US20140190496A1 - Methods and devices for compound delivery - Google Patents

Methods and devices for compound delivery Download PDF

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Publication number
US20140190496A1
US20140190496A1 US14/092,405 US201314092405A US2014190496A1 US 20140190496 A1 US20140190496 A1 US 20140190496A1 US 201314092405 A US201314092405 A US 201314092405A US 2014190496 A1 US2014190496 A1 US 2014190496A1
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Prior art keywords
passageway
heater element
cases
nicotine
agent
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Abandoned
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US14/092,405
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English (en)
Inventor
Martin Wensley
Michael Hufford
Jeffrey Williams
Peter Lloyd
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Fontem Ventures BV
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E Nicotine Technology Inc
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Filing date
Publication date
Application filed by E Nicotine Technology Inc filed Critical E Nicotine Technology Inc
Priority to US14/092,405 priority Critical patent/US20140190496A1/en
Publication of US20140190496A1 publication Critical patent/US20140190496A1/en
Assigned to E-NICOTINE TECHNOLOGY, INC. reassignment E-NICOTINE TECHNOLOGY, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: LLOYD, PETER, WENSLEY, MARTIN, WILLIAMS, JEFFREY, HUFFORD, MICHAEL
Assigned to FONTEM HOLDINGS 1 B.V. reassignment FONTEM HOLDINGS 1 B.V. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: E-NICOTINE TECHNOLOGY INC.
Abandoned legal-status Critical Current

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    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
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    • A—HUMAN NECESSITIES
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    • A61M11/04—Sprayers or atomisers specially adapted for therapeutic purposes operated by the vapour pressure of the liquid to be sprayed or atomised
    • A61M11/041—Sprayers or atomisers specially adapted for therapeutic purposes operated by the vapour pressure of the liquid to be sprayed or atomised using heaters
    • A24F47/008—
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    • A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
    • A24B15/10—Chemical features of tobacco products or tobacco substitutes
    • A24B15/16—Chemical features of tobacco products or tobacco substitutes of tobacco substitutes
    • A24B15/167—Chemical features of tobacco products or tobacco substitutes of tobacco substitutes in liquid or vaporisable form, e.g. liquid compositions for electronic cigarettes
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    • A61M2205/00—General characteristics of the apparatus
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    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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Definitions

  • NRTs Current nicotine replacement therapies
  • eCigs electronic cigarettes
  • Smokers also vary widely in terms of their daily nicotine intake, ranging from “social smokers” who may only consume 1 or 2 cigarettes in the presence of friends and/or with alcohol, to heavy smokers who consume 60 or more cigarettes per day.
  • social smokers who may only consume 1 or 2 cigarettes in the presence of friends and/or with alcohol
  • heavy smokers who consume 60 or more cigarettes per day.
  • Deep lung absorption of nicotine can facilitate rapid delivery of nicotine to the brain, which can result in a subsequent cessation of nicotine cravings.
  • nicotine laden smoke particles are carried proximally on tar droplets (0.1-1.0 ⁇ M in diameter), are inhaled and travel to the small airways and alveoli in the deep lung. Nicotine off-gasses from particles and defuses to, and deposits on, the alveoli wall where it can be rapidly absorbed into the blood stream.
  • a typical electronic cigarette does not produce an aerosol of nicotine with a particle size for deep lung delivery. Aerosol particles with an aerodynamic diameter larger than 5 ⁇ m can be too large to reach the deep lung because the particles can impact in the mouth and upper airway, resulting in a slow PK. Conversely, aerosol particles with a median aerodynamic diameter of less than 1 ⁇ m can be small enough to reach the deep lung but can be too light to gravitationally settle and can be exhaled, which can result in low dose delivery. Additionally, aerosols with small aerosol particle size can contain a larger percentage of the mass in the gas phase, which rapidly diffuses to the mouth and upper airway.
  • Aerosol particles with an aerodynamic diameter of about 1 ⁇ m to about 5 ⁇ m can be small enough to reach the deep lung but large enough to gravitationally settle in alveoli, which can result in a rapid PK.
  • a condensation aerosol generating device for generating a condensation aerosol from a liquid formulation, the device comprising: a) a reservoir comprising a liquid formulation; and b) a passageway comprising a heater element, an inlet, and an outlet, wherein the heater element is disposed in the passageway between the inlet and the outlet, wherein the reservoir is in fluid communication with the heater element, and wherein the passageway is configured to produce a condensation aerosol in the device, wherein the condensation aerosol has a mass median aerodynamic diameter (MMAD) of from about 1 ⁇ m to about 5 ⁇ m.
  • the heater element comprises a wick element.
  • the heater element comprises a coil.
  • the heater element comprises a wick element and a coil.
  • the wick element comprises an electrically resistive material.
  • the wick element and coil are formed from the same rod.
  • the rod comprises a pliable material.
  • the coil is wrapped around the wick element.
  • the wick element is capable of being heated.
  • the coil spans a length of from about 0.25 cm to about 0.39 cm (from about 0.1 inch to about 0.15 inches) along the length of the wick element.
  • the heater element comprises a wire coil.
  • the device further comprises a positive displacement pump in fluid communication with the reservoir.
  • the displacement pump is configured to pump the liquid formulation comprising the liquid formulation to the heater element.
  • the positive displacement pump comprises a peristaltic pump.
  • the passageway has an internal diameter of from 0.20 cm to about 1.3 cm (about 0.08 inches to about 0.5 inches). In some cases, an internal diameter of the passageway where the heater element is located is from about 0.44 cm to about 0.64 cm (about 0.175 to about 0.25 inches). In some cases, an internal diameter of the passageway before and after the heater element is from about 0.07 cm to about 1.3 cm (about 0.03 to about 0.5 inches). In some cases, the length of the passageway is from about 0.5 cm to about 15.3 cm (from about 0.2 inches to about 6 inches). In some cases, the device further comprises a baffle disposed in the passageway between the outlet and the heater element. In some cases, the baffle inhibits flow of particles having an MMAD of greater than 5 ⁇ m.
  • the device further comprises a second passageway connected to the passageway.
  • the second passageway connects with the passageway between the outlet and the heater element.
  • the second passageway connects with the passageway between the air inlet and the heater element.
  • the device further comprises a power source in electric communication with the heater element.
  • the power source is a battery.
  • the device further comprises a tube disposed within the passageway and connected to the reservoir, wherein the tube is configured to deliver the liquid formulation to the heater element.
  • the tube is a capillary.
  • the tube comprises a valve.
  • the tube comprises a second heater element.
  • the tube comprises a heatable region.
  • the device further comprises a valve located in the tube between the heatable region and the reservoir.
  • the tube comprises an electrically resistive material.
  • the device further comprises a flow restrictor disposed in the passageway.
  • a flow rate of a gas through the device is capable of delivering the condensation aerosol of the liquid formulation to a deep lung of a user of the device.
  • a flow rate of gas through the device that is capable of delivering the condensation aerosol of the liquid formulation to a deep lung of a user of the device is from about 20 liters per minute (LPM) to about 80 LPM.
  • the device permits a flow resistance of from about 0.05 to about 0.15 sqrt (cm-H2O)/LPM.
  • the device permits a flow resistance of from about 0.08 to about 0.12 sqrt (cm-H2O)/LPM.
  • the condensation aerosol is formed at a flow rate of about 1 LPM to about 10 LPM past the heater element under a vacuum of between about 249 Pa to about 3738 Pa (about 1 inch of water to about 15 inches of water).
  • the device further comprises a mouthpiece attached to the outlet.
  • the liquid formulation comprises a flavoring.
  • the liquid formulation comprises a pharmaceutically active agent.
  • the liquid formulation comprises nicotine and a carrier.
  • the carrier comprises propylene glycol or vegetable glycerin.
  • the device further comprises a programmable controller.
  • the programmable controller comprises a non-transitory computer readable medium, wherein the non-transitory computer readable medium comprises one or more algorithms for regulating dosage of the condensation aerosol of the liquid formulation, frequency of administration of the condensation aerosol of the liquid formulation, or a delivery schedule of the condensation aerosol of the liquid formulation.
  • the programmable controller is connected to one or more electronic devices.
  • the one or more electronic devices comprise a computer, a smartphone, or a mobile phone.
  • the reservoir is within the passageway.
  • the device further comprises a sensor to detect inhalation. In some cases, the sensor comprises an optical path. In some cases, the device further comprises a second heater element. In some cases, the heater element is a aerosol generating heater element. In some cases, the heater element is capable of vaporizing the liquid formulation when the liquid formulation is delivered to the heater element, wherein the vaporized liquid formulation is condensed into aerosol particles in the passageway. In some cases, the device further comprises an air flow regulator. In some cases, the device further comprises a second passageway, wherein the air flow regulator is capable of directing air through the second passageway in response to a pressure drop across the air flow regulator. In some cases, the air flow regulator comprises one or more gas control valves.
  • the device further comprises a controller, wherein the controller comprises a non-transitory computer readable medium comprising one or more algorithms, wherein the one or more algorithms regulate dosing or a delivery schedule of the condensation aerosol of the liquid formulation.
  • the device further comprises an interface for communicating with the controller.
  • the controller is removably attached to the passageway and the reservoir. In some cases, the controller is capable of communicating with one or more electronic devices.
  • a condensation aerosol generating device for generating a condensation aerosol comprising a pharmaceutically active agent, the device comprising: a) a housing comprising a heater element for vaporizing a liquid formulation comprising the pharmaceutically active agent, wherein the heater element is located between an outlet and an air inlet in the housing; b) a reservoir comprising the liquid formulation, wherein the reservoir is in fluid communication with the heater element; c) a passageway for condensing a vaporized liquid formulation comprising the pharmaceutically active agent, wherein the passageway is in fluid communication with the heater element; and d) a programmable controller.
  • the programmable controller comprises a non-transitory computer readable medium.
  • the non-transitory computer readable medium comprises one or more algorithms for regulating dosage of the pharmaceutically active agent, frequency of administration of the pharmaceutically active agent, or a delivery schedule of the pharmaceutically active agent. In some cases, the one or more algorithms regulate dosage of the pharmaceutically active agent, frequency of administration of the pharmaceutically active agent, or delivery schedule of the pharmaceutically active agent based on data provided to the device. In some cases, the device further comprises an interface for communicating with the programmable controller.
  • the programmable controller comprises a non-transitory computer readable medium, wherein the non-transitory computer readable medium comprises sequences of instructions, which, when executed by the device, cause the device to a) record data on use of the device; b) generate date on use of the device; c) retrieve data on use of the device; d) communicate data on use of the device; or e) input data regarding use of the device into one or more algorithms.
  • the programmable controller is connected to one or more electronic devices.
  • the connection is local or remote.
  • the connection comprises a wired connection.
  • the connection comprises a wireless connection.
  • the one or more electronic devices comprise a computer, smartphone, or a mobile phone.
  • the device further comprises the ability to access the Internet.
  • the heater element comprises a wick element and a coil. In some cases, the wick element and the coil are formed from the same rod. In some cases, the coil is wrapped around the wick element.
  • the device further comprises a positive displacement pump in fluid communication with the reservoir. In some cases, the device further comprises a baffle disposed in the passageway between the outlet and the heater element. In some cases, the device further comprises a second passageway, wherein the second passageway connects with the passageway between the outlet and the heater element. In some cases, the device further comprises a second passageway, wherein the second passageway connects with the passageway between the inlet and the heater element.
  • the device further comprises a tube disposed within the passageway and connected to the reservoir, wherein the tube is configured to deliver the liquid formulation comprising the pharmaceutically active agent to the heater element.
  • the device further comprises a mouthpiece attached to the outlet.
  • the liquid formulation comprises a flavoring.
  • the pharmaceutically active agent is nicotine.
  • the liquid formulation comprises nicotine and a carrier.
  • the device produces condensation aerosol particles having a mass median aerodynamic diameter (MMAD) of from about 1 ⁇ m to about 5 ⁇ m.
  • MMAD mass median aerodynamic diameter
  • a flow rate of gas in the device is capable of delivering the condensation aerosol of the liquid formulation comprising the pharmaceutically active agent to a deep lung of a user, wherein the flow rate is from about 20 LPM to about 80 LPM at a vacuum of about 249 Pa to about 3738 Pa (about 1 inch of water to about 15 inches of water).
  • the device permits a flow resistance of from about 0.05 to about 0.15 sqrt (cm-H 2 O)/LPM.
  • a method for generating a condensation aerosol of a liquid formulation comprising: a) generating a condensation aerosol, wherein the generating comprises vaporizing a liquid formulation using a heater element, wherein the heater element is disposed in a passageway of a condensation aerosol generating device, wherein the condensation aerosol has an MMAD of from about 1 ⁇ m to about 5 ⁇ m; and b) flowing a gas through the condensation aerosol generating device at a flow rate effective to allow delivery of the condensation aerosol.
  • the delivery is to the deep lung of a subject using the device.
  • the subject is a human.
  • the flowing comprises flowing a gas at a rate of about 20 LPM to about 80 LPM.
  • the condensation aerosol generating device permits a flow resistance of from about 0.05 to about 0.15 sqrt (cm-H 2 O)/LPM.
  • the condensation aerosol is formed at a flow rate of about 1 LPM to about 10 LPM past the heater element under a vacuum of between about 1 to about 249 Pa to about 3737 Pa (about 1 to about 15 inches of water).
  • the subject is a human.
  • the liquid formulation comprises a pharmaceutically active agent.
  • the pharmaceutically active agent is delivered orally to the subject.
  • the heater element comprises a wick element and a coil.
  • the wick element comprises an electrically resistive material.
  • the wick element and coil are formed from the same rod. In some cases, the coil is wrapped around the wick element.
  • the condensation aerosol generating device comprises a programmable controller.
  • the programmable controller comprises a non-transitory computer readable medium.
  • the non-transitory computer readable medium comprises one or more algorithms for regulating dosage of a pharmaceutically active agent, frequency of administration of a pharmaceutically active agent, or a delivery schedule of a pharmaceutically active agent.
  • the method further comprises programming the condensation aerosol generating device to deliver a dose of the pharmaceutically active agent.
  • the method further comprises programming a delivery schedule for the condensation aerosol generating device.
  • method further comprises programming a dosing schedule for the condensation aerosol generating device.
  • the passageway comprises an inlet and an outlet. In some cases, the passageway is disposed between the inlet and the outlet.
  • the deep lung comprises alveoli.
  • the liquid formulation comprises a pain medication.
  • the liquid formulation comprises a flavoring.
  • the liquid formulation comprises nicotine.
  • the liquid formulation comprises nicotine and a carrier.
  • the administering produces a nicotine blood concentration in the subject that is substantially similar to the nicotine blood concentration of a subject after smoking a cigarette.
  • the nicotine blood concentration is an arterial or venous nicotine blood concentration.
  • the administering produces a nicotine blood concentration in the subject that is at least 50% of the nicotine blood concentration of a subject after smoking a cigarette.
  • the condensation aerosol generating device further comprises a baffle located in the passageway, wherein the baffle inhibits flow of particles having an MMAD of greater than 5 ⁇ m.
  • the condensation aerosol generating device further comprises a reservoir comprising the liquid formulation.
  • the reservoir is disposed an inlet and outlet.
  • the condensation aerosol generating device further comprises a tube located within the passageway and connected to the reservoir.
  • the tube is configured to deliver the liquid formulation to the heater element.
  • the tube is a capillary.
  • the tube is in fluid communication with the heater element.
  • the tube comprises a heatable region.
  • the condensation aerosol generating device further comprises a valve located in the tube between the heatable region and the reservoir.
  • the condensation aerosol generating device further comprises a controller, wherein the controller comprises a non-transitory computer readable medium comprising one or more algorithms, wherein the one or more algorithms regulate dosing or a delivery schedule of the condensation aerosol of the liquid formulation.
  • the condensation aerosol generating device further comprises an interface for communicating with the controller.
  • the controller is removably attached to the passageway and the reservoir. In some cases, the controller is capable of communicating with one or more electronic devices.
  • the condensation aerosol generating device further comprises an air flow regulator located in the passageway. In some cases, the condensation aerosol generating device further comprises a second passageway, wherein an air flow regulator is capable of directing air through the second passageway in response to a pressure drop across the air flow regulator. In some cases, the air flow regulator comprises one or more gas control valves. In some cases, the heater element comprises a wire coil.
  • a method for treating a condition comprising: a) producing a condensation aerosol, wherein the producing comprises vaporizing a liquid formulation using a heater element, wherein the heater element is disposed in a passageway of a condensation aerosol generating device, wherein the condensation aerosol has an MMAD of from about 1 ⁇ m to about 5 ⁇ m; and b) flowing a gas through the condensation aerosol generating device at a flow rate effective to allow delivery of the condensation aerosol comprising the pharmaceutically active agent to the deep lung of a user of the device, thereby treating the condition.
  • the flowing comprises flowing a gas at a rate of about 20 LPM to about 80 LPM at a vacuum of about 249 Pa to about 3738 Pa (about 1 inch of water to about 15 inches of water).
  • the device permits a flow resistance of from about 0.05 to about 0.15 sqrt (cm-H 2 O)/LPM.
  • the condensation aerosol is formed at a flow rate of about 1 LPM to about 10 LPM past the heater element under a vacuum of between about 249 Pa to about 3738 Pa (about 1 inch of water to about 15 inches of water).
  • the condensation aerosol generating device comprises a programmable controller. In some cases, the method further comprises programming the condensation aerosol generating device to deliver a dose of the pharmaceutically active agent. In some cases, method further comprises programming a delivery schedule for the condensation aerosol generating device. In some cases, the method further comprises programming a dosing schedule for the condensation aerosol generating device.
  • the subject is a human.
  • the deep lung comprises alveoli.
  • the condition is pain. In some cases, the liquid formulation comprises a pain medication. In some cases, the pharmaceutically active agent is delivered orally to the subject. In some cases, the condition is addiction to smoking. In some cases, the condition is nicotine addiction. In some cases, the treating the condition comprises smoking cessation. In some cases, the treating the condition comprises transitioning a subject who smokes from use of cigarettes to use of the condensation aerosol generating device. In some cases, the liquid formulation comprises a flavoring. In some cases the liquid formulation comprises nicotine. In some cases, the liquid formulation comprises nicotine and a carrier. In some cases, the condition is addiction to smoking or nicotine addiction, and the delivery produces a nicotine blood concentration in the subject that is substantially similar to a nicotine blood concentration of a subject after smoking a cigarette. In some cases, the nicotine blood concentration is an arterial or venous nicotine blood concentration. In some cases, the delivery produces a nicotine blood concentration in the subject that is at least 50% of the nicotine blood concentration of a subject after smoking a cigarette.
  • a heater element comprising: a) a coil comprising an electrically resistive material; and b) a wick element capable of being heated, wherein the coil is wrapped around the wick element.
  • the wick element comprises an electrically resistive material.
  • the wick element and the coil are independent.
  • the wick element and the coil are formed from the same rod.
  • the wick element and the coil are wire.
  • the coil comprises 1 to 9 turns.
  • a distance between each turn in a coil is from about 0.01 to about 0.02 inches.
  • the coil has a length to width aspect ratio of at least 2.
  • the coil comprises an inner diameter of from about 0.027 inches to about 0.040 inches.
  • the coil comprises an outside diameter of from about 0.047 inches to about 0.080 inches.
  • a method comprising producing a nicotine blood concentration in a subject that is substantially similar to a nicotine blood concentration of a subject after smoking a cigarette, the method comprising delivering a condensation aerosol comprising nicotine to a subject, wherein the condensation aerosol has a MMAD of from about 1 ⁇ m to about 5 ⁇ m.
  • the nicotine blood concentration is an arterial or venous nicotine blood concentration.
  • the condensation aerosol is produced from a condensation aerosol generating device.
  • the condensation aerosol generating device comprises a) a passageway comprising a heater element, an inlet, and an outlet, wherein the heater element is disposed in the passageway between the inlet and the outlet; and b) a reservoir comprising a liquid formulation comprising nicotine, wherein the reservoir is in fluid communication with the heater element, wherein the heater element is capable of vaporizing the liquid formulation comprising the pharmaceutically active agent when the liquid formulation comprising nicotine is delivered to the heater element, wherein the vaporized liquid formulation comprising nicotine is condensed into aerosol particles.
  • a condensation aerosol generating device for generating a condensation aerosol of a liquid formulation
  • the device comprising: a) a passageway comprising a heater element; and b) a reservoir comprising the liquid formulation, wherein the reservoir is in fluid communication with the heater element, wherein the heater element is capable of vaporizing the liquid formulation when the liquid formulation is delivered to the heater element, and wherein a flow of air through the device delivers the condensation aerosol of the liquid formulation to the deep lung of a subject using the device.
  • the device permits a flow resistance of from about 0.08 to about 0.12 sqrt (cm-H 2 O)/LPM.
  • the passageway comprises an upstream opening and a downstream opening, wherein the upstream opening comprises an inlet for the air and the downstream opening serves as an outlet for the air, and wherein the heater element is located in the passageway between the upstream and downstream openings.
  • the reservoir is located within the passageway between the upstream and downstream openings.
  • the device further comprises an air flow regulator located in the passageway. In some cases, the device further comprises a second passageway, wherein an air flow regulator is capable of directing the air through the second passageway in response to a pressure drop across the air flow regulator. In some cases, the air flow regulator comprises one or more gas control valves. In some cases, the heater element comprises a wire coil.
  • the device further comprises a tube in fluid communication with the reservoir.
  • tube is a capillary.
  • the tube is in fluid communication with the heater element.
  • the tube comprises a heatable region.
  • the device further comprises a controller, wherein the controller comprises a non-transitory computer readable medium comprising one or more algorithms wherein the one or more algorithms regulate dosing or a delivery schedule of the condensation aerosol of the liquid formulation.
  • the device further comprises an interface for communicating with the controller.
  • the controller is removably attached to the passageway and the reservoir.
  • the controller is capable of communicating with one or more electronic devices.
  • the liquid formulation comprises a flavoring.
  • a condensation aerosol generating device for producing a condensation aerosol
  • the device comprising: a) a passageway comprising an aerosol generating heater element, an inlet, and an outlet, wherein the aerosol generating heater element is between the inlet and the outlet in the passageway, wherein the device is configured to produce a condensation aerosol from a liquid formulation in the device, wherein the condensation aerosol has a mass median aerodynamic diameter (MMAD) of from 1 ⁇ M to 5 ⁇ M; and b) one or more additional airflow regulating inlets for air located between the outlet and the heater element in the passageway, wherein the total airflow rate out of the outlet is between 20 LPM and 80 LPM at a vacuum of about 249 Pa to about 3738 Pa (about 1 inch of water to about 15 inches of water).
  • MMAD mass median aerodynamic diameter
  • the device further comprises a reservoir comprising the liquid formulation, wherein the reservoir is in fluid communication with the aerosol generating heater element.
  • the device further comprises a tube located within the passageway and connected to the reservoir, wherein the tube is configured to deliver the liquid formulation to the aerosol generating heater element.
  • the reservoir is located within the passageway.
  • the passageway further comprises a positive displacement pump configured to pump the liquid formulation comprising through the tube to the heater element.
  • the positive displacement pump comprises a peristaltic pump.
  • the passageway has an internal diameter of from about 0.20 cm to about 1.3 cm (about 0.08 inches to about 0.5 inches).
  • an internal diameter of the passageway where the heater element is located is from about 0.44 cm to about 0.64 cm (about 0.175 to about 0.25 inches).
  • an internal diameter of the passageway before and after the heater element is from about 0.07 cm to about 1.3 cm (about 0.03 to about 0.5 inches).
  • the length of the passageway is from about 0.5 cm to about 15.3 cm (from about 0.2 inches to about 6 inches).
  • the passageway comprises a baffle located between the outlet and the heater element, wherein the baffle is configured to remove aerosol particles with an MMAD of greater than 5 ⁇ m from the aerosol.
  • the aerosol generating heater element comprises a wick element.
  • the aerosol generating heater element comprises a coil.
  • the aerosol generating heater element comprises a coil wrapped around a wick element, wherein the coil and the wick element are formed from the same rod.
  • the coil spans a length of from about 0.1 to about 0.15 inches along the length of the wick element.
  • the wick element comprises an electrically resistive material.
  • the rod comprises a pliable material.
  • the device further comprises a sensor to detect inhalation. In some cases, the sensor comprises an optical path. In some cases, the device further comprises a power source to power the heater element. In some cases, the power source is a battery. In some cases, the tube is a capillary tube. In some cases, the tube comprises a valve. In some cases, the tube comprises an electrically resistive material.
  • the device further comprises a programmable controller. In some cases, the device is connected to one or more electronic devices. In some cases, the one or more electronic devices comprise a computer, smartphone, or mobile phone. In some cases, the device further comprises a second heater element. In some cases, the passageway is configured to produce a flow rate of from about 1 to about 10 LPM at the heater element under a vacuum of between about 249 Pa to about 3738 Pa (about 1 inch of water to about 15 inches of water).
  • the liquid formulation comprises nicotine. In some cases, the liquid formulation comprises a carrier. In some cases, the carrier comprises propylene glycol or vegetable glycerin.
  • a condensation aerosol generating device for producing a condensation aerosol
  • the device comprising: a passageway comprising an aerosol generating heater element, an inlet, and an outlet, wherein the aerosol generating heater element is between the inlet and the outlet in the passageway, wherein the passageway is configured to produce a condensation aerosol from a liquid formulation, wherein the condensation aerosol has a mass median aerodynamic diameter (MMAD) of from about 1 ⁇ m to about 5 ⁇ m, wherein the device is configured to produce an internal air resistance of from 0.05 to 0.15 sqrt (cm-H 2 O)/LPM.
  • the device further comprises a reservoir comprising a liquid formulation, wherein the reservoir is in fluid communication with the heater element.
  • the device further comprises a tube located within the passageway and connected to the reservoir, wherein the tube is configured to deliver the liquid formulation comprising to the heater element.
  • the reservoir is located within the passageway.
  • the passageway further comprises a positive displacement pump configured to pump the liquid formulation comprising through the tube to the heater element.
  • the positive displacement pump comprises a peristaltic pump.
  • the passageway has an internal diameter of from about 0.20 cm to about 1.3 cm (about 0.08 inches to about 0.5 inches). In some cases, an internal diameter of the passageway where the heater element is located is from about 0.44 cm to about 0.64 cm (about 0.175 to about 0.25 inches). In some cases, an internal diameter of the passageway before and after the heater element is from about 0.07 cm to about 1.3 cm (about 0.03 to about 0.5 inches). In some cases, the length of the passageway is from about 0.5 cm to about 15.3 cm (from about 0.2 inches to about 6 inches).
  • the passageway comprises a baffle located between the outlet and the heater element, wherein the baffle is configured to remove aerosol particles with an MMAD of greater than 5 ⁇ m from the aerosol.
  • the heater element comprises a wick element.
  • the heater element comprises a coil.
  • the heater element comprises a coil wrapped around a wick element, wherein the coil and the wick element are formed from the same rod.
  • the coil spans a length of from about 0.25 cm to about 0.39 cm (about 0.1 to about 0.15 inches) along the length of the wick element.
  • the wick element comprises an electrically resistive material.
  • the rod comprises a pliable material.
  • the device further comprises a sensor to detect inhalation. In some cases, the sensor comprises an optical path. In some cases, the device further comprises a power source to power the heater element. In some cases, the power source is a battery. In some cases, the tube is a capillary tube. In some cases, the tube comprises a valve. In some cases, the tube comprises an electrically resistive material. In some cases, the device further comprises a second passageway connected to the passageway. In some cases, the second passageway connects between the outlet and the heater element in the passageway. In some cases, the second passageway connects to the passageway between the inlet and the heater element.
  • the device further comprises a programmable controller. In some cases, the device is connected to one or more electronic devices. In some cases, the one or more electronic devices comprise a computer, smartphone, or mobile phone. In some cases, the device further comprises a second heater element. In some cases, the passageway is configured to produce a flow rate of from 1 to 10 LPM past the heater element under a vacuum of between about 249 Pa to about 3738 Pa (about 1 inch of water to about 15 inches of water). In some cases, the liquid formulation comprises nicotine. In some cases, the liquid formulation comprises a carrier. In some cases, the carrier comprises propylene glycol or vegetable glycerin.
  • FIG. 1 illustrates an embodiment of an electronic nicotine delivery device.
  • FIGS. 2A and 2B illustrate an embodiment of electronic agent (e.g., nicotine) delivery device.
  • electronic agent e.g., nicotine
  • FIGS. 3A and 3B illustrate embodiments of a heater element.
  • FIG. 4 illustrates an embodiment of an agent (e.g., nicotine) reservoir.
  • agent e.g., nicotine
  • FIG. 5 illustrates another embodiment of an agent (e.g., nicotine) reservoir.
  • agent e.g., nicotine
  • FIG. 6 illustrates another embodiment of an agent (e.g., nicotine) reservoir.
  • agent e.g., nicotine
  • FIG. 7 illustrates an embodiment of a heater element.
  • FIG. 8 illustrates an embodiment of an electronic agent (e.g., nicotine) delivery device.
  • an electronic agent e.g., nicotine
  • FIG. 9 illustrates another embodiment of a heater element.
  • FIGS. 10A and 10B illustrate additional embodiments of a heater element.
  • FIG. 11 illustrates inertial impaction
  • FIG. 12 illustrates an embodiment of a method of removal of an agent (e.g., nicotine) mixture from a reservoir and dispensing the nicotine into desired doses.
  • an agent e.g., nicotine
  • FIG. 13 illustrates another embodiment of a method for measuring an agent (e.g., nicotine) dose.
  • an agent e.g., nicotine
  • FIG. 14 illustrates another embodiment for measuring an agent (e.g., nicotine) dose.
  • agent e.g., nicotine
  • FIG. 15 illustrates another embodiment for measuring an agent (e.g., nicotine) dose.
  • agent e.g., nicotine
  • FIGS. 16A and 16B illustrate embodiments for applying an agent (e.g., nicotine) to a heater element.
  • an agent e.g., nicotine
  • FIGS. 17A and 17B illustrate embodiments of mechanisms for generating an aerosol.
  • FIG. 18 illustrates an embodiment of a mechanism for dispensing an agent (e.g., nicotine) mixture.
  • an agent e.g., nicotine
  • FIG. 19 illustrates feedback to a nicotine user regarding nicotine intake and mean craving over time.
  • FIG. 20 illustrates customized feedback to a user of an electronic nicotine delivery device.
  • FIG. 21 illustrates an embodiment of a method for flow control.
  • FIG. 22 illustrates an embodiment of a heater element.
  • FIG. 23 illustrates another embodiment for measuring an agent (e.g., nicotine) dose.
  • agent e.g., nicotine
  • FIG. 24 illustrates another embodiment for measuring an agent (e.g., nicotine) dose.
  • agent e.g., nicotine
  • FIGS. 25A and 25B illustrate another embodiment of a method of removal of an agent (e.g., nicotine) mixture from a reservoir.
  • an agent e.g., nicotine
  • FIG. 26 illustrates a schematic of a test apparatus used for testing the effects of altering system parameters of an aerosol delivery device on particle size distribution.
  • FIGS. 27A , 27 B, 27 C, and 27 D illustrate a schematic of a test bed used for generating an aerosol in the test apparatus of FIG. 26 .
  • FIG. 28 shows a comparison of particle sizes of an aerosol created by an e-cigarette (e-cig) vs. an aerosol created by a device as provided herein.
  • FIG. 29A illustrate a schematic of a test apparatus used for testing flow control.
  • FIG. 29B illustrates a close-up of the valve ( 2904 a ) that is part of the test apparatus in FIG. 29A .
  • FIG. 30A illustrates an alternative valve flap for use in the valve ( 2904 a ) in FIG. 29A .
  • FIG. 30B illustrates a slot for use in the bypass ( 2908 a ) in FIG. 29A .
  • FIGS. 31A , 31 B, 31 C, 31 D, and 31 E illustrate embodiments of airflow configurations and heater element.
  • FIGS. 32A , 32 B, 32 C, 32 D, and 32 E illustrate embodiments of flow-through passageways.
  • FIG. 33 illustrates an additional embodiment of a flow-through passageway.
  • FIG. 34 illustrates an embodiment of a flow control valve.
  • FIG. 35 illustrates an embodiment of a device comprising a primary and secondary airway.
  • FIG. 36 illustrates another embodiment of a heater element.
  • FIGS. 37A and 37B illustrate embodiments of a heater element similar to that shown in FIG. 36 .
  • FIG. 37A depicts a wire coil spanning a large percentage of the length of one end of the wire.
  • FIG. 37B depicts a wire coil spanning a smaller percentage of the length of one end of the wire than shown in FIG. 37A .
  • FIG. 38 is an enlarged representation of the wire coil from the heater element of FIG. 36 .
  • FIG. 39 illustrates components of eHealth-enabled electronic agent (e.g., nicotine) delivery system, in accordance with an embodiment.
  • eHealth-enabled electronic agent e.g., nicotine
  • FIG. 40 illustrates example components of an electronic agent (e.g., nicotine) delivery system, in accordance with an embodiment.
  • an electronic agent e.g., nicotine
  • FIG. 41 illustrates example components of an electronic agent (e.g., nicotine) delivery device for implementing aspects described herein, in accordance with an embodiment.
  • an electronic agent e.g., nicotine
  • FIG. 42 illustrates an escalating dose protocol utilized during part 1 of a two part study for assessing the safety, tolerability, pharmacokinetics, and pharmacodynamics of a condensation aerosol comprising nicotine and propylene glycol produced from an electronic agent (e.g., nicotine) delivery device as provided herein.
  • an electronic agent e.g., nicotine
  • FIG. 43 illustrates a trial design for part 2 of a two part study for assessing the safety, tolerability, pharmacokinetics, and pharmacodynamics of a condensation aerosol comprising nicotine and propylene glycol produced from an electronic agent (e.g., nicotine) delivery device as provided herein.
  • an electronic agent e.g., nicotine
  • FIGS. 44A , 44 B, and 44 C illustrate embodiments of a passageway comprising a baffle for removing particles of a non-optimal size.
  • FIGS. 44A and 44B illustrate exterior views of a passageway comprising a baffle.
  • FIG. 44C illustrates an interior view of a passageway comprising a baffle.
  • devices, systems, kits, compositions, computer readable medium, and methods for electronic delivery of an agent to a subject can be used for electronic nicotine delivery, which can facilitate recreational nicotine delivery, full or partial smoking cessation, or facilitate full or partial cessation of nicotine intake.
  • the subject can be a human.
  • the human subject can be a smoker or an individual who uses tobacco or nicotine containing products.
  • Devices described herein can generate an aerosol comprising an agent (e.g., nicotine), and the agent (e.g., nicotine) aerosol can have a known and consistent amount of agent (e g., nicotine).
  • agents e.g., nicotine
  • devices and methods for dose titration are provided.
  • the devices, systems, kits, compositions, and computer readable medium provided herein can be part of an electronic agent (e.g., nicotine) delivery platform.
  • the electronic platform for delivering an agent e.g., nicotine
  • the electronic delivery platform regulates a schedule of delivery of an agent (e.g., nicotine) to a user over time.
  • methods of tracking usage of an agent (e.g., nicotine) to suggest a dosing strategy based on the goal or goals of the user.
  • a user is a human.
  • a user is a human who smokes or otherwise uses tobacco or a nicotine containing product.
  • a subject is a human.
  • a subject is a human who smokes or otherwise uses tobacco or nicotine containing products.
  • the particles can be of a size suitable to delivery to the deep lung (i.e., alveoli) of the subject.
  • the particles can be any of the sizes provided herein.
  • the particles can comprise a mass median aerodynamic diameter (MMAD) of from about 1 to about 5 ⁇ m.
  • the particles can have a geometric standard deviation (GSD) of less than 2.
  • the condensation aerosol can be generated from a formulation comprising a pharmaceutically active agent.
  • the formulation can be in a liquid or solid phase prior to vaporization.
  • the agent can be any agent as provided herein; in some cases, the agent is nicotine, and in some cases the nicotine is stabilized using one or more carriers (e.g., vegetable glycerin and/or propylene glycol).
  • the device can comprise a heater element as provided herein and a configuration of flow-through passages or chambers suitable for generating condensation aerosols comprising particles of a size suitable for delivery to the deep lungs of a subject.
  • a device can comprise a primary flow-through chamber in fluid communication with a secondary flow-through chamber.
  • the primary flow-through chamber can comprise an upstream and downstream opening, and the upstream opening can be an inlet for a carrier gas.
  • the device can comprise an aerosol generation chamber, wherein the aerosol generation chamber is located (disposed) between the upstream and downstream openings within the primary flow through chamber.
  • the aerosol generation chamber can comprise a heater element as provided herein and a source of a formulation comprising a pharmaceutically active agent (e.g. nicotine) as provided herein.
  • the aerosol generation chamber can further comprise a configuration whereby the flow rate of the carrier gas entering the aerosol generation chamber is effective to condense a vapor generated from a formulation comprising a pharmaceutically active agent (e.g. nicotine) as provided herein within the aerosol generation chamber.
  • Devices and methods for aliquoting an agent e.g., nicotine
  • an agent e.g., nicotine
  • devices and methods are provided herein for sensing an inhalation by a user and triggering a device.
  • Devices and methods are also provided herein for inhalation flow control.
  • a device provided herein can incorporate electronics that control for variability in battery condition and ensure consistent heating by direct measurement of resistance through the heater element to control for changes in battery voltage/charge.
  • Devices and methods are provided herein for transitioning a smoker away from cigarettes. For example, devices and methods are provided for enabling a subject to achieve full smoking or nicotine cessation. Devices and methods are provided for enabling a subject to achieve full smoking or nicotine cessation without relapse. Also, devices and methods are provided for enabling a subject to achieve full smoking or nicotine cessation with reduced, minimal, or no withdrawal symptoms.
  • a subject is a human. In some cases, a subject is a human who smokes or otherwise uses tobacco or a nicotine containing product.
  • eHealth tools can yield customized doses of an agent (e.g., nicotine) to a subject.
  • customized dosing regimens are provided, which can include instructions to dose at specific intervals, driven by reminders on the device.
  • Devices and methods for providing customized feedback and behavioral support to a subject are also provided.
  • the customized feedback and/or behavioral support comprise simple instructions.
  • the customized feedback and/or behavioral support can comprise use of social media to leverage social networks to help induce and/or maintain behavior change.
  • an individual is a human. In some cases, an individual is a human who smokes or otherwise uses tobacco or a nicotine containing product.
  • FIG. 1 illustrates an embodiment of an electronic agent (e.g., nicotine) delivery device for controlling and reducing aerosol particle size for deep lung delivery and rapid pharmacokinetics.
  • An agent e.g., nicotine ( 102 ) is held in an agent (e.g., nicotine) reservoir ( 104 ), and can be wicked into a dosing mechanism ( 106 ).
