not include pressurized oxygen or chemical storage for oxygen contained in the aerosol. In embodiments, the aerosol comprises, consists essentially of, or consists of an aerosolized nicotine liquid formulation, optionally in combination with ambient air.
Term(s) for
When a feature or element is referred to herein as being "on" another feature or element, the feature or element may be directly on the other feature or element or intervening features and/or elements may also be present. In contrast, when a feature or element is referred to as being "directly on" another feature or element, there are no intervening features or elements present. It will also be understood that when a feature or element is referred to as being "connected," "attached," or "coupled" to another feature or element, it can be directly connected, attached, or coupled to the other feature or element or intervening features or elements may be present. In contrast, when a feature or element is referred to as being "directly connected," "directly attached," or "directly coupled" to another feature or element, there are no intervening features or elements present.
Although described or illustrated with respect to one embodiment, the features and elements so described or illustrated may be applicable to other embodiments. It will also be understood by those skilled in the art that references to a structure or feature that is disposed "adjacent" another feature may have portions that overlap or underlay the adjacent feature.
The terminology used herein is for the purpose of describing particular embodiments and implementations only and is not intended to be limiting. For example, as used herein, the singular forms "a", "an" and "the" are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms "comprises" and/or "comprising," when used in this specification, specify the presence of stated features, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, steps, operations, elements, components, and/or groups thereof. As used herein, the term "and/or" includes any and all combinations of one or more of the associated listed items and may be abbreviated as "/".
In the description above and in the claims, phrases such as "at least one of … …" or "one or more of … …" may appear after a consecutive listing of elements or features. The term "and/or" may also be present in a list of two or more elements or features. Such phrases are intended to mean any of the recited elements or features individually or in any combination with any of the other recited elements or features, unless otherwise implicitly or explicitly contradicted by context in which such phrase is used. For example, the phrases "at least one of a and B", "one or more of a and B", and "a and/or B" are each intended to mean "a alone, B alone, or a and B together". Similar interpretations are also intended to include more than three items. For example, the phrases "at least one of A, B and C", "one or more of A, B and C", and "A, B and/or C" are each intended to mean "a alone, B alone, C alone, a and B together, a and C together, B and C together, or a and B and C together". The use of the term "based on" above and in the claims is intended to mean "based at least in part on" such that non-recited features or elements are also permitted.
Spatially relative terms such as "forward", "rearward", "below … …", "below … …", "below", "over … …", "over", and the like may be used herein for ease of description to describe one element or feature's relationship to another element or feature as illustrated in the figures. It will be understood that the spatially relative terms are intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the figures. For example, if the device is turned over in the drawings, elements described as "below" or "beneath" other elements or features would then be oriented "above" the other elements or features. Thus, the exemplary term "below … …" can encompass both an orientation of "above … …" and an orientation of "below … …". The device may be otherwise oriented (rotated 90 degrees or at other orientations) and the spatially relative descriptors used herein interpreted correspondingly. Similarly, the terms "upward," "downward," "vertical," "horizontal," and the like are used herein for the purpose of illustration only, unless explicitly indicated otherwise.
Although the terms "first" and "second" may be used herein to describe different features/elements (including steps), these features/elements should not be limited by these terms unless the context indicates otherwise. These terms may be used to distinguish one feature/element from another feature/element. Thus, a first feature/element discussed below could be termed a second feature/element, and similarly, a second feature/element discussed below could be termed a first feature/element, without departing from the teachings provided herein.