  • agent e.g., nicotine
  • agent e.g., nicotine
  • Small droplets are entrapped in airflow in the airway ( 108 ).
  • a heater ( 110 ) can be in electrical communication with a battery ( 112 ). Larger droplets inertially impact with a heater ( 110 ), deposit, and are vaporized and reduced in size. Vapor condenses to form an optimum size aerosol by controlling airflow and vaporization rate.
  • An electronic agent (e.g., nicotine) delivery device can provide doses of agent (e.g., nicotine) in a consistent and known amount.
  • a dose of an agent (e.g., nicotine) can about, more than, less than, or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 94, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96,
  • a device can deliver a dose of an agent of about, more than, less than, or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 94, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, or 100 mg.
  • a dose of an agent is about 1 ⁇ g to about 1000 ⁇ g, about 1 ⁇ g to about 500 ⁇ g, about 1 ⁇ g to about 1000 ⁇ g, about 10 ⁇ g to about 500 ⁇ g, about 20 ⁇ g to about 500 ⁇ g, about 25 ⁇ g to about 500 ⁇ g, about 30 ⁇ g to about 500 ⁇ g, about 40 ⁇ g to about 500 ⁇ g, about 50 ⁇ g to about 500 ⁇ g, about 10 ⁇ g to about 250 ⁇ g, about 20 ⁇ g to about 250 ⁇ g, about 30 ⁇ g to about 250 ⁇ g, about 40 ⁇ g to about 250 ⁇ g, about 50 ⁇ g to about 250 ⁇ g, about 1 ⁇ g to about 200 ⁇ g, about 10 ⁇ g to about 200 ⁇ g, about 20 ⁇ g to about 200 ⁇ g, about 30 ⁇ g to about 200 ⁇ g, about 40 ⁇ g to about 200 ⁇ g, about 50 ⁇ g to about 250 ⁇ g, about 1 ⁇ g to about
  • a dose of an agent is about 1 mg to about 100 mg, about 1 mg to about 50 mg, about 10 mg to about 50 mg, about 20 mg to about 50 mg, about 25 mg to about 50 mg, about 30 mg to about 50 mg, about 40 mg to about 50 mg, about 50 mg to about 100 mg, about 1 mg to about 25 mg, about 2 mg to about 25 mg, about 3 mg to about 25 mg, about 4 mg to about 25 mg, about 5 mg to about 25 mg, about 1 mg to about 20 mg, about 1 mg to about 20 mg, about 2 mg to about 20 mg, about 3 mg to about 20 mg, about 4 mg to about 20 mg, or about 5 mg to about 20 mg of agent.
  • An emitted dose of an agent can be about, more than, less than, or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 94, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108,
  • an emitted dose of an agent is about, more than, less than, or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 94, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, or 100 mg.
  • an emitted dose of an agent is about 1 ⁇ g to about 1000 ⁇ g, about 1 ⁇ g to about 500 ⁇ g, about 1 ⁇ g to about 1000 ⁇ g, about 10 ⁇ g to about 500 ⁇ g, about 20 ⁇ g to about 500 ⁇ g, about 25 ⁇ g to about 500 ⁇ g, about 30 ⁇ g to about 500 ⁇ g, about 40 ⁇ g to about 500 ⁇ g, about 50 ⁇ g to about 500 ⁇ g, about 10 ⁇ g to about 250 ⁇ g, about 20 ⁇ g to about 250 ⁇ g, about 30 ⁇ g to about 250 ⁇ g, about 40 ⁇ g to about 250 ⁇ g, about 50 ⁇ g to about 250 ⁇ g, about 1 ⁇ g to about 200 ⁇ g, about 10 ⁇ g to about 200 ⁇ g, about 20 ⁇ g to about 200 ⁇ g, about 30 ⁇ g to about 200 ⁇ g, about 40 ⁇ g to about 200 ⁇ g, about 50 ⁇ g to about 250 ⁇ g, about 1 ⁇ g
  • an emitted dose of an agent is about 1 mg to about 100 mg, about 1 mg to about 50 mg, about 10 mg to about 50 mg, about 20 mg to about 50 mg, about 25 mg to about 50 mg, about 30 mg to about 50 mg, about 40 mg to about 50 mg, about 50 mg to about 100 mg, about 1 mg to about 25 mg, about 2 mg to about 25 mg, about 3 mg to about 25 mg, about 4 mg to about 25 mg, about 5 mg to about 25 mg, about 1 mg to about 20 mg, about 1 mg to about 20 mg, about 2 mg to about 20 mg, about 3 mg to about 20 mg, about 4 mg to about 20 mg, or about 5 mg to about 20 mg of agent.
  • a device delivers only a single emitted dose of an agent (e.g., nicotine).
  • the emitted dose can be about, more than, less than, or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 94, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, or 100% of the dose (or loaded dose).
  • the emitted dose can be between 1%-10%, 10%-20%, 20%-30%, 30%-40%, 40%-50%, 50%-60%, 60%-70%, 70%-80%, 80%-90%, or 90%-100% of the dose (or loaded dose). In some cases, the emitted dose is more than 20% of the dose (or loaded dose). In some cases, the emitted dose is less than 20% of the dose (or loaded dose).
  • the dose (or loaded dose) is the amount of nicotine solution delivered onto the heater element prior to the creation of the aerosol and can be about 2% of the target dose (the label claimed dose or goal dose). The emitted dose can be 92% to 97% of the dose. For example, the amount actually delivered to the lung if the label claim dose is 100 ⁇ g can be between 90% and 99%.
  • a subject is a human.
  • a subject is a human who smokes or otherwise uses tobacco or nicotine containing products.
  • Methods are provided herein for generating condensation aerosols comprising particles comprising a mass median aerodynamic diameter (MMAD) effective for delivery to the deep lung of a subject.
  • the methods can comprise supplying or delivering a liquid formulation comprising a pharmaceutically active agent (e.g.
  • the size of the particles following condensation can be an MMAD of from about 1 to about 5 ⁇ m.
  • the flow rate can be about 1 to about 10 liters per minute (LPM) (a range from about 1.667 ⁇ 10 ⁇ 5 m 3 /s to about 1.667 ⁇ 10 ⁇ 4 m 3 /s), e.g., at a vacuum of about 1 to about 15 inches of water (a range from about 249 Pa to about 3738 Pa).
  • the flow resistance of the device can be about 0.05 to about 0.15 (cm of H 2 O) 1/2 /LPM.
  • the liquid formulation can be supplied or delivered from a reservoir.
  • the reservoir can comprise a tube, e.g., a capillary tube.
  • the reservoir can be in fluid communication with the heater element.
  • the liquid formulation comprising a pharmaceutically active agent e.g., nicotine
  • the positive displacement pump can be a reciprocating, metering, rotary-type, hydraulic, peristaltic, gear, screw, flexible impeller, diaphragm, piston, or progressive cavity pump, or any other pump utilizing positive displacement as known in the art.
  • the positive displacement pump can be in fluid communication with the heater element.
  • the positive displacement pump can be in fluid communication or fluidically coupled to a reservoir comprising a pharmaceutically active agent (e.g., nicotine).
  • the positive displacement pump can be in fluid communication with the heater element and a reservoir comprising a pharmaceutically active agent (e.g., nicotine).
  • the pharmaceutically active agent e.g., nicotine
  • the positive displacement pump can be within the passageway or external to the passageway.
  • the heater element can be any heater element as provided herein.
  • the carrier gas can be air.
  • an element comprising porous materials can wick out fluid comprising agent (e.g., nicotine) at a particular rate in order to measure out a dose to provide dose-to-dose uniformity.
  • a tube e.g., a capillary tube can be used to measure out a dose.
  • heat is used as a means of ejecting a dose.
  • a material or geometry of a device can be used to measure out a dose.
  • providing dose consistency controls for variability in environment and device.
  • inhalation flow control ensures that variability in inhalations by a user are controlled and corrected for, which can result in dose-to-dose consistency and predictable and desirable aerosol particle sizes.
  • an agent e.g., nicotine
  • a device dosing mechanism
  • the metering can occur between inhalations of a user of a device.
  • an agent e.g., nicotine
  • an agent e.g., nicotine
  • the agent can be a pharmaceutically active agent.
  • the agent can be in a formulation that is liquid.
  • the liquid formulation comprising a pharmaceutically active agent e.g., nicotine
  • the subject can be a human.
  • the human subject can be a smoker or user of tobacco or nicotine containing substances.
  • the agent (e.g., nicotine) in the vaporization chamber or heater element can be vaporized and subsequently condense to form an aerosol.
  • the aerosol can comprise agent (e.g., nicotine) particles of an optimum size to achieve certain biological effects (e.g., deep lung delivery producing rapid pharmacokinetics).
  • Devices described herein can comprise a mechanism for separating out and reducing large aerosol particles to a size that can navigate to the deep lung of a subject. In the deep lung, the particles can settle and be rapidly absorbed. Also provided herein are methods for controlling aerosol particle size, pH, and other inhalation characteristics, which can ensure deep lung delivery and rapid pharmacokinetics.
  • the aerosol size control can result in rapid, cigarette-like nicotine absorption, which can help to satisfy nicotine cravings.
  • aerosol particles comprising nicotine produced by a heater element or device as provided herein can achieve peak plasma concentrations similar to peak plasma concentrations achieved by smoking a cigarette.
  • aerosol particles comprising nicotine produced by a heater element or device as provided herein can achieve peak plasma concentrations in a time frame similar to the time frame required to achieve peak plasma concentrations achieved by smoking a cigarette.
  • the condensation aerosol comprising nicotine produced by any of the devices provided herein can result in rapid, cigarette-like nicotine absorption resulting in nicotine plasma concentrations similar or substantially similar to the nicotine plasma concentration achieved from smoking a cigarette.
  • the plasma concentration can be an arterial plasma concentration.
  • the plasma concentration can be a venous plasma concentration.
  • Smoking a single cigarette can produce peak increments of plasma nicotine concentration of 5-30 ng/ml.
  • use of a device described herein can produce an arterial plasma nicotine concentration in the user of the device of about 1 ng/mL to about 200 ng/mL, about 1 ng/mL to about 150 ng/mL, about 1 ng/mL to about 100 ng/mL, about 1 ng/mL to about 75 ng/mL, about 1 ng/mL to about 50 ng/mL, about 1 ng/mL to about 40 ng/mL, about 1 ng/mL to about 30 ng/mL, about 1 ng/mL to about 20 ng/mL, about 1 ng/mL to about 10 ng/mL, about 10 ng/mL to about 200 ng/mL, about 10 ng/mL to about 150 ng/mL, about about 10 ng/mL to about 100 ng/mL, about 10 ng/mL to about 75 ng/mL, about 10 ng/mL to about 50 ng/mL, about 10 ng
  • use of a device described herein can produce an arterial plasma nicotine concentration in a user of the device of about, more than, less than, or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100 ng/mL.
  • the arterial plasma nicotine concentration can be produced after receiving at least
  • use of a device described herein can produce a peak plasma nicotine concentration in a user of the device within about 30 seconds to 30 minutes, 30 seconds to 20 minutes, 30 seconds to 10 minutes, 30 seconds to 5 minutes, 30 seconds to 2 minutes, 1 to about 30 minutes, about 1 minute to about 25 minutes, about 1 minute to about 20 minutes, about 1 minute to about 15 minutes, about 1 minute to about 10 minutes, about 5 minutes to about 30 minutes, about 5 minutes to about 25 minutes, about 5 minutes to about 20 minutes, about 5 minutes to about 15 minutes, about 5 minutes to about 10 minutes, about 10 minutes to about 30 minutes, about 10 minutes to about 25 minutes, about 10 minutes to about 20 minutes, or about 10 minutes to about 15 minutes of use of the device.
  • a use of the device can be an inhalation of a dose delivered by the device.
  • the peak increments of plasma nicotine concentration from smoking a cigarette can be achieved within 10 minutes.
  • the nicotine arterial plasma concentration can be about, more than, less than, or at least 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, 41%, 42%, 43%, 44%, 45%, 46%, 47%, 48%, 49%, 50%, 51%, 52%, 53%, 54%, 55%, 56%, 57%, 58%, 59%, 60%, 61%, 62%, 63%, 64%, 65%, 66%, 67%, 68%, 69%, 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%
  • the nicotine arterial plasma concentration can be between 1%-10%, 10%-20%, 20%-30%, 30%-40%, 40%-50%, 50%-60%, 60%-70%, 70%-80%, 80%-90%, or 90%-100% of the nicotine plasma concentration achieved by smoking a cigarette.
  • the nicotine arterial plasma concentration can be about 1% to about 10%, about 10% to about 20%, about 20% to about 30%, about 30% to about 40%, about 40% to about 50%, about 50% to about 60%, about 60% to about 70%, about 70% to about 80%, about 80% to about 90%, or about 90% to about 100% of the nicotine plasma concentration achieved by smoking a cigarette.
  • FIG. 12 illustrates an embodiment of a method of removal of an agent (e.g., nicotine) mixture from a reservoir and dispensing the agent (e.g., nicotine) into desired doses.
  • FIG. 12 shows an agent (e.g., nicotine) reservoir ( 1202 ) next to a frit ( 1204 ) or porous material, such as a metal (stainless steel) or a ceramic, and allowing the agent (e.g., nicotine) to wick into it. Then, upon inhalation, the air can draw the agent (e.g., nicotine) into the airway ( 1208 ) and onto the heater element ( 1206 ).
  • the mixture is a liquid formulation comprising an agent (e.g., nicotine).
  • FIG. 13 illustrates another embodiment of a method for measuring a dose. Another method of dosing out the mixture is to draw the material out using a venturi.
  • the device can comprise a tube, e.g., a capillary tube ( 1302 ), an agent (e.g., nicotine) reservoir ( 1304 ), and a heater element ( 1306 ).
  • the mixture is a liquid formulation comprising an agent (e.g., nicotine).
  • FIG. 14 illustrates another embodiment of a method for measuring a dose.
  • an agent e.g., nicotine
  • the device can comprise a heater element ( 1402 ), plates ( 1404 ), tube, e.g., capillary tube ( 1406 ), and an agent (e.g., nicotine) reservoir ( 1408 ).
  • the mixture is a liquid formulation comprising an agent (e.g., nicotine).
  • FIG. 15 illustrates another embodiment for measuring a dose.
  • An agent e.g., nicotine
  • An agent e.g., nicotine
  • the device can comprise an agent (e.g., nicotine) reservoir ( 1508 ) and a heater element ( 1504 ).
  • a piezo electric device is mounted on an end or a side of the reservoir and receipt of an electrical pulse causes the piezo to deflect and push a small amount of the agent (e.g., nicotine) formulation out of a tube, e.g., capillary tube mounted on another end of the reservoir onto a heater element.
  • the agent formulation is liquid.
  • All of the forgoing mechanisms to power the dispensing of a mixture can be powered by a user performing a maneuver such as pushing a button or lever.
  • Mechanical energy from the user can also allow for alternative methods of applying agent (e.g., nicotine) to a heater surface.
  • agent e.g., nicotine
  • An agent e.g., nicotine
  • the heater surface can be etched or pitted to accept the mixture.
  • a movable member e.g., vane ( 1702 a or 1702 b )
  • This member can break an optical path ( 1706 a ) (e.g., when no inhalation is occurring), move out of an optical path ( 1706 a ) when inhalation occurs (see e.g., FIG. 17A ), or can complete an optical path when inhalation occurs (by, e.g., reflection; see e.g., FIG. 17B ).
  • An LED ( 1708 a or 1708 b ) can be used to generate the light. To ensure that a sensor or detector ( 1710 a or 1710 b ) does not get confused by stray light, the LED ( 1708 a or 1708 b ) can be strobed in a particular pattern and only when that pattern is detected is an inhalation present. In some cases, optical light pipes can be used to route the light to the valve and to route the light back to the detector.
  • a valve can be designed to create increased pressure in the initial part of the inhalation and decrease the resistance for the duration of the inhalation (see e.g., FIG. 18 ).
  • an electronic agent (e.g., nicotine) delivery device that provides a dose of from 25 to 200 ⁇ g of freebase agent (e.g., nicotine).
  • the agent e.g., nicotine
  • the agent can be in a mixture of propylene glycol at a ratio of agent (e.g., nicotine) to propylene glycol of from about 1:1 to about 1:20, or about 1:5 to about 1:10.
  • a mixture comprises propylene glycol and about 1.25% to about 20% nicotine.
  • the mixture is liquid formulation comprising an agent (e.g., nicotine).
  • the mixture is liquid formulation comprising an agent (e.g., nicotine) during use of the device.
  • An aerosol can have an MMAD of about 1 to about 5 microns with a geometric standard deviation (GSD) of less than 2.0.
  • Dose to dose consistency over the lifetime of the product can be no greater than ⁇ 30%.
  • the device can have a dose to dose consistency over the lifetime of the product that can be about, more than, less than, at least, or at most ⁇ 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, 41%, 42%, 43%, 44%, 45%, 46%, 47%, 48%, 49%, or 50%.
  • the device can be activated by an inhalation.
  • the device can have an interior air resistance (to inhalation) no greater than that of a cigarette.
  • the device can have an interior air resistance (to inhalation) no greater than 0.08 (cm H 2 O) 1/2 /LPM.
  • the device can have an interior air resistance (to inhalation) about, more than, less than, at least, or at most 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.10, 0.11, 0.12, 0.13, 0.14, 0.15, 0.16, 0.17, 0.18, 0.19, or 0.20 (cm H 2 O) 1/2 /LPM.
  • FIG. 23 illustrates another embodiment of a method for measuring a dose. Another method of dosing out the mixture is to draw the material out using a peristaltic pump comprising a rotatable cam.
  • the device can comprise a tube, e.g., capillary tube ( 2302 ), agent (e.g., nicotine) reservoir ( 2304 ), and a rotatable cam ( 2306 ) to pull or draw an agent (e.g., nicotine) mixture from the nicotine reservoir.
  • agent e.g., nicotine
  • an agent (e.g., nicotine) delivery device comprises a disposable component that comprises the tube, e.g., capillary tube, and agent (e.g, nicotine) reservoir and a reusable component comprising the rotatable cam, wherein the tube, e.g., capillary tube and agent (e.g., nicotine) reservoir are mechanically connected to the rotatable cam by mating the disposable component to the reusable component.
  • the mixture is a liquid formulation comprising an agent (e.g., nicotine).
  • FIG. 24 illustrates another embodiment of a method for measuring a dose.
  • the device can comprise a tube, e.g, capillary tube ( 2402 ), agent (e.g., nicotine) reservoir ( 2404 ), and a cam made of variable durometer material ( 2406 ).
  • the cam can comprise an area of high durometer material surrounded by low durometer material, wherein the tube, e.g., capillary tube can be sealed within the high durometer material.
  • an agent (e.g., nicotine) mixture can be pushed out of the tube, e.g., capillary tube by compression, wherein pressure is exerted on the low durometer material of the cam to cause compression of the tube, e.g., capillary tube, within the high durometer material.
  • an agent (e.g., nicotine) delivery device comprises a disposable component that comprises the tube, e.g., capillary tube and the agent (e.g., nicotine) reservoir and a reusable component comprising the cam made of variable durometer material, wherein the tube, e.g., capillary tube and agent (e.g., nicotine) reservoir are mechanically connected to the cam made of variable durometer material by mating the disposable component to the reusable component.
  • the mixture is a liquid formulation comprising an agent (e.g., nicotine).
  • FIG. 25 illustrates an embodiment of a method of removal of an agent (e.g., nicotine) mixture from a reservoir.
  • FIG. 25A shows a tube, e.g., capillary tube ( 2502 a ) adjacent to, but separate from, an agent (e.g., nicotine) reservoir ( 2504 a ) comprising an agent (e.g., nicotine) mixture ( 2506 a ).
  • FIG. 25A shows a tube, e.g., capillary tube ( 2502 a ) adjacent to, but separate from, an agent (e.g., nicotine) reservoir ( 2504 a ) comprising an agent (e.g., nicotine) mixture ( 2506 a ).
  • an agent e.g., nicotine
  • the tube, e.g., capillary tube ( 2502 b ) can pierce the agent (e.g., nicotine) reservoir ( 2504 b ) such that the agent (e.g., nicotine) mixture ( 2506 b ) within the agent (e.g., nicotine) reservoir can move into the tube, e.g., capillary tube and subsequently onto a heater element as provided herein.
  • the agent (e.g., nicotine) reservoir comprises a septum or seal, wherein the tube, e.g., capillary tube pierces the septum or seal.
  • the agent (e.g., nicotine) reservoir is a collapsible bag or container.
  • the collapsible bag or container is made of plastic, foil, or any other collapsible material known in the art.
  • the tube e.g., capillary tube can directly pierce an agent (e.g., nicotine) reservoir that is made of a collapsible material.
  • the tube, e.g., capillary tube is not inserted into the agent (e.g., nicotine) reservoir prior to a first use of the device, wherein upon first use, the tube, e.g., capillary tube, is inserted into the agent (e.g., nicotine) reservoir such that an agent (e.g., nicotine) mixture can move from the agent (e.g., nicotine) reservoir into the tube, e.g., capillary tube and subsequently onto a heater element as provided herein.
  • the mixture is a liquid formulation comprising an agent (e.g., nicotine).
  • an agent e.g., nicotine
  • the mixture can be liquid at room temperature.
  • an agent e.g., nicotine
  • the mixture can be liquid during use of the device such that the liquid mixture is delivered to the heater element during use of the device.
  • the one or more other substances can be pharmaceutically acceptable excipients or carriers.
  • the suitable pharmaceutically acceptable excipients or carriers can be volatile or nonvolatile. The volatile excipients, when heated, can be volatilized, aerosolized and inhaled with the agent (e.g. nicotine).
  • excipients include, without limitation, gaseous, supercritical fluid, liquid and solid solvents.
  • the excipient/carriers can be water; terpenes, such as menthol; alcohols, such as ethanol, propylene glycol, glycerol and other similar alcohols; dimethylformamide; dimethylacetamide; wax; supercritical carbon dioxide; dry ice; and mixtures or combinations thereof.
  • the one or more other substances can be, e.g., propylene glycol (1,2-dihydroxypropane, 1,2-propanediol, methyl glycol, or trimethyl glycol).
  • the ratio of agent (e.g., nicotine) to propylene glycol can be about, more than, less than, or at least 100:1, 95:1, 90:1, 85:1, 80:1, 75:1, 70:1, 65:1, 60:1, 55:1, 50:1, 45:1, 40:1, 35:1, 30:1, 25:1, 20:1, 15:1, 10:1, 5:1, 2:1, 1:1, 1:2, 1:5, 1:10, 1:15, 1:20, 1:25, 1:30, 1:35, 1:40, 1:45, 1:50, 1:55, 1:60, 1:65, 1:70, 1:75, 1:80, 1:85, 1:90, 1:95, or 1:100.
  • the ratio of agent (e.g., nicotine) to propylene glycol can be from about 100:1 to about 1:100, about 75:1 to about 1:100, about 50:1 to about 1:100, about 25:1 to about 1:100, about 25:1 to about 1:50, about 10:1 to about 1:100, about 10:1 to about 1:50, about 10:1 to about 1:20, about 5:1 to about 1:20, or about 1:1 to about 1:20.
  • a 100 ⁇ g dose of agent (e.g., nicotine) and 1:10 ratio yields a volume of 1 mm 3 (1 mg).
  • a mixture of agent (e.g., nicotine) and another substance, e.g., propylene glycol can be held in an agent (e.g., nicotine) reservoir (e.g., as a liquid).
  • the one or more other substances is vegetable glycerin.
  • the ratio of an agent (e.g., nicotine) to vegetable glycerin can be about, more than, less than, or at least 100:1, 95:1, 90:1, 85:1, 80:1, 75:1, 70:1, 65:1, 60:1, 55:1, 50:1, 45:1, 40:1, 35:1, 30:1, 25:1, 20:1, 15:1, 10:1, 5:1, 2:1, 1:1, 1:2, 1:5, 1:10, 1:15, 1:20, 1:25, 1:30, 1:35, 1:40, 1:45, 1:50, 1:55, 1:60, 1:65, 1:70, 1:75, 1:80, 1:85, 1:90, 1:95, or 1:100.
  • the ratio of an agent (e.g., nicotine) to vegetable glycerin can be from about 100:1 to about 1:100, about 75:1 to about 1:100, about 50:1 to about 1:100, about 25:1 to about 1:100, about 25:1 to about 1:50, about 10:1 to about 1:100, about 10:1 to about 1:50, about 10:1 to about 1:20, about 5:1 to about 1:20, or about 1:1 to about 1:20.
  • a 100 ⁇ g dose of agent (e.g., nicotine) and 1:10 ratio yields a volume of 1 mm 3 (1 mg).
  • a mixture of agent (e.g., nicotine) and vegetable glycerin can be held in an agent (e.g., nicotine) reservoir (e.g., as a liquid).
  • the one or more other substances comprise vegetable glycerin and propylene glycol.
  • the ratio of vegetable glycerin to propylene glycol can be about, more than, less than, or at least 100:1, 95:1, 90:1, 85:1, 80:1, 75:1, 70:1, 65:1, 60:1, 55:1, 50:1, 45:1, 40:1, 35:1, 30:1, 25:1, 20:1, 15:1, 10:1, 5:1, 2:1, 1:1, 1:2, 1:5, 1:10, 1:15, 1:20, 1:25, 1:30, 1:35, 1:40, 1:45, 1:50, 1:55, 1:60, 1:65, 1:70, 1:75, 1:80, 1:85, 1:90, 1:95, or 1:100.
  • the ratio of agent (e.g., nicotine) to vegetable glycerin can be from about 100:1 to about 1:100, about 75:1 to about 1:100, about 50:1 to about 1:100, about 25:1 to about 1:100, about 25:1 to about 1:50, about 10:1 to about 1:100, about 10:1 to about 1:50, about 10:1 to about 1:20, about 5:1 to about 1:20, or about 1:1 to about 1:20.
  • the ratio of agent (e.g., nicotine) to mixture of vegetable glycerin and propylene glycol can be about, more than, less than, or at least 100:1, 95:1, 90:1, 85:1, 80:1, 75:1, 70:1, 65:1, 60:1, 55:1, 50:1, 45:1, 40:1, 35:1, 30:1, 25:1, 20:1, 15:1, 10:1, 5:1, 2:1, 1:1, 1:2, 1:5, 1:10, 1:15, 1:20, 1:25, 1:30, 1:35, 1:40, 1:45, 1:50, 1:55, 1:60, 1:65, 1:70, 1:75, 1:80, 1:85, 1:90, 1:95, or 1:100.
  • agent e.g., nicotine
  • the ratio of agent (e.g., nicotine) to vegetable glycerin and glycerin can be from about 100:1 to about 1:100, about 75:1 to about 1:100, about 50:1 to about 1:100, about 25:1 to about 1:100, about 25:1 to about 1:50, about 10:1 to about 1:100, about 10:1 to about 1:50, about 10:1 to about 1:20, about 5:1 to about 1:20, or about 1:1 to about 1:20.
  • the one or more other substances can be polyethylene glycol (PEG).
  • PEG polyethylene glycol
  • the PEG can be PEG200, PEG300, PEG400, PEG600, PEG1000, PEG2000, PEG4000, or PEG6000.
  • the one or more other substances is glycerol.
  • an electronic agent (e.g., nicotine) delivery device comprises a mixture of agent (e.g., nicotine) and polyethylene glycol.
  • a mixture can comprise an agent (e.g., nicotine), polyethylene glycol, and vegetable glycerin.
  • a mixture can comprise an agent (e.g., nicotine), polyethylene glycol, vegetable glycerin, and propylene glycol.
  • a mixture comprises an agent (e.g., nicotine), polyethylene glycol, and propylene glycol.
  • a mixture can comprise an agent (e.g., nicotine), propylene glycol, and vegetable glycerin.
  • the percentage of an agent (e.g., nicotine) in a formulation (e.g., solution) comprising an agent (e.g., nicotine) can be about, more than, less than, or at least 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.25, 4.5, 4.75, 5, 5.25, 5.5, 5.75, 6, 6.25, 6.5, 6.75, 7, 7.25, 7.5, 7.75, 8, 8.25, 8.5, 8.75, 9, 9.25, 9.5, 9.75, 10, 10.25, 10.5, 10.75, 11, 11.25, 11.5, 11.75, 12, 12.25, 12.5, 12.75, 13, 13.25, 13.5, 13.75, 14, 14.25, 14.5, 14.75, 15, 15.25, 15.5, 15.75, 16, 16.25, 16.5, 16.75, 17, 17.25, 17.5, 17.75, 18, 18.25, 18.5, 18.75, 19, 19.25, 19.5, 19.75, 20, 20.5, 21, 21.5, 22, 22.5, 23,
  • the percentage of an agent (e.g., nicotine) in a formulation (e.g., solution) comprising an agent (e.g., nicotine) can be from about 0.25 to about 1.25, about 1.25 to about 2.5, about 2.5 to about 5, about 5 to about 7.5, about 7.5 to about 10, about 10 to about 12.5, about 12.5 to about 15, about 15 to about 17.5, about 17.5 to about 20, or about 20 to about 25% by volume.
  • the formulation (e.g., solution) can further comprise one or more substances.
  • the one or more substances can be propylene glycol and/or vegetable glycerin.
  • the formulation can be liquid at room temperature or at temperatures at which the device is generally used by a subject.
  • the source of nicotine for use in the devices and methods as provided herein can be a tobacco or tobacco material.
  • a tobacco or tobacco material can be defined as any combination of natural and synthetic material that can be vaporized for pleasure or medicinal use.
  • the formulation comprising nicotine can comprise flue-cured tobacco, glycerin, and flavorings.
  • the formulation comprising nicotine can comprise flue-cured tobacco, propylene glycol, and flavorings.
  • a liquid formulation comprising nicotine can be produced by chopping tobacco into fine pieces (less than 3 mm diameter, less than 2 mm), adding the other ingredients (e.g., propylene glycol, vegetable glycerin, water, and/or flavorings), and mixing until even consistency is achieved.
  • An electronic agent (e.g., nicotine) delivery device described herein can control a pH of an agent (e.g., nicotine) mixture or aerosol.
  • the pH of the agent (e.g., nicotine) mixture or aerosol can be about, more than, less than, or at least 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 5.6, 5.7, 5.8, 5.9, 6, 6.1, 6.2, 6.3, 6.4, 6.5, 6.6, 6.7, 6.8, 6.9, 7, 7.1, 7.2, 7.3, 7.4, 7.5, 7.6, 7.7, 7.8, 7.9, 8, 8.1, 8.2, 8.3, 8.4, 8.5, 8.6, 8.7, 8.8, 8.9 9, 9.5, 10, 10.5, 11, 11.5, 12, 12.5, 13, 13.5, or 14.
  • the pH of an agent (e.g., nicotine) mixture or aerosol can be about 1 to about 14, about 2 to about 13, about 3 to about 12, about 4 to about 11, about 5 to about 10, about 6 to about 9, about 6 to about 8, about 6 to about 7, about 4 to about 6, about 4 to about 8, about 5 to about 8, about 5 to about 7, about 7 to about 9, about 5.5 to about 8.5, about 6.5 to about 8.5, about 6.5 to about 7.5, about 7.5 to about 9, or about 7 to about 8.5.
  • One or more buffers can be added to a mixture to adjust the pH of the mixture.
  • the one or more buffers can be any buffers known in the art.
  • the one or more buffers can be acidic buffers or alkaline buffers.
  • the one or more buffers can be a phosphate, bicarbonate or protein buffer system.
  • buffers can include, but are not limited to, TAPS (3- ⁇ tris(hydroxymethyl)methyl]amino ⁇ propanesulfonic acid), Bicine (N,N-bis(2-hydroxyethyl)glycine), Tris (tris(hydroxymethyl)methylamine), Tricine (N-tris(hydroxymethyl)methylglycine), TAPSO (3-N-Tris(hydroxymethyl)methylamino]-2-hydroxypropanesulfonic Acid), HEPES (4-2-hydroxyethyl-1-piperazineethanesulfonic acid), TES (2- ⁇ [tris(hydroxymethyl)methyl]amino ⁇ ethanesulfonic acid), MOPS (3-(N-morpholino)propanesulfonic acid), PIPES (piperazine
  • a mixture comprises one or more flavorings.
  • the one or more flavorings can be a flavor offered by, e.g., Flavourart (Italy), Flavor Apprentice, or LorAnn
  • a flavor can be, e.g., almond, almond amaretto, apple, Bavarian cream, black cherry, black sesame seed, blueberry, brown sugar, bubblegum, butterscotch, cappuccino, caramel, caramel cappuccino, cheesecake (graham crust), cinnamon redhots, cotton candy, circus cotton candy, clove, coconut, coffee, clear coffee, double chocolate, energy cow, graham cracker, grape juice, green apple, Hawaiian punch, honey, Jamaican rum, Kentucky bourbon, kiwi, koolada, lemon, lemon lime, tobacco, maple syrup, maraschino cherry, marshmellow, menthol, milk chocolate, mocha, Mountain Dew, peanut butter, pecan, peppermint, raspberry, banana, ripe banana, root beer, RY4, spearmint
  • a flavoring can be used to pair nicotine administration with certain gustatory and/or olfactory sensations. Subsequent administration of agent (e.g., nicotine) doses can be reduced while retaining the flavoring to help the user reduce their agent (e.g., nicotine) dependency and enable cravings to be fully or partially sated using the flavoring as a conditioned stimulus.
  • agent e.g., nicotine
  • a device provided herein can generate an aerosol that can be particles of an optimum size for delivery to the deep lung.
  • the aerosol can be a condensation aerosol.
  • the particle size can be about, more than, less than, or at least 0.01, 0.015, 0.02, 0.025, 0.03, 0.035, 0.04, 0.045, 0.05, 0.055, 0.06, 0.065, 0.07, 0.075, 0.08, 0.085, 0.09, 0.095, 0.1, 0.11, 0.12, 0.13, 0.14, 0.15, 0.16, 0.17, 0.18, 0.19, 0.2, 0.21, 0.22, 0.23, 0.24, 0.25, 0.26, 0.27, 0.28, 0.29, 0.3, 0.31, 0.32, 0.33, 0.34, 0.35, 0.36, 0.37, 0.38, 0.39, 0.4, 0.41, 0.42, 0.43, 0.44, 0.45, 0.46, 0.47, 0.48, 0.49, 0.5, 0.51, 0.52, 0.53, 0.54,
  • the particle size can be from about 1 to about 10 microns, about 1 to about 9 microns, about 1 to about 7 microns, about 1 to 6 microns, about 1 to about 5 microns, about 1 to about 4 microns, about 1 to about 3 microns, or about 1 to about 2 microns.
  • the particle size can be from about 0.5 to about 10 microns, about 0.5 to about 9.5 microns, about 0.5 to about 9 microns, about 0.5 to about 8.5 microns, about 0.5 to about 8 microns, about 0.5 to about 7.5 microns, about 0.5 to about 7 microns, about 0.5 to about 6.5 microns, about 0.5 to about 6 microns, about 0.5 to about 5.5 microns, about 0.5 to about 5 microns, about 0.5 to about 4.5 microns, about 0.5 to about 4.0 microns, about 0.5 to about 3.5 microns, about 0.5 to about 3 microns, about 0.5 to about 2.5 microns, about 0.5 to about 2 microns, about 0.5 to about 1.5 microns, or about 0.5 to about 1 microns.
  • the particle size can be less than 1 micron.
  • the particle size can be greater than 5 microns.
  • the particle size can be less than 5 microns.
  • the particle size can be greater than 1 micron.
  • the particle size is from about 1 to about 5 microns.
  • the particle size is from about 1 to about 3 microns.
  • the particle size is a mass median aerodynamic diameter (MMAD).
  • a device provided herein can generate an aerosol that can create particles of an optimum size for delivery to the deep lung.
  • the geometric standard deviation (GSD) of the particles can be about, more than, less than, or at least 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, or 3.
  • the GSD can be from about 1 to about 3 or about 1 to about 2.
  • the GSD can be between about 1 to about 1.5, about 1.5 to about 2, or about 2 to about 3. In one embodiment, the GSD is less than 2.
  • FIG. 4 illustrates an embodiment of an agent (e.g., nicotine) reservoir ( 404 ) that can be used in an electronic agent (e.g., nicotine) delivery device provided herein.
  • a tube e.g., capillary tube ( 400 ) with a valve ( 402 ) does not need to be inserted into a separate reservoir, but can be the reservoir ( 404 ) itself by extending away from the ejection end.
  • the diameter of the tube, e.g., capillary tube can be increased to store more mixture.
  • the back end can have a vent ( 406 ).
  • the agent (e.g., nicotine) reservoir is cylindrical.
  • the agent (e.g., nicotine) reservoir holds a formulation comprising 200 mg of agent (e.g., nicotine) mixed with 1000 mg of propylene glycol.
  • the agent (e.g., nicotine) reservoir holds a formulation comprising 200 ug of agent (e.g., nicotine) mixed with 1000 ug of propylene glycol.
  • the agent (e.g., nicotine) formulation is a liquid formulation.
  • FIG. 5 illustrates another embodiment of a reservoir.
  • An agent e.g., nicotine
  • reservoir ( 500 ) can be a porous, open cell foam ( 502 ) within a cartridge; a tube, e.g., capillary tube ( 504 ) can extend from the reservoir.
  • FIG. 6 illustrates another embodiment of an agent (e.g., nicotine) reservoir.
  • the mixture can be held in a collapsible bag ( 602 ) which can be held within a secondary container ( 600 ).
  • a tube, e.g., capillary tube ( 604 ) can extend from the reservoir.
  • doses of a liquid agent are held in a safe dose cartridge container until needed.
  • a container for an agent e.g., nicotine
  • the sealing mechanism comprises septum sealing. Methods are provided herein for safely puncturing and reclosing access to a drug (e.g., nicotine) cartridge.
  • a septum and a puncturing needle is used to extract an agent (e.g., nicotine) from a cartridge.
  • a semi-porous material can be used to ensure that the rate of agent (e.g., nicotine) transfer is safe.
  • materials can include a frit or other material (e.g., ceramic, foam, or metal) that has a convoluted or open structure.
  • a device comprises a dose cartridge.
  • the dose cartridge is a disposable dose cartridge.
  • the dose cartridge houses an agent (e.g., nicotine) formulation and an aerosol creation mechanism as described herein.
  • the agent (e.g., nicotine) formulation is housed in a reservoir.
  • the dose cartridge comprises a reservoir comprising an agent (e.g., nicotine) formulation.
  • the dose cartridge comprises a reservoir comprising an agent (e.g., nicotine) formulation and dispensing tube, e.g., capillary tube, for dispensing the agent (e.g., nicotine) formulation.