As used in this specification and the claims, including as used in the examples, and unless otherwise expressly specified, all numbers may be read as if prefaced by the word "about" or "approximately", even if the term does not expressly appear. When describing sizes and/or locations, the phrase "about" or "approximately" may be used to indicate that the described values and/or locations are within a reasonably expected range of values and/or locations. For example, a numerical value may have a value (or range of values) that is +/-0.1% of the stated value, a value (or range of values) that is +/-1% of the stated value, a value (or range of values) that is +/-2% of the stated value, a value (or range of values) that is +/-5% of the stated value, a value (or range of values) that is +/-10% of the stated value, and the like. Any numerical value given herein is also to be understood as including about that value or about that value unless the context indicates otherwise. For example, if the value "10" is disclosed, then "about 10" is also disclosed. Any numerical range recited herein is intended to include all sub-ranges subsumed therein. It is also understood that when values are disclosed that "less than or equal to" the recited value, "greater than or equal to" the recited value, and possible ranges between values are also disclosed, as is well understood by those of skill in the art. For example, if the value "X" is disclosed, "less than or equal to X" and "greater than or equal to X" (e.g., where X is a numerical value) are also disclosed. It is also understood that throughout this application, data is provided in a number of different forms, and that the data represents endpoints and starting points and ranges for any combination of data points. For example, if a particular data point "10" and a particular data point "15" are disclosed, it is understood that greater than, greater than or equal to, less than or equal to, and equal to 10 and 15 are also considered disclosed, along with between 10 and 15. It is also understood that each unit between two particular units is also disclosed. For example, if 10 and 15 are disclosed, 11, 12, 13 and 14 are also disclosed.
Although various illustrative embodiments have been described above, any number of variations may be made in the various embodiments without departing from the teachings herein. For example, the order in which the different described method steps are performed may often be varied in alternative embodiments, and in other alternative embodiments one or more method steps may be skipped entirely. Optional features in different device and system embodiments may be included in some embodiments and not in others. Accordingly, the foregoing description is provided primarily for the purpose of illustration and should not be construed to limit the scope of the claims.
One or more aspects or features of the subject matter described herein may be implemented as follows: digital electronic circuitry, integrated circuitry, specially designed Application Specific Integrated Circuits (ASICs), Field Programmable Gate Arrays (FPGAs) computer hardware, firmware, software, and/or combinations thereof. These various aspects or features may include embodiments that employ one or more computer programs that are executable and/or interpretable on a programmable system including at least one programmable processor, which may be special or general purpose, coupled to receive data and instructions from, and to transmit data and instructions to, a storage system, at least one input device, and at least one output device. A programmable or computing system may include clients and servers. A client and server are conventionally remote from each other and typically interact through a communication network. The association of client and server arises by virtue of computer programs running on the respective computers and having a client-server relationship to each other.
These computer programs, which may also be referred to as "programs," "software applications," "components," or "code," include machine instructions for a programmable processor, and may be implemented in a high-level programming language, an object-oriented programming language, a functional programming language, a logical programming language, and/or in assembly/machine language. As used herein, the term "machine-readable medium" refers to any computer program product, apparatus and/or device for providing machine instructions and/or data to a programmable processor, such as, for example, magnetic disks, optical disks, memory, and Programmable Logic Devices (PLDs), including a machine-readable medium that receives machine instructions as a machine-readable signal. The term "machine-readable signal" refers to any signal used to provide machine instructions and/or data to a programmable processor. A machine-readable medium may store such machine instructions non-transitory, such as, for example, non-transitory solid state memory or a magnetic hard drive or any equivalent storage medium. A machine-readable medium may alternatively or additionally store such machine instructions in a transitory manner, such as, for example, a processor cache or other random access memory associated with one or more physical processor memories.
The examples and illustrations contained herein show by way of illustration, and not limitation, specific embodiments in which the subject matter may be practiced. As mentioned, other embodiments may be utilized and derived from the specific embodiments, such that structural and logical substitutions and changes may be made without departing from the scope of this disclosure. Such embodiments of the inventive subject matter may be referred to herein, individually or collectively, by the term "invention" merely for convenience and without intending to voluntarily limit the scope of this application to any single invention or inventive concept if more than one is in fact disclosed. Thus, although specific embodiments have been illustrated and described herein, any arrangement calculated to achieve the same purpose may be substituted for the specific embodiments shown. This disclosure is intended to cover any and all adaptations or variations of various embodiments. Combinations of the above embodiments, and other embodiments not specifically described herein, will be apparent to those of skill in the art upon reviewing the above description.
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