  • the dose cartridge comprises a mouthpiece.
  • the mouthpiece comprises a cap.
  • the cap can help prevent contamination.
  • the cap can provide a tamper resistance feature.
  • the cap can provide a child resistance feature.
  • the cap covers both the mouthpiece and any air inlets.
  • the cap is reusable.
  • the dose cartridge comprises a mouthpiece at one end and a mating mechanism whereby the dose cartridge can connect to a controller at another end.
  • the dose cartridge comprises a mechanism for breath detection.
  • the dose cartridge comprises a flow control valve.
  • the dose cartridge comprises a flow control valve that can regulate inhalation.
  • the mechanism for breath detection or inhalation sensing can comprise breath sensory components.
  • the breath sensory components can comprise an optical chase whereby light can be routed to and from a flow sensor.
  • the dose cartridge comprises a heater element.
  • the heater element comprises a metal foil.
  • the metal foil can be made of stainless steel or any other electrically resistive material.
  • the metal foil is made of stainless steel.
  • the heater element comprises a steel or metal foil that can be about 0.013 mm thick in order to ensure rapid vaporization.
  • the heater element comprises a coil of wire or wire coil.
  • the coil of wire or wire coil can be from about 0.12 to about 0.5 mm in diameter.
  • the dose cartridge comprises more than one heater element.
  • the dose cartridge comprises two heater elements. In some cases, the heater element can be rapidly heated.
  • a heating element can comprise a heating rate of about 1600° C.
  • a heater element is activated for a duration of about 10 msec to about 2000 msec, about 10 msec to about 1000 msec, about 10 msec to about 500 msec, about 10 msec to about 250 msec, about 10 msec to about 100 msec, about 50 msec to about 1000 msec, about 50 msec to about 500 msec, about 50 msec to about 250 msec, about 100 msec to about 1000 msec, about 100 msec to about 500 msec, about 100 msec to about 400 msec, or about 100 msec to about 300 msec.
  • a heater element is activated for about 10, 50, 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950, or 1000 msec. In some cases, a heater element is activated for at least 10, 50, 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950, or 1000 msec. In some cases, the maximum temperature of the heater element is about 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600° C. (a range from about 373.15° K to about 873.15° K). In some cases, the maximum temperature of the heater element is at least 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600° C. (a range from about 373.15° K to about 873.15° K).
  • a device provided herein is made up of multiple components.
  • the device provided herein is comprised of two components wherein one component comprises a controller and the other component comprises a dose cartridge.
  • the controller is reusable and the dose cartridge is replaceable.
  • the dose cartridge is mated to the controller. Mating of the dose cartridge to the controller can be accomplished by inserting the dose cartridge into an interlocking channel in the controller and engaging a locking mechanism.
  • the locking mechanism can comprise a tab or button on the controller which can be depressed.
  • the dose cartridge is detachable from the controller. In one embodiment, detachment of the dose cartridge is accomplished by releasing the locking mechanism.
  • releasing the locking mechanism entails depressing the tab or button on the controller. Electrical connection between the dose cartridge and the controller can be accomplished through a set of mating electrical contacts.
  • attachment or mating of the dose cartridge to the controller establishes a breath detection mechanism.
  • the breath detection mechanism can comprise breath sensory components.
  • the breath detection mechanism comprises detecting an alteration in an optical signal, wherein attachment or mating of the dose cartridge to the controller establishes an optical path through which the optical signal can be sent and received.
  • a source and detector of an optical signal is present in the controller, while the dose cartridge comprises an optical path.
  • the optical path can comprise reflectors for reflecting an optical signal.
  • the optical path can comprise a vane, wherein an inhalation can move the vane in such a way as to cause an alteration in an optical signal.
  • the dose cartridge comprises a vane, wherein an inhalation can move the vane in such a manner as to cause an alteration in an optical signal.
  • the optical signal can be light of any wavelength.
  • Tube e.g., Capillary Tube
  • FIGS. 2A and 2B illustrate embodiments of components of an electronic nicotine delivery device.
  • FIG. 2A illustrates an agent (e.g., nicotine) reservoir ( 202 ) and a tube, e.g., capillary tube ( 204 ).
  • FIG. 2B illustrates an expanded view of the device.
  • the agent (e.g., nicotine) reservoir can comprise an agent (e.g., nicotine)/propylene glycol (PG) mixture ( 206 ).
  • the tube, e.g., capillary tube can comprise a region on the interior which has been coated with an agent (e.g., nicotine)/PG philic material ( 208 ) to promote wicking out of a reservoir.
  • a region on the interior which has been coated with an agent (e.g., nicotine)/PG phobic material ( 210 ) can lie at the open end.
  • This coating can cause the agent (e.g., nicotine)/PG to stop wicking short of the open end, thereby reducing the surface area of the mixture exposed to air, and air devoid of agent (e.g., nicotine) vapor.
  • the tube, e.g., capillary tube can comprise a heated section ( 212 ) of the tube, e.g., capillary tube which, upon heating, can cause the mixture in the tube to vaporize and expand, pushing the mixture from the open end.
  • a ball valve ( 214 ) can be trapped between two indentations in the tube, e.g., capillary tube, the end indentation being such that the ball, if pushed by fluid, will form a seal.
  • This configuration can allow the liquid to be ejected from the end upon heating rather than back into the reservoir. All four of these elements can form a pump which can eject a known dose of the mixture from the end of the tube, e.g., capillary tube.
  • 1 mm 3 of material can be in the tube, e.g., capillary tube.
  • the length can be ⁇ 5 mm.
  • a valve can be a check valve, and the check valve can be a ball which can be made of a metal, such as stainless steel or can be made of a plastic, such as nylon, delrin, or a homopolymer acetal.
  • the ball can have a diameter less than the interior diameter of the tube, e.g., capillary tube sufficient to allow an agent (e.g., nicotine)/PG mix to wick by it.
  • a heater element can be any heater element as provided herein.
  • the heater element can be used to generate a condensation aerosol from a liquid formulation comprising a pharmaceutically active agent as provided herein.
  • the condensation aerosol can comprise particles of a size suitable for delivery to the lungs of a subject as provided herein.
  • the heater element comprises a coil.
  • the coil can be a wire coil.
  • the coil can further comprise a wick element capable of being heated.
  • the heater element can vaporize the liquid formulation when the liquid formulation is delivered to the heater element.
  • the liquid formulation comprising a pharmaceutically active agent e.g., nicotine
  • the positive displacement pump can be a reciprocating, metering, rotary-type, hydraulic, peristaltic, gear, screw, flexible impeller, diaphragm, piston, or progressive cavity pump, or any other pump utilizing positive displacement as known in the art.
  • the positive displacement pump can be in fluid communication with the heater element.
  • the positive displacement pump can be in fluid communication or fluidically coupled to a reservoir comprising a pharmaceutically active agent (e.g., nicotine).
  • the positive displacement pump can be in fluid communication with the heater element and a reservoir comprising a pharmaceutically active agent (e.g., nicotine).
  • the pharmaceutically active agent e.g., nicotine
  • the pharmaceutically active agent e.g., nicotine
  • the positive displacement pump can be within the passageway or external to the passageway.
  • the heater element can comprise a rod comprising electrically resistive material.
  • the rod can be a wire.
  • the rod can be a pliable rod.
  • the rod can comprise a coil, wherein a segment of the rod can pass through the interior of the coil.
  • the coil can be a wire coil.
  • the heater element can comprise a wick element capable of being heated.
  • the wick element capable of being heated can pass through and exit the center of the coil.
  • the heater element comprises a heatable wick element.
  • the rod can comprise the heatable wick element.
  • the rod comprises a coil and a heatable wick element, wherein the heatable wick element is a segment of the rod that passes through the interior or center of the coil.
  • FIGS. 3A and 3B illustrate configurations of a heater element.
  • the tube, e.g., capillary tube can be made of stainless steel, or a similar matter, which has an electrical resistance substantially greater than other metals (aluminum, brass, iron).
  • the tube, e.g., capillary tube can be made of a thin wall material ( FIG. 3A ), or a section of the wall can be narrowed ( FIG. 3B ) to result in that section having an electrical resistance such that when an electrical current is passed across the section heating happens.
  • the tube, e.g., capillary tube can be wrapped with a heater wire.
  • This configuration can allow for the tube, e.g., capillary tube to be made of a non-electrically conductive material such as Kapton (polyimide), which can withstand heat. Electrical heating can be powered directly from a battery or can be powered from a charged capacitor.
  • a non-electrically conductive material such as Kapton (polyimide)
  • Kapton polyimide
  • agent e.g., nicotine
  • FIG. 7 illustrates a configuration of a heater element ( 704 ) in an airway ( 706 ).
  • the heater element can be made of a thin stainless steel foil.
  • the foil can be of a thickness of about 0.0005 to about 0.005 inches (a range from about 0.01 mm to about 0.13 mm) thick, or from about 0.0005 to about 0.001 inches (a range from about 0.01 mm to about 0.025 mm) so that less electrical current is needed to vaporize the mixture.
  • the foil can be of a thickness of about, less than, more than, at least or at most 0.0005, 0.0006, 0.0007, 0.0008, 0.0009, 0.001, 0.002, 0.003, 0.003, 0.004, or 0.005 inches (a range from about 0.01 mm to about 0.13 mm).
  • the heater element ( 704 ) can be positioned at the exit of the tube, e.g., capillary tube ( 710 ) so that the mixture can deposit ( 708 ) on the heater element ( 704 ).
  • the heater element ( 704 ) can be positioned in an airway ( 706 ) so that a user upon inhalation can cause the aerosol to pass through the mouthpiece ( 702 ) and be drawn into the lungs.
  • the agent (e.g., nicotine) reservoir ( 712 ) can be in the airway.
  • FIG. 8 illustrates that in some cases, an agent (e.g., nicotine) reservoir ( 802 ) can be placed outside of an airway ( 804 ), while the heater element ( 806 ) can be in the airway ( 804 ).
  • a tube, e.g., capillary tube ( 808 ) can enter the airway ( 804 ).
  • FIGS. 31A-D illustrates another configuration of a heater element ( 3106 a - d ) in an airway ( 3112 a - d ).
  • FIG. 31A depicts a device (ENT-100-A), comprising a primary carrier gas inlet ( 3112 a ), positive and negative brass contacts ( 3110 a ), a heater element ( 3106 a ) comprising a coil located distally from the inlet to the primary airway ( 3112 a ) and two bypass inlets ( 3104 a ) located (disposed) downstream of the heater element but prior to the outlet ( 3102 a ).
  • FIG. 31B depicts a device designated ENT-100-B, which is the same as ENT-100-A except that the heater element has been moved to be proximal to the inlet of the primary airway ( 3112 b ).
  • FIG. 31C depicts a device designated ENT-100-C, which is similar to the ENT-100-A device except that the wire coil heater element has been moved to an intermediate position relative to the location of the coil in ENT-100-A and ENT-100-B.
  • Any of the devices depicted in FIG. 31A-C can comprise the wire coil heater element designated “A Coil” ( 3114 e ) or “B Coil” ( 3116 e ) as illustrated in FIG. 31E .
  • FIG. 31D depicts a device designated ENT-100-D with a primary passageway ( 3112 d ) for air to flow through, brass contacts (+/ ⁇ ) embedded within the wall of the primary passageway, and a heater element ( 3106 d ) comprising a wire wherein one end of the wire wraps around another segment of the wire, wherein a wire coil is formed with an end of the wire passes through the center of the wire coil.
  • a liquid formulation comprising a pharmaceutically active agent (e.g., nicotine) is delivered to the heater element of FIGS. 31A-D from a reservoir comprising the liquid formulation comprising a pharmaceutically active agent (e.g., nicotine) through the use of a tube, e.g., capillary tube as provided herein, wherein the tube, e.g., capillary tube is coupled or capable of being coupled to the reservoir.
  • a liquid formulation comprising a pharmaceutically active agent e.g., nicotine
  • a positive displacement pump as provided herein, wherein the positive displacement pump is fluidically coupled to the reservoir.
  • FIG. 9 illustrates another embodiment for a heater element.
  • an agent e.g., nicotine
  • the heater element can be positioned to cover the end of the tube, e.g., capillary tube when cold.
  • the heater would move away from the end ( 908 ) due to thermal expansion, opening up the end and allowing the mixture to leave.
  • the position of deposited material ( 910 ) is shown.
  • FIGS. 10A and 10B illustrate additional configurations of a heater element.
  • FIG. 10A illustrates that a heater element ( 1006 a ) can be positioned at the end of the tube, e.g., capillary tube ( 1004 a ), where the tube, e.g., capillary tube can be attached to an agent (e.g., nicotine) reservoir ( 1002 a ).
  • FIG. 10B illustrates an agent (e.g., nicotine) reservoir ( 1002 b ) and a tube, e.g., capillary tube ( 1004 b ), where the geometry of the tube, e.g., capillary tube is modified at the end ( 1006 b ) by narrowing or flattening to aid in vaporization.
  • FIG. 22 illustrates another embodiment of a heater element.
  • the heater element ( 2200 ) can be a rod comprising a coil ( 2202 ) that can be made of stainless steel, or a similar matter, which has an electrical resistance substantially greater than other metals (aluminum, brass, iron).
  • the rod is a wire, wherein the coil is a wire coil.
  • the rod can comprise an electrically resistive material.
  • the electrically resistive material can have an electrical resistance such that when an electrical current is passed across the rod heating happens.
  • the rod is connected to brass contacts ( 2204 ) through segments of the rod that do not form the coil. In some cases, the segments of the rod that connect to the brass contacts comprise leads. The brass contacts can serve to pass electrical current across the rod, including the coil.
  • the electrical current can serve to heat the coil and vaporize material (i.e. an agent (e.g., nicotine) mixture) that contacts or is delivered to the coil.
  • the coil can be an open coil that can allow for air to flow between the coils and carry away the vaporized material.
  • the brass contacts ( 2204 ) are located (disposed) on either side of an airflow channel and the rod, including the coil, span the channel.
  • the coil can be oriented parallel to the flow of a carrier gas (e.g, air).
  • the coil can be oriented perpendicular to the flow of a carrier gas (e.g., air).
  • a carrier gas e.g., air
  • a tube, e.g., capillary tube ( 2206 ) attached to a reservoir ( 2208 ) comprising an agent (e.g., nicotine) mixture is located at one end of the coil and an agent (e.g., nicotine) mixture is dispensed from the end of the tube, e.g., capillary tube onto the coil.
  • the agent (e.g., nicotine) mixture once dispensed, can wick along the coil to cover the entire or part of the coil.
  • the coil can be heated which can vaporize the agent (e.g., nicotine) mixture.
  • FIGS. 36-38 illustrate yet another embodiment of a heater element.
  • a first ( 3602 a ; +) and a second ( 3602 b ; ⁇ ) brass contact or terminal are located adjacent to each other.
  • the brass contacts can be embedded within or placed proximal to a wall of a housing or channel of a device for generating an aerosol as provided herein.
  • the heater element can be a rod comprising electrically resistive material, wherein a first end or lead ( 3604 a ) is connected to one brass contact ( 3602 a ; +), while a second end or lead ( 3604 b ) is connected to another, separate brass contact ( 3602 b ; ⁇ ). As illustrated in FIG.
  • a portion or segment of the rod between the leads is configured into a coil ( 3606 ).
  • a separate portion or segment ( 3608 ) of the rod passes through the interior of the coil ( 3606 ).
  • Supplying current to the rod through the brass contacts ( 3602 a,b ) can serve to heat both the coil ( 3606 ) as well as the segment ( 3608 ) of the rod that passes through the interior of the coil ( 3606 ).
  • the segment of the rod that runs through the center of the coil is capable of holding a liquid formulation comprising an agent (i.e. nicotine) as provided herein.
  • the liquid formulation can wick or be delivered by any of dosing mechanisms provided herein onto the segment of the rod that runs through the center of the coil from a source of the liquid formulation (e.g., a reservoir).
  • a source of the liquid formulation e.g., a reservoir
  • supplying current to the rod through the brass contacts ( 3602 a,b ) serves to heat both the coil ( 3606 ) as well as the segment ( 3608 ) of the rod that passes through the interior of the coil ( 3606 ), wherein a liquid formulations that wicks or is delivered by any of dosing mechanisms provided herein onto the segment of the rod running through the coil is vaporized.
  • the coil is oriented perpendicular to the flow of a carrier gas (e.g. air flow) ( 3610 ).
  • FIGS. 37A and 37B depict alternate embodiments to the heater element illustrated in FIG. 36 , wherein the number of coils shown in the heater element of FIG. 37A is reduced in the heater element of FIG. 37B .
  • alternating the number of coils ( 3702 b , 3702 b ) in the coil serves to increase the length of the non-coil segments ( 3704 a , 3704 b ) of the rod and decrease the length of the rod covered by the coil.
  • FIG. 38 illustrates components of the rod and coil in the heater element illustrated in FIG.
  • the diameter of the rod ( 3802 ), total length of the coil ( 3804 ) e.g., 0.1 to 0.15 inches (a range from about 2.54 mm to about 3.81 mm)
  • inner diameter of the coil ( 3808 ) e.g., 0.027-0.040 inches (about 0 6 mm to about 1.02 mm)
  • outer diameter of the coil ( 3806 ) e.g., 0.047-0.06 inches (a range from about 1.19 mm to about 1.53 mm)
  • An electronic agent (e.g., nicotine) delivery device can comprise a heater element comprising a coil, wherein the coil comprises electrically resistive material.
  • the coil can be a wire coil.
  • the electrically resistive material can include but is not limited to: semiconductors such as doped ceramics, electrically conductive ceramics such as molybdenum disilicide, carbon, graphite, metals, metal alloys and composite materials made of a ceramic material and a metallic material. Such composite materials may comprise doped or undoped ceramics. Examples of suitable doped ceramics include doped silicon carbides. Examples of suitable metals include titanium, zirconium, tantalum and metals from the platinum group.
  • suitable metal alloys include stainless steel-, Constantan-, nickel-, cobalt-, chromium-, aluminium-titanium- zirconium-, hafnium-, niobium-, molybdenum-, tantalum-, tungsten-, tin-, gallium-, manganese- and iron-containing alloys, and super-alloys based on nickel, iron, cobalt, stainless steel, Timetal® and iron-manganese-aluminium based alloys. Timetal® is a registered trade mark of Titanium Metals Corporation, 1999 Broadway Suite 4300, Denver Colo.
  • the electrically resistive material can optionally be embedded in, encapsulated or coated with an insulating material or vice-versa, depending on the kinetics of energy transfer and the external physicochemical properties required.
  • the coil comprises stainless steel.
  • a heater element comprising a rod as provided herein can comprise a coil and a wick element around which the coil can be wrapped.
  • the wick element can be capable of being heated.
  • the wick element can be connected to the rod.
  • the wick element can be independent of the rod. In some cases, the wick element is capable of being heated, and wherein the wick element is connected to the rod.
  • the rod can be a wire.
  • the coil can be a wire coil.
  • the rod can comprise a coil along the entire length of the wick element.
  • the wick element can be capable of wicking or holding a liquid formulation comprising an agent as provided herein.
  • the wick element can be a capillary (a self wicking tube).
  • the liquid formulation comprising an agent as provided herein can be in fluid communication with a source of the liquid formulation.
  • the source of the liquid formulation can be any source as provided herein, including but not limited to, a reservoir.
  • the liquid formulation comprising an agent as provided herein can be delivered to the wick element by any means known in the art. The delivery can be through capillary action or through the use of a pump.
  • the rod comprises a capillary wherein the capillary is in fluid communication with a reservoir, wherein the reservoir comprises a liquid formulation comprising a pharmaceutically active agent (e.g. nicotine), and wherein the capillary is capable of holding the liquid formulation comprising a pharmaceutically active agent (e.g. nicotine).
  • the wick element can be made of any material known in the art capable of wicking or holding a liquid formulation comprising an agent as provided herein.
  • the coil connects to a source of electricity.
  • the coil can connect to the source of electricity through one or more leads protruding from both ends of the coil.
  • the source of electricity can be a battery or a charged capacitor.
  • the battery can be rechargeable.
  • the coil can wrap around or span exactly, about, more than, less than, at least, or at most 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 21%, 22%, 23%, 24%, 25%, 26%, 27%, 28%, 29%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, 41%, 42%, 43%, 44%, 45%, 46%, 47%, 48%, 49%, 50%, 51%, 52%, 53%, 54%, 55%, 56%, 57%, 58%, 59%, 60%, 61%, 62%, 63%, 64%, 65%, 66%, 67%, 68%, 69%, 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%,
  • the coil can wrap around or span between 1-10%, 10-20%, 20-30%, 30-40%, 40-50%, 50-60%, 60-70%, 70-80%, 80-90%, or 90-100%, 10-20% of the length of the wick element. In some cases, the coil can wrap around or span of about 1 to about 10%, about 10 to about 20%, about 20 to about 30%, about 30 to about 40%, about 40 to about 50%, about 50 to about 60%, about 60 to about 70%, about 70 to about 80%, about 80 to about 90%, or about 90 to about 100% of the length of the wick element.
  • the total length of the coil can be exactly, about, more than, less than, at least, or at most 0.01, 0.0125, 0.015, 0.0175, 0.02, 0.0225, 0.025, 0.0275, 03, 0.0325, 0.035, 0.0375, 0.04, 0.0425, 0.045, 0.0475, 0.05, 0.0525, 0.055, 0.0575, 0.06, 0.0625, 0.065, 0.0675, 0.07, 0.0725, 0.075, 0.0775, 0.08, 0.0825, 0.085, 0.0875, 0.09, 0.0925, 0.095, 0.0975, 0.1, 0.11, 0.115, 0.12, 0.125, 0.13, 0.135, 0.14, 0.145, 0.15, 0.155, 0.16, 0.165, 0.17, 0.175, 0.18, 0.185, 0.19, 0.195 or 0.2 inches (a range from about 0.25 mm to about 5.08 mm).
  • the total length of the coil can be between 0.01-0.015, 0.015-0.02, 0.02-0.025, 0.025-030, 0.03-0.035, 0.035-0.04, 0.04-0.045, 0.045-0.05, 0.05-0.055, 0.055-0.06, 0.06-0.065, 0.065-0.07, 0.07-0.075, 0.075-0.08, 0.08-0.085, 0.085-0.09, 0.09-0.095, 0.095-0.1, 0.1-0.12, 0.12-0.13, 0.13-0.14, 0.14-0.15, 0.15-0.16, 0.16-0.17, 0.17-0.18, 0.18-0.19, or 0.19-0.2 inches (a range from about 0.25 mm to about 5.08 mm).
  • the total length of the coil can be about 0.01 to about 0.015, about 0.015 to about 0.02, about 0.02 to about 0.025, about 0.025 to about 03, about 0.03 to about 0.035, about 0.035 to about 0.04, about 0.04 to about 0.045, about 0.045 to about 0.05, about 0.05 to about 0.055, about 0.055 to about 0.06, about 0.06 to about 0.065, about 0.065 to about 0.07, about 0.07 to about 0.075, about 0.075 to about 0.08, about 0.08 to about 0.085, about 0.085 to about 0.09, about 0.09 to about 0.095, about 0.095 to about 0.1, about 0.1 to about 0.12, about 0.12 to about 0.13, about 0.13 to about 0.14, about 0.14 to about 0.15, about 0.15 to about 0.16, about 0.16 to about 0.17, about 0.17 to about 0.18, about 0.18 to about 0.19, or about 0.19 to about 0.2 inches (a range from about 0.25 mm to about 5.08
  • a heater element comprising a rod as provided herein can comprise one or more segments comprising a coil and one or more segments not comprising a coil (i.e. non-coil segment).
  • the rod can be a wire.
  • the coil can be a wire coil.
  • One or more non-coil segments of the rod can be capable of wicking or holding a liquid formulation comprising an agent as provided herein.
  • the non-coil segment can act as a capillary or wick.
  • one or more non-coil segments of the rod comprise a wick element.
  • One or more wick elements can be capable of being heated, thereby forming one or more heated wick elements.
  • the liquid formulation comprising an agent as provided herein can be in fluid communication with a source of the liquid formulation.
  • the source of the liquid formulation can be any source as provided herein, including, but not limited to, a reservoir.
  • the liquid formulation comprising an agent as provided herein can be delivered to a non-coil segment of the rod by any means known in the art. The delivery can be through capillary action or through the use of a pump.
  • the non-coil segment is in fluid communication with a reservoir, wherein the reservoir comprises a liquid formulation comprising a pharmaceutically active agent (e.g. nicotine), and wherein the non-coil segment is capable of holding the liquid formulation comprising a pharmaceutically active agent (e.g., nicotine).
  • a pharmaceutically active agent e.g. nicotine
  • the non-coil segments can serve as electrical leads for connecting the rod to a source of electricity.
  • the rod can comprise a coil along the entire length of the rod. In some cases, the coil connects to the source of electricity.
  • the source of electricity can be a battery or a charged capacitor.
  • the battery can be rechargeable.
  • a distance between the first and second leads of the rod when the first lead is connected to either the first or second terminal of the power source while the second lead is connected to the other of the first or second terminal of the power source is about, more than, less than, or at least 0.01, 0.015, 0.02, 0.025, 0.03, 0.035, 0.04, 0.045, 0.05, 0.055, 0.06, 0.065, 0.07, 0.075, 0.08, 0.085, 0.09, 0.095, 0.1, 0.11, 0.12, 0.13, 0.14, 0.15, 0.16, 0.17, 0.18, 0.19, or 0.2 inches (a range from about 0.254 mm to about 5.08 mm)
  • a distance between the first and second leads of the rod when the first lead is connected to either the first or second terminal of the power source while the second lead is connected to the other of the first or second terminal of the power source is from about 0.01 to about 0.1 inches, about 0.02 to about 0.09 inches, or about 0.025 to about 0.8 inches (
  • the coil can wrap around a non-coil segment of the rod, wherein the non-coil segment passes through the coil.
  • the coil can wrap around or span exactly, about, more than, less than, at least, or at most 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 21%, 22%, 23%, 24%, 25%, 26%, 27%, 28%, 29%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, 41%, 42%, 43%, 44%, 45%, 46%, 47%, 48%, 49%, 50%, 51%, 52%, 53%, 54%, 55%, 56%, 57%, 58%, 59%, 60%, 61%, 62%, 63%, 64%, 65%, 66%, 67%, 68%
  • the coil can wrap around or span between 1-10%, 10-20%, 20-30%, 30-40%, 40-50%, 50-60%, 60-70%, 70-80%, 80-90%, or 90-100%, 10-20% of the length a non-coil segment of the rod.
  • the coil can wrap around or span of about 1 to about 10%, about 10 to about 20%, about 20 to about 30%, about 30 to about 40%, about 40 to about 50%, about 50 to about 60%, about 60 to about 70%, about 70 to about 80%, about 80 to about 90%, or about 90 to about 100% of the length of a non-coil segment of the rod.
  • the total length of the coil can be exactly, about, more than, less than, at least, or at most 0.01, 0.0125, 0.015, 0.0175, 0.02, 0.0225, 0.025, 0.0275, 03, 0.0325, 0.035, 0.0375, 0.04, 0.0425, 0.045, 0.0475, 0.05, 0.0525, 0.055, 0.0575, 0.06, 0.0625, 0.065, 0.0675, 0.07, 0.0725, 0.075, 0.0775, 0.08, 0.0825, 0.085, 0.0875, 0.09, 0.0925, 0.095, 0.0975, 0.1, 0.11, 0.115, 0.12, 0.125, 0.13, 0.135, 0.14, 0.145, 0.15, 0.155, 0.16, 0.165, 0.17, 0.175, 0.18, 0.185, 0.19, 0.195 or 0.2 inches (a range from about 0.254 mm to about 5.08 mm).
  • the total length of the coil can be between 0.01-0.015, 0.015-0.02, 0.02-0.025, 0.025-030, 0.03-0.035, 0.035-0.04, 0.04-0.045, 0.045-0.05, 0.05-0.055, 0.055-0.06, 0.06-0.065, 0.065-0.07, 0.07-0.075, 0.075-0.08, 0.08-0.085, 0.085-0.09, 0.09-0.095, 0.095-0.1, 0.1-0.12, 0.12-0.13, 0.13-0.14, 0.14-0.15, 0.15-0.16, 0.16-0.17, 0.17-0.18, 0.18-0.19, or 0.19-0.2 inches (a range from about 0.254 mm to about 5.08 mm).
  • the total length of the coil can be about 0.01 to about 0.015, about 0.015 to about 0.02, about 0.02 to about 0.025, about 0.025 to about 03, about 0.03 to about 0.035, about 0.035 to about 0.04, about 0.04 to about 0.045, about 0.045 to about 0.05, about 0.05 to about 0.055, about 0.055 to about 0.06, about 0.06 to about 0.065, about 0.065 to about 0.07, about 0.07 to about 0.075, about 0.075 to about 0.08, about 0.08 to about 0.085, about 0.085 to about 0.09, about 0.09 to about 0.095, about 0.095 to about 0.1, about 0.1 to about 0.12, about 0.12 to about 0.13, about 0.13 to about 0.14, about 0.14 to about 0.15, about 0.15 to about 0.16, about 0.16 to about 0.17, about 0.17 to about 0.18, about 0.18 to about 0.19, or about 0.19 to about 0.2 inches (a range from about 0.254 mm to about 5.
  • a heater element comprising a rod as provided herein can comprise one or more coils.
  • the rod can be a wire.
  • the coil can be a wire coil.
  • the coil can have exactly, about, more than, less than, at least or at most 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5 10, 10.5, 11, 11.5, 12, 12.5, 13, 13.5, 14, 14.5, 15, 15.5, 16, 16.5, 17, 17.5, 18, 18.5, 19, 19.5, 20, 20.5, 21, 21.5, 22, 22.5, 23, 23.5, 24, 24.5, 25, 25.5, 26, 26.5, 27, 27.5, 28, 28.5, 29, 29.5, 30, 30.5, 31, 31.5, 32, 32.5, 33, 33.5, 34, 34.5, 35, 35.5, 36, 36.5, 37, 37.5, 38, 38.5, 39, 39.5, 40, 41, 42, 43, 44, 45, 46, 47, 4, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58,
  • the coil can comprise 1-2, 2-4, 4-6, 6-8, 8-10, 10-12, 12-14, 14-16, 16-18, or 18-20 coils.
  • the coil can comprise 2-20, 4-20, 6-20, 8-20, 10-20, 12-20, 14-20, or 16-20 coils.
  • the coil can comprise between 1-5, 5-10, 10-15, or 15-20 coils.
  • the coil can comprise between 1-10, 1-20, 1-30, 1-40, 1-60, 1-70, 1-80, 1-90, 1-100 coils.
  • the coil can comprise from about 1 to about 5, about 5 to about 10, about 10 to about 15, or about 15 to about 20 coils.
  • the coil can comprise from about 1 to about 10, about 1 to about 20, about 1 to about 30, about 1 to about 40, about 1 to about 60, about 1 to about 70, about 1 to about 80, about 1 to about 90, or about 1 to about 100 coils. In one embodiment, the coil comprises from about 5 to about 10 coils. In one embodiment, the coil comprises from about 1 to about 10 coils.
  • the distance between successive coils or the pitch of the coils can be exactly, about, more than, less than, at least or at most 0.01, 0.0125, 0.015, 1.17, 0.0175, 0.02, 0.0225, 0.025, 0.0275, 03, 0.0325, 0.035, 0.0375, 0.04, 0.0425, 0.045, 0.0475, 0.05, 0.0525, 0.055, 0.0575, 0.06, 0.0625, 0.065, 0.0675, 0.07, 0.0725, 0.075, 0.0775, 0.08, 0.0825, 0.085, 0.0875, 0.09, 0.0925, 0.095, 0.0975, 0.1, 0.11, 0.115, 0.12, 0.125, 0.13, 0.135, 0.14, 0.145, 0.15, 0.155, 0.16, 0.165, 0.17, 0.175, 0.18, 0.185, 0.19, 0.195 or 0.2 inches (a range from about 0.254 mm to about 5.08 mm).
  • the distance between successive coils or the pitch of the coils can be between 0.01-0.015, 0.015-0.3, 0.01-0.02, 0.015-0.02, 0.020-0.025, 0.025-03, 0.03-0.035, 0.035-0.04, 0.04-0.045, 0.045-0.05, 0.05-0.055, 0.055-0.06, 0.06-0.065, 0.065-0.07, 0.07-0.075, 0.075-0.08, 0.08-0.085, 0.085-0.09, 0.09-0.095, 0.095-0.1, 0.1-0.12, 0.12-0.13, 0.13-0.14, 0.14-0.15, 0.15-0.16, 0.16-0.17, 0.17-0.18, 0.18-0.19, or 0.19-0.2 inches (a range from about 0.254 mm to about 5.08 mm).
  • the distance between successive coils or the pitch of the coils can be about 0.01 to about 0.015, about 0.01 to about 0.02, about 0.015 to about 0.3, about 0.015 to about 0.02, about 0.02 to about 0.025, about 0.025 to about 03, about 0.03 to about 0.035, about 0.035 to about 0.04, about 0.04 to about 0.045, about 0.045 to about 0.05, about 0.05 to about 0.055, about 0.055 to about 0.06, about 0.06 to about 0.065, about 0.065 to about 0.07, about 0.07 to about 0.075, about 0.075 to about 0.08, about 0.08 to about 0.085, about 0.085 to about 0.09, about 0.09 to about 0.095, about 0.095 to about 0.1, about 0.1 to about 0.12, about 0.12 to about 0.13, about 0.13 to about 0.14, about 0.14 to about 0.15, about 0.15 to about 0.16, about 0.16 to about 0.17, about 0.17 to about 0.18, about 0.18 to about 0.
  • the rod can have a diameter between 0.005 and 0.01, 0.01 and 0.015, or 0.015 and 0.02 inches (a range from about 0.127 mm to about 0.51 mm). In one embodiment, the rod has a diameter between 0.005 and 0.02 inches (a range from about 0.127 mm to about 0.51 mm). In one embodiment, the rod has a diameter between 0.008 and 0.0012 inches (a range from about 0.2032 mm to about 0.03 mm). The rod can have a diameter of about 0.005 to about 0.01, about 0.01 to about 0.015, or about 0.015 to about 0.02 inches (a range from about 0.127 mm to about 0.508 mm).
  • the rod has a diameter of about 0.005 to about 0.02 inches (a range from about 0.127 mm to about 0.508 mm). In one embodiment, the rod has a diameter of about 0.008 to about 0.0012 inches (a range from about 0.2031 mm to about 0.03 mm).
  • the rod can be a wire.
  • a heater element comprising a coil as provided herein can have a coil with an inner or internal diameter of exactly, about, more than, less than, at least or at most 0.01, 0.012, 0.0125, 0.015, 0.0175, 0.02, 0.022, 0.0225, 0.025, 0.0275, 03, 0.032, 0.0325, 0.035, 0.0375, 0.04, 0.042 0.0425, 0.045, 0.0475, 0.05, 0.0520.0525, 0.055, 0.0575, 0.06, 0.062, 0.0625, 0.065, 0.0675, 0.07, 0.072, 0.0725, 0.075, 0.0775, 0.08, 0.0825, 0.085, 0.0875, 0.09, 0.0925, 0.095, 0.0975, 0.1, 0.11, 0.115, 0.12, 0.125, 0.13, 0.135, 0.14, 0.145, 0.15, 0.155, 0.16, 0.165, 0.17, 0.175, 0.18, 0.185, 0.19, 0.
  • the inner or internal diameter of the coil can be between 0.01-0.015, 0.015-0.02, 0.02-0.025, 0.0250-03, 0.03-0.035, 0.035-0.04, 0.04-0.045, 0.045-0.05, 0.05-0.055, 0.055-0.06, 0.06-0.065, 0.065-0.07, 0.07-0.075, 0.075-0.08, 0.08-0.085, 0.085-0.09, 0.09-0.095, 0.095-0.1, 0.1-0.12, 0.12-0.13, 0.13-0.14, 0.14-0.15, 0.15-0.16, 0.16-0.17, 0.17-0.18, 0.18-0.19, 0.19-0.2, 0.2-0.21, 0.21-0.22, 0.22-0.23, 0.23-0.24, 0.24-0.25, 0.25-0.26, 0.26-0.27, 0.27-0.28, 0.28-0.29, 0.29-0.3, 0.3-0.35, 0.35-0.4, 0.4-0.45, or 0.45-0.5 inches (a range from about 0.2
  • the inner or internal diameter of the coil can be about 0.01 to about 0.015, about 0.015 to about 0.02, about 0.02 to about 0.025, about 0.025 to about 0.3, about 0.03 to about 0.035, about 0.035 to about 0.04, about 0.04 to about 0.045, about 0.045 to about 0.05, about 0.05 to about 0.055, about 0.055 to about 0.06, about 0.06 to about 0.065, about 0.065 to about 0.07, about 0.07 to about 0.075, about 0.075 to about 0.08, about 0.08 to about 0.085, about 0.085 to about 0.09, about 0.09 to about 0.095, about 0.095 to about 0.1, about 0.1 to about 0.15, about 0.15 to about 0.2, about 0.2 to about 0.25, about 0.25 to about 0.3, about 0.3 to about 0.35, about 0.35 to about 0.4, about 0.4 to about 0.45, or about 0.45 to about 0.5 inches (a range from about 0.254 mm to about 12.7 mm).
  • the inner or internal diameter of the coil can be between 0.02 and 0.04, 0.04 and 0.06, or 0.02 and 0.06 inches (a range from about 0.508 mm to about 1.524 mm). In one embodiment, the inner or internal diameter of the coil is between 0.03 and 0.04 inches (a range from about 0.3 mm to about 1.02 mm). The inner or internal diameter of the coil can be about 0.02 to about 0.04, about 0.04 to about 0.06, or about 0.02 to about 0.06 inches (a range from about 0.508 mm to about 1.524 mm). In one embodiment, the inner or internal diameter of the coil is about 0.03 to about 0.04 inches (a range from about 0.3 mm to about 1.02 mm).
  • the inner or internal diameter of the coil is about 0.02 to about 0.04 inches (a range from about 0.508 mm to about 1.02 mm). In one embodiment, the inner or internal diameter of the coil is between 0.02 to about 0.04 inches (a range from about 0.508 mm to about 1.02 mm).
  • the coil can be a wire coil.
  • a heater element comprising a coil as provided herein can have a coil with an outer or external diameter of exactly, about, more than, less than, at least or at most 0.01, 0.0125, 0.015, 0.0175, 0.02, 0.0225, 0.025, 0.0275, 0.03, 0.0325, 0.035, 0.0375, 0.04, 0.0425, 0.045, 0.0475, 0.05, 0.0525, 0.055, 0.0575, 0.06, 0.0625, 0.065, 0.0675, 0.07, 0.0725, 0.075, 0.0775, 0.08, 0.0825, 0.085, 0.0875, 0.09, 0.0925, 0.095, 0.0975, 0.1, 0.11, 0.115, 0.12, 0.125, 0.13, 0.135, 0.14, 0.145, 0.15, 0.155, 0.16, 0.165, 0.17, 0.175, 0.18, 0.185, 0.19, 0.195, 0.2, 0.21, 0.22, 0.23, 0.24, 0.25, 0.26, 0.
  • the outer or external diameter of the coil can be between 0.01-0.015, 0.015-0.02, 0.02-0.025, 0.025-0.03, 0.03-0.035, 0.035-0.04, 0.04-0.045, 0.045-0.05, 0.05-0.055, 0.055-0.06, 0.06-0.065, 0.065-0.07, 0.07-0.075, 0.075-0.08, 0.08-0.085, 0.085-0.09, 0.09-0.095, 0.095-0.1, 0.1-0.12, 0.12-0.13, 0.13-0.14, 0.14-0.15, 0.15-0.16, 0.16-0.17, 0.17-0.18, 0.18-0.19, 0.19-0.2, 0.2-0.21, 0.21-0.22, 0.22-0.23, 0.23-0.24, 0.24-0.25, 0.25-0.26, 0.26-0.27, 0.27-0.28, 0.28-0.29, 0.29-0.3, 0.3-0.35, 0.35-0.4, 0.4-0.45, or 0.45-0.5 inches (a range from about 0.2
  • the outer or external diameter of the coil can be about 0.01 to about 0.015, about 0.015 to about 0.02, about 0.02 to about 0.025, about 0.025 to about 0.3, about 0.03 to about 0.035, about 0.035 to about 0.04, about 0.04 to about 0.045, about 0.045 to about 0.05, about 0.05 to about 0.055, about 0.055 to about 0.06, about 0.06 to about 0.065, about 0.065 to about 0.07, about 0.07 to about 0.075, about 0.075 to about 0.08, about 0.08 to about 0.085, about 0.085 to about 0.09, about 0.09 to about 0.095, about 0.095 to about 0.1, about 0.1 to about 0.15, about 0.15 to about 0.2, about 0.2 to about 0.25, about 0.25 to about 0.3, about 0.3 to about 0.35, about 0.35 to about 0.4, about 0.4 to about 0.45, or about 0.45 to about 0.5 inches (a range from about 0.254 mm to about 12.7 mm).
  • the outer or external diameter of the coil can be between 0.02 and 0.04, 0.04 and 0.06, or 0.02 and 0.06 inches (a range from about 0.02 mm and 1.02 mm to about 0.02 mm and 1.524 mm). In one embodiment, the outer or external diameter of the coil is between 0.03 and 0.04 inches (a range from about 0.0.762 mm to about 1.02 mm). The outer or external diameter of the coil can be about 0.02 to about 0.04, about 0.04 to about 0.06, about 0.02 to about 0.06 inches, about 0.02 to about 0.08 inches, about 0.02 to about 0.1 inches (a range from about 0.508 mm to about 2.54 mm).
  • the outer or external diameter of the coil is about 0.03 to about 0.04 inches (a range from about 0.762 mm to about 1.02 mm). In one embodiment, the outer or external diameter of the coil is about 0.02 to about 0.04 inches (a range from about 0.508 mm to about 1.02 mm). In one embodiment, the outer or external diameter of the coil is between 0.02 to about 0.04 inches (a range from about 0.508 mm to about 1.02 mm).
  • the coil can be a wire coil.
  • a heater element comprising a coil as provided herein can have a coil with a length to width aspect ratio exactly, about, more than, less than, at least or at most 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 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, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4, 4.5, 4.6, 4.7, 4.8, 4.9, 5, 5.1, 5.2, 5.3, 5.4, 5.5, 5.6, 5.7, 5.8, 5.9, 6, 6.1, 6.2, 6.3, 6.4, 6.5, 6.6, 6.7, 6.8, 6.9, 7, 7.1, 7.2, 7.3, 7.4, 7.5, 7.6, 7.7, 7.8,
  • the length to width aspect ratio of the coil can be between 0.1-0.15, 0.15-0.2, 0.2-0.25, 0.25-0.3, 0.3-0.35, 0.35-0.4, 0.4-0.45, 0.45-0.5, 0.5-0.55, 0.55-0.6, 0.6-0.65, 0.65-0.7, 0.7-0.75, 0.75-0.8, 0.8-0.85, 0.85-0.9, 0.9-0.95, 0.95-1, 1-1.5, 1.5-2, 2-2.5, 2.5-3, 3-3.5, 3.5-4, 4-4.5, 4.5-5, 5-5.5, 5.5-6, 6-6.5, 6.5-7, 7-7.5, 7.5-8, 8-8.5, 8.5-9, 9-9.5, 9.5-10, 10-10.5, 10.5-11, 11-11.5, 11.5-12, 12.5-13, 13-13.5, 13.5-14, 14-14.5, or 14.5-15.
  • the length to width aspect ratio of the coil can be about 0.1 to about 0.15, about 0.15 to about 0.2, about 0.2 to about 0.25, about 0.25 to about 0.3, about 0.3 to about 0.35, about 0.35 to about 0.4, about 0.4 to about 0.45, about 0.45 to about 0.5, about 0.5 to about 0.55, about 0.55 to about 0.6, about 0.6 to about 0.65, about 0.65 to about 0.7, about 0.7 to about 0.75, about 0.75 to about 0.8, about 0.8 to about 0.85, about 0.85 to about 0.9, about 0.9 to about 0.95, about 0.95 to about 1, about 1 to about 1.5, about 1.5 to about 2, about 2 to about 2.5, about 2.5 to about 3, about 3 to about 3.5, about 3.5 to about 4, about 4 to about 4.5, about 4.5 to about 5, about 5 to about 5.5, about 5.5 to about 6, about 6 to about 6.5, about 6.5 to about 7, about 7 to about 7.5, about 7.5 to about 8, about 8 to about 8.5, about 8.5 to about 9, about
  • a heater element comprising a rod as provided herein, wherein the rod can have a coil wherein a ratio of the diameter of the rod to the diameter of the coil can be exactly, about, more than, less than, at least or at most 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4, 4.5, 4.6, 4.7, 4.8, 4.9, 5, 5.1, 5.2, 5.3, 5.4, 5.5, 5.6, 5.7, 5.8, 5.9, 6, 6.1, 6.2, 6.3, 6.4, 6.5, 6.6, 6.7, 6.8, 6.9, 7, 7.1, 7.2,
  • the ratio of the diameter of the rod to the diameter of the coil can be between 0.1-0.15, 0.15-0.2, 0.2-0.25, 0.25-0.3, 0.3-0.35, 0.35-0.4, 0.4-0.45, 0.45-0.5, 0.5-0.55, 0.55-0.6, 0.6-0.65, 0.65-0.7, 0.7-0.75, 0.75-0.8, 0.8-0.85, 0.85-0.9, 0.9-0.95, 0.95-1, 1-1.5, 1.5-2, 2-2.5, 2.5-3, 3-3.5, 3.5-4, 4-4.5, 4.5-5, 5-5.5, 5.5-6, 6-6.5, 6.5-7, 7-7.5, 7.5-8, 8-8.5, 8.5-9, 9-9.5, 9.5-10, 10-10.5, 10.5-11, 11-11.5, 11.5-12, 12.5-13, 13-13.5, 13.5-14, 14-14.5, or 14.5-15.
  • the ratio of the diameter of the rod to the diameter of the coil can be about 0.1 to about 0.15, about 0.15 to about 0.2, about 0.2 to about 0.25, about 0.2 to about 0.4, about 0.25 to about 0.3, about 0.3 to about 0.35, about 0.35 to about 0.4, about 0.4 to about 0.45, about 0.45 to about 0.5, about 0.5 to about 0.55, about 0.55 to about 0.6, about 0.6 to about 0.65, about 0.65 to about 0.7, about 0.7 to about 0.75, about 0.75 to about 0.8, about 0.8 to about 0.85, about 0.85 to about 0.9, about 0.9 to about 0.95, about 0.95 to about 1, about 1 to about 1.5, about 1.5 to about 2, about 2 to about 2.5, about 2.5 to about 3, about 3 to about 3.5, about 3.5 to about 4, about 4 to about 4.5, about 4.5 to about 5, about 5 to about 5.5, about 5.5 to about 6, about 6 to about 6.5, about 6.5 to about 7, about 7 to about 7.5, about 7.5 to about 8, about
  • a heater element comprising a rod wherein the rod can have a coil wherein the volume of the rod can be less than the volume of the coil.
  • the volume of the rod can be exactly, about, more than, less than, at least or at most 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 21%, 22%, 23%, 24%, 25%, 26%, 27%, 28%, 29%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, 41%, 42%, 43%, 44%, 45%, 46%, 47%, 48%, 49%, 50%, 51%, 52%, 53%, 54%, 55%, 56%, 57%, 58%, 59%, 60%, 61%, 62%, 63%, 64%, 65%, 66%, 67%, 6
  • the volume of the rod can be between 1-10%, 10-20%, 20-30%, 30-40%, 40-50%, 50-60%, 60-70%, 70-80%, 80-90%, or 90-100% of the volume of the coil.
  • the volume of the rod can be about 1 to about 10%, about 10 to about 20%, about 20 to about 30%, about 30 to about 40%, about 40 to about 50%, about 50 to about 60%, about 60 to about 70%, about 70 to about 80%, about 80 to about 90%, or about 90 to about 100% of the volume of the coil.
  • the rod can be a wire.
  • the coil can be a wire coil.
  • the volume of the coil be about, more than, less than, at least, or no greater than 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, or 10 times the volume of the rod.
  • a heater element comprising a rod is provided herein, wherein the rod can have a coil, wherein the surface area of the rod can be less than, greater than or equal to the surface area of the outer or external surface of the coil.
  • the surface area of the rod can be exactly, about, more than, less than, at least or at most 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 21%, 22%, 23%, 24%, 25%, 26%, 27%, 28%, 29%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, 41%, 42%, 43%, 44%, 45%, 46%, 47%, 48%, 49%, 50%, 51%, 52%, 53%, 54%, 55%, 56%, 57%, 58%, 59%, 60%, 61%,
  • the surface area of the rod can be between 1-10%, 10-20%, 20-30%, 30-40%, 40-50%, 50-60%, 60-70%, 70-80%, 80-90%, or 90-100% greater than or less than the outer surface area of the coil.
  • the surface area of the rod can be about 1 to about 10%, about 10 to about 20%, about 20 to about 30%, about 30 to about 40%, about 40 to about 50%, about 50 to about 60%, about 60 to about 70%, about 70 to about 80%, about 80 to about 90%, or about 90 to about 100% greater than or less than the outer surface area of the coil.
  • the rod can be a wire.
  • the coil can be a wire coil.
  • a surface area of a rod can be 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4, 4.5, 4.6, 4.7, 4.8, 4.9, 5, 5.1, 5.2, 5.3, 5.4, 5.5, 5.6, 5.7, 5.8, 5.9, 6, 6.1, 6.2, 6.3, 6.4, 6.5, 6.6, 6.7, 6.8, 6.9, 7, 7.1, 7.2, 7.3, 7.4, 7.5, 7.6, 7.7, 7.8, 7.9, 8, 8.1, 8.2, 8.3, 8.4, 8.5, 8.6, 8.7, 8.8, 8.9, 9, 9.1, 9.2, 9.3, 9.4, 9.5, 9.6, 9.7, 9.8, 9.9, or 10 times greater than a surface
  • a heater element as provided herein can comprise an electrical resistance that can be exactly, about, more than, less than, at least or at most 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4, 4.5, 4.6, 4.7, 4.8, 4.9, 5, 5.1, 5.2, 5.3, 5.4, 5.5, 5.6, 5.7, 5.8, 5.9, 6, 6.1, 6.2, 6.3, 6.4, 6.5, 6.6, 6.7, 6.8, 6.9, 7, 7.1, 7.2, 7.3, 7.4, 7.5, 7.6, 7.7, 7.8, 7.9, 8, 8.1, 8.2, 8.3,
  • the electrical resistance can be between 0.1-0.15, 0.15-0.2, 0.2-0.25, 0.25-0.3, 0.3-0.35, 0.35-0.4, 0.4-0.45, 0.45-0.5, 0.5-0.55, 0.55-0.6, 0.6-0.65, 0.65-0.7, 0.7-0.75, 0.75-0.8, 0.8-0.85, 0.85-0.9, 0.9-0.95, 0.95-1, 1-1.5, 1.5-2, 2-2.5, 2.5-3, 3-3.5, 3.5-4, 4-4.5, 4.5-5, 5-5.5, 5.5-6, 6-6.5, 6.5-7, 7-7.5, 7.5-8, 8-8.5, 8.5-9, 9-9.5, or 9.5-10 Ohms.
  • the electrical resistance can be about 0.1 to about 0.15, about 0.15 to about 0.2, about 0.2 to about 0.25, about 0.25 to about 0.3, about 0.3 to about 0.35, about 0.35 to about 0.4, about 0.4 to about 0.45, about 0.45 to about 0.50, about 0.5 to about 0.55, about 0.55 to about 0.6, about 0.6 to about 0.65, about 0.65 to about 0.7, about 0.7 to about 0.75, about 0.75 to about 0.8, about 0.8 to about 0.85, about 0.85 to about 0.9, about 0.9 to about 0.95, about 0.95 to about 1, about 1 to about 1.5, about 1.5 to about 2, about 2 to about 2.5, about 2.5 to about 3, about 3 to about 3.5, about 3.5 to about 4, about 4 to about 4.5, about 4.5 to about 5, about 5 to about 5.5, about 5.5 to about 6, about 6 to about 6.5, about 6.5 to about 7, about 7 to about 7.5, about 7.5 to about 8, about 8 to about 8.5, about 8.5 to about 9, about 9 to about 9.5,
  • a heater element as provided herein can vaporize a liquid formulation comprising a pharmaceutically active agent (e.g., nicotine) as provided herein, wherein substantially all of the liquid formulation in contact with or delivered to the heater element is vaporized.
  • the vaporization of the liquid formulation that contacts or is delivered to a heater element as provided herein can be exactly, about, more than, less than, at most, or at least 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, 41%, 42%, 43%, 44%, 45%, 46%, 47%, 48%, 49%, 50%, 51%, 52%, 53%, 54%, 55%, 56%, 57%, 58%, 59%, 60%, 61%, 62%, 63%
  • the vaporization of the liquid formulation that contacts or is delivered to a heater element as provided herein can be between 1%-10%, 10%-20%, 20%-30%, 30%-40%, 40%-50%, 50%-60%, 60%-70%, 70%-80%, 80%-90%, or 90%-100%.
  • the vaporization of the liquid formulation that contacts or is delivered to a heater element as provided herein can be about 1% to about 10%, about 10% to about 20%, about 20% to about 30%, about 30% to about 40%, about 40% to about 50%, about 50% to about 60%, about 60% to about 70%, about 70% to about 80%, about 80% to about 90%, or about 90% to about 100%.
  • the vaporization of the liquid formulation that contacts or is delivered to a heater element as provided herein can be greater than 95%, 99%, or 99.5%.
  • the amount of residue or build-up of non-vaporized liquid formulation comprising a pharmaceutically active agent (e.g., nicotine) that contacts or is delivered to a heater element as provided herein can be reduced by exactly, about, more than, less than, at most, or at least 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, 41%, 42%, 43%, 44%, 45%, 46%, 47%, 48%, 49%, 50%, 51%, 52%, 53%, 54%, 55%, 56%, 57%, 58%, 59%, 60%, 61%, 62%, 63%, 64%, 65%, 66%, 67%, 68%, 69%, 70%, 71%, 72%, 73%, 74%, 75%
  • the amount of residue or build-up of non-vaporized liquid formulation comprising a pharmaceutically active agent that contacts or is delivered to a heater element as provided herein can be between 1%-10%, 10%-20%, 20%-30%, 30%-40%, 40%-50%, 50%-60%, 60%-70%, 70%-80%, 80%-90%, or 90%-100%.
  • the amount of residue or build-up of non-vaporized liquid formulation comprising a pharmaceutically active agent that contacts or is delivered to a heater element as provided herein can be reduced by about 1% to about 10%, about 10% to about 20%, about 20% to about 30%, about 30% to about 40%, about 40% to about 50%, about 50% to about 60%, about 60% to about 70%, about 70% to about 80%, about 80% to about 90%, or about 90% to about 100%.
  • the amount of residue or build-up of non-vaporized liquid formulation comprising a pharmaceutically active agent that contacts or is delivered to a heater element as provided herein can be reduced by greater than 95%, 99%, or 99.5%.
  • Heating elements can be renewed with changes in an agent (e.g., nicotine) dose cartridge to ensure dose consistency by removal of any build up of combusted material on the heater element.
  • agent e.g., nicotine
  • the heater element comprises a coil and a wick element, wherein the coil wraps around the wick element, and wherein the liquid formulation wicks onto the heated wick element, wherein the liquid formulation is vaporized through heating of the coil and wick element.
  • the heater element can be in fluid communication with a source of liquid formulation comprising an agent (e.g., nicotine) as provided herein.
  • the heater element further comprises a source of a liquid formulation comprising an agent (e.g., nicotine), wherein the source is in fluid communication with the wick element capable of being heated, wherein the liquid formulation comprising an agent (e.g., nicotine) wicks onto the wick element capable of being heated, whereby the liquid formulation is aerosolized by heating of the coil and wick element capable of being heated upon activation of a power source, wherein the power source is electrically coupled to the heater element.
  • an agent e.g., nicotine
  • the heater element further comprises a source of a liquid formulation comprising an agent, wherein the source is in fluid communication with the heatable wick element, wherein the liquid formulation comprising an agent wicks onto the heatable wick element, wherein the heatable wick element is heated after the formulation has wicked onto the heatable wick element, whereby the liquid formulation is aerosolized by heating of the coil and heatable wick element upon activation of the power source.
  • the heater element comprising a coil with a center exit wick element capable of being heated as described herein can vaporize substantially all of the liquid formulation comprising the pharmaceutically active agent (e.g., nicotine) that wicks onto the center wick element.
  • the heater element comprising a coil with a center exit wick element capable of being heated can have a reduced or substantially no splatter.
  • the heater element comprises a coil with a center exit wick element capable of being heated, wherein a liquid formulation comprising a pharmaceutically active agent (e.g., nicotine) is held or wicks onto the center exit wick element capable of being heated, and wherein both the wick element capable of being heated and coil are heated, thereby vaporizing the liquid formulation, wherein substantially all of the liquid formulation is vaporized.
  • the heater element comprising a coil with a center exit wick element capable of being heated can vaporize greater than 95% of the liquid formulation wicked onto the wick element.
  • the amount of residue or build-up of non-vaporized liquid formulation comprising a pharmaceutically active agent (e.g., nicotine) can be substantially reduced. Following vaporization of a liquid formulation as provided herein by a heater element comprising a coil and a center exit wick element capable of being heated less than 5% residue of non-vaporized liquid formulation can remain on the heater element.
  • a heater element is connected to a timing device.
  • FIG. 11 shows an agent (e.g., nicotine) reservoir ( 1104 ), tube, e.g., capillary tube ( 1106 ), heater element 1 ( 1108 ), and a heater element 2 ( 1110 ).
  • agent e.g., nicotine
  • FIG. 11 shows an agent (e.g., nicotine) reservoir ( 1104 ), tube, e.g., capillary tube ( 1106 ), heater element 1 ( 1108 ), and a heater element 2 ( 1110 ).
  • One consideration is whether a restriction in a nozzle ( 1102 ) can cause an unacceptable increase in the air flow resistance.
  • the following formula can be used to calculate the diameter of an orifice (D J ) ( 1112 ).
  • d 50 is the average aerosol practice size.
  • a nozzle with a diameter of about 6 mm can be used, which can be acceptable for a pressure drop at 15 L/min (about 2.5 ⁇ 10 ⁇ 4 m 3 /s) flow rate of inhalation.
  • a device for generating a condensation aerosol from a liquid formulation comprising a pharmaceutically active agent (e.g., nicotine) as provided herein comprises a means for removing aerosol particles of a size not optimal for deep lung delivery and subsequent rapid PK.
  • the non-optimal particles can have an MMAD of greater than 5 ⁇ m.
  • the means for removing the non-optimal particles can be a solid structure within a passageway in which a condensation aerosol generated as provided herein flows.
  • the structure is a planar surface attached to one or more walls of the passageway, wherein the planar structure comprises one or more holes wherein particles of specific sizes (e.g. less than 5 ⁇ m) pass through.
  • the structure comprises a planar surface attached to the passageway such that the planar surface has a diameter or width that occupies a portion of the diameter or width of the passageway such that only particles of an optimal size flow or are diverted around the planar surface while non-optimally sized particles impact the surface and are incapable of flowing around the surface.
  • the optimally sized particles have an MMAD of less than or equal to 5 ⁇ m. In some cases, the optimally sized particles have an MMAD of about 1 to about 5 ⁇ m. In some cases, the optimally sized particles have an MMAD of greater than 5 ⁇ m.
  • the structure can be a baffle or baffle plate. FIGS.
  • FIGS. 44A and B illustrate exterior views of the passageway comprising the baffle
  • FIG. 44C provides an interior view of a cone shaped baffle ( 4402 ) and its orientation within a passageway through which a condensation aerosol flows ( 4410 ).
  • a condensation aerosol comprising a pharmaceutically active agent (e.g., nicotine) generated by any means as provided herein enters a portion of a passageway comprising the baffle ( 4402 ) through an aerosol inlet ( 4404 ).
  • a pharmaceutically active agent e.g., nicotine
  • the aerosol inlet can be a portion of a passageway downstream of a heater element that narrows following the area of the passageway that comprises the heater element.
  • the aerosol inlet ( 4404 ) serves to funnel the aerosol through a narrowed passageway prior to the aerosol encountering the planar surface of the cone-shaped baffle ( 4402 ). Prior to the baffle ( 4402 ), the passageway widens, wherein the diameter of the planar surface of the baffle occupies a substantial portion of the diameter of the widened passageway.
  • the aerosol flows toward the baffle ( 4402 ), wherein large particles (>5 ⁇ m) flow into the planar surface of the baffle, while small particles ( ⁇ 5 ⁇ m), flow around the edges of the baffle ( 4402 ).
  • large particles >5 ⁇ m
  • small particles ⁇ 5 ⁇ m
  • the widened passageway downstream of the baffle ( 4402 ) entrains the small particles into additional carrier gas ( 4408 ) that enters through secondary carrier gas ( 4408 ) inlets.
  • a flow of carrier gas through the passageway is about 1 to about 10 LPM (a range from about 1.667 ⁇ 10 ⁇ 5 m 3 /s to about 1.667 ⁇ 10 ⁇ 4 m 3 /s) (e.g., at a vacuum of about 1 to about 15 inches of water (a range from about 249 Pa to about 3738 Pa)), while the carrier gas ( 4408 ) entering through the secondary carrier gas ( 4408 ) inlets entrains the small particles in an air flow of about 20 to about 80 LPM (a range from about 3 ⁇ 10 ⁇ 4 m 3 /s to about 1.3 ⁇ 10 ⁇ 3 m 3 /s).
  • the passageway depicted in FIG. 44C is connected to and downstream of the passageways depicted in any one of FIGS. 31A-D , wherein the passageway depicted in FIG. 44C is connected at the aerosol inlet ( 4404 ). In some cases, the aerosol inlet of the passageway depicted in FIG. 44C is a downstream extension of the passageways depicted in any one of FIGS. 31A-D .
  • the inner diameter of the passageway at the aerosol inlet of FIG. 44C and downstream of the narrow channel can be can be exactly, about, more than, less than, at least or at most 0.2, 0.21, 0.22, 0.23, 0.24, 0.25, 0.26, 0.27, 0.28, 0.29, 0.3, 0.35, 0.4, 0.45, or 0.5 inches (a range from about 0.508 mm to about 12.7 mm).
  • 44C and downstream of the narrow channel can be between 0.2-0.21, 0.21-0.22, 0.22-0.23, 0.23-0.24, 0.24-0.25, 0.25-0.26, 0.26-0.27, 0.27-0.28, 0.28-0.29, 0.29-0.3, 0.3-0.35, 0.35-0.4, 0.4-0.45, or 0.45-0.5 inches (a range from about 0.508 mm to about 12.7 mm).
  • the inner diameter of the outlet ( 4406 ) can be exactly, about, more than, less than, at least or at most 0.2, 0.21, 0.22, 0.23, 0.24, 0.25, 0.26, 0.27, 0.28, 0.29, 0.3, 0.35, 0.4, 0.45, or 0.5 inches (a range from about 0.508 mm to about 12.7 mm).
  • the inner diameter of the outlet ( 4406 ) can be between 0.2-0.21, 0.21-0.22, 0.22-0.23, 0.23-0.24, 0.24-0.25, 0.25-0.26, 0.26-0.27, 0.27-0.28, 0.28-0.29, 0.29-0.3, 0.3-0.35, 0.35-0.4, 0.4-0.45, or 0.45-0.5 inches (a range from about 0.508 mm to about 12.7 mm).
  • the inner diameter of the outlet ( 4406 ) can be about 0.2 to about 0.25, about 0.25 to about 0.3, about 0.3 to about 0.35, about 0.35 to about 0.4, about 0.4 to about 0.45, or about 0.45 to about 0.5 inches (a range from about 0.508 mm to about 12.7 mm).
  • the inner diameter of the narrow channel can be exactly, about, more than, less than, at least or at most 0.01, 0.0125, 0.015, 0.0175, 0.02, 0.0225, 0.025, 0.0275, 0.03, 0.0325, 0.035, 0.0375, 0.04, 0.0425, 0.045, 0.0475, 0.05, 0.0525, 0.055, 0.0575, 0.06, 0.0625, 0.065, 0.0675, 0.07, 0.0725, 0.075, 0.0775, 0.08, 0.0825, 0.085, 0.0875, 0.09, 0.0925, 0.095, 0.0975, 0.1, 0.11, 0.115, 0.12, 0.125, 0.13, 0.135, 0.14, 0.145, or 0.15 inches (a range from about 0.254 mm to about 3.81 mm).
  • the inner diameter of the narrow channel can be between 0.01-0.015, 0.015-0.02, 0.02-0.025, 0.025-0.03, 0.03-0.035, 0.035-0.04, 0.04-0.045, 0.045-0.05, 0.05-0.055, 0.055-0.06, 0.06-0.065, 0.065-0.07, 0.07-0.075, 0.075-0.08, 0.08-0.085, 0.085-0.09, 0.09-0.095, 0.095-0.1, 0.1-0.12, 0.12-0.13, 0.13-0.14, or 0.14-0.15 inches (a range from about 0.254 mm to about 3.81 mm).
  • the inner diameter of the narrow channel can be about 0.01 to about 0.015, about 0.015 to about 0.02, about 0.02 to about 0.025, about 0.025 to about 03, about 0.03 to about 0.035, about 0.035 to about 0.04, about 0.04 to about 0.045, about 0.045 to about 0.05, about 0.05 to about 0.055, about 0.055 to about 0.06, about 0.06 to about 0.065, about 0.065 to about 0.07, about 0.07 to about 0.075, about 0.075 to about 0.08, about 0.08 to about 0.085, about 0.085 to about 0.09, about 0.09 to about 0.095, about 0.095 to about 0.1, or about 0.1 to about 0.15 inches (a range from about 0.254 mm to about 3.81 mm).
  • a device provided herein can be configured to limit a flow of a carrier gas through the passageway or aerosol generation area/chamber to permit condensation of the vaporized liquid formulation.
  • the carrier gas can be air.
  • the flow of a carrier gas through the aerosol generation chamber or passageway comprising or in fluid communication with the heater element can be limited to about 1 to about 10 liters per minute (LPM) (a range from about 1.667 ⁇ 10 ⁇ 5 m 3 /s to about 1.667 ⁇ 10 ⁇ 4 m 3 /s).
  • LPM liters per minute
  • the device can be configured to comprise a flow resistance (to inhalation) of about 0.05 to about 0.15 sqrt (cm-H 2 O)/LPM.
  • the device can be configured to comprise an inhalation resistance comprising a vacuum pressure of about 1 to about 10 inches of H 2 O (a range from about 249 Pa to about 2488 Pa).
  • an optical sensor that uses a deformable member (e.g., a vane) that moves during inhalation can be used to either open or close an optical path.
  • a Hall effect sensor is used to measure inhalation.
  • inhalation sensing is accomplished using an optical signal wherein a unique pattern of light pulses is sent along an optical path or light pipe and resent back along the optical path to a light detector.
  • the optical signal is sent from a controller into a dose cartridge whereby it is resent back into the controller to a light detector.
  • a vane is positioned in the path of an airway such that when an inhalation occurs, the vane is deflected out of the way and interrupts the optical signal.
  • the device notes the absence of the optical signal and triggers the creation of an aerosol.
  • a valve system to allow for a user to experience an initial high pressure and low flow rates, followed by low pressure is used.
  • An initial high-pressure drop through the device to facilitate the ejection of an agent (e.g., nicotine) from a dosing mechanism can be used.
  • the following high flow rate can facilitate deep lung delivery.
  • a slide valve with an attached piston mechanism is used to eject an agent (e.g., nicotine) from a dosing reservoir.
  • air flow over a vaporizing agent (e.g., nicotine) formulation is regulated and controlled to an optimum level using a valve system, resulting in optimum particle sizing and dosing effectiveness.
  • a valve system is used to create an internal air or inhalation resistance that is low (e.g., 0.08 to 0.12 (cm H 2 O) 1/2 /LPM).
  • a device for generating a condensation aerosol as provided herein can comprise a heater element.
  • a device provided herein can comprise a passageway, wherein the passageway comprises a heater element and a reservoir.
  • the device comprises a passageway, a reservoir, and a housing which comprises a heater element, wherein the passageway is in fluid communication with the heater element.
  • the passageway comprising the heater element or in fluid communication with the heater element can comprise an aerosol generation area or chamber.
  • the aerosol generation area or chamber comprises the heater element.
  • the aerosol generation area or chamber comprises the heater element and a source of a formulation comprising an agent as provided herein.
  • the source can be a tube, e.g., capillary tube, or a reservoir.
  • the tube, e.g., capillary tube can be coupled to the reservoir.
  • the reservoir can comprise the liquid formulation.
  • the reservoir can be in fluid communication with the heater element.
  • the reservoir can serve to deliver the liquid formulation to the heater element, wherein the liquid formulation can wick onto the heater element.
  • the reservoir can comprise a tube, e.g., capillary tube, wherein the tube, e.g., capillary tube can deliver the liquid formulation onto the heater element.
  • a device for generating a condensation aerosol as provided herein comprises an aerosol generation chamber.
  • the aerosol generation chamber can comprise a heater element.
  • the aerosol generation chamber can comprise a source of a liquid formulation comprising a pharmaceutically active agent (e.g. nicotine).
  • the aerosol generation chamber comprises a heater element and a source of a liquid formulation comprising a pharmaceutically active agent (e.g. nicotine).
  • the aerosol generation chamber can be within a primary flow-through passageway.
  • a device for producing a condensation aerosol as provided herein comprises a flow-through passageway, wherein the flow-through passageway comprises an upstream opening and a downstream opening, wherein the flow-through passageway comprises an aerosol generation chamber between the upstream and downstream openings of the flow-through passageway.
  • the passageway can be a primary flow-through passageway.
  • the primary flow-through passageway can be in fluid communication with a secondary flow-through passageway as provided herein.
  • the aerosol generation chamber further comprises a nozzle as provided herein.
  • a device for generating a condensation aerosol as provided herein comprises an aerosol generation chamber, wherein the aerosol generation chamber is within a passageway configured to limit the flow of a carrier gas through the aerosol generation chamber to a flow rate effective for producing a condensation aerosol comprising particles of a size suitable for delivery to the deep lung of a subject.
  • the flow rate can be limited to about 1 to about 10 liters per minute (LPM) (a range from about 1.667 ⁇ 10 ⁇ 5 m 3 /s to about 1.667 ⁇ 10 ⁇ 4 m 3 /s) at, e.g., a vacuum of about 1 to about 15 inches of water (a range from about 249 Pa to about 3738 Pa).
  • LPM liters per minute
  • a device for producing a condensation aerosol as provided herein comprises a primary flow-through passageway, wherein the primary flow-through passageway comprises an upstream opening and a downstream opening, wherein the upstream opening comprises an inlet for a carrier gas (e.g., air) and the downstream opening comprises an outlet for the carrier gas (e.g., air).
  • the passageway can be a primary flow-through passageway.
  • the primary flow-through passageway can be in fluid communication with a secondary flow-through passageway as provided herein.
  • the inlet can comprise a flow restrictor configured to limit the flow of the carrier gas through primary flow-through passageway to a flow rate effective for producing a condensation aerosol comprising particles of a size suitable for delivery to the deep lung of a subject.
  • the flow restrictor can limit the flow rate to about 1 to about 10 liters per minute (LPM) (a range from about 1.667 ⁇ 10 ⁇ 5 m 3 /s to about 1.667 ⁇ 10 ⁇ 4 m 3 /s), e.g., at a vacuum of about 1 to about 15 inches of water (a range from about 249 Pa to about 3738 Pa).
  • the flow restrictor can be a valve or an orifice comprising dimensions that limit the flow of a carrier gas (e.g., air) to a rate suitable for producing a condensation aerosol comprising particles of a size suitable for delivery to the deep lung of a subject.
  • a carrier gas e.g., air
  • An orifice for air that passes over the heater element can have a diameter of about, more than, less than, or at least 0.01, 0.012, 0.015, 0.02, 0.022, 0.025, 0.03, 0.032, 0.035, 0.04, 0.042, 0.045, 0.05, 0.052, 0.055, 0.06, 0.062, 0.065, 0.07, 0.075, 0.08, 0.085, 0.09, 0.1, 0.105, 0.11, 0.12, 0.13, 0.14, 0.15, 0.16, 0.17, 0.18, 0.19, 0.2, 0.21, 0.22, 0.23, 0.24, 0.25, 0.26, 0.27, 0.28, 0.29, 0.3, 0.31, 0.32, 0.33, 0.34, 0.35, 0.36, 0.37, 0.38, 0.39, 0.4, 0.41, 0.42, 0.43, 0.44, 0.45, 0.46, 0.47, 0.48, 0.49, 0.5, 0.51, 0.52, 0.53, 0.54, 0.55, 0.56,
  • an orifice for air that passes over a heater element has a diameter of about 0.01 to about 0.12 inches, about 0.02 to about 0.1 inches, about 0.03 to about 0.09 inches, about 0.04 to about 0.08 inches, or about 0.05 to about 0.07 inches, or about 0.15 to about 3 inches (a range from about 0.254 mm to about 76.2 mm).
  • An orifice for bypass air (air that is routed around a heater element) can have a diameter of about, more than, less than, or at least 0.02, 0.04, 0.06, 0.08, 0.1, 0.12, 0.14, 0.16, 0.18, 0.2, 0.22, 0.24, 0.26, 0.28, 0.3, 0.32, 0.34, 0.36, 0.38, 0.4, 0.42, 0.44, 0.46, 0.48, 0.5, 0.52, 0.54, 0.56, 0.58, 0.6, 0.62, 0.64, 0.66, 0.68, 0.7, 0.8, 0.9, 1, or 1.2 inches (a range from about 0.508 mm to about 30.48 mm).
  • an orifice for bypass air (air that is routed around a heater element) has a diameter of about 0.05 to about 0.4 inches, about 0.1 to about 0.3 inches, or about 0.1 to about 0.4 inches (a range from about 1.27 mm to about 10.16 mm).
  • a device for producing a condensation aerosol as provided herein comprises a flow-through passageway, wherein the flow-through passageway comprises an upstream opening and a downstream opening, wherein the flow-through passageway is configured to facilitate formation of a condensation aerosol comprising particles of a size effective for delivery to the deep lung of a subject.
  • the particles can comprise an MMAD of about 1 to about 5 ⁇ m.
  • the subject can be a human.
  • the subject can be a human who smokes and/or uses tobacco or nicotine containing products.
  • the condensation aerosol can comprise a pharmaceutically active agent (e.g. nicotine).
  • the passageway can be a primary flow-through passageway.
  • the primary flow-through passageway can be in fluid communication with a secondary flow-through passageway as provided herein.
  • the upstream opening can be an inlet.
  • the inlet can comprise a flow restrictor as provided herein.
  • the downstream opening can comprise an outlet.
  • the outlet can be a mouthpiece.
  • the flow-through passageway can be configured to form a narrow channel between the upstream and downstream openings.
  • the passageway can be further configured to widen downstream of the narrow channel prior to the downstream opening of the passageway.
  • the narrow channel can comprise an inner diameter and an outer diameter (see, e.g., FIGS. 32 and 33 ).
  • the inner diameter of the narrow channel can be exactly, about, more than, less than, at least or at most 0.01, 0.0125, 0.015, 0.0175, 0.02, 0.0225, 0.025, 0.0275, 0.03, 0.0325, 0.035, 0.0375, 0.04, 0.0425, 0.045, 0.0475, 0.05, 0.0525, 0.055, 0.0575, 0.06, 0.0625, 0.065, 0.0675, 0.07, 0.0725, 0.075, 0.0775, 0.08, 0.0825, 0.085, 0.0875, 0.09, 0.0925, 0.095, 0.0975, 0.1, 0.11, 0.115, 0.12, 0.125, 0.13, 0.135, 0.14, 0.145, or 0.15 inches (a range from about 0.254 mm to about 3.81 mm).
  • the inner diameter of the narrow channel can be between 0.01-0.015, 0.015-0.02, 0.02-0.025, 0.025-0.03, 0.03-0.035, 0.035-0.04, 0.04-0.045, 0.045-0.05, 0.05-0.055, 0.055-0.06, 0.06-0.065, 0.065-0.07, 0.07-0.075, 0.075-0.08, 0.08-0.085, 0.085-0.09, 0.09-0.095, 0.095-0.1, 0.1-0.12, 0.12-0.13, 0.13-0.14, or 0.14-0.15 inches (a range from about 0.254 mm to about 3.81 mm).
  • the inner diameter of the narrow channel can be about 0.01 to about 0.015, about 0.015 to about 0.02, about 0.02 to about 0.025, about 0.025 to about 03, about 0.03 to about 0.035, about 0.035 to about 0.04, about 0.04 to about 0.045, about 0.045 to about 0.05, about 0.05 to about 0.055, about 0.055 to about 0.06, about 0.06 to about 0.065, about 0.065 to about 0.07, about 0.07 to about 0.075, about 0.075 to about 0.08, about 0.08 to about 0.085, about 0.085 to about 0.09, about 0.09 to about 0.095, about 0.095 to about 0.1, or about 0.1 to about 0.15 inches (a range from about 0.254 mm to about 3.81 mm).
  • the outer diameter of the narrow channel can be exactly, about, more than, less than, at least or at most 0.08, 0.0825, 0.085, 0.0875, 0.09, 0.0925, 0.095, 0.0975, 0.1, 0.11, 0.115, 0.12, 0.125, 0.13, 0.135, 0.14, 0.145, or 0.15 inches (a range from about 2.0 mm to about 3.81 mm).
  • the outer diameter of the narrow channel can be between 0.08-0.085, 0.085-0.09, 0.09-0.095, 0.095-0.1, 0.1-0.12, 0.12-0.13, 0.13-0.14, or 0.14-0.15 inches (a range from about 2.0 mm to about 3.81 mm).
  • the outer diameter of the narrow channel can be about 0.08 to about 0.085, about 0.085 to about 0.09, about 0.09 to about 0.095, about 0.095 to about 0.1, or about 0.1 to about 0.15 inches (a range from about 2.0 mm to about 3.81 mm).
  • the inner diameter of the flow-through passageway prior to and/or downstream of the narrow channel can be exactly, about, more than, less than, at least or at most 0.2, 0.21, 0.22, 0.23, 0.24, 0.25, 0.26, 0.27, 0.28, 0.29, 0.3, 0.35, 0.4, 0.45, or 0.5 inches (a range from about 5.08 mm to about 12.7 mm).
  • the inner diameter of the flow-through passageway prior to and/or downstream of the narrow channel can be between 0.2-0.21, 0.21-0.22, 0.22-0.23, 0.23-0.24, 0.24-0.25, 0.25-0.26, 0.26-0.27, 0.27-0.28, 0.28-0.29, 0.29-0.3, 0.3-0.35, 0.35-0.4, 0.4-0.45, or 0.45-0.5 inches (a range from about 5.08 mm to about 12.7 mm).
  • the inner diameter of the flow-through passageway prior to and/or downstream of the narrow channel can be about 0.2 to about 0.25, about 0.25 to about 0.3, about 0.3 to about 0.35, about 0.35 to about 0.4, about 0.4 to about 0.45, or about 0.45 to about 0.5 inches (a range from about 5.08 mm to about 12.7 mm).
  • a device for generating a condensation aerosol comprising a primary flow-through passageway as provided herein further comprises a secondary flow-through passageway.
  • the secondary flow-through passageway can be in fluid communication with the primary flow through passageway.
  • the secondary flow-through passageway can comprise one or more channels.
  • the secondary flow-through channel comprises a first, a second, and a third channel.
  • the first channel can be in fluid communication with a primary flow-through chamber upstream of an aerosol generation chamber as provided herein.
  • the second channel can be in fluid communication with a primary flow through passageway between an aerosol generation chamber as provided herein and a downstream opening of the primary flow through passageway.
  • the third channel can comprise a second inlet for a carrier gas (e.g.
  • the secondary flow-through passageway can also comprise an articuable element.
  • the articuable element can be a diaphragm.
  • the articuable element can be further connected to springs.
  • the springs can control the movement of the articuable element.
  • the articuable element can be articulated by changes in pressure within the device.
  • the pressure that articulates the articuable element can be inhalation resistance or vacuum pressure.
  • the inhalation resistance can be a vacuum of about 1 to about 10 inches of H 2 O (a range from about 249 Pa to about 2488 Pa).
  • An increase in pressure can compress the springs.
  • Inhalation through a device for generating a condensation aerosol as provided herein can increase the pressure in the device.
  • the articuable element can comprise a protruding member.
  • one or more springs are located on a first side of an articuable element, while the protruding member is located on a second side opposite the first side.
  • the protruding member can be configured to enter and block the third channel.
  • a pressure differential between primary and secondary flow-through passageways within the device can cause articulation or movement of the articuable element.
  • the pressure differential can be affected by inhalation through the downstream opening of the primary flow chamber.
  • the pressure differential can be across the first channel of the secondary flow chamber. Under conditions of low pressure or inhalation resistance, the articuable element can block the third channel, thereby preventing entry of the carrier gas (e.g. air).
  • the carrier gas e.g. air
  • the articuable element can be articulated or removed from blocking the third channel, thereby allowing the carrier gas to enter the device.
  • inhalation through the downstream opening of the primary flow-through passageway serves to articulate the articuable element, whereby the articulation serves to open the third channel, wherein the opening permits the carrier gas (e.g. air) to flow through the third channel of the secondary flow-through passageway and enter the primary flow through passageway through the second channel in the secondary flow-through passageway, thereby entraining the condensation aerosol in the carrier gas from the secondary flow-through passageway.
  • the carrier gas e.g. air
  • Additional carrier gas entering the primary flow-through passageway through the secondary flow-through passageway as described herein can entrain the condensation aerosol in the carrier gas (e.g. air) to produce a total flow rate of about 20 to about 80 LPM (a range from about 3 ⁇ 10 ⁇ 4 m 3 /s to about 1.3 ⁇ 10 ⁇ 3 m 3 /s).
  • the device can have an interior air resistance (to inhalation) no greater than that of a cigarette.
  • the device can have an interior air resistance (to inhalation) of about 0.05 to about 0.15 (cm H 2 O) 1/2 /LPM.
  • a device for generating condensation aerosols comprising a primary flow-through passageway as provided herein can further comprise one or more additional sources of carrier gas, wherein the additional sources permit the flow of carrier gas to enter the device in addition to the carrier gas flowing through the primary flow-through passageway.
  • the one or more additional sources can be inlets or channels.
  • the one or more additional sources can be bypass inlets or bypass channels, wherein carrier gas entering a device through the bypass inlets or channels is bypass carrier gas.
  • the bypass carrier gas can be air.
  • the one or more sources can be within one or more walls of the primary flow-through passageway.
  • the one or more sources can be components of a secondary flow-through passageway as provided herein, wherein the secondary flow-through passageway can be in fluid communication with the primary flow-through passageway.
  • the one or more sources can be within one or more walls of the secondary flow-through passageway.
  • the one or more sources can be within one or more walls of a housing, wherein the housing surrounds or encompasses the primary flow-through passageway.
  • the one or more sources can be flow regulators.
  • the carrier gas entering the device through the one or more sources can be the same type or a different type of carrier gas as that flowing through a primary flow-through passageway.
  • the carrier gas entering through the one or more sources can be air.
  • the one or more sources permit flow of carrier gas to enter the device downstream of a heater element or aerosol generation chamber or area as provided herein.
  • the flow of carrier gas entering the device through the one or more sources can mix with the carrier gas flowing through a primary flow through passageway.
  • the mixing can be downstream of a heater element or aerosol generation chamber as provided herein but before a downstream opening or outlet of a primary passageway comprising the heater element or aerosol generation chamber.
  • the mixing of the carrier gases can produce a total flow rate exiting the device that can be similar to normal breathing of a subject.
  • the total flow rate can be about 20 to about 80 LPM (a range from about 3 ⁇ 10 ⁇ 4 m 3 /s to about 1.3 ⁇ 10 ⁇ 3 m 3 /s).
  • the subject can be a human.
  • the subject can be a human who smokes and/or uses tobacco or nicotine containing products.
  • FIG. 21 illustrates an embodiment of an electronic agent (e.g., nicotine) delivery device comprising a valve system ( 2100 ) for controlling air flow for deep lung delivery and rapid PK.
  • a valve system 2100 for controlling air flow for deep lung delivery and rapid PK.
  • negative pressure in a mouthpiece ( 2102 ) increases causing a pressure drop across a gas control valve ( 2104 ).
  • An increase in the pressure drop can cause the valve ( 2104 ) to close and prevent airflow ( 2106 ) into an aerosol generating area ( 2108 ) within a flow through chamber ( 2110 ).
  • the aerosol generating area ( 2108 ) can comprise an agent (e.g., nicotine) reservoir comprising an agent (e.g., nicotine) formulation, any of the dosing mechanisms described herein, and a heater for vaporizing an agent (e.g., nicotine) droplets that can be released from the dosing mechanism.
  • Closing of the valve ( 2104 ) can subsequently cause an increase in airflow ( 2106 ) from an air inlet ( 2112 ) across a backflow valve ( 2114 ) through a diversion air orifice ( 2116 ) and into a diversion air channel ( 2118 ).
  • the airflow over a vaporizing agent e.g., nicotine
  • a vaporizing agent e.g., nicotine
  • the valve system produces an inhalation resistance no greater than that of a cigarette. In one embodiment, the valve system produces an inhalation resistance no greater than 0.08 (cm H 2 O) 1/2 /LPM.
  • FIG. 32 A-E illustrates multiple embodiments of a device for regulating the flow of a carrier gas (e.g. air).
  • the device comprises a primary flow-through passageway ( 3202 A-E) and one or more sources of bypass or additional carrier gas ( 3204 A-E).
  • the one or more sources of bypass or additional carrier gas ( 3204 A-E) permit an additional or bypass flow of carrier gas (e.g. air) to mix with the carrier gas flowing through the primary flow-through passageway ( 3202 A-E).
  • the mixing occurs downstream of an aerosol generation chamber, thereby mixing a condensation aerosol produced in the aerosol generation chamber with a larger volume of carrier gas (e.g. air).
  • FIG. 32A shows a device comprising a primary flow-through passageway ( 3202 a ) comprising an upstream and downstream section comprising an inner diameter of 0.25 inches (about 6.35 mm), and two secondary flow-through chambers ( 3204 a ), wherein bypass or additional carrier gas enters the device through two inlets ( 3206 a ) adjacent to the primary flow-through chamber ( 3202 a ).
  • the inner diameter of the primary flow through chamber ( 3202 a ) narrows just prior to entry of the bypass carrier gas.
  • the narrowing of the primary flow-through passageway permits formation of condensation aerosol particles comprising particles with an MMAD of about 1 to about 5 uM.
  • the device in FIG. 32A can permit the mixing of the bypass carrier gas with the carrier gas flow through the primary chamber at a ratio of 10:1.
  • FIG. 32B shows a device comprising a primary flow-through passageway ( 3202 b ) comprising an upstream and downstream section comprising an inner diameter of 0.25 inches (about 6.35 mm), and two inlets ( 3204 b ) within the wall of the primary flow-through chamber ( 3202 b ), wherein bypass or additional carrier gas enters the device.
  • the primary flow through chamber ( 3202 b ) narrows just prior to entry of the bypass carrier gas to comprise an inner diameter of 0.084 inches (about 2.13 mm) and an outer diameter of 0.108 inches (about 2.74 mm). In some cases, the narrowing of the primary flow-through passageway ( 3202 b ) permits formation of condensation aerosol particles comprising particles with an MMAD of about 1 to about 5 um.
  • the device in FIG. 32B can permit the mixing of the bypass carrier gas with the carrier gas flow through the primary chamber at a ratio of 7:1.
  • FIG. 32C shows a device comprising a primary flow-through passageway ( 3202 c ) comprising an upstream and downstream section comprising an inner diameter of 0.5 inches (about 12.7 mm), and two inlets ( 3204 c ) within the wall of the primary flow-through chamber ( 3202 c ), wherein bypass or additional carrier gas enters the device.
  • the primary flow through chamber ( 3202 c ) narrows just prior to entry of the bypass carrier gas to comprise an inner diameter of 0.084 inches (about 2.13 mm) and an outer diameter of 0.108 inches (about 2.74 mm). In some cases, the narrowing of the primary flow-through passageway ( 3202 c ) permits formation of condensation aerosol particles comprising particles with an MMAD of about 1 to about 5 ⁇ m.
  • the device in FIG. 32C can permit the mixing of the bypass carrier gas with the carrier gas flow through the primary chamber at a ratio of 28:1.
  • FIG. 32D shows a device comprising a primary flow-through passageway ( 3202 d ) comprising an upstream and downstream section comprising an inner diameter of 0.25 inches (about 6.35 mm), and two sets of two inlets ( 3204 d ) adjacent to the primary flow-through chamber ( 3202 d ), wherein bypass or additional carrier gas enters the device.
  • the flow through chamber narrows just prior to entry of the bypass carrier gas from each set of two inlets to comprise an inner diameter of 0.096 inches (about 2.44 mm) and an outer diameter of 0.125 inches (about 3.175 mm).
  • the primary flow through passageway widens to an inner diameter of 0.250 inches (about 6.35 mm), before narrowing again.
  • the narrowing of the primary flow-through passageway permits formation of condensation aerosol particles comprising particles with an MMAD of about 1 to about 5 ⁇ m.
  • the device in FIG. 32D can permit the mixing of the bypass carrier gas with the carrier gas flow through the primary chamber at a ratio of 35:1.
  • FIG. 32E The device in FIG. 32E is similar to the device in FIG. 32D , wherein FIG. 32E shows a device comprising a primary flow-through passageway ( 3202 e ) comprising an upstream and downstream section comprising an inner diameter of 0.250 inches (about 6.35 mm), and two sets of two inlets ( 3204 e ) adjacent to the primary flow-through chamber ( 3202 e ), wherein bypass or additional carrier gas enters the device.
  • the primary flow through chamber ( 3202 e ) narrows just prior to entry of the bypass carrier gas from the first set of two inlets to comprise an inner diameter of 0.096 inches (about 2.44 mm) and an outer diameter of 0.125 inches (about 3.175 mm).
  • the primary flow through passageway ( 3202 e ) widens to an inner diameter of 0.250 inches (about 6.35 mm) and an out diameter of 0.280 inches (about 7.112 mm). Subsequently, the primary flow-through passageway ( 3202 e ) opens into a secondary housing ( 3206 e ), which has an inner diameter of 0.466 inches (about 11.8 mm) In FIG. 32E , the second pair of inlets ( 3204 e ) are located in the wall of a secondary housing ( 3206 e ), which is coupled to and encompasses the primary flow-through passageway.
  • FIG. 33 illustrates another embodiment of a device for regulating the flow of a carrier gas (e.g. air).
  • FIG. 33 shows a device comprising a primary flow-through passageway ( 3302 ) comprising an upstream and downstream section comprising an inner diameter of 0.25 inches (about 6.35 mm), and two inlets ( 3306 ) within the wall of the primary flow-through chamber ( 3302 ), wherein bypass or additional carrier gas enters the device.
  • the primary flow-through chamber narrows ( 3302 ) just prior to entry of the bypass carrier gas to comprise an inner diameter of 0.086 inches (about 2.18 mm) and an outer diameter of 0.106 inches (about 2.69 mm). As depicted in FIG.
  • the section of the primary flow-through chamber ( 3302 ) is coupled to and encased by a secondary housing ( 3308 ).
  • the secondary housing comprises a bypass inlet ( 3304 ), which permits entry of bypass or additional carrier gas (e.g. air) to enter the primary flow-through passageway through the inlets ( 3306 ).
  • bypass or additional carrier gas e.g. air
  • the narrowing of the primary flow-through passageway permits formation of condensation aerosol particles comprising particles with an MMAD of about 1 to about 5 ⁇ m.
  • FIG. 35 illustrates another embodiment a device for regulating the flow of a carrier gas (e.g. air).
  • the device comprises a primary airway ( 3504 ) that comprises an aerosol generation chamber ( 3528 ) comprising a heater element ( 3502 ), a restrictive orifice ( 3514 ) and a mouthpiece ( 3506 ).
  • the heater element ( 3502 ) comprises a coil.
  • the heater element can be any heater element comprising a coil as provided herein.
  • the primary airway ( 3504 ) is fluidically connected to a secondary airway ( 3516 ), through a first channel ( 3518 ) located (disposed) between the restrictive orifice ( 3514 ) and heater element ( 3502 ), and a second channel ( 3520 ) located (disposed) between the heater element ( 3502 ) and the mouthpiece ( 3506 ).
  • the secondary airway ( 3516 ) further comprises a third channel ( 3530 ) that is a secondary inlet ( 3508 ) for a carrier gas (e.g. air) and a diaphragm ( 3510 ).
  • the diaphragm ( 3510 ) comprises a base member that is connected to a pair of springs ( 3512 ) on a first side and a protruding member ( 3524 ) on a second side.
  • the springs ( 3512 ) are additionally connected to a wall opposite the first side of the base member that is part of the housing of the secondary airway ( 3516 ).
  • the base member of the diaphragm ( 3510 ) is also connected to a pair of lateral springs ( 3526 ) on its lateral edges, which are further connected to the walls of the housing of the secondary airway ( 3516 ) opposite the lateral edges of the base member.
  • the restrictive orifice ( 3514 ) is configured to limit the flow rate of the carrier gas (e.g.
  • the restrictive orifice ( 3514 ) limits the flow rate of the carrier gas (i.e. air) about 1 to about 10 liters per minute (LPM) (a range from about 1.667 ⁇ 10 ⁇ 5 m 3 /s to about 1.667 ⁇ 10 ⁇ 4 m 3 /s) at, e.g., a vacuum of about 1 to about 15 inches of water (a range from about 249 Pa to about 3738 Pa).
  • the carrier gas i.e. air
  • LPM liters per minute
  • Inhalation through the mouthpiece ( 3506 ) can produce a flow of carrier gas (e.g. air) through the restrictive orifice ( 3514 ) that can produce an inhalation resistance.
  • the inhalation resistance produces a pressure differential across the opening of the first channel ( 3518 ) connecting the primary airway ( 3504 ) with the secondary airway ( 3516 ).
  • the inhalation resistance causes the springs ( 3512 ) coupled to the first side of the diaphragm ( 3510 ) to compress and the lateral springs ( 3526 ) coupled to the lateral edges of the diaphragm ( 3510 ) to extend, whereby the protruding member of coupled to the second side of the diaphragm ( 3510 ) is removed from the third channel ( 3530 ) of the secondary airway ( 3516 ). Removal of the protruding member ( 3524 ) causes an additional flow of carrier gas (e.g. air) to enter the device.
  • the additional flow of carrier gas e.g.
  • the additional flow of carrier gas e.g. air
  • a device for producing a condensation aerosol as provided herein can have an interior air resistance (to inhalation) no greater than 0.08 (cm H 2 O) 1/2 /LPM.
  • the device can have an interior air resistance (to inhalation) exactly, about, more than, less than, at least, or at most 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.10, 0.11, 0.12, 0.13, 0.14, 0.15, 0.16, 0.17, 0.18, 0.19, 0.20, or 0.25 (cm H 2 O) 1/2 /LPM.
  • the device can have an interior air resistance (to inhalation) between 0.01-0.02, 0.02-0.03, 0.03-0.04, 0.04-0.05, 0.05-0.06, 0.06-0.07, 0.07-0.08, 0.08-0.09, 0.09-0.10, 0.1-0.11, 0.11-0.12, 0.12-0.13, 0.13-0.14, 0.14-0.15, 0.15-0.16, 0.16-0.17, 0.17-0.18, 0.18-0.19, 0.19-0.20, or 0.20-0.25 (cm H 2 O) 1/2 /LPM.
  • the device can have an interior air resistance (to inhalation) of about 0.01 to about 0.03, about 0.03 to about 0.05, about 0.05 to about 0.07, about 0.07 to about 0.09, about 0.09 to about 0.11, about 0.11 to about 0.13, about 0.13 to about 0.15, about 0.15 to about 0.17, about 0.17 to about 0.19, or about 0.19 to about 0.25 (cm H 2 O) 1/2 /LPM.
  • a device for producing a condensation aerosol as provided herein can produce a total flow rate of a carrier gas (e.g. air) of exactly, about, more than, less than, at least, or at most 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, or 100 liters per
  • the total flow rate can be between 1-10, 10-20, 20-30, 30-40, 40-50, 50-60, 60-70, 70-80, 80-90, or 90-100 LPM (a range from about 1.667 ⁇ 10 ⁇ 5 m 3 /s to about 1.667 ⁇ 10 ⁇ 3 m 3 /s).
  • the total flow rate can be about 1 to about 10, about 10 to about 20, about 20 to about 30, about 30 to about 40, about 40 to about 50, about 50 to about 60, about 60 to about 70, about 70 to about 80, about 80 to about 90, or about 90 to about 100 LPM (a range from about 1.667 ⁇ 10 ⁇ 5 m 3 /s to about 1.667 ⁇ 10 ⁇ 3 m 3 /s).
  • the device can comprise a primary flow-through passageway for a carrier gas and one or more sources of additional or bypass carrier gas as provided herein. These flow rates can be at a vacuum of about 1 to about 15 inches of water (a range from about 249 Pa to about 3738 Pa).
  • the one or more sources of additional or bypass carrier gas can be configured to limit the flow rate of additional or bypass carrier gas to produce a total flow rate as provided herein.
  • the flow rate can be limited by using a restrictive orifice on the one or more sources of additional or bypass carrier gas (e.g. air).
  • the restrictive orifice can comprise any valve or flap as known in the art.
  • the valve or flap can be moderated at specific flow rates.
  • the flow rates that moderate the valve or flap can be the limited to flow rates provided herein.
  • the valve or flap can be opened at specific inhalation resistance levels.
  • the restrictive orifice can be opened at inhalation resistances comprising a vacuum of about 1 to about 10 inches of water (a range from about 249 Pa to about 2488 Pa).
  • a device for producing a condensation aerosol as provided herein can be configured to limit the flow rate of a carrier gas across or through a aerosol generation area or heater element as provided herein to a flow rate of exactly, about, more than, less than, at least, or at most 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 10.5, 11, 11.5, 12, 12.5, 13, 13.5, 14, 14.5, 15, 15.5, or 16 liters per minute (LPM) (a range from about 1.667 ⁇ 10 ⁇ 5 m 3 /s to about 2.667 ⁇ 10 ⁇ 4 m 3 /s).
  • LPM liters per minute
  • a device for producing a condensation aerosol as provided herein can be configured to limit the flow rate of a carrier gas across or through a aerosol generation area or heater element to between 1-2, 2-4, 4-6, 6-8, 8-10, 10-12, 12-14, or 14-16 LPM a range from (about 1.667 ⁇ 10 ⁇ 5 m 3 /s to about 2.667 ⁇ 10 ⁇ 4 m 3 /s).
  • a device for producing a condensation aerosol as provided herein can be configured to limit the flow rate of a carrier gas across or through a aerosol generation area or heater element to about 1 to about 2, about 2 to about 4, about 4 to about 6, about 6 to about 8, about 8 to about 10, about 10 to about 12, about 12 to about 14, or about 14 to about 16 LPM (a range from about 1.667 ⁇ 10 ⁇ 5 m 3 /s to about 2.667 ⁇ 10 ⁇ 4 m 3 /s).
  • the flow rate can be limited by using a restrictive orifice on the inlet for a carrier gas (e.g. air).
  • the restrictive orifice can comprise any valve or flap as known in the art.
  • the valve or flap can be moderated at specific flow rates.
  • the flow rates that moderate the valve or flap can be the limited flow rates provided herein.
  • the valve or flap can be opened at specific inhalation resistance levels.
  • the restrictive orifice can be opened at inhalation resistances comprising a vacuum of about 1 to about 10 inches of water (a range from about 249 Pa to about 2488 Pa).
  • the restrictive orifice can be configured to limit the flow rates to flow rates as provided herein.
  • the restrictive orifice can be configured into a slot as depicted in FIG. 30B .
  • An aerosol generation area or heater element as provided herein can be within a flow-through passageway.
  • the flow-through passageway can be a primary flow through passageway.
  • a device for producing a condensation aerosol comprising a primary flow-through passageway and one or more sources of additional or bypass carrier gas (e.g. air) as provided herein can produce a mixing ratio of bypass or additional carrier gas to carrier gas flowing through the primary flow through chamber of 1:1, 2:1, 3:1, 4:1, 5:1, 6:1, 7:1, 8:1, 9:1, 10:1, 11:1, 12:1, 13:1, 14:1, 15:1, 16:1, 17:1, 18:1, 19:1, 20:1, 21:1, 22:1, 23:1, 24:1, 25:1, 26:1, 27:1, 28:1, 29:1, 30:1, 31:1, 32:1, 33:1, 34:1, 35:1, 36:1, 37:1, 38:1, 39:1, 40:1, 41:1, 42:1, 43:1, 44:1, 45:1, 46:1, 47:1, 48:1, 49:1, or 50:1.
  • additional or bypass carrier gas e.g. air
  • the mixing ratio can be between 1:1 and 5:1, 5:1 and 10:1, 10:1 and 15:1, 15:1 and 20:1; 20:1 and 25:1, 25:1, and 30:1, 30:1, and 35:1, 35:1 and 40:1, 40:1 and 45:1, or 45:1 and 50:1.
  • the mixing ratio can be about 1:1 to about 5:1, about 5:1 to about 10:1, about 10:1 to about 15:1, about 15:1 to about 20:1; about 20:1 to about 25:1, about 25:1 to about 30:1, about 30:1 to about 35:1, about 35:1 to about 40:1, about 40:1 to about 45:1, or about 45:1 to about 50:1.
  • an electronic agent (e.g., nicotine) delivery device comprises the dimensions of an electronic cigarette.
  • the electronic agent (e.g., nicotine) delivery device can have an overall cylindrical shape.
  • the electronic agent (e.g., nicotine) delivery device can resemble a combustible cigarette.
  • An electronic agent (e.g., nicotine) delivery device as provided herein can have an outer diameter of about, more than, less than, or at least 0.001, 0.0015, 0.002, 0.0025, 0.003, 0.0035, 0.004, 0.0045, 0.005, 0.0055, 0.006, 0.0065, 0.007, 0.0075, 0.008, 0.0085, 0.009, 0.0095, 0.01, 0.015, 0.02, 0.025, 0.03, 0.035, 0.04, 0.045, 0.05, 0.055, 0.06, 0.065, 0.07, 0.075, 0.08, 0.085, 0.09, 0.095, 0.1, 0.11, 0.12, 0.13, 0.14, 0.15, 0.16, 0.17, 0.18, 0.19, 0.2, 0.21, 0.22, 0.23, 0.24, 0.25, 0.26, 0.27, 0.28, 0.29, 0.3, 0.31, 0.32, 0.33, 0.34, 0.35, 0.36, 0.37, 0.38, 0.39, 0.4,
  • An electronic agent (e.g., nicotine) delivery device as provided herein can have a length of about, more than, less than, or at least 20, 21, 22, 23, 24, 25, 26 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114
  • An electronic agent (e.g., nicotine) delivery device as provided herein can have a length of about 25 mm to about 75 mm, about 75 mm to about 125 mm, about 125 mm to about 150 mm, or about 75 mm to about 150 mm
  • An electronic agent (e.g., nicotine) delivery device as provided herein can have a transverse dimension of about, more than, less than, or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, or 40 mm.
  • Agents e.g., pharmaceutically active agents
  • drugs include, for example, drugs of one of the following classes: anesthetics, antibiotic, anticonvulsants, antidepressants, antidiabetic agents, antidotes, antiemetics, antihistamines, anti-infective agents, antineoplastics, antiparkisonian drugs, antirheumatic agents, antipsychotics, anxiolytics, appetite stimulants and suppressants, blood modifiers, cardiovascular agents, central nervous system stimulants, drugs for Alzheimer's disease management, a cold medication, COPD (chronic obstructive pulmonary disease) drug, cough medication, drugs for cystic fibrosis management, diagnostics, dietary supplements, drugs for erectile dysfunction, gastrointestinal agents, hormones, drugs for the treatment of alcoholism, drugs for the treatment of addiction, immunosuppressives, mast cell stabilizers, migraine preparations, motion sickness products, drugs
  • An anesthetic can be ketamine, procaine, amethocaine, cocaine, prilocaine, bupivacaine, levobupivacaine, ropivacaine, mepivacaine, dibucaine, or lidocaine.
  • An anesthetic can be desflurane, enflurane, halothane, isofurane, methoxyflurane, or sevoflurane, amobaribital, methohexital, thiamylal, thiopental, diazepam, lorazepam, midzolam, etomidate, or propofol.
  • An anesthetic can be atracurium, ciastracurium besyalte, rapacuronium, rocuronium, succinylcholine, or suxamethonium chloride.
  • An anesthetic can be articaine, benzocaine, benzonatate, butacaine, butanilicaine, chloroprocaine, cinchocaine, dimethocaine, eucaine, etidocaine, hexylcaine, levobupivacaine, mepivacaine, meprylcaine, metabutoxycaine, orthocaine, oxybuprocaine, phenacaine, piperocaine, pramocaine, prilocaine, procaine, proparacaine, propoxycaine, quinisocaine, ropivacaine, trimecaine, or tetracaine.
  • An antibiotic can be an aminoglycoside (e.g., amikacin, gentamicin, kanamycin, neomycin, netilmicin, tobramycin, paromomycin, spectinomycin); an ansamycin (e.g., geldanamycin, herbimycin, rifaximin, streptomycin); a carbacephem (e.g., loracarbef); a carbapenem (e.g., ertapenem, doripenem, imipenem/cilastatin, meropenem); a cephalosporin (first generation) (e.g., cefadroxil, cefazolin, cefalotin or cefalothin, cefalexin); a cephalosporin (second generation) (e.g., cefaclor, cefamandole, cefoxitin, cefprozil, cefuroxime); a cephalosporin (third generation) (
  • An anticonvulsant can be an aldehyde (e.g., paraldehyde), an aromatic allylic alcohol (e.g., stiripentol), a GABA analog (e.g., gabapentin, pregabalin); a barbiturate (e.g., pentobarbital, methylpenobarital, or barbexaclone); a benzodiazepine (e.g., clonazepam, clobazam, clorazepate, diazepam, midazolam, nitrazepam, warmthzepam, nimetazepam, or lorazepam); a bromide (e.g., potassium bromide), a carbamate (e.g., felbamate), a caroxamide (e.g., carbamazepine, oxcarbazepine, eslicarbazepine acetate), a fatty acid (e
  • An antidepressant can be a selective serotonin reuptake inhibitor (SSRI, e.g., citalopram, escitalopram, paroxetine, fluoxetine, fluvoxamine, sertraline), a norepinephrine reuptake inhibitor (NRI, e.g., atomoxetine, reboxetine, viloxazine), a noradrenergic and specific serotonergic antidepressant (NaSSA e.g., mianserin, mirtazapine), a serotonin-norepinephrine reuptake inhibitor (SNRIs, e.g., desvenlafaxine, duloxetine, milnacipran, venlafaxine), a serotonin antagonist and reuptake inhibitor (SARIs, e.g., etoperidone, nefazodone, trazodone), a norepinephrine-dopamine
  • the antidepressant is agomelatine, amitriptyline, amoxapine, atomoxetine, buspirone, benmoxine, butriptyline, citalopram, clomipramine, desipramine, dosulepin, doxepin, duloxetine, escitalopram, etoperidone, femoxetine, fluovoxamine, imipramine, kitanserin, lofepramine, medifoxamine, mianserin, maprotoline, mazindol, milnacipran, mirtazapine, nefzaodone, nisoxetine, nomifensine, nortriptyline, protriptyline, oxaprotiline, paroxetine, reboxetine, sertaline, trazodone, trimipramine, venlafaxine, viloxazine, zimelidine, citalopram
  • An antidiabetic agent can be insulin, a sufonylurea (e.g., tolbutamide, acetohexamide, tolazmide, chlorpropamide, glyburide, glibenclamide, glimepiride, gliclazide, glycopyramide, gliquidone, or glipizide), a biguanide (e.g., metformin, phenformin, or buformin), an alpha-glucosidase inhibitor (e.g., acarbose, miglitol, or voglibose), a meglitinide (e.g., repaglinide, nateglinide), or a thiazolidinedione (e.g., pioglitazone rosiglitazone, or troglitazone).
  • a sufonylurea e.g., tolbutamide, acetohexamide, tolazmide, chlor
  • An antidiabetic agent can be an injectable glucagon-like peptide analog (e.g., exenatide, liraglutide), or a dipeptidyl peptidase-4 inhibitor (e.g., vildagliptin, sitagliptin, saxagliptin, linagliptin, allogliptin, septagliptin).
  • injectable glucagon-like peptide analog e.g., exenatide, liraglutide
  • a dipeptidyl peptidase-4 inhibitor e.g., vildagliptin, sitagliptin, saxagliptin, linagliptin, allogliptin, septagliptin.
  • An antidote can be edrophonium chloride, flumazenil, deferoxamine, nalmefene, naloxone, or naltrexone.
  • An antidote can be activated charcoal (e.g., with sortibal), adenosine, atropine, beta blocker, calcium chloride, calcium gluconate, a chelator (e.g, EDTA, dimercaptrol, penicillamine, EGTA, or 2,3-dimercaptosuccinic acid), a cyanide antidote (amyl nitrite, sodium nitrite, thiosulfate), cyproheptadine, deferoxamine mesylate, digoxin immune Fab antibody, diphenhydramine hydrochloride, benztorpine mesylate, ethanol, fomepizole, flumazenil, glucagon, insulin, insulin with glucagon, leu
  • An antiemetic can be a 5-HT3 receptor antagonist (e.g., dolasetron, granisetron, ondansetron, tropisetron, palonosetron, or mirtazapine), a dopamine antagonist (e.g., doperidone, olanzapine, droperidol, haloperidol, chlorpormaine, promethazine, prochloperazine, alizapride, prochlorperazine, metoclopramide), an NK1 receptor antagonist (e.g., aprepitant, casopitant), an antihistamine (H1 histamine receptor antagonist; e.g., cyclizine, diphenhydramine, dimenhydrinate, doxylamine, meclozine, promethazine, hydroxyzine), a cannabinoid (e.g., cannabis, dronabinol, nabilone, one of a JWH cannabinoid series), a benzodiazepine (
  • the antiemetic is alizapride, azasetron, benzquinamide, bromopride, buclizine, chlorpromazine, cinnarizine, clebopride, cyclizine, diphenhydramine, diphenidol, dolasetron, droperidol, granisetron, hyoscine, lorazepam, dronabinol, metoclopramide, metopimazine, ondansetron, perphenazine, promethazine, prochlorperazine, scopolamine, triethylperazine, trifluoperazine, triflupromazine, trimethobenzamide, tropisetron, domperidone, or palonosetron.
  • An antihistamine can be an H1-receptor antagonist (e.g., acrivastine, azelastine, bromopheniramine, buclizine, bromodiphenhydramine, carbinoxamine, cetirizine, chlorpromazine, cyclizine, chlorpheniramine, chlorodiphenhydramine, celmastine, cyproheptadine, desloratadine, dexbrompheniramine, dexchlorpheniramine, dimenhydramine, doxylamine, ebastine, embramine, fexofenadine, levocetirizine, loratadine, meclozine, mirtazapine, olopatadine, orphenadrine, pheninadamine, pheniramine, phenyltooxamine, promethazine, pyrilamine, quetiapine, rupatadine, tripelennamine, triprolidine), an H2-re
  • an antihistamine can be astemizole, azatadine, brompheniramine, carbinoxamine, cetrizine, chlorpheniramine, cinnarizine, clemastine, cyproheptadine, dexmedetomidine, diphenhydramine, doxylamine, fexofenadine, hydroxyzine, loratidine, hyroxyizine, promethazine, pyrilamine or terfenidine.
  • a drug can be an allergy medication.
  • the allergy medication can be an antihistamine, montelukast, azelastine/fluticaseon propionate, beclomethasone dipropionate, budesonide, ciclesonide, cromlyn sodium, flunisollide, fluticaonse furoate, fluticasone propionate, ipratropium bromide, mometasone furoate monohydrate, olopatadine, oxymetazoline, triamcinolone acetonide, azelastine, cromolyn, emadastine, epinastine, ketorolac, ketotifen, lodoxamine, loteprednol, naphazoline, naphazoline/pheniramine, nedocromil, olopatadine, pemirolast, epinephrine, aclometasone, fluocinolone, fluocinonide, triamcino
  • An anti-infective agent can be selected from one of the following classes: antivirals (e.g., abacavir, acyclovir, acyclovir, adefovir, amadtadine, amprenavir, ampligen, arbidol, atazanavir, atripla, balavir, boceprevirertet, cidofovir, combivir, darunavir, delavirdine, didanosine, docosanol, edoxudine, efavirenz, emtricitabine, enfuvirtide, entecavir, famciclovir, fomivirsen, fosamprenavir, foscarnet, fosfonet, ganciclovir, ibacitabine, imunovir, idoxuridine, imiquimod, indinavir, inosine, lamivudine, lipinavir, loviride, maraviroc,
  • An anti-neoplastic agent can be, e.g., lomustine, carmustine, steptozocin, mechlorethamine, melphalan, uracil nitrogen mustard, chlorambucil, cyclophosphamide, iphosphamide, cisplatin, carboplatin, mitomycin, thiotepa, dacarbazin, procarbazine, hexamethyl melamine, triethylene melamine, busulfan, pipobroman, mitotane, methotrexate, trimetrexate, pentostatin, cytarabine, Ara-CMP, fludarabine phosphate, hydroxyurea, fluorouracil, floxuridine, chlorodeoxyadenosine, gemcitabine, thioguanine, 6-mercaptopurine, bleomycin, toptecan, irinotecan, camptothecin sodium salt, daunorubicin, doxor
  • An antiparkisonian drug can be amantadine, baclofen, biperiden, benztropine, orphenadrine, procyclidine, trihexyphenidyl, levodopa, carbidopa, andropinirole, apomorphine, benserazide, bromocriptine, budipine, cabergoline, eliprodil, eptastigmine, ergoline, galanthamine, lazabemide, lisuride, mazindol, memantine, mofegiline, pergolide, piribedil, pramipexole, propentofylline, rasagiline, remacemide, ropinerole, selegiline, spheramine, terguride, entacapone, or tolcapone.
  • An antirheumatic agent can be abatacept, adalimumab, azathioprine, chloroquine, diclofenac, hydroxychloroquine, methotrexate, ciclosporin, D-penicillamine, etanercept, golimumab, infliximab, leflunomide, miocyline, rituximab, or sulfasalzine.
  • An antipsychotic can be acetophenazine, alizapride, amisulpride, amoxapine, amperozide, aripiprazole, asenapine, benperidol, benzquinamide, bromperidol, buramate, butaclamol, butaperazine, carphenazine, carpipramine, chlorpromazine, chlorprothixene, clocapramine, clomacran, clopenthixol, clospirazine, clothiapine, clopenthixol, clozapine, cyamemazine, droperidol, flupenthixol, fluphenazine, fluspirilene, haloperidol, loxapine, melperone, mesoridazine, levomepromazine, pimozide, metofenazate, molindrone, olanzapine, paliperidone, l
  • An anxiolytic can be a benzodiazepine (e.g., alprazolam, chlordiazepoxide, clonazepam, diazepam, etizolam, lorazepam, oxazepam); tofisopam; a selective serotonin reuptake inhibitor (SSRI); afobazole; selank; bromantane; an azapirone (e.g., buspirone, tandospirone, gipeirone); a barbiturate; hydroxyzine; pregalalin; validol; an herbal treatment (e.g., Bacopa monnieri, Lactuca virosa, Rohodiola rosea, Hypericum perforatum, Matricaria recutita, Passiflora incarnate, Piper methysticum; Sceletium tortuosum, Scutellaria lateriflora; Valeriana officinalis; Sal
  • an anxiolytic can be alprazolam, bromazepam, oxazepam, buspirone, hydroxyzine, mecloqualone, medetomidine, metomidate, adinazolam, chlordiazepoxide, clobenzepam, flurazepam, lorazepam, loprazolam, midazolam, alpidem, alseroxlon, amphenidone, azacyclonol, bromisovalum, captodiamine, capuride, carbcloral, carbromal, chloral betaine, enciprazine, flesinoxan, ipsapiraone, lesopitron, loxapine, methaqualone, methprylon, propanolol, tandospirone, trazadone, zopiclone, or zolpidem.
  • An appetite stimulant can be ghrelin, orexin, neuropeptide Y; a 5-HT2c receptor antagonist (e.g., mirtazapine, alanzapine, quetiapin, amitriptyline, cyrpoheptadine); an H1 receptor antagonist (e.g., mirtazapine, olanzapine, quetiapine, amitriptyline, cyproheptadine); a dopamine antagonist (e.g., haloperidol, chlorpromazine, olanzapine, risperidone, quetiapine); an adrenergic antagonist (e.g., carvedilol, propranolol; alpha2-adrenergi agonist (e.g., clonidine); a CB1 receptor agonist (e.g., THC/dronabinol, nabilone); a corticosteroid
  • An appetite suppressant can be diethylpropion, rimonabant, oxymetazoline, fenfluramine, phentermine, sibutramine, benfluorex, butenolide, cathine, diethylpropion, FG-7142, phenmetrazine, phenylpropanolamine, pryoglutamyl-histidyl-glycine, amfepramon, amphetamine, benzphetamine, dexmethylphenidate, dextroamphetamine, glucagon, lisdexamfetamine, methamphetamine, methylphenidate, phendimetrazine, phenethylamine, or bupropion.
  • a blood modifier can be an anticoagulant (e.g., heparin); colony stimulating factor (e.g., fligrastim, pegfilgrastim; sargramostim); phytonadione (Vitamin K); iron; iron combination (e.g., iron+vitamin C) cilostazol, dipyridamol, abbokinase, abciximab, activase, advate, aggrastat, aggrenox, agrylin, albumin, alteplase, amicar, aminocaproic acid, anadrol, anagrelide, angiomax, anti-inhibitor coagulant complex; antihemophilic factor, antithrombin III, aprotinin, aquamephyton, aranesp, argtroban, arixtra, aspirin, aspirin+dipryidamole, benefix, bivalirudin, buminate 25%, buminate 5%, cath
  • An asthma agent can be fluticaone, budeonside, mometasone, beclomethasone, zariflukast, zileuton, flunisolide, ciclesonide, triamcinolone, ipratropium, dyphylllin/guaifenesin, dexamethasone, prednisone, methylprednisolne, formoterol/mometeasone, triamcinolone, montelukast, isoetharine, dyphylline, salmeterol, budeonside/formoterol, mometasone/formoterol, theophylline, albuterol, levabulterol, ipratropium, omalizumab, or guaifenesin/theophylline.
  • the asthma medication can be an inhaled corticosteroid (e.g., beclomethasone propionate, budesonide, budesonide/formoterol, ciclesonide, blunisolide, fluticasone propionate, fluticaonse/salmeterol, mometasone, memetasone/formoterol, or triamcinolone acetonide).
  • the asthma agent can be a long-acting beta-agonist (LABA; e.g., albuterol sulfate, formoterol fumarate, salmeterol xinafoate, or arformoterol tartrate).
  • the asthma agent can be cromolyn sodium or theophylline.
  • an asthma agent can be a leukotriene modifier (e.g., montelukast, zafirlukast, zileuton).
  • an asthma agent can be an immunomodulator (e.g., omalizumab).
  • an asthma agent can be a short-acting beta-agonist (SABA; e.g., albuterol sulfate, ipratropium bromide/albuterol sulfate, ipratropium bromide HFA, levalbuterol HCl, pirbuterol, tiotropium bromide).
  • SABA short-acting beta-agonist
  • an asthma agent is duplilumab.
  • the asthma agent is bambuterol, bitolerol, doxofylline, ephedrine, epinephrine/chlorpheniramine, erythromycin, hydrocortisone, ipratropium bromide, isoetharine, isoprenaline, isoproterenol, ketotifen, metaproterenol, mometasone furoate and formoterol fumarate, nedocromil, oxtriphylline, salmeterol/fluticasone, terbutaline, tinocordin, triamcinolone, zafirlukast, or zileuton.
  • a cardiovascular agent can be fenoldopam, diazoxide, nitroprusside, ambrisentan, epoprostenol, treprostinil, sildenafil, bosentan, iloprost, treprostinil, epoprostenol; an aldosterone receptor antagonist (e.g., spironolactone, eplerenone); an angiotensin converting enzyme inhibitor (e.g., fosinopril, ramipril, captopril, trandolapril, moexipril, lisinopril, quinapril, enalapril, lisinopril, perinodpril, benazepril); an angiontensin II inhibitor (e.g., eprosartan, olemsartan, azilsartan medoxomil, telmisartan, losartan, valsartan
  • the cardiovascular agent can be benazepril, captopril, enalapril, quinapril, ramipril, doxazosin, prazosin, clonidine, labetolol, candesartan, irbesartan, losartan, telmisartan, valsartan, disopyramide, flecanide, mexiletine, procainamide, propafenone, quinidine, tocamide, amiodarone, dofetilide, ibutilide, adenosine, gemfibrozil, lovastatin, acebutalol, atenolol, bisoprolol, esmolol, metoprolol, nadolol, pindolol, propranolol, sotalol, diltiazem, nifedipine, verapamil, spironolactone, bumetanide,
  • a central nervous system stimulant can be phendimetrazine, methamphetamine, diethylpropion, amphetamine/dextroamphetamine, benzphetamine, phendimetrazine, lisdexamfetamine, diethylpropion, phendimetrazine, dexmethylphenidate, armodafinil, atomexetine, doxapram, amphetamine, brucine, caffeine, dexfenfluramine, dextroamphetamine, ephedrine, fenfluramine, mazindol, methyphenidate, pemoline, phentermine, sibutramine, or modafinil.
  • An agent for Alzheimer's disease management can be donepezil, galanthamine, rivastigmine, tacrine, or memantine.
  • An agent for cystic fibrosis management can be an antibiotic (e.g., ciprofloxacin, tobramycin); a bronchodilator (e.g., albuterol or salmeterol); an anticholinergic (e.g., atrovent); a DNase (e.g., pulmozyme); a mucolytic (e.g., acetylcysteine); a saltwater solution (e.g., hypertonic saline); a nonsteroidal anti-inflammatory (NSAID; e.g., ibuprofen); a corticosteroid (e.g., fluticasone or prednisone); an enzyme replacement therapy (e.g., creon or pancreaze); CPX, IBMX, XAC and analogues; 4-phenylbutyric acid; genistein and analogous isoflavones; azithromycin, aztreonam, pancrelipase, genta
  • a diagnostic agent can be adenosine or aminohippuric acid.
  • a homeopathic cold medication can be Aconitum napellus, Allium cepa, Antimonium tartaricum, Apsi mellifica, Arsenicum album, Arum triphyllum, Belladonna, Bryonia alba, Dulcamara, Eupatorium perforliaturn, Euphrasia, Ferrum phosphoricum, Gelsemium, Hepar sulphuris, Kali bichromicum, Mercurius solubilis, Natrum muriaticum, Nux vomica, Oscillococinum ( Anas barbariase ), phosphorus, Rhus toxicodendron , sulphur, or Pulsatilla Sticta.
  • a COPD drug can be montelukast, budesonide/formoterol, roflumilast, aclidinium, prednisone, isoetharine, dyphylline, guaifenesin/theophylline, or fluticasone/vilanterol.
  • a COPD drug is a bronchodilator (e.g., albuterol, levabuterol, ipratropium; or a long-acting bronchodilator (e.g., tiotropium, salmeterol, formoterol, arformoterol, indacaterol, aclidinium).
  • a COPD drug is a steroid (e.g., fluticasone, budesonide). In some cases, a COPD drug is a combination (e.g., salmeterol/fluticasone and formoterol/budesonide). In some cases a COPD drug is a phosphodiesterase-4 inhibitor (e.g., roflumilast). In some cases, a COPD drug is theophylline or an antibiotic.
  • a cough medication can be guaifenesin/hydrocodone, acetaminophen/codeine, diphenhydramine, guaifenesin/potassium guaiacolsulfonate, carbetapentane/guaifenesin, codeine/guaifenesin, dextromethorphan/guaifenesin, guaifenesin, carbinoxamine/dextromethorphan/pseudoephedrine, dextromethorphan, brompheniramine/codeine, carbetapentane/chlorpheniramine/phenylephrine, benzocaine/dextromethorphan, menthol, acetaminophen/dextromethorphan, chlophedianol/guaifenesin, acetaminophen/dextromethrophan/doxylamine, aceteaminophen/hydrocodone,
  • the cough medication can be dextromethorphan, codeine, noscapine, bromhexine, acetylcysteine, ephedrine, guaifenesin, honey, cinnaomon, honey/cinnamon, lemon, elderberry syrup, tea, Slippery Elm, peppermint, Chinese Hot Mustard, cayenne pepper (capsaicin), apple cider vinegar, wasabi, horseradish, Echinacea , vitamin c, zinc, ginger ( zingiber officinale ), vinegar, water, red onion, garlic, hyssop, or mullein.
  • a cough medication can be an antihistamine, decongestant, inhaled asthma drug, antibiotic, acid blocker, or cough suppressant.
  • a cough medication is licorice, horehound, mullein, peppermint, elderflower, yarrow, Belladonna, bryonia, Gelsemium, Coccus catcti, Drosera, Dulcamara, Eupatorium, Euphrasia , hepar suphuratum, Kali bic, Nux vomica , phosphorus, Pulsatilla, Antimonium tartaricu, Rhus tox, Spongia , or Vincetoxicum.
  • a dietary supplement can be acai, aloe vera, an anabolic steroid, astragalus, vitamin A, bilberry, beta carotene, bitter orange, Black Cohosh, Butterbur, vitamin B12, vitamin B6, calcium, carnitine, cartilage, cat's claw, chamomile, chasteberry, chondroitin, chromium, cinnamon, coenzyme Q10, colloidal silver, cranberry, vitamin C, dandelion, vitamin C, Echinacea , ephedra, essiac/flor-essence, European elder, evening primrose oil, vitamin E, fenugreek, feverfew, fish oil, flaxseed, folate, folic acid, garlic, ginger, ginkgo, ginseng, glucosamine, glucosamine with chondroitin sulfate, goldenseal, grape seed extract, green tea, hawthorn, hoodia, horse chestnut,
  • An agent for erectile dysfunction can be tadalafil, sildenafil, vardenafil, alprostadil, avanafil, apomorphine, apomorphine diacetate, phentolamine, and yohimbine.
  • a gastrointestinal agent can be a 5-aminosalicylate (e.g., mesalamine, balsalazide, sulfasalazine, olsalazine), an antacid (e.g., aluminum hydroxide/magnesium hydroxide/simethicone; sodium barcarbonate, magaldrate/simethicone, calcium carbonate, aluminum hydroxide/magnesium hydroxide/simethicone, magnesium hydroxide, aluminum hydroxide/magnsesium hydroxide, magnesium hydroxide, alginic acid/aluminum hydroxide/magnesium trisilicate, alginic acid/aluminum hydroxide/magnesium carbonate, aluminum hydroxide/magnesium hydroxide/simethicone, calcium carbonate/magnesium hydroxide, magaldrate, magaldrate/simethicon), an antidiarrheal (e.g., bismuth subsalicylate, atropine
  • pylori eradication agent e.g., amoxicillin/clarithromycin/lansoprazole, bismuth subcitrate potassium/metronidazole/tetracycline, bismuth subsalicylate/metronidazole/tetracycline, amoxicillin/clarithromycin/omeprazole
  • an H2 antagonist e.g., nizatidine, cimetidine, ranitidine, famotidine, cimetidine, calcium carbonate/famotdine/magnesium hydroxide
  • a laxative e.g., magnesium citrate, polyethylene glycol 3350, lactulose, senna, bisacodyl, psyllium, methylcellulose, docusate, polycarbophil, sodium biphophate/sodium phosphate, docusate/senna, sodium biphosphate/sodium phosphate, polyethylene glycol 3350 with electrolytes, bisacody
  • a hormone can be estrogen, progesterone, hydrocortisone, fludocortisone, throxine, progestin, testosterone, estradiol, cortisone, 1-androstendediol, 1-androstenedione, bolandiol, bolasterone, boldenone, boldione, calusterone, clostebol, danazol, dehydrochlormethyltestosterone, desoxymethyltestosterone, drostanolone, ethylestrenol, fluoxymesterone, formeboone, furazabol, gestrinone, 4-hydroxytestosterone, mestanolone, mesterolone, meenolone, methandienone, methandriol, methasterone, methyldienolone, methyl-1-testosterone, methylnortestosterone, methyltestosterone, mitribolone, mibolerone, nandrolone, 19-noradrostenedione
  • An agent for the treatment of alcoholism can be naloxone, naltrexone, acamprostate, or disulfuram.
  • An agent for the treatment of addiction can be disulfiram, naltrexone, acamprosate, methadone, levo-alph acetyl methadol (LAAM), or buprenorphine.
  • An immunosupressive can be a glucocorticoid, a cytostatic (e.g., alkyating agent, antimetabolite (e.g., methotrexate, azathiopurine, mercaptopurine, fluorouracil, a cytotoxic antibiotic (e.g., dactinomycin, an antracycline, mitomycin C, bleomycin, mithramycin), an antibody (e.g., a monoclonal antibody (e.g., IL-2 receptor directed antibody, CD3 directed antibody; a T-cell receptor directed antibody (e.g., muromonab-CD3)), a drug acting on immunophilin (e.g., ciclosporin, tacrolimus, sirolimus), other drugs (e.g., an interferon, an opioid, a TNF binding protein, a mycophenolate).
  • a cytostatic e.g., alkyating agent, antimetabolite (e.g.,
  • the immunosuppressive is mycophenolic acid, cyclosporin, azathioprine, tacrolimus, everolimus, or rapamycin.
  • the immunosuppressive agent is a calcineurin inhibitor (e.g., cyclosporine, tacrolimus), an interleukin inhibitor (e.g., rilonacept, tocilizumab, anakinra, ustekinumab, canakinumab, basiliximab, daclizumab), omalizumab, lenalidomide, azathioprine, methotrexate, pomalidomide, thalidomide, alefacept, efalizumab, mycophenolic acid, mycophenolate mofetil, fingolimod, natalizumab, belimumab, lefunomide, abatacept, lymphocyte immune globulin anti-thy (equine), teriflunomide,
  • a mast cell stabilizer can be cromolyn, pemirolast, or nedocromil.
  • An agent for migraine headache can be naproxen, ibuprofen, acetaminophen, almotriptan, alperopride, codeine, dihydroergotamine, ergotamine, eletriptan, frovatriptan, isometheptene, lidocaine, lisuride, metoclopramide, naratriptan, oxycodone, propoxyphene, rizatriptan, sumatriptan, tolfenamic acid, zolmitriptan, amitriptyline, atenolol, clonidine, cyproheptadine, diltiazem, doxepin, fluoxetine, lisinopril, methysergide, metoprolol, nadolol, zolmitriptan, nortriptyline, paroxetine, pizotifen, pizotyline, propanolol, protripty
  • An agent that can be used to treat motion sickness can be diphenhydramine, dimehydrinate, cinnaizine, meclozine, promethazine, metoclopramide, prochlorperazine, ginger root, or scopolamine
  • An agent for managing multiple sclerosis can be corticotropin, dalfampridine, teriflunomide, interferon beta-1a, interferon beta-1b, glatiramer, cyclophosphamide, dexamethasone, prednisone, fingolimod, azathioprine, natalizumab, bencyclane, methylprednisolone, azathioprine, mitoxantrone, or prednisolone.
  • a muscle relaxant can be a neuromuscular blocking agent (e.g., succinylcholine, mivacurium, cisatracurium, vecuronium, doxacurium, pancuronium, atracurium); a skeletal muscle relaxant combination (e.g., aspirin/caffeine/orphenadrine, aspirin/carisoprodol, aspirin/carisoprodol/codeine, aspirin/methocarbamol, aspirin/meprobamate); or a skeletal muscle relaxant (e.g., dantrolene, botulinum toxin type b, carisprodol, onabotulinumtoxin A, cyclobenzaprine, chlorzoxazone, chlrophenesin, tizanidine, baclofen, cyclobenzaprine, metaxalone, methocarbamol, cyclobenzaprine, orphenadrine, carisopro
  • the muscle relaxant is decamethonium, rapacuronium, atracurium, rocuronium, alcuronium, gallamine, metocurine, pipecuronium, bubocurarine, baclofen, chlorzoxazone, cyclobenzaprine, methocarbamol, orphenadrine, quinine, carisoprodol, gabapentin, metaxalone, diazepam, dantrolene, botulinum toxin type b, onabotulinumtoxinA, chloroxazone, chlorphenesin, baclofen, methocarbamol, or ortizanidine.
  • a drug for treating mycocardial infarction can be urokinase, perindopril, alteplase, ramipril, aspirin, aluminum hydroxide/aspirin/calcium carbonate/magnesium hydroxide, timolol, magnesium chloride, warfarin, dalteparin, heparin, propranolol, eptifibatide, metoprolol, enoxaparin, trandolapril, nitroglycerin, clopidogrel, lisinopril, reteplase, streptokinase, atenolol, tenecteplase, or moexipril.
  • the drug for treating myocardial infarction can be a vasodilator.
  • a vasodilator can be an alpha-adrenoceptor antagonist (e.g., prazosin, terazosin, doxazosin, trimazosin, phentolamine, phenoxybenzamine); an angiotensin converting enzyme (ACE) inhibitor (e.g., benazepril, captopril, enalapril, fosinopril, lisinopril, moexipril, quinapril, ramipril); an angiotensin receptor blocker (ARB) (e.g., candesartan, eprosartan, irbesartan, losartan, olmesartan, telmisartan, valsartan); a beta2-adrenoceptor agonist (beta2-agonist) (e.g., epinephrine, nore
  • a drug for treating myocardial infarction can be a cardiac depressant drug (e.g., a beta-adrenoceptor antagonist (beta-blocker), e.g., a non-selective beta1/beta2 drug (e.g., carteolol, carvedilol, labetalol, nadolol, penbutolol, pindolol, propranolol, sotalol, timolol) or a beta1-selective drug (e.g., acebutolol, atenolol, betaxolol, bisoprolol, esmolol, metoprolol, nebivolol); a calcium-channel blocker (e.g., amlodipine, felodipine, isradipine, nicardipine, nifedipine, nimodipine, ni
  • a drug for treating myocardial infarction can be an antiarrhythmic drug (e.g., Class I—sodium-channel blocker (e.g., Class 1A (e.g., quinidine, procainamide, disopryamide); Class 1B (e.g., lidocaine, tocainide, mexiletine); Class 1C (e.g., flecainide, propafenone, moricizine); Class II—beta blocker (e.g., a non-selective beta1/beta2 drug (e.g., carteolol, carvedilol, labetalol, nadolol, penbutolol, pindolol, propranolol, sotalol, timolol) or a beta1-selective drug (e.g., acebutolol, atenolol, betaxolol, bisoprolo
  • the drug for treating myocardial infarction is a thrombolytic drug (e.g., a tissue plasmiogen activator (e.g., alteplase, retaplase, tenecteplase); streptokinase, anistreplase, or urokinase.
  • a tissue plasmiogen activator e.g., alteplase, retaplase, tenecteplase
  • streptokinase anistreplase
  • urokinase urokinase.
  • a nonsteroidal anti-inflammatory can be a salicylate (e.g., aspirin (acetylsalicylic acid), diflunisal, salsalate); a propionic acid derivative (e.g., ibuprofen, dexibuprofen, naproxen, fenoprofen, ketoprofen, dexketoprofen, flurbiprofen, oxaprozin, loxoprofen); an acetic acid derivative (e.g., indomethacin, tolmetin, sulindac, etodolac, ketorolac, diclofeanc, nabumetone) a enolic acid (oxicam) derivative (e.g., piroxicam meloxicam, tenoxicam, droxicam, lornoxicam, isoxicam); a fenamic acid derivative (fenamate; e.g., mefenamic acid, meclofena
  • a nonsteroidal anti-inflammatory can be aceclofenac, alminoprofen, amfenac, aminopropylon, amixetrine, aspirin, benoxaprofen, bromfenac, bufexamac, carprofen, celecoxib, choline salicylate, cinchophen, cinmetacin, clopriac, clometacin, diclofenac, diclofenac potassium, diclofenac sodium, diclofenac sodium with misoprostol, diflunisal, etodolac, fenoprofen, fenoprofen calcium, flurbiprofen, ibuprofen, indomethacin, indoprofen, ketoprofen, ketorolac, magnesium salicylate, mazipredone, meclofenamate, meclofenamate sodium, mefanamic acid, meloxicam, nabumetone, nap
  • An opioid, opioid antagonist, or inverse agonist can be an opium alkaloid (e.g., codeine, morphine, oripavine, pseudomorphine, thebaine); an alkaloid salt mixture (e.g., pantopon, papaveretum); 14-hydroxymorphine, 2,4-dinitorphenylmorphe, 6-methyldihydromorphine, 6-methylenedihydrodesoxymorphine, acetyldihydromorphine, azidomorphine, chlornaltrexamine, chloroxymorphamine, desomorphine, dihydromorphine, ehtyldihydromorphine, hydromorphinol, methyldesorphine, N-henethylnormorphine, RAM-378, 6-nicotinoyldihydromorphine, acetlypropionylmorphin, diacetyldihydromorphine, dibutyrylmorphine, dibenzoylmorphine, diformylmorphine, dipropanoy
  • An analgesic can be merperidine, hydromorphone, fentanyl, codeine, methadone, morphine, oxycodone, oxycodone and ASA, oxycodone and acetaminophen, pentazocine, acetaminophen/caffeine/codeine, acetaminophen/codeine, acetaminophen, acetylsalicylic acid, ibuprofen, naproxen sodium, naproxen, indomethacin, diclofenac, mefenamic acid, ketorolac, celecoxib, erotamin, sumatriptan, butorphanol, zolmitriptan, naratriptan, rizatriptan, almotriptan, apazone, benzpiperylon, benzydramine, caffeine, clonixin, ethoheptazine, flupirtine, nefopam, orphenadrine,
  • An opthalmic preparation can be an anti-angiogenic ophthalmic agent (e.g., aflibercept, ranibizumab, pegaptanib); cysteamine, ocriplasmin, mitomycin, dapiprazole; a mydriatic (e.g., cyclpentolate, phenylephrine, atropine, cyclopentolate/phenylephrine, homatropine, scopolamine, phenylephrine/scopolamine, tropicamide, hydroxyamphetamine/tropicamide, tropicamide); an ophthalmic anesthetic (e.g, lidocaine, proparacaine, tetracaine); ophthalmic anti-infectives (e.g., levofloxacin, natamycin, bactiracin/neomycin/polymyxin b, bactiracin/polymyxin b, tobramycin, moxifloxacin, cip
  • An osteoporosis preparation can be alendronate, ibandronate, calcium carbonate, calcium/vitamin D, estradiol, teriparatide, hydrochlorothiazide, calcitonin, conjugated estrogens, conjugated estrogens/medroxyprogesterone, denosumab, zoledronic acid, ibandronate, calcium glubionate, dihydrotachysterol, etidronate, esterified estrogens, raloxifene, alendronate/cholecalciferol, calcium phosphate tribasic, conjugated estrogens/medroxyprogesterone, calcium lactate, estropitate, risedronate or raloxifene.
  • a pain medication can be ibuprofen, hydroxyzine, celecoxib, meperidien, hydromorphone, amitriptyline, acetaminophen/hydrocodone, acetaminophen/codeine, tapentadol, acetaminophen/diphenhydramine, oxymorphone, oxycodone, acetaminophen, ketorolac, tramadol, diclonfenac, diphenhydramine/ibuprofen, naproxen, acetaminophen/phenyltoloxamine, aspirin/hydrocodone, acetaminophen/pheyltoloxamine, aspirin/caffeine, lidocaine, flurbiprofen, fentanyl, ketoprofen, aluminum hydroxide/aspirin/calcium carbonate/magnesium, trolamine salicylate, morphine, nortriptyline, capsaicin, aspirin/hydr
  • An anti-anxiety or panic disorder medication can be alprazolam, clomipramin, lorazepma, nortriptyline, buspirone, venlafaxine, clonazepam, lorazepam, maprotiline, paroxetine, fluoxetine, nefazodone, imipramine, sertraline; a serotonin and norepinephrine reuptake inhibitor (e.g., venlafaxine hydrochloride); a benzodiazepine (e.g., alprazolam, clonazepam, or lorazepam); or a selective serotonin reuptake inhibitor (SSRI; e.g., fluoxetine, paroxetine, or sertraline).
  • SSRI selective serotonin reuptake inhibitor
  • a panic disorder medication can be a tricyclic antidepressant (TCA; imipramine hydrochloride, desipramine, clomipramine) or a monoamine oxidase inhibitor (MAOI; e.g., isocaroxazid, phenelzine, tranylcypromine).
  • TCA tricyclic antidepressant
  • MAOI monoamine oxidase inhibitor
  • An anti-anxiety or panic medication can be lemon balm ( Melissa officinalis ), ibergoast (caraway, chamomile, licorice, milk thistle, and peppermint), hops ( Humulus lupulus ), lemon juice, ground ginger, honey, catnip, chamomile ( Matricaria recutita ), fennel, L-theanine, Kava Kava, Motherwort, Passionflower, Skullcap ( Scutellaria lateriflora ), omega-3, Valerian ( Valeriana officinalis ), lavender ( Lavandula hybrida ), St.
  • John's Wort magnesium vitamin B12, vitamin B1 , Aconitum napellus, Argentum nitricum, Arsesnicum album, Gelsemium sempervirens, Natrum muriaticum, Calcarea carbonica, Ignatia amara, Kali arsenicosum, Kali phosphoricum, Lycopodium clavatum, Natrum muriaticum , phosphorus, Pulsatilla, Silicea (Silica), Aconite ( Aconitum napellus ), Ignatia amara, Mercurius solubilis , phosphorus, sulphur, borax, Bryonia , Casticum, Anacardium, or Valerian Root.
  • a prostaglandin can be epoprostanol, dinoprostone, misoprostol, or alprostadil.
  • a respiratory agent can be an antiasthmatic combination (e.g., dyphylline/guaifensin, guaifenesin/theophylline), an antihistamine (e.g., fexofenadine, loratadine, phenindamine, dexchlorpheniramine, terfenadine, triprolidine, promethazine, brompheniramine, chlorpheniramine, cetirizine, diphenhydramine, carbinoxamine, diphenhydramine, chlorpheniramine, cyproheptadine, levocetirizine, desloratadine, clemastine, astemizole, tripelennamine, carboxamine, pheniramine/phenyltoloxamine/pyrilamine); an antitussive (e.g., carbetapentane, benzonatate, dextromethorphan); a bronchodilator (e.g., an
  • the respiratory agent is albuterol, ephedrine, epinephrine, fomoterol, metaproterenol, terbutaline, budesonide, ciclesonide, dexamethasone, flunisolide, fluticasone propionate, triamcinolone acetonide, ipratropium bromide, pseudoephedrine, theophylline, montelukast, zafirlukast, ambrisentan, bosentan, enrasentan, sitaxsentan, tezosentan, iloprost, treprostinil, or pirfenidone.
  • a sedative or hypnotic can be a barbiturate (e.g., amobarbital, pentobarbital, secobarbital, phenobarbitol); a benzodiazepine (e.g., clonazepam, diazepam, estrazolam, flunitrazepam, lorazepam, midazolam, nitrazepam, oxazepma, trazolam, temazepma, chlordiazepoxide, alprazolam,); an herbal sedative (e.g., ashwagandha, Duboisia hopwoodii, Prosanthera striatiflora, catnip, kava, mandrake, valerian, marijuana); a non-benzodiazpein “z-drug” sedative (e.g., eszopiclone, zaleplon, zolpidem, zopiclone
  • the sedative or hypnotic is butalbital, chlordiazepoxide, diazepam, estazolam, flunitrazepam, flurazepam, lorazepam, midazolam, temazepam, triazolam, zaleplon, zolpidem, zolpidem tartrate, butisol sodim, pentobarbital or zopiclone.
  • a skin or mucous membrane agent can be an antibiotic (e.g., bacitracin, bacitracin zinc/polymyxin B sulfate; clindamycin phosphate, erythromycin/tretinoin, fusidate sodium, fusidic acid; gramicidin/polymyxin B sulfate; mupirocin; polymyxin B sulfate/bacitracin); an antiviral (e.g., acyclovir, idoxuridine); an antifungal (e.g., clotrimazole, ketoconazole, miconazole nitrate, nystatin, terbinafine HCl, terconazole, tolnaftate); a scabicide or pediculicide (e.g., crotamiton, isopropyl myristate, lindane, permethrin; piperonyl butoxide/pyrethrins
  • a smoking cessation aid can be topiramate, fluphenazine, varenicline, nortriptyline, bupropion, clonidine, nicotine, or tryptophan.
  • a Tourette's syndrome agent can be pimozide, topiramate, olanzapine, clonidine, guanfacine, haloperidol, botulinum toxin type A, methylphenidate, dextroamphetamine, or pergolide.
  • a urinary tract agent can be lactobacillus acidophilus , amoxicillin, cefazolin, amoxicillin/clavulante, sulfamethoxazole/trimethoprim, cefuroxime, ciprofloxacin, ertapenem, levofloxacin, nitrofurantoin, ceftriaxone, cefixime, ampicillin/sulbactam, doxycycline, piperacillin/tazobactam, hyoscyamine/methenamine/methylene blue/phenyl salicylate, doripenem, cefadroxil, acetohydroxamic acid, nitrofurantoin, methenamine, lomefloxacin, cefepime, cefoxitin, tolteridine, darifenicin, propantheline bromide, or oxybutynin.
  • a vertigo agent can be promethazine, diphenidol, betahistine or meclizine.
  • An insomnia medication can be 5-hydroxytryptophan, diphenhydramine/ibuprofen, zolpidem, lorazepam, flurazepam, amitriptyline, triazolam, eszopiclone, estazolam, temezepam, ramelteon, doxepin, doxylamine, zaleplon, acetaminophen/diphenhydramine, diphenhydramine, 5-hydroxytryptophan, tryptophan, chloral hydrate, diphenhydramine/magnesium salicylate, quazepam, eszopiclone, secobarbital, doxepin, olanzapine, clonazepam, quazepam, lorazepam, alprazolam, oxazepam, prazepam, flunitrazepam, melatonin, valerian root, chamomile tea, lemon balm, or 5-L-5-hydroxytryptophan
  • a weight loss drug can be megestrol, phentermine/topirmate, phentermine, phenylpropanolamine, lorcaserin, oxandrolone, megestrol, mazindol, orlistat, sibutramine, rimonabant, metformin, exenatide, pramlintide, conjugated linoleic acid, green tea extract, khat, lipoic acid, ECA stack, or raspberry ketone.
  • An herb, supplement, or vitamin can be aloe, arginine, beta-carotene, black cohosh, chocolate, chondriotin sulfate, coca, coenzyme Q10, cranberry, creatine, DHEA (dehydroepiandrosterone), dong quai, Echinacea , ephedra, evening primrose oil, flaxseed, flaxseed oil, folate, ginkgo, glucosamine, honey, Lactobacillus acidophilus , lycopene, marijuana, melatonin, milk thistle, niacin, omega-3 fatty acid, fish oil, alpha-linolenic acid, red yeast rice, SAMe (adenosylmethionine), saw palmetto , soy, St.
  • DHEA dehydroepiandrosterone
  • An herb can be a medicinal herb.
  • a medicinal herb can be absinthe wormwood ( Artemisia absinthium ), agrimony ( Agrimonia eupatoria ), aloe vera ( Aloe barbadensis Miller), alpine rose ( Rhododendron ferrugineum ), angelica ( Angelica silvestris ), anise ( Pimpinella anisum ), arnica ( Arnica montana ), ash ( Fraxinus excelsior ), asparagus ( Asparagus officinalis ), barberry ( Berberis vulgaris ), barley ( Hordeum sativum ), basil ( Ocimum basilicum ), bean ( Phaseolus vulgaris ), bearberry ( Arctostaphylos uva ursi ), beet ( Beta vulgaris ), betony
  • An agent can be one that is, or can be made to be, vaporizable.
  • the drug can be a heat stable drug.
  • Exemplary drugs include acebutolol, acetaminophen, alprazolam, amantadine, amitriptyline, apomorphine diacetate, apomorphine hydrochloride, atropine, azatadine, betahistine, brompheniramine, bumetanide, buprenorphine, bupropion hydrochloride, butalbital, butorphanol, carbinoxamine maleate, celecoxib, chlordiazepoxide, chlorpheniramine, chlorzoxazone, ciclesonide, citalopram, clomipramine, clonazepam, clozapine, codeine, cyclobenzaprine, cyproheptadine, dapsone, diazepam, diclofenac ethyl ester, diflu
  • an agent is a parasympathomimetic alkaloid.
  • the parasympathomimetic alkaloid is nicotine, arecoline, muscarine, or pilocarpine.
  • an agent is a nicotinic acetylcholine receptor agonist.
  • the nicotinic acetylcholine receptor agonist is nicotine, acetylcholine, choline, epibatidine, lobeline, or varenicline.
  • an agent inhibits chromatin modifying enzymes (e.g., class I and II histone deaceytlases). In some cases, an agent that inhibits chromation modifying enzymes is nicotine.
  • an agent is a nicotine analog or derivative.
  • the nicotine analog is EVP-6124.
  • a nicotine analog or derivative is described, e.g., in U.S. Patent Application Publication Nos. 20130157995, 20090234129, 20080108822, 20070186940, or 20080227088 or U.S. Pat. Nos. 4,243,605, 5,015,741, 6,503,922, 6,995,265, or 7,132,545.
  • a combination of at least or at most 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 agents is used. In some cases, a combination of between 1-2, 2-4, 4-6, 6-8, 8-10, 10-12, 12-14, 14-16, 16-18, or 18-20 agents is used. In some cases, a combination of between 1-5, 5-10, 10-15, or 15-20 agents is used.
  • any agent as provided herein for use in the methods and devices described herein can be in a formulation comprising one or more additional substances as provided herein.
  • the formulation comprising an agent (e.g., nicotine) and one or more additional substances is a liquid formulation.
  • the formulation is liquid at room temperature.
  • the liquid formulation is contained in a reservoir as provided herein in a device as provided herein and is liquid at an operating temperature of the device. The operating temperature of any of the devices as described herein can be at, below, or above room temperature.
  • the liquid formulation comprising a pharmaceutically active agent (e.g., nicotine) as provided herein is delivered as a liquid to a heater element as provided herein in a device as provided herein when a user inhales from the outlet or mouthpiece of the device.
  • the liquid formulation is not a viscous liquid.
  • the liquid formulation is not gel-like or a gel.
  • a liquid formulation comprising a pharmaceutically active agent (e.g., nicotine) as provided herein is not coated as a solid or film of any thickness onto a heater element as provided herein.
  • a liquid formulation comprising nicotine for use in the methods and devices described herein is not admixed with thickening agents and thereby has a viscosity that is reduced or is less than a liquid formulation comprising nicotine that has been admixed with a thickening agent.
  • a liquid formulation for use in the methods and devices as provided herein is not applied to or coated on a heater element as provided herein prior to use of the device by a user or subject as provided herein.
  • the liquid formulation comprising a pharmaceutically active agent is delivered as a liquid to a heater element in a device as provided herein only upon use of the device.
  • the device can be a user as provided herein inhaling or drawings on an outlet or mouthpiece on a device as provided herein.
  • inhalation on the outlet or mouthpiece draws carrier gas (e.g., air) ino the device through an inlet on the device as provided herein, wherein the flow of the carrier gas (e.g., air) through the inlet triggers delivery of a liquid formulation comprising a pharmaceutically active agent (e.g., nicotine) by any of the means provided herein to a heater element contained within the device.
  • the device can comprise one or more inlets as provided herein, wherein inhalation on an outlet draws carrier gas (e.g., air) through the one or more inlets simultaneously.
  • one or more carriers or excipients is added to a liquid formulation to change a property of the formulation.
  • One or more carrriers can be used to change the density, compressibility, specific weight, viscosity, surface tension, or vapor pressure of a liquid formulation.
  • eHealth tools which can include mobile devices, web-based devices, computer readable medium, and an eHealth-enabled electronic agent (e.g., nicotine) delivery platform.
  • an eHealth-enabled electronic nicotine delivery platform can help a smoker transition to clean nicotine delivery by delivering a pre-determined nicotine dose with a pre-determined nicotine particle size at a pre-determined time for an individual user of a device.
  • the eHealth-enabled electronic nicotine delivery platform can provide nicotine to an individual user on a particular schedule, which may involve varying the number of doses per day, timing of doses within the day, or amount of nicotine per dose over time.
  • the eHealth-enabled electronic nicotine delivery platform is used to achieve full smoking cessation.
  • the eHealth-enabled electronic nicotine delivery platform is used to achieve full nicotine or smoking cessation without relapse to smoking. In another embodiment, the eHealth-enabled electronic nicotine delivery platform is used to achieve full nicotine withdrawal without nicotine withdrawal symptoms. In another embodiment, the eHealth-enabled electronic nicotine delivery platform is used in conjunction with other nicotine replacement therapies, nicotinic agonist or partial agonists (e.g., varenicline or any other ⁇ 4 ⁇ 2 subtype of the nicotinic acetylcholine receptor) to help achieve a particular smoking goal (e.g., complete cessation). In another embodiment, the eHealth tools can help to ensure user safety when administering doses of nicotine from an electronic nicotine delivery device, so as to prevent overdose.
  • nicotinic agonist or partial agonists e.g., varenicline or any other ⁇ 4 ⁇ 2 subtype of the nicotinic acetylcholine receptor
  • the methods can be applied to a variety of types of classifications of users of combustible tobacco products, including a new smoker, a trough maintainer smoker, an intermittent smoker, a light smoker, a weight-loss smoker, a heavy smoker, or a very heavy smoker.
  • An intermittent smoker can be an individual who does not smoke every day.
  • a light smoker can be an individual who smokes 1 to 9 cigarettes per day.
  • a moderate smoker can be an individual who smokes 10 to 19 cigarettes a day.
  • a heavy smoker can be an individual who smokes 20 to 29 cigarettes per day.
  • a very heavy smoker can be an individual who smokes 30 or more cigarettes per day. Different smokers may require different approaches to facilitate their transition from smoking.
  • the method can comprise providing a device for generating a condensation aerosol comprising a pharmaceutically active agent.
  • the pharmaceutically active agent can be an agent as provided herein.
  • the condition is smoking or nicotine addiction.
  • the pharmaceutically active agent is nicotine.
  • the device for generating the condensation aerosol can be device as provided herein.
  • the device can comprise a heater element.
  • the heater element can be any heater element as provided herein.
  • the heater element can vaporize a composition comprising the pharmaceutically active agent.
  • the formulation is a liquid formulation.
  • the heater element can be in fluid communication with a source of the formulation.
  • the source of the formulation can be a reservoir.
  • the heater element can be in fluid communication with a passageway configured for permiting the condensation of the vaporized formulation to produce particles comprising a size effective for deep lung delivery.
  • the size of the particles can have an MMAD of about 1 to about 5 um.
  • the device can further comprise a programmable controller, wherein the programmable controller comprises a non-transitory computer readable medium comprising one or more algorithms, and an interface for communicating with the programmable controller, wherein the interface is capable of receiving information from and/or transmitting information to a source.
  • the source can be a user of the device, a healthcare provider and/or a counselor.
  • the methods provided herein can include inputting, receiving and/or recording data on the device; analyzing the data; and regulating a dosage, frequency of administration and/or delivery schedule of the condensed formulation comprising the pharmaceutically active agent based on the analysis of the data by the one or more algorithms.
  • the method as provided herein can also comprise adjusting the dosage, frequency of administration and/or delivery schedule of the condensed formulation comprising the pharmaceutically active agent based on the information received from the source.
  • the inputting, analysis, regulating, and, optionally, adjusting can be repeated in order to manage treatment of the condition.
  • the dosage, frequency of administration and/or delivery schedule of the condensed formulation comprising the pharmaceutically active agent can be pre-set by a source.
  • the analysis of the data can be performed by the one or more algorithms.
  • the regulation the dosage, frequency of administration and/or delivery schedule of agent as provided herein can be based on an analysis of the data by the one or more algorithms.
  • the method can comprise providing any device for generating a condensation aerosol comprising a pharmaceutically active agent as provided herein, wherein the device comprises a programmable controller.
  • the pharmaceutically active agent can be nicotine.
  • the subject inhales the condensation aerosol produced by the device a plurality of times, wherein inhaling a plurality of times produces a desired nicotine blood concentration.
  • the desired nicotine plasma concentration can be a plasma concentration.
  • the desired plasma concentration can be an arterial plasma concentration.
  • the desired plasma concentration can be a venous plasma concentration.
  • the desired nicotine plasma concentration can be about, more than, less than, or at least 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, 41%, 42%, 43%, 44%, 45%, 46%, 47%, 48%, 49%, 50%, 51%, 52%, 53%, 54%, 55%, 56%, 57%, 58%, 59%, 60%, 61%, 62%, 63%, 64%, 65%, 66%, 67%, 68%, 69%, 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%
  • the desired nicotine plasma concentration can be between 1%-10%, 10%-20%, 20%-30%, 30%-40%, 40%-50%, 50%-60%, 60%-70%, 70%-80%, 80%-90%, or 90%-100% of the nicotine plasma concentration achieved by smoking a cigarette.
  • the desired nicotine plasma concentration can be about 1% to about 10%, about 10% to about 20%, about 20% to about 30%, about 30% to about 40%, about 40% to about 50%, about 50% to about 60%, about 60% to about 70%, about 70% to about 80%, about 80% to about 90%, or about 90% to about 100% of the nicotine plasma concentration achieved by smoking a cigarette.
  • Smoking a single cigarette can produce peak increments of plasma nicotine concentration of 5-30 ng/ml. The peak increments of plasma nicotine concentration from smoking a cigarette can be achieved within 10 minutes.
  • the methods provided herein further comprise altering the dosage, frequency of administration, and/or delivery schedule of the condensation aerosol in order to alter the arterial nicotine plasma concentration.
  • the alteration of the dosage, frequency of administration, and/or delivery schedule of the condensation aerosol can facilitate smoking cessation.
  • the dosage of the pharmaceutically active agent inhaled during each of the plurality of inhalations can be a percentage of a total dosage required for a specific period of time.
  • the period of time can be a day, wherein each inhalation of the plurality of inhalations can be a percentage of the daily dosage.
  • Each inhalation can be about, more than, less than, or at least 1%, 5%, 10%, 15%, 20%, 25%, 30%, 33%, 50%, or 100% of a total dosage.
  • An eHealth tool can be a healthcare practice supported by electronic processes and/or communication.
  • eHealth tools comprise healthcare practice using the Internet.
  • the eHealth tools can be formatted for use by different types of smokers, including a new smoker, a weight loss smoker, a trough maintainer, a light smoker, a heavy smoker, or a very heavy smoker.
  • the eHealth tools can be formatted for use by different types of patients who may be using nicotine to enhance their cognition or otherwise improve other symptoms of their illness (ulcerative colitis).
  • the eHealth tools can communicate with a device described herein (e.g., through Bluetooth connectivity), or eHealth tools can be incorporated into a device described herein.
  • the eHealth tools provided herein include mechanisms for tracking use of a device. For example, the frequency of use of a device can be tracked. Also, provided herein are algorithms for analyzing the use of a device. The algorithms can be used to generate goals for a user of the device. In some cases, the algorithms can suggest a recommended dose of an agent (e.g., nicotine) for a user. The algorithms can suggest an agent (e.g., nicotine) delivery schedule for a user. Algorithms provided herein can change over time based on input from a device or feedback from the user over time. An eHealth nicotine delivery platform described herein can track use of a nicotine delivery device, assess the user in terms of their subjective nicotine craving, mood, or other psychological or behavioral parameters, and adjust nicotine delivery to accomplish desired effects. Smoking behavior can be tracked, as can other symptoms of a disease where nicotine is being used either as a treatment or to enhance deficiencies in cognition associated with a specific illness.
  • agents e.g., nicotine
  • Algorithms provided herein can change over
  • a smoking pattern of a user can be monitored, or use of a device described herein can be monitored.
  • tools provided herein can be used to determine if smoking or use of a device provided herein was used to satisfy a morning craving, determine if smoking occurred, or a device was used, while a subject was bored, drinking, under stress.
  • Tools can be used to assess whether a subject smoked or used a device described herein alone or in the presence of others (e.g., friends), or whether the dose of nicotine administered was successful in enhancing cognition or improving another target medical or psychiatric symptom.
  • One or more algorithms can be used to devise a plan (e.g., nicotine dose, nicotine delivery schedule) for a user.
  • a plan e.g., nicotine dose, nicotine delivery schedule
  • web-based tools can be used to transition a smoker to use of an electronic nicotine delivery device described herein along with customized behavioral input.
  • the eHealth tools provided herein can be used to enable smoking cessation, partial smoking cessation (e.g., use of an electronic nicotine delivery device at work, in public places, or on a plane), or full nicotine cessation.
  • eHealth tools provided herein can be used to engage smokers, including teenagers and a person in their 20s to alter their smoking habits.
  • the eHealth tools are web-based tools.
  • the web-based tools can enable an appropriate dosing of nicotine for a user of a device described herein.
  • the web-based tools can track experiences of a user.
  • a web-based tool can track success in making a transition from smoking.
  • Web-based tools described herein can track health benefits derived from using devices described herein. Such tracking can enable generation of rewards (e.g., decreased health premiums).
  • Web-based tools can enable development of constantly-improving use algorithms by obtaining use profiles from a multitude of users in the field, and can provide feedback to users.
  • web-based tools described herein can leverage social media to produce ideal health outcomes.
  • the social media can be a social networking site (e.g., Facebook, Google+, MySpace, Bebo), blog or microblog (e.g., Twitter), a content community (e.g., YouTube), a virtual social world (e.g., Second Life), a virtual game world (e.g., World of Warcraft), or a collaborative project (e.g., Wikipedia).
  • Social media can include technologies such as a blog, picture-sharing, vlog, wall-posting, email, instant messaging, music-sharing, crowdsourcing, voice over IP, Internet forums, weblog, social blog, microblog, wiki, podcast, and social bookmarking.
  • the customized feedback can also be specific for users suffering from a medical or psychiatric disorder.
  • nicotine has been shown to have beneficial effects on cognition among patients with schizophrenia.
  • the device could be used to deliver nicotine and also provide therapeutic input to patients to help them manage their nicotine intake in such a way as to provide maximum therapeutic advantage to their cognition or psychiatric symptom control.
  • Other disorders where nicotine has been shown to have beneficial effects on cognition include Parkinson's disease, attention deficient disorder, mild cognitive impairment, and Alzheimer's disease.
  • an eHealth tool is a mobile device.
  • the mobile device is an electronic nicotine delivery device.
  • the mobile device can ensure dosing occurs at an appropriate time.
  • the mobile device can comprise on-board tracking of dosing, can provide reminders to a subject, and can provide nicotine craving assessments.
  • a mobile device can comprise complementary advertising opportunities.
  • the devices provided herein can comprise electronics that control for variability in battery condition and ensure consistent heating.
  • Customized goals can enable the same nicotine delivery platform to be used to achieve multiple beneficial health benefits for different smokers, from full smoking cessation, to partial cessation (e.g., no smoking during the workday), to partial or full nicotine cessation (i.e., stopping nicotine intake entirely), to cognition remediation.
  • the customized goals enable the same nicotine delivery platform to be used to achieve full smoking cessation.
  • the customized goals enable the same nicotine delivery platform to be used to achieve full nicotine or smoking cessation without relapse.
  • the customized goals enable the same nicotine delivery platform to be used to achieve full nicotine withdrawal without nicotine withdrawal symptoms.
  • eHealth tools can include Web based and mobile tools.
  • self-report measures can be used to help a smoker or new user of a device provided herein identify a target goal based on their degree of nicotine dependency, health status, health goals, economic goals (i.e., decrease the amount of money spent on cigarettes), target body weight or change in body weight, or other factors.
  • Tests of attentional bias for smoking stimuli, and other cognitive measures of nicotine dependency can be assessed on the web backend or an electronic nicotine delivery device to assess risk for relapse upon smoking cessation, which can then be used to identify a pattern of use that will minimize the odds of relapse to smoking.
  • biomarkers such as nicotine receptor polymorphisms, information can also be added to a user's profile to help identify the optimal outcome for an individual user.
  • smoking patterns can be tracked prior to the transition to an electronic nicotine delivery platform, which can enable a real world, ecologically valid assessment of actual behavior to be used as a foundation for a subsequent prescribed pattern of use of an electronic nicotine delivery device.
  • data can be captured from individual users in the field and can be sent to a backend web-based central database for algorithm development.
  • the mobile device can also assess the ecological risk factors for relapse and adjust the dose or dose characteristics of nicotine accordingly to help achieve the desired outcome. An initial trial of several different types of dose characteristics may also be helpful in determining the ideal use algorithm.
  • data from real world use of the electronic nicotine delivery device can be collected and used to predict outcomes. Users can also pick from one of several established algorithms that they think will best suit their health or other goals.
  • the central database can issue instructions back to the electronic nicotine device, either in the form of explicit compliance reminders to use the device to achieve the optimal nicotine absorption, or implicit dosing instructions to the device to gradually taper the dose (or other characteristics of the nicotine dose, including its concentration, pH, particle size, flavorings, or flow characteristics coming from the device which can affect back of the throat impaction, which in turn can affect subjective sensations associated with the nicotine dose (i.e., tingling or burning in the back of the throat)) over the days or weeks to help achieve various health or nicotine-related goals.
  • a user's goal when transitioning off of combustible tobacco products may change over time (e.g., a user initially wanting to quit smoking only at work may come to choose full cessation over time).
  • a user initially wanting to quit smoking only at work may come to choose full cessation over time.
  • feedback from the mobile device can be used help identify an initial use algorithm, as well as make changes to the use algorithm or switch to a new algorithm entirely.
  • a web-based backend database can communicate subtle and/or gross changes in prescribed use algorithms to the device to help enhance the probability that a target goal will be achieved. In this way, each user can become part of a community helping to refine his/her own and others optimal algorithms to achieve a variety of goals.
  • a differentially reinforcing subjective reward from the nicotine can be created.
  • dose characteristics e.g., dose, particle size, pH, amount of nicotine in the gas vs. particulate phase, air speed velocity coming out of a nicotine delivery device, flavorings, etc.
  • the probability that certain goals will be achieved e.g., smoking cessation
  • dose characteristics of nicotine can be maximized by varying dose characteristics of nicotine.
  • the electronic nicotine delivery device can modify dose characteristics of nicotine. These modifications can occur gradually over time (e.g., slowly decreasing the dose of nicotine over days or weeks) to eventually help the user stop all nicotine intake or transition to other forms of nicotine replacement.
  • the modifications can change in response to environmental triggers (e.g., by altering the mean particle size of the dose to provide an especially reinforcing dose if the subject reports on the electronic nicotine delivery device a strong craving to return to smoking, or if their pattern of use is indicative of someone likely to return to smoking).
  • the modifications can change to help the initial transition off of combustible tobacco (e.g., by altering the pH or flavor of the dose to help match previous stimulus characteristics of smoking).
  • An electronic nicotine delivery device can be used to administer challenge doses of nicotine to a user in order to assess their readiness to change use algorithms, assess physical and psychological aspects of nicotine dependency, or, for example, to demonstrate to users that they are increasingly able to wean themselves off of nicotine administration entirely.
  • the electronic nicotine delivery device can administer one or more nicotine challenge doses.
  • These challenge doses may contain no nicotine, less nicotine than previous doses, or doses of nicotine that vary in regards to other important characteristics (e.g., dose, particle size, pH, amount of nicotine in the gas vs. particulate phase, air speed velocity coming out of a nicotine delivery device, flavorings, etc).
  • An electronic nicotine delivery device can then assess self-reported cravings or changes in a pattern of use that suggests increased or decreased nicotine administration. This feedback can then be used as real world data to help maintain or change the use algorithm to increase the probability that the user will achieve certain health or other nicotine-related goals.
  • feedback to the user can be customized to help promote the achievement of certain health goals.
  • This customized feedback can be used in multiple ways. For example, achieving certain use patterns (e.g., sufficient nicotine administration to forestall strong cravings after initially transitioning from smoking, or administering a new minimum amount of nicotine in accordance with a planned taper to nicotine cessation) can result in a virtual credit or actual monetary reward that can reinforce the user's pattern of nicotine administration.
  • Customized feedback can also be used to leverage psychological principles important in smoking cessation. For example, a user could be given feedback that his/her pattern of use is consistent with his/her goals (e.g., quitting smoking) or aim to enhance his/her self-efficacy by demonstrating that the user is becoming less dependent on nicotine based on a real world nicotine challenge presented by an electronic nicotine delivery device described herein (e.g., by administering a test dose containing no nicotine or less nicotine than the user had been administering and demonstrating that their nicotine craving did not increase, or significantly increase, after that challenge dose; see FIG. 19 ).
  • Feedback could also engage users using game theory, including the earning of virtual points, which, for example, can be used to enable other actions of the device or to enhance one's standing in a virtual online world, or be redeemed for real-world reinforcements.
  • the electronic nicotine delivery device or web backend system can reinforce a user's self-efficacy by giving him/her feedback that his/her pattern of use is indicative of other users who successfully abstain from smoking.
  • an electronic nicotine delivery device or web backend system can give the user feedback that his/her mean nicotine dose is decreasing over time, despite it initially remaining constant or nearly constant, so as to enhance self-efficacy and increase his/her resilience in the face of environmental smoking cues that could otherwise trigger a smoking lapse or relapse ( FIG. 20 ).
  • “About” can mean a referenced numeric indication plus or minus 10% of that referenced numeric indication.
  • the term about 4 can include a range of 3.6 to 4.4.
  • FIG. 39 illustrates an example environment 3900 for implementing devices and methods described herein in accordance with an embodiment.
  • one or more user devices 3902 connect via a network 3904 to an electronic agent (e.g., nicotine) delivery device 3906 as provided herein which can be configured to produce a condensation aerosol comprising a pharmaceutically active agent (e.g., nicotine) as provided herein.
  • the electronic agent (e.g., nicotine) delivery device 3906 can comprise a controller, which can be programmable, as provided herein and the electronic agent (e.g., nicotine) delivery device 3906 can be connected to the network 3904 through the programmable controller.
  • the condensation aerosol comprising the pharmaceutically active agent is produced from a liquid formulation comprising the pharmaceutically active agent (e.g., nicotine) as provided herein.
  • the user devices 3902 can include any device capable of communicating with the network 3904 , such as personal computers, workstations, laptops, smartphones, mobile phones, tablet computing devices, smart TVs, game consoles, internet-connected set up boxes, and the like.
  • the user devices 3902 can include applications such as web browsers and/or applications (e.g., mobile apps) that are capable of communicating with the electronic agent (e.g., nicotine) delivery device 3906 and/or a system that uses the electronic agent (e.g., nicotine) delivery device 3906 .
  • the user devices 3902 communicate with the electronic agent (e.g., nicotine) delivery device 3906 via the programmable controller as provided herein.
  • the user can be a patient, and/or a healthcare provider (e.g., physician, physician's assistant, nurse, nurse practitioner, pharmacist or other medical professional).
  • a first user uses the device, while a second user uses the other user devices 3902 .
  • a first user uses the device and the other user devices 3902 , while the second user also uses the user devices 3902 .
  • the electronic agent (e.g., nicotine) delivery device 3906 can communicate with a data store 3908 in order perform the functionalities described herein (e.g., track device usage, adjust dose, frequency of administration, delivery schedule, customize feedback, administer challenge doses, etc.).
  • the data store 3908 can be used to store historical (e.g. user use history, dosage history, delivery schedule history, frequency of administration history, etc.), evaluation rules, and the like.
  • the data store 3908 can include one or more data files, databases, (e.g., SQL database), data storage devices (e.g., tape, hard disk, solid-state drive), data storage servers, or the like.
  • the data store 3908 can be connected to the electronic agent (e.g., nicotine) delivery device 3906 locally or remotely via a network.
  • data store 3908 , or any other data stores discussed herein can comprise one or more storage services provisioned from a “cloud storage” provider, for example, Amazon Simple Storage Service (“Amazon S3”), provided by Amazon.com, Inc. of Seattle, Wash., Google Cloud Storage, provided by Google, Inc. of Mountain View, Calif., and the like.
  • Amazon Simple Storage Service (“Amazon S3”), provided by Amazon.com, Inc. of Seattle, Wash.
  • Google Cloud Storage provided by Google, Inc. of Mountain View, Calif., and the like.
  • the network 3904 can include the Internet, a local area network (“LAN”), a wide area network (“WAN”), a cellular network, wireless network or any other public or private data and/or telecommunication network.
  • LAN local area network
  • WAN wide area network
  • cellular network wireless network or any other public or private data and/or telecommunication network.
  • FIG. 40 illustrates example components of an electronic agent (e.g., nicotine) delivery system 4000 , in accordance with an embodiment.
  • the electronic agent (e.g., nicotine) delivery system 4000 includes a data collector 4002 residing on a user or client device 4004 .
  • the system further comprises an electronic agent (e.g., nicotine) delivery device 4006 , which can be the same as 3906 as depicted in FIG. 39 .
  • the electronic agent (e.g., nicotine) delivery device 4006 can comprise a programmable controller, wherein the data collector resides on the programmable controller.
  • the data collector can be implemented as a browser script using JavaScript or any other scripting language.
  • the data collector can be configured to communicate with a web-based backend database.
  • the data collector can be configured to collect parameter information about the electronic agent (e.g., nicotine) delivery device 4006 such as discussed herein and transmit such parameter information to the web-based backend database, for example, using an application programming interface (API) provided by the user device 4004 .
  • the collection and/or communication with the user device 4004 can be triggered by an event on the electronic agent (e.g., nicotine) delivery device 4006 .
  • the event can include a click on a portion (e.g., a button or a link) of a user display on the electronic agent (e.g., nicotine) delivery device 4006 , use of the delivery device by a user or patient, and the like.
  • the user display can be on the programmable controller as provided herein.
  • the electronic agent (e.g., nicotine) delivery device 4006 can be configured to receive parameter information (e.g., dosage, frequency of administration, dosing schedule, etc.) provided by the data collector of the user device and to compare and/or analyze the parameter information received from the data collector of the user device to the parameter information from use of the electronic agent (e.g., nicotine) delivery device 4006 .
  • the electronic agent (e.g., nicotine) delivery device 4006 can utilize an evaluation engine 4008 .
  • the evaluation engine 4008 can be configured to analyze the parameter information in order to customize or adjust output parameters of the electronic agent (e.g., nicotine) delivery device 4006 .
  • the evaluation engine 4008 can be implemented using one or more server-side library files.
  • the evaluation engine 4008 can be implemented using one or more algorithms as provided herein for analyzing the respective parameter.
  • customized feedback or a treatment regimen can be evaluated based on some or all of the parameters as provided herein.
  • a lookup table e.g., stored in memory
  • the weight values may or may not be further weighted, combined or otherwise processed to derive a final customized feedback or treatment regimen.
  • the lookup table and the one or more algorithms for deriving the customized feedback or treatment regimen can be included on one or more rules that are pre-determined based on historical data such as past usage and/or user activities.
  • analysis of parameter information and/or generation of customized feedback or treatment regimen can be performed in real time or nearly real time with respect to the receipt of the parameter information.
  • any or all of the above operations may be performed in an asynchronous mode, for example, using batch processing.
  • the generated feedback and/or treatment regimen can be stored in a data store 4010 .
  • the data store 4010 can include a memory of a server, one or more data storage device (e.g., SSD, hard disk, taps), or a cloud-based storage service such as discussed in connection with FIG. 39 .
  • the data store 4010 may or may not be owned and/or operated by the same as the provider of the electronic agent (e.g., nicotine) delivery device 4006 .
  • FIG. 41 illustrates example components of a computer device 4100 for implementing aspects of devices and methods described herein, in accordance with an embodiment.
  • the computer device 4100 may be configured to implement a user device such as a user device 3902 discussed in connection with FIG. 39 and/or components or aspects of the electronic agent (e.g., nicotine) delivery device 3906 such as described in connection with FIGS. 39 and 40 .
  • computing device 4100 can include many more components than those shown in FIG. 4100 . However, it is not necessary that all of these components be shown in order to disclose an illustrative embodiment.
  • computing device 4100 includes a network interface 4102 for connecting to a network such as discussed above.
  • the computing device 4100 is housed on a programmable controller on an electronic agent (e.g., nicotine) delivery device as provided herein.
  • the computing device 4100 may include one or more network interfaces 4102 for communicating with one or more types of networks such as the Internet, wireless networks, cellular networks, and any other network.
  • computing device 4100 also includes one or more processing units 4104 , a memory 4106 , and an optional display or user interface as provided herein 4108 , all interconnected along with the network interface 4102 via a bus 4110 .
  • the processing unit(s) 4104 can be capable of executing one or more methods or routines stored in the memory 4106 .
  • the display 4108 can be configured to provide a graphical user interface to a user operating the computing device 4100 for receiving user input, displaying output, and/or executing applications. In some cases, such as when the computing device 4100 is a server, the display 4108 may be optional.
  • the memory 4106 can generally comprise a random access memory (“RAM”), a read only memory (“ROM”), and/or a permanent mass storage device, such as a disk drive.
  • the memory 4106 may store program code for an operating system 4112 , one or more agent (e.g., nicotine) delivery routines 4114 , and other routines.
  • the program code can be stored on a computer-readable storage medium, for example, in the form of a computer program comprising a plurality of instructions executable by one or more processors.
  • the computer-readable storage medium can be non-transitory.
  • the one or more agent (e.g., nicotine) delivery routines 4114 when executed, can provide various functionalities associated with the electronic agent (e.g., nicotine) delivery device as described herein.
  • the software components discussed above can be loaded into memory 4106 using a drive mechanism associated with a non-transient computer readable storage medium 4118 , such as a floppy disc, tape, DVD/CD-ROM drive, memory card, USB flash drive, solid state drive (SSD) or the like.
  • the software components can alternatively be loaded via the network interface 4102 , rather than via a non-transient computer readable storage medium 4118 .
  • the computing device 4100 can also include an optional time keeping device (not shown) for keeping track of the timing of usage of the electronic agent (e.g., nicotine) delivery device.
  • the computing device 4100 also communicates via bus 4110 with one or more local or remote databases or data stores such as an online data storage system via the bus 4110 or the network interface 4102 .
  • the bus 4110 can comprise a storage area network (“SAN”), a high-speed serial bus, and/or via other suitable communication technology.
  • SAN storage area network
  • databases or data stores may be integrated as part of the computing device 4100 .
  • FIG. 26 shows a schematic of the entire test apparatus while FIG. 27 shows alternates views of the test airway used in the test apparatus.
  • the test bed has an airway created between a block of Delrin (bottom) and a sheet of clear plexiglass (top) with brass sides used to clamp and make electrical contact with a heater element.
  • the heater element is a stainless steel foil of variable thickness (0.0005 inches (about 0.013 mm) or 0.001 inches (about 0.025 mm)), and the formulation used to generate an aerosol is composed of propylene glycol.
  • FIG. 27A shows a top view, with airflow ( 2702 a ) into an an inlet ( 2704 a ).
  • a hole to deposite drug ( 2706 a ) is provided and foil is shown ( 2708 a ).
  • Brass contacts ( 2710 a ) are provided.
  • the length of the device is 6 inches (about 152.4 mm), and the width is 2.25 inches (about 57.15 mm)
  • FIG. 27B shows a side view of the inlet ( 2704 b ), foil ( 2708 b ), brass electrical contacts ( 2710 b ), and outlet ( 2712 b ).
  • FIG. 27C shows and end view of the foil ( 2708 c ) and ( 2712 c ).
  • FIG. 27D shows an isometric view.
  • Table 2 shows the results of altering heater element thickness, air flow rate, current, and duration of heating on particle size distribution. Based on the results in Table 2, as the air flow rate is increased, the particle size diameter (PSD) decreases when the other parameters are held constant.
  • This example describes how changes in specific parameters (i.e. air flow rate, and electrical current to a heater element) affect the size of aerosol particles generated from a 10% nicotine/propylene glycol formulation by a test apparatus as described in Example 1.
  • Table 3 shows the results of altering heater element thickness, air flow rate, current, and duration of heating on particle size distribution. As shown in Table 3, when air flow rate is altered while other parameters are held constant, the higher the air flow rate, the smaller the average particle size diameter (PSD).
  • This example describes the particle size diameters of aerosols generated from either a PG formulation or 10% nicotine/PG formulation using a test apparatus as shown in FIGS. 26 and 27 and described in Example 1.
  • the heater element is a stainless steel coil comprising 3.5 coils and a diameter of 0.10 inches (about 2.54 mm).
  • the heater element is heated using a current of 2.5 Amps and the air flow rate is 4 Liters/min (about 6.7 ⁇ 10 ⁇ 5 m 3 /s). Table 4 shows the results.
  • This example describes the particle size diameters of aerosols generated from either one of two brands of eCigs (Finiti and BLU).
  • a 50 ml volume of an aerosol was pulled from either one of the two brands of eCigs over a period of 3 seconds in order to simulate a human breath.
  • the collected aerosol was then injected into a laser particle size detector set at a flow rate of 14 Liters/min (about 2.33 ⁇ 10 ⁇ 4 m 3 /s).
  • Table 5 shows the particle size diameter of the aerosols generated from two brands of eCigs.
  • FIG. 28 shows a comparison of the particle size distribution for aerosols created by eCigs vs. aerosol created by devices provided herein (devices). As shown in FIG. 28 , the particle size distribution of aerosols generated by devices provided herein is shifted toward larger particle sizes vs. those generated by eCigs.
  • FIG. 29A shows a schematic of the entire test apparatus while FIG. 29B shows an internal view of the valve ( 2904 a ) used in the test apparatus.
  • the valve flap ( 2902 b ) has a 3 ⁇ 4 inch diameter and the diameter of the channel downstream of the valve is 0.375 inches (about 9.53 mm) in length and 0.090 inches (about 2.29 mm) in width.
  • the test bed has a primary airway ( 2906 a ), and a bypass airway ( 2908 a ), an aerosol generation chamber ( 2912 a ) and vacuum source ( 2910 a ).
  • the aerosol generation chamber comprises a heater element.
  • the inlet to the bypass airway is a slot of varying dimensions (L ⁇ W).
  • Table 6 shows the results using a valve of 3 ⁇ 4 inch (about 19.05 mm) diameter and altering valve material and bypass orifice diameter. As shown in Table 6, regardless of valve material type and bypass orifice diameter, above inhalation pressures of about 2 inches of H 2 O (about 498 Pa), the primary flow remains relatively constant, while the bypass flow increases with increasing vacuum pressure.
  • Table 7 shows the results using a valve of 3 ⁇ 8 inch diameter, a bypass orifice of varying dimensions, and altering the orifice dimensions for the inlet of the primary airway. As shown in Table 7, reducing the size of the orifice of the primary airway consistently reduces the flow rate through the primary airway regardless of varying vacuum pressure, dimensions of the bypass orifice, or varying the valve material
  • FIG. 31A depicts a device designated ENT-100-A, (two inches (about 50.8 mm) long) comprising a primary carrier gas inlet ( 3112 a ), positive and negative brass contacts ( 3110 a ), a heater element ( 3106 a ) comprising a coil located distally from the inlet to the primary airway ( 3112 a ) and two bypass inlets ( 3104 a ) located (disposed) downstream of the heater element but prior to the outlet ( 3102 a ).
  • FIG. 31A depicts a device designated ENT-100-A, (two inches (about 50.8 mm) long) comprising a primary carrier gas inlet ( 3112 a ), positive and negative brass contacts ( 3110 a ), a heater element ( 3106 a ) comprising a coil located distally from the inlet to the primary airway ( 3112 a ) and two bypass inlets ( 3104 a ) located (disposed) downstream of the heater element but prior to the outlet ( 3102 a ).
  • FIG. 31B depicts a device designated ENT-100-B, which is the same as ENT-100-A except that the heater element has been moved to be proximal to the inlet of the primary airway ( 3112 b ).
  • FIG. 31C depicts a device designated ENT-100-C, which is similar to the ENT-100-A device except that the wire coil heater element has been moved to an intermediate position relative to the location of the coil in ENT-100-A and ENT-100-B.
  • Any of the devices depicted in FIG. 31A-C can comprise the wire coil heater element designated “A Coil” ( 3114 e ) or “B Coil” ( 3116 e ) as illustrated in FIG. 31E .
  • the coil in both types of heater elements comprise inner diameter of 0.26 inches (about 6.604 mm).
  • the “A Coil” comprises a stretch of coil followed by a straight lead on either end of the coil which connects to the brass contacts.
  • the “B Coil” comprises a stretch of coil, wherein the coil itself connects to the brass contacts.
  • Tables 8-12 shows the particle size diameter of the aerosols generated from the devices depicted in FIG. 31A-C .
  • Table 8 shows the PSD of particles generated using an ENT-100-A device with the “B Coil”.
  • Table 9 shows the PSD of particles generated using an ENT-100-B device with the “A Coil”.
  • Table 10 shows the PSD of particles generated using an ENT-100-B device with the “B Coil”.
  • Table 11 shows the PSD of particles generated using an ENT-100-C device with the “A-Coil”.
  • Table 12 shows the PSD of particles generated using an ENT-100-C device with the “B-Coil”.
  • This example describes the particle size diameters (PSD) of aerosols generated from a heater element comprising a wire wherein one end of the wire wraps around another segment of the wire, wherein a wire coil is formed with an end of the wire passes through the center of the wire coil.
  • FIGS. 36-38 An example of this type of heater element is shown in FIGS. 36-38 .
  • the heater element is inserted into the device depicted in FIG. 31D .
  • FIG. 31D depicts a device designated ENT-100-D with a primary passageway for air to flow through, brass contacts (+/ ⁇ ) embedded within the wall of the primary passageway, and a heater element as described in this example.
  • the wire of the heater element has a diameter of 0.10 inches (about 2.54 mm).
  • the wire coil of the heater element has 9 coils, and the wire coil has an inner diameter of 0.032 inches (about 0.813 mm).
  • the liquid formulation comprises propylene glycol and it wicks onto the ends of the wire of the heater element and onto the brass contacts.
  • Table 13 shows the particle size diameter of the aerosols generated from a device comprising the heater element. As shown in Table 13, the particle size distribution of aerosols generated by devices with the heater element is unaffected by alterations in current used to heat the wire.
  • FIG. 31D depicts a device designated ENT-100-D with a primary passageway for air to flow through, brass contacts (+/ ⁇ ) embedded within the wall of the primary passageway, and a heater element as described in this example.
  • the diameter of the inlet is varied from 0.060 inches to either 0.070, 0.071, or 0.041 inches (a range from about 1.524 mm to either 1.78, 1.80, or 1.04 mm.
  • the wire of the heater element has a diameter of 0.10 inches (about 0.254 mm).
  • the wire coil of the heater element has a reduced number of coils, and the wire coil has an inner diameter of 0.032 inches (about 0.813 mm).
  • the liquid formulation comprises propylene glycol and it wicks onto the ends of the wire of the heater element and onto the brass contacts. Table 14 shows the particle size diameter of the aerosols generated from a device comprising the heater element.
  • Table 14 the particle size distribution of aerosols generated by device with the heater element is unaffected by alterations in current used to heat the wire.
  • Table 14 also shows the effects of altering the airway configuration in the ENT-100-D device. As shown in Table 14, altering the configuration of the airway of the ENT-100-D device by adding the airway depicted in FIG. 32E (designated the MARK V adders in Table 14) downstream of the heater element produces particles with a PSD of about 1 to about 2 ⁇ m.
  • FIG. 31D depicts a device designated ENT-100-D with a primary passageway for air to flow through, brass contacts (+/ ⁇ ) embedded within the wall of the primary passageway, and a heater element as described in this example.
  • the wire of the heater element has a diameter of 0.10 inches (about 2.54 mm).
  • the wire coil of the heater element has an increased number of coils relative to example 8, and the wire coil has an inner diameter of 0.032 inches (about 0.813 mm).
  • the liquid formulation comprises propylene glycol and it wicks onto the ends of the wire of the heater element and onto the brass contacts.
  • the dose of the formulation is 2 mg.
  • Table 15 shows the particle size diameter of the aerosols generated from the device described in this example. As shown in Table 15, the particle size diameter distribution of aerosols generated by this device is unaffected by alterations in current used to heat the wire.
  • FIG. 31D depicts a device designated ENT-100-D with a primary passageway for air to flow through, brass contacts (+/ ⁇ ) embedded within the wall of the primary passageway, and a heater element as described in this example.
  • the wire of the heater element has a diameter of 0.10 inches (about 2.54 mm).
  • the wire coil of the heater element has an inner diameter of 0.032 inches (about 0.813 mm).
  • the liquid formulation comprises propylene glycol and it wicks onto the ends of the wire of the heater element and onto the brass contacts.
  • the dose of the formulation in this example is 2 mg.
  • Table 16 shows the particle size diameter of the aerosols generated from a device comprising the heater element described in this example. As shown in Table 16, the particle size distribution of aerosols generated by devices with the heater element is unaffected by alterations in current used to heat the wire. Also as shown in Table 16, altering the configuration of the airway of the ENT-100-D device by adding the airway depicted in FIG. 33 (designated the MARK VI adder in Table 15) downstream of the heater element produces particles with a PSD of about 1 to about 2 uM, which matches the PSD of the particles generated without the MARK VI adder.
  • the MARK VI adder comprises a primary airway with an internal diameter of 0.25 inches (about 6.35 mm), which narrows to an airway comprising an internal diameter of 0.086 inches (about 2.18 mm) and an external diameter of 0.106 inches (about 2.69 mm)
  • the particle size diameters (PSD) of a condensation aerosol generated by a device comprising the airway configuration depicted in FIG. 33 are tested.
  • the device comprises a primary airway with an internal diameter of 0.25 inches (about 6.35 mm), which narrows to an airway comprising an internal diameter of 0.086 inches (about 2.18 mm) and an external diameter of 0.106 inches (about 2.69 mm).
  • the airway configuration is coupled to a heater element comprising a wire coil, wherein the heater element vaporizes a liquid formulation comprising propylene glycol upstream of where the primary airway narrows. The vaporized formulation then enters the narrowed airway and condenses into particles.
  • the narrowed primary airway is designed to carry the vaporized formulation in a carrier gas (e.g. air) at a flow rate suitable for condensing the vapor into particles of a desired size (e.g. an MMAD of about 1 to about 5 um).
  • a carrier gas e.g. air
  • the narrowed primary airway opens up into a wide downstream airway comprising an internal diameter of 0.25 inches (about 6.35 mm) and the condensed particles are mixed with bypass carrier gas (e.g. air) that enters the widened primary airway from inlets located (disposed) in the walls of the primary airway.
  • bypass carrier gas e.g. air
  • Table 17 shows the results. As shown in Table 17, different rates of B flow have no effect on the PSD. Moreover, the PSD at each B flow rate is between 1 and 3 uM. Table 18 shows the effect on PSD of limiting the flow of bypass carrier gas through the bypass inlet on the secondary housing. The flow of bypass gas through the bypass inlet is limited by using either a valve or by altering the geometry of the orifice (i.e. forming a slot of different dimensions. As shown in Table 18, either the use of a valve or slot to control the flow of bypass gas is effective in producing particles with a PSD of about 1 to about 5 ⁇ m.
  • the effects of gravity on the particle size diameters (PSD) of a condensation aerosol generated by an ENT-100-D device as depicted in FIG. 31D are tested.
  • the ENT-100-D device is loaded with 2 mg of a liquid propylene glycol formulation and the device is rotated during the use of the device.
  • the device is rotated 90 degrees in all dimensions from a stable baseline position.
  • the particle size diameter is measured at each rotation and found not to change. As a result, the device produces particles of a consistent size regardless of the orientation in space of the device.
  • condensation aerosol comprising nicotine produced from a liquid nicotine formulation using the ENT-100 nicotine inhaler.
  • One primary objective is to establish the maximally tolerated dose in the range of 25-100 ⁇ g of a condensation aerosol comprising nicotine and propylene glycol (PG) from the eNT-100 nicotine inhaler.
  • a second primary objective is to establish the plasma level-time profiles of nicotine administered as 10 inhalations (single dose) using ⁇ g doses from the eNT-100 nicotine inhaler.
  • Part 1 will be a single-blind, placebo and vehicle-controlled, escalating, single dose design to assess the safety, tolerability, nicotine concentrations, and pharmacodynamics of a condensation aerosol comprising nicotine produced from a liquid nicotine formulation using the eNT-100 nicotine inhaler.
  • Subjects will be abstinent from smoking for at least 12 hours prior to the experimental session. Groups of 12 subjects will be assigned to one of up to seven experimental groups, depending on the maximally tolerated dose within the predetermined range of 25-100 ⁇ g of nicotine per inhalation (less than a typical cigarette inhalation per puff).
  • Subjects will complete predose assessments of their exhaled CO, smoking urge, nicotine concentrations, spirometry, and pulse oximetry, and a brief training including practice inhalations, and then complete 10 inhalations from the eNT-100 inhaler at approximately 30-second intervals over a 4.5-minute period.
  • Postdose assessments will include nicotine concentrations, safety, tolerability, liking, smoking urge, spirometry, and pulse oximetry assessments.
  • Subjects will receive a follow-up phone call approximately 24 hours after dosing to assess any adverse events (AEs) that have occurred since dosing. Escalation to the next dose group will not take place until adequate safety and tolerability from the previous group has been demonstrated.
  • AEs adverse events
  • a final cohort of subjects Upon reaching the maximally tolerated dose (within the predetermined range of 25-100 ⁇ g of nicotine per inhalation), a final cohort of subjects will be run at the same nicotine dose, but at twice the nicotine concentration (e.g., if 100 ⁇ g of nicotine is well tolerated within 1 mg of PG, [i.e., 10% solution], then an additional group would be run using 100 ⁇ g of nicotine within 0.5 mg of PG [i.e., 20% solution]).
  • Part 2 will be a randomized, single-blind, within-subject, 5-way crossover, vehicle-, e-cig-, and combustible cigarette-controlled design to assess the safety, tolerability, pharmacokinetics and pharmacodynamic effects of the eNT-100 nicotine inhaler.
  • the selected nicotine aerosol concentrations and doses to be administered during Part 2 will be determined upon completion of Part 1 of the study.
  • Subjects will complete predose assessments of exhaled CO, their smoking urge, nicotine PK, spirometry, and pulse oximetry, and a brief training including practice inhalations.
  • Each administration of the study products will include 10 inhalations at approximately 30-second intervals over a 4.5-minute period (or completion of one conventional cigarette).
  • Postdose assessments will include nicotine PK, safety, tolerability, liking, smoking urge, exhaled CO, spirometry, and pulse oximetry assessments. A 36-hour wash-out from nicotine will be required prior to each product administration. See FIG. 43 for the trial design of this portion of the trial.
  • Parts 1 and 2 will include approximately 48-84 (depending on the maximally tolerated aerosol administration) and 15 subjects, respectively.
  • Subjects will be healthy, adult males and females, 21-65 years of age inclusive, who smoke at least 10 cigarettes per day (CPD) for the last 12 months. Ideally, subjects participating in Part 1 will serve as the pool of subjects for Part 2; however, additional subjects will be recruited following completion of Part 1 if necessary to better ensure that 15 subjects are administered study product in Part 2. Potential subjects must fulfill all of the following inclusion criteria to be eligible for participation in the study. Inclusion criteria include: 1. Healthy adult male and female smokers, 21 to 65 years of age, inclusive, at Screening. 2. At least a 12-month smoking history prior to Check-in with a cigarette smoked per day average of 10 or more manufactured cigarettes per day (no restriction on brand).
  • Female subjects who are heterosexually active and of childbearing potential e.g., not surgically sterile [bilateral tubal ligation, hysterectomy, or bilateral oophorectomy at least 6 months prior to Check-in] or at least 2 years naturally postmenopausal
  • hormonal method e.g., oral, vaginal ring, transdermal patch, implant, or injection
  • double barrier method i.e., condom with spermicide or diaphragm with spermicide
  • intrauterine device for at least 3 months prior to Check-in
  • Essure® procedure at least 6 months prior to Check-in
  • Subjects may be excluded from the study if there is evidence of any of the following criteria at Screening, Check-in, or at any time during the study as appropriate, in the opinion of the principal investigator (PI): History or presence of clinically significant gastrointestinal, renal, hepatic, neurologic, hematologic, endocrine, oncologic, urologic, pulmonary (especially bronchospastic diseases), immunologic, psychiatric, or cardiovascular disease, or any other condition that, in the opinion of the PI, would jeopardize the safety of the subject or impact the validity of the study results; (Part 2 only) clinically significant abnormal findings on the physical examination, ECG, or clinical laboratory results, in the opinion of the PI; (Part 2 only) positive test for human immunodeficiency virus (HIV), hepatitis B surface antigen (HbsAg), or hepatitis C virus (HCV); positive urine screen for alcohol or drugs of abuse at Screening or any Check-in; history of drug or alcohol abuse within 24 months of Check-in
  • Stable doses i.e., no dosage adjustments within 30 days prior to Check-in
  • over-the-counter medications e.g., hypertension
  • Hormonal contraceptives e.g., oral, transdermal patch, implant, injection
  • hormonal replacement therapy e.g., oral, transdermal patch, implant, injection
  • Occasional use of over-the-counter analgesics e.g., acetaminophen, ibuprofen
  • antihistamines e.g., antihistamines
  • nasal decongestants e.g., Exceptions may be permitted at the discretion of the PI in consultation with the Sponsor, providing the medication in question would have no impact on the study. Any exceptions will be documented.
  • Subjects will be assigned a unique screening number and subject numbers for each part of the study.
  • Replacement subjects if used, will be assigned a number 1000 higher than the subject being replaced (e.g., Subject 1110 would replace Subject 110).
  • Eligibility for inclusion into Part 1 will be based on a screening visit(s) to assess medical history, concomitant medications, demographics, and smoking history (including the Fagerstrom Test for Nicotine Dependence [FTND]), an exhaled CO test, urine cotinine and drugs of abuse test, urine pregnancy test, vital signs, and BMI determination.
  • FTND Fagerstrom Test for Nicotine Dependence
  • Part 2 Subjects participating in Part 2 will complete additional screening events including a physical examination, ECG, clinical laboratory, and serology evaluations. If the pool of subjects from Part 1 is deemed not sufficient to successfully complete Part 2, then additional subjects will be recruited.
  • Part 1 will be completed during a Screening visit, a single study visit and a follow-up phone call. Subjects entering into Part 2 will complete an additional 11-day in-clinic confinement. Overall the study is expected to take place over approximately 10 weeks.
  • Placebo eNT-100 inhaler delivering air only
  • Vehicle control eNT-100 inhaler delivering PG only
  • eNT-100 Nicotine Inhaler potential nicotine concentration range depending on tolerability: 1.25-20% nicotine solution in PG vehicle
  • Subjects will participate in one of the experimental groups using the eNT-100 nicotine inhaler involving 10 inhalations resulting in the total nicotine delivery as listed in Table 19 below.
  • the total amount of solution aerosolized (starting at 1.0 mg but adjustable to a minimum of 0.5 mg or a maximum of 2.0 mg of total nicotine plus PG solution), as well as the nicotine concentration of the aerosol, can be adjusted following a review of the safety and tolerability from the previous group.
  • the final maximally tolerated dose (MTD) nicotine group (e.g., Group #7), will evaluate the nicotine concentration for the eNT-100 with the nicotine concentration based on the safety and tolerability from the previous groups.
  • the maximum nicotine concentration that would be evaluated in any scenario is 20.0%.
  • Dose-escalation decisions within part 1 will be made based on evaluation of safety data, AEs, and the pharmacodynamic (PD) assessments.
  • the selected nicotine aerosol concentration and doses to be administered during Part 2 will be determined upon completion of Part 1.
  • % nicotine is % by volume.
  • serial blood samples will be collected within 15 minutes prior to product administration, and at approximately 5 and 10 minutes after the start of each product administration, and will be used to determine plasma nicotine concentrations.
  • Table 22 outlines the blood sample collection protocol for Part 1.
  • serial blood samples will be collected within 15 minutes prior to product administration and at approximately 3, 5, 10, 15, 20, 25, 30, and 60 minutes after the start of each product administration and will be used to determine plasma nicotine concentrations.
  • Table 23 outlines the blood sample collection protocol for Part 2.
  • noncompartmental PK parameters of C5, C max , t max , and AUC 0-t will be calculated from plasma concentrations of nicotine. Additional PK parameters may be calculated if deemed appropriate.
  • Nicotine concentrations and PK parameters will be summarized by study product using descriptive statistics.
  • Analyses of variance or other appropriate statistical tests will be performed on the PK parameters.
  • the ANOVA model will include sequence, study product, and period as fixed effects, and subject nested within sequence as a random effect. Sequence will be tested using subject nested within sequence as the error term.
  • Each ANOVA will include calculation of least-squares means (LSM), differences between product LSM, and the standard error associated with these differences. The above statistical analyses will be performed using the appropriate SAS procedures.
  • Part 1 Prior to inclusion into Part 1 of the study, medical history, vital signs, urine drug and alcohol screen, and pregnancy test (females only) will be performed. Part 1 Check-in evaluations will include vital signs, urine drug and alcohol screen, and a pregnancy test (females only).
  • Part 2 Additional safety evaluations performed prior to inclusion in Part 2 will include a physical examination, electrocardiogram (ECG), clinical laboratory (clinical chemistry, hematology, urinalysis), and serology.
  • ECG electrocardiogram
  • Part 2 Check-in evaluations will include a brief physical examination (symptom-driven), vital signs, clinical laboratory (clinical chemistry, hematology, and urinalysis), urine drug and alcohol screen, and a pregnancy test (females only).
  • End-of-Study (or Early Termination) evaluations will include a brief physical examination (symptom-driven) and vital signs.
  • AEs Adverse events spontaneously reported by the subjects or observed by the PI or other study personnel will be monitored and followed up until the symptoms or values return to normal or acceptable levels or until lost to follow-up, as appropriate in the opinion of the PI or his designee.
  • Spirometry, pulse oximetry, and expired CO values for both Part 1 and Part 2 will be listed by subject and time point. Postdose to predose difference in each assessment will be summarized by time point using descriptive statistics and analyzed using an appropriate statistical method.
  • the aerosol is created inside the eNT-100 inhaler, which is itself inside a small cylindrical plastic housing that is used to blind the test subject from the test article.
  • the test subject will inhale from a plastic tube that slides over the stainless-steel mouthpiece shown.
  • Inside of the aerosol-generating inhaler is a small heater element that is used to vaporize the nicotine solution under flow conditions that result is a 1.4 to 2.5 micron aerosol particle.
  • the nicotine inhaler further comprises a positive displacement pump to meter out a dose of the nicotine solution onto the heater element.
  • the eNT-100 is designed to create the aerosol when the inhalation rate reaches 20 lpm (about 3 ⁇ 10 ⁇ 4 m 3 /s). At that flow rate the aerosol produced has a particle size of 2.5 micron volume median diameter (VMD) with a GSD of 1.6.
  • VMD micron volume median diameter
  • the upper end of the inhalation flow rate is determined by the flow rate that can be produced under what is considered an upper limit of vacuum that the human lung can produce by inhalation (13 inches of water is considered that upper limit (about 3235 Pa)). At that vacuum, the inhalation flow rate is 50 lpm (about 8.33 ⁇ 10 ⁇ 4 m 3 /s) and the particle size is 1.4 micron VMD with a GSD of 1.2.
  • the bulk of the aerosol is created within 1 second of the inhaler being breath-activated. Within 1.4 seconds the entire aerosol is created. An estimate of the aerosol produced between the 1 second and the 1.4 second time point is around 5-10% of the total amount of the aerosol. As a result, the bulk of the aerosol is delivered to the respiratory tract in the first 1 ⁇ 3 to 1 ⁇ 2 of the volume of the total inhalation volume, thereby allowing the aerosol to be “chased” down into the deep lung by the balance of the inhalation.
  • the eNT-100 system can generate an emitted dose of +/ ⁇ 20% of the dose (or loaded dose).
  • the dose (or loaded dose) can be the amount of nicotine solution pumped onto the heater element prior to the creation of the aerosol and can be +/ ⁇ 2% of the target dose (the label claimed dose or goal dose).
  • the emitted dose can be 92% to 97% of the dose. For example, the amount actually delivered to the lung if the label claim dose is 100 ⁇ g would be between 90% and 99%.

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Cited By (164)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140255525A1 (en) * 2012-05-16 2014-09-11 Louise M Smith Beverages with compositions of vinegar
US20150027455A1 (en) * 2013-07-24 2015-01-29 Sis Resources, Ltd. Solid core electronic cigarette
US20150196060A1 (en) * 2013-09-20 2015-07-16 E-Nicotine Technology, Inc. Devices and methods for modifying delivery devices
US20150217068A1 (en) * 2014-02-04 2015-08-06 George Wakalopulos Electric wick and heater for portable vaporizer
US20150245659A1 (en) * 2014-02-28 2015-09-03 R.J. Reynolds Tobacco Company Atomizer for an aerosol delivery device and related input, aerosol production assembly, cartridge, and method
US20150272216A1 (en) * 2014-03-31 2015-10-01 Westfield Limited (Ltd.) Personal vaporizer with liquid supply by suction
US20150335074A1 (en) * 2014-05-22 2015-11-26 Nuryan Holdings Limited Handheld vaporizing device
US20150351457A1 (en) * 2013-01-05 2015-12-10 Qiuming Liu Electronic cigarette and method for adjusting flow rate of gas flow of electronic cigarette
WO2016019353A1 (en) * 2014-07-31 2016-02-04 MJAR Holdings, LLC Electronic cigarettes, cartridges, and inhalable formulations of medicinal cannabis compounds, and apparatuses and methods for making and using the same
US20160045685A1 (en) * 2014-08-13 2016-02-18 Elwha Llc Methods, systems, and devices related to a supplemental inhaler
WO2016040575A1 (en) * 2014-09-10 2016-03-17 Fontem Holdings 1 B.V. Methods and devices for modulating air flow in delivery devices
US20160136213A1 (en) * 2014-11-14 2016-05-19 Charles William Paul Process to suspend cannabis oil in glycerin
WO2016096497A1 (en) * 2014-12-15 2016-06-23 Philip Morris Products S.A. An aerosol-generating system using the venturi effect to deliver substrate to a heating element
WO2016096728A1 (en) * 2014-12-15 2016-06-23 Philip Morris Products S.A. Aerosol-generating system comprising moveable cartridge
WO2016096762A1 (en) * 2014-12-15 2016-06-23 Philip Morris Products S.A. E-liquid collapsible cartridge
US20160219936A1 (en) * 2015-01-30 2016-08-04 Fontem Holdings 2 B.V. Wick-positioning cartomizer
EP3066941A1 (en) * 2015-03-13 2016-09-14 Fontem Holdings 1 B.V. Aerosol generating component for an electronic smoking device, electronic smoking device and method for generating an inhalant
US20160270446A1 (en) * 2014-11-03 2016-09-22 Yuval Shenkal E-Cigarette with Valve Allowing Exhale Filter
US20160284197A1 (en) * 2014-06-19 2016-09-29 Kimree Hi-Tech Inc. Data communication method and system
US20160295917A1 (en) * 2013-12-05 2016-10-13 Philip Morris Products S.A. Heated aerosol generating article with air-flow barrier
WO2016200382A1 (en) * 2015-06-10 2016-12-15 Evolv, Llc Electronic vaporizer having reduced particle size
US20170006917A1 (en) * 2015-07-07 2017-01-12 Altria Client Services Inc. E-vapor device including capsule containing pre-vapor formulation
US20170013878A1 (en) * 2015-07-16 2017-01-19 Njoy, Inc. Vaporizer tank with atomizer
WO2017048972A1 (en) * 2015-09-16 2017-03-23 Sansa Corporation (Barbados) Inc. Nicotine formulations and methods of making and using the same
WO2017046400A1 (en) * 2015-09-18 2017-03-23 Philip Morris Products S.A. Liquid formulation of an electronic vapor device
US20170095005A1 (en) * 2013-12-23 2017-04-06 James Monsees Vaporization device systems and methods
WO2017059571A1 (en) 2015-10-08 2017-04-13 Fontem Holdings 1 B.V. Liquid supply for an electronic smoking device
US20170105452A1 (en) * 2014-05-21 2017-04-20 Philip Morris Products S.A. Aerosol-generating system comprising a cartridge with an internal air flow passage
US20170135402A1 (en) * 2014-06-27 2017-05-18 Fontem Holdings 1 B.V. Electronic smoking device and capsule system
US20170157343A1 (en) * 2014-06-30 2017-06-08 Syqe Medical Ltd. Methods, devices and systems for pulmonary delivery of active agents
WO2017093535A1 (en) * 2015-12-03 2017-06-08 Jt International S.A. Heating system and method for an inhaler device
US20170208867A1 (en) * 2016-01-25 2017-07-27 Shenzhen First Union Technology Co., Ltd. Smart control method and control system for an electronic cigarette, and electronic cigarette
US20170251722A1 (en) * 2016-03-03 2017-09-07 Altria Client Services Llc Flavor assembly for electronic vaping device
US20170251723A1 (en) * 2016-03-03 2017-09-07 Altria Client Services Llc Methods to add menthol, botanic materials, and/or non-botanic materials to a cartridge, and/or an electronic vaping device including the cartridge
WO2017167647A1 (en) * 2016-03-31 2017-10-05 Philip Morris Products S.A. Vaporizing assembly comprising sheet heating element and liquid delivery device for an aerosol generating system
US9802011B2 (en) 2014-06-30 2017-10-31 Syqe Medical Ltd. Drug dose cartridge for an inhaler device
US20170318863A1 (en) * 2016-07-27 2017-11-09 Shenzhen First Union Technology Co., Ltd. Electronic cigarette, control method and control system having same
US20170319797A1 (en) * 2016-05-03 2017-11-09 Pneuma Respiratory, Inc. Droplet delivery device for delivery of fluids to the pulmonary system and methods of use
US9839241B2 (en) 2014-06-30 2017-12-12 Syqe Medical Ltd. Methods, devices and systems for pulmonary delivery of active agents
US20170360089A1 (en) 2010-12-22 2017-12-21 Syqe Medical Ltd. Method and system for drug delivery
WO2018007887A1 (en) * 2016-07-07 2018-01-11 Philip Morris Products S.A. Nicotine particle delivery consumable
WO2018007886A1 (en) * 2016-07-07 2018-01-11 Philip Morris Products S.A. Nicotine inhaler system
US20180007969A1 (en) * 2016-07-08 2018-01-11 Rai Strategic Holdings, Inc. Radio frequency to direct current converter for an aerosol delivery device
US20180080559A1 (en) * 2015-04-17 2018-03-22 Fontem Holdings 1 B.V. Liquid supply with spiral container
US20180092402A1 (en) * 2015-05-22 2018-04-05 Japan Tobacco Inc. Method for manufacturing atomizing unit, atomizing unit, and non-combustion type flavor inhaler
WO2018067579A1 (en) 2016-10-03 2018-04-12 Neto Jorge Neval Moll Devices, systems and methods for delivering coffee-derived volatiles
US20180110725A1 (en) * 2016-10-21 2018-04-26 Somniferum Labs LLC Compositions, methods and kits for the safe inhaled delivery of targeted opioids for the treatment of pain and addiction
CN107995846A (zh) * 2015-01-22 2018-05-04 方特慕控股第私人有限公司 电子蒸发装置
CN108024575A (zh) * 2015-08-25 2018-05-11 富特姆控股第有限公司 电子吸烟装置的液体供应器
US9993602B2 (en) 2014-06-30 2018-06-12 Syqe Medical Ltd. Flow regulating inhaler device
US10034988B2 (en) 2012-11-28 2018-07-31 Fontem Holdings I B.V. Methods and devices for compound delivery
USD825102S1 (en) 2016-07-28 2018-08-07 Juul Labs, Inc. Vaporizer device with cartridge
US10045567B2 (en) 2013-12-23 2018-08-14 Juul Labs, Inc. Vaporization device systems and methods
US10058130B2 (en) 2013-12-23 2018-08-28 Juul Labs, Inc. Cartridge for use with a vaporizer device
US10076139B2 (en) 2013-12-23 2018-09-18 Juul Labs, Inc. Vaporizer apparatus
US10080851B2 (en) 2014-06-30 2018-09-25 Syqe Medical Ltd. Method and device for vaporization and inhalation of isolated substances
US20180271172A1 (en) * 2015-03-04 2018-09-27 Altria Client Services Llc E-vaping cartridge
US10104915B2 (en) 2013-12-23 2018-10-23 Juul Labs, Inc. Securely attaching cartridges for vaporizer devices
US10111470B2 (en) 2013-12-23 2018-10-30 Juul Labs, Inc. Vaporizer apparatus
USD836541S1 (en) 2016-06-23 2018-12-25 Pax Labs, Inc. Charging device
US20180369508A1 (en) * 2015-12-28 2018-12-27 Koninklijke Philips N.V. Air-flow in a nebulizer head
US10188148B2 (en) 2014-11-17 2019-01-29 Mcneil Ab Electronic nicotine delivery system
USD842536S1 (en) 2016-07-28 2019-03-05 Juul Labs, Inc. Vaporizer cartridge
US20190069603A1 (en) * 2014-02-28 2019-03-07 Beyond Twenty Ltd. E-cigarette personal vaporizer
US10226076B2 (en) 2014-11-17 2019-03-12 Mcneil Ab Disposable cartridge for use in an electronic nicotine delivery system
US20190082740A1 (en) * 2013-11-12 2019-03-21 VMR Products LLC. Vaporizer
US10244793B2 (en) 2005-07-19 2019-04-02 Juul Labs, Inc. Devices for vaporization of a substance
US10244795B2 (en) 2016-03-31 2019-04-02 Altria Client Services Llc Vaporizing assembly comprising sheet heating element and liquid delivery device for an aerosol generating system
US10251425B2 (en) 2015-07-06 2019-04-09 Njoy, Llc Vaporizing device with power component
US10258087B2 (en) 2016-03-10 2019-04-16 Altria Client Services Llc E-vaping cartridge and device
US10266388B2 (en) 2014-02-28 2019-04-23 Beyond Twenty Ltd. Electronic vaporiser system
US10264820B2 (en) 2011-10-28 2019-04-23 Evolv, Llc Electronic vaporizer that simulates smoking with power control
US10279934B2 (en) 2013-03-15 2019-05-07 Juul Labs, Inc. Fillable vaporizer cartridge and method of filling
USD848057S1 (en) 2016-06-23 2019-05-07 Pax Labs, Inc. Lid for a vaporizer
US10285430B2 (en) 2014-02-28 2019-05-14 Ayr Ltd. Electronic vaporiser system
US10285449B2 (en) 2015-09-01 2019-05-14 Ayr Ltd. Electronic vaporiser system
USD849996S1 (en) 2016-06-16 2019-05-28 Pax Labs, Inc. Vaporizer cartridge
US10306924B2 (en) 2013-03-14 2019-06-04 Rai Strategic Holdings, Inc. Atomizer for an aerosol delivery device formed from a continuously extending wire and related input, cartridge, and method
USD851830S1 (en) 2016-06-23 2019-06-18 Pax Labs, Inc. Combined vaporizer tamp and pick tool
CN110022703A (zh) * 2016-12-19 2019-07-16 菲利普莫里斯生产公司 具有外部筒的气溶胶生成系统
US10357060B2 (en) 2016-03-11 2019-07-23 Altria Client Services Llc E-vaping device cartridge holder
US10362803B2 (en) 2015-06-10 2019-07-30 Evolv, Llc Electronic vaporizer having reduced particle size
US10368581B2 (en) 2016-03-11 2019-08-06 Altria Client Services Llc Multiple dispersion generator e-vaping device
US10368580B2 (en) 2016-03-08 2019-08-06 Altria Client Services Llc Combined cartridge for electronic vaping device
US10405582B2 (en) 2016-03-10 2019-09-10 Pax Labs, Inc. Vaporization device with lip sensing
US10449310B2 (en) 2018-02-08 2019-10-22 Optimist Inhaler LLC Security features for an electronic metered-dose inhaler system
US10455863B2 (en) 2016-03-03 2019-10-29 Altria Client Services Llc Cartridge for electronic vaping device
US10492531B2 (en) * 2014-05-28 2019-12-03 Huizhou Kimree Technology Co., Ltd., Shenzhen Branch Information pushing method and communication system
US10512282B2 (en) 2014-12-05 2019-12-24 Juul Labs, Inc. Calibrated dose control
EP3607985A1 (en) 2018-08-09 2020-02-12 GSW Creative Corporation A vaporization device
US10588176B2 (en) 2014-02-28 2020-03-10 Ayr Ltd. Electronic vaporiser system
US10588344B2 (en) 2017-01-31 2020-03-17 Philter Labs, Inc. Low emissions electronic smoking device and emissions filtering device
WO2020058881A1 (en) * 2018-09-20 2020-03-26 Rai Strategic Holdings, Inc. Flavorants for smoking articles
WO2020081527A1 (en) * 2018-10-15 2020-04-23 Juul Labs, Inc. Cartridges for vaporized devices
USD887632S1 (en) 2017-09-14 2020-06-16 Pax Labs, Inc. Vaporizer cartridge
US10687561B2 (en) 2017-01-31 2020-06-23 Philter Labs, Inc. Low emissions electronic smoking device and emissions filtering device
CN111372511A (zh) * 2017-05-23 2020-07-03 莱战略控股公司 用于气溶胶递送设备的心率监测器
US10709173B2 (en) 2014-02-06 2020-07-14 Juul Labs, Inc. Vaporizer apparatus
US10736359B2 (en) 2016-12-02 2020-08-11 VMR Products, LLC Cartridge-based vaporizers
US10765817B2 (en) 2014-08-13 2020-09-08 Elwha, Llc Methods, systems, and devices related to delivery of alcohol with an inhaler
CN111670027A (zh) * 2018-02-01 2020-09-15 赛德玛公司 环肽在美容中的用途
EP3711800A1 (en) * 2019-03-21 2020-09-23 Nerudia Limited Aerosol delivery system
EP3711799A1 (en) * 2019-03-21 2020-09-23 Nerudia Limited Aerosol delivery system
EP3711593A1 (en) * 2019-03-21 2020-09-23 Nerudia Limited Aerosol delivery system
EP3711598A1 (en) * 2019-03-21 2020-09-23 Nerudia Limited Aerosol delivery system
EP3711798A1 (en) * 2019-03-21 2020-09-23 Nerudia Limited Aerosol delivery system
EP3711802A1 (en) * 2019-03-21 2020-09-23 Nerudia Limited Aerosol delivery system
WO2020187937A1 (en) * 2019-03-21 2020-09-24 Nerudia Limited Aerosol delivery system
US20200315253A1 (en) * 2019-04-02 2020-10-08 Juul Labs, Inc. Fixed dose cartridge for vaporizer device
US10820855B2 (en) 2014-08-13 2020-11-03 Elwha Llc Systems, methods, and devices to incentivize inhaler use
CN111920096A (zh) * 2019-05-13 2020-11-13 西姆雷尔收藏有限责任公司 具有混合室的汽化器冷却系统
CN111990695A (zh) * 2015-05-06 2020-11-27 奥驰亚客户服务有限责任公司 非燃烧吸烟装置及其元件
US10865001B2 (en) 2016-02-11 2020-12-15 Juul Labs, Inc. Fillable vaporizer cartridge and method of filling
US10912333B2 (en) 2016-02-25 2021-02-09 Juul Labs, Inc. Vaporization device control systems and methods
CN112512347A (zh) * 2018-08-21 2021-03-16 菲利普莫里斯生产公司 用于气溶胶生成装置的消耗品以及填充和制造用于气溶胶生成装置的消耗品的方法
IT201900018632A1 (it) * 2019-10-11 2021-04-11 Matteo Ratti Composizione per trattare le corde vocali di un soggetto
US11019685B2 (en) 2014-02-06 2021-05-25 Juul Labs, Inc. Vaporization device systems and methods
USD920570S1 (en) 2019-11-13 2021-05-25 Canopy Growth Corporation Vaporizer cartridge
USD920571S1 (en) 2019-11-20 2021-05-25 Canopy Growth Corporation Vaporizer cartridge
US11026451B2 (en) 2017-06-01 2021-06-08 Fontem Holdings 1 B.V. Electronic cigarette fluid pump
US11033049B2 (en) 2018-08-01 2021-06-15 R.J. Reynolds Tobacco Company Apparatus for recovering tobacco material and related method
US11053395B2 (en) 2017-06-12 2021-07-06 Altria Client Services Llc Corrosion-resistant reservoir for an e-vaping device and method of manufacturing thereof
CN113208148A (zh) * 2021-05-12 2021-08-06 云南中烟工业有限责任公司 一种协同释放尼古丁和致香成分的超分子凝胶
US11085550B2 (en) 2014-02-28 2021-08-10 Ayr Ltd. Electronic vaporiser system
US20210299366A1 (en) * 2020-03-31 2021-09-30 Pu Yuan Biotech Co., Ltd. Breathing airflow detecting device for a nebulizing device
US20210338948A1 (en) * 2020-04-30 2021-11-04 Mcneil Ab Biomarker Based Nicotine Replacement Therapy
CN113840547A (zh) * 2019-05-06 2021-12-24 进立有限公司 用于微型蒸发器的平板加热元件
US11241044B2 (en) 2018-07-23 2022-02-08 Juul Labs, Inc. Airflow management for vaporizer device
US11253001B2 (en) 2019-02-28 2022-02-22 Juul Labs, Inc. Vaporizer device with vaporizer cartridge
US11300114B2 (en) * 2018-12-24 2022-04-12 Zhenjiang Chen Automatic e-liquid transportation system and method of electronic cigarette as well as peristaltic pump
US11298477B2 (en) * 2014-06-30 2022-04-12 Syqe Medical Ltd. Methods, devices and systems for pulmonary delivery of active agents
US20220125109A1 (en) * 2019-01-15 2022-04-28 Philip Morris Products S.A. Aerosol-generating device with movable top cover
US11317654B2 (en) * 2016-07-07 2022-05-03 Altria Client Services Llc Additive assembly for electronic vaping device
US11351314B2 (en) * 2016-08-09 2022-06-07 Hauni Maschinenbau Gmbh Inhaler and fluid reservoir for an inhaler
US20220202097A1 (en) * 2019-09-20 2022-06-30 Nerudia Limited Smoking substitute apparatus
US20220256919A1 (en) * 2019-09-20 2022-08-18 Nerudia Limited Smoking substitute apparatus
US20220273020A1 (en) * 2013-07-19 2022-09-01 Altria Client Services Llc Liquid aerosol formulation of an electronic smoking article
RU213319U1 (ru) * 2022-02-21 2022-09-06 Общество с ограниченной ответственностью "Небулайзер" Портативный компрессорный ингалятор с подогревом аэрозоля
US11446244B2 (en) * 2020-01-17 2022-09-20 Matthew McLeay Compositions containing verteporfin, ribavirin, gemcitabine, or combinations thereof and methods of use for treating COVID-19, cancer, or non cancer diseases
US20220295896A1 (en) * 2019-07-03 2022-09-22 Airja, Inc. Aerosol delivery devices and methods of using same
US20220295905A1 (en) * 2016-07-25 2022-09-22 Altria Client Services Llc Manufacturing a fluid permeable heater assembly with cap
US11464082B2 (en) 2018-07-31 2022-10-04 Juul Labs, Inc. Cartridge-based heat not burn vaporizer
US11458267B2 (en) 2017-10-17 2022-10-04 Pneuma Respiratory, Inc. Nasal drug delivery apparatus and methods of use
US11464921B2 (en) 2018-11-05 2022-10-11 Juul Labs, Inc. Cartridges for vaporizer devices
US11529476B2 (en) 2017-05-19 2022-12-20 Pneuma Respiratory, Inc. Dry powder delivery device and methods of use
US11564287B2 (en) 2018-11-05 2023-01-24 Juul Labs, Inc. Cartridges with vaporizable material including at least one ionic component
IT202100021824A1 (it) * 2021-08-12 2023-02-12 E Liquid Labs S R L Formulazione liquida aromatizzata per sigaretta elettronica
US11589621B2 (en) 2017-05-23 2023-02-28 Rai Strategic Holdings, Inc. Heart rate monitor for an aerosol delivery device
US20230063372A1 (en) * 2015-02-20 2023-03-02 Zorday IP, LLC Systems and methods for intelligent vaporizers
WO2023039266A1 (en) * 2021-09-12 2023-03-16 Niconox Llc Delivery devices and compositions
US11612185B2 (en) * 2016-06-29 2023-03-28 Nicoventures Trading Limited Article for use with apparatus for heating smokable material
WO2023052097A1 (en) * 2021-09-28 2023-04-06 Nerudia Limited Smoking substitute apparatus
US20230112752A1 (en) * 2015-02-19 2023-04-13 Zorday IP, LLC Systems and methods for intelligent vaporizers
US11684080B2 (en) * 2018-10-24 2023-06-27 Zanoprima Lifesciences Limited Electronic cigarette compositions, devices, and related methods
US11690396B2 (en) 2018-10-24 2023-07-04 Zanoprima Lifesciences Limited Electronic cigarette compositions, devices, and related methods
US11738158B2 (en) 2017-10-04 2023-08-29 Pneuma Respiratory, Inc. Electronic breath actuated in-line droplet delivery device and methods of use
US11771852B2 (en) 2017-11-08 2023-10-03 Pneuma Respiratory, Inc. Electronic breath actuated in-line droplet delivery device with small volume ampoule and methods of use
US11793945B2 (en) 2021-06-22 2023-10-24 Pneuma Respiratory, Inc. Droplet delivery device with push ejection
US11806331B2 (en) 2016-01-06 2023-11-07 Syqe Medical Ltd. Low dose therapeutic treatment
US11825565B2 (en) 2014-06-14 2023-11-21 Evolv, Llc Electronic vaporizer having temperature sensing and limit
US11838997B2 (en) 2018-11-05 2023-12-05 Juul Labs, Inc. Cartridges for vaporizer devices
US11911557B2 (en) 2018-10-15 2024-02-27 Juul Labs, Inc. Heating element
US20240114949A1 (en) * 2019-10-09 2024-04-11 Nicoventures Trading Limited Aerosolizable material
US11998681B2 (en) 2019-07-03 2024-06-04 Airja, Inc. Aerosol delivery devices and methods of using same

Families Citing this family (71)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11517042B2 (en) 2012-04-25 2022-12-06 Altria Client Services Llc Digital marketing applications for electronic cigarette users
JP6689188B2 (ja) 2013-03-15 2020-04-28 ザ ジェネラル ホスピタル コーポレイション 一酸化窒素の吸気合成
MX370384B (es) 2013-03-15 2019-12-11 Massachusetts Gen Hospital Sintesis de gas de oxido nitrico para inhalacion.
CA2913000A1 (en) 2013-05-20 2014-12-11 Sis Resources, Ltd. Application development for a network with an electronic cigarette
PL3698832T3 (pl) * 2014-01-22 2023-01-30 Fontem Ventures B.V. Sposoby i urządzenia do łagodzenia potrzeby palenia
CA2953073A1 (en) * 2014-06-30 2016-01-07 Syqe Medical Ltd. Methods, devices and systems for pulmonary delivery of active agents
WO2016050245A1 (en) * 2014-10-03 2016-04-07 Fertin Pharma A/S Electronic nicotine delivery system
AU2015336055B2 (en) * 2014-10-20 2020-07-16 The General Hospital Corporation Systems and methods for the synthesis of nitric oxide
GB201501951D0 (en) 2015-02-05 2015-03-25 Jt Int Sa Aerosol guiding device and aerosol generating system comprising said aerosol guiding device
GB201501950D0 (en) * 2015-02-05 2015-03-25 Jt Int Sa Aerosol guiding device and aerosol generating system comprising said aerosol guiding device
MY184410A (en) 2015-04-02 2021-04-01 Japan Tobacco Inc Flavor inhaler
KR102643274B1 (ko) * 2015-04-15 2024-03-05 필립모리스 프로덕츠 에스.에이. 이중 저항 건조 분말 흡입기
EP3135137B1 (en) * 2015-08-28 2021-04-28 Fontem Holdings 1 B.V. Electronic smoking device with additive reservoir
EP3135136B1 (en) * 2015-08-28 2018-07-11 Fontem Holdings 1 B.V. Liquid reservoir with two storage volumes and atomizer/liquid reservoir portion as well as electronic smoking device with liquid reservoir
GB2542389A (en) * 2015-09-17 2017-03-22 Kind Consumer Ltd Simulated cigarette
MX2018009248A (es) * 2016-02-01 2019-01-21 Incarda Therapeutics Inc Combinacion de monitoreo electronico con terapia farmacologica inhalada para manejar arritmias cardiacas incluyendo fibrilacion auricular.
CN105597201A (zh) * 2016-02-04 2016-05-25 深圳金亿帝医疗设备股份有限公司 雾化器及雾化器主体
DE202016100917U1 (de) 2016-02-22 2016-03-09 Türk & Hillinger GmbH Luft- und/oder Aerosolerhitzer
GB201605105D0 (en) 2016-03-24 2016-05-11 Nicoventures Holdings Ltd Vapour provision apparatus
GB201605100D0 (en) * 2016-03-24 2016-05-11 Nicoventures Holdings Ltd Vapour provision system
GB201605101D0 (en) 2016-03-24 2016-05-11 Nicoventures Holdings Ltd Electronic vapour provision system
KR20190005839A (ko) 2016-03-25 2019-01-16 더 제너럴 하스피탈 코포레이션 산화질소의 전기 플라즈마 합성을 위한 전달 시스템 및 방법
ITUA20162410A1 (it) 2016-04-08 2017-10-08 Gd Spa Metodo ed unità di ispezione di un organo riscaldante per sigaretta elettronica.
CN109561732B (zh) * 2016-07-27 2021-06-29 日本烟草产业株式会社 香味吸入器、烟弹及香味单元
CA3026391A1 (en) * 2016-08-10 2018-02-15 Gary Stephen Shuster Vaporization improvements
WO2018045263A1 (en) * 2016-09-02 2018-03-08 Inspirx, Inc. Breath-enhanced jet nebulizer
ES2924804T3 (es) 2016-12-27 2022-10-11 Juul Labs Inc Mecha térmica para vaporizadores electrónicos
GB201700136D0 (en) 2017-01-05 2017-02-22 British American Tobacco Investments Ltd Aerosol generating device and article
GB201700620D0 (en) 2017-01-13 2017-03-01 British American Tobacco Investments Ltd Aerosol generating device and article
MX2020010523A (es) 2017-02-27 2021-02-09 Third Pole Inc Sistemas y metodos para generar oxido nitrico.
WO2018157172A1 (en) 2017-02-27 2018-08-30 Third Pole, Inc. Systems and methods for generating nitric oxide
AU2018224329B2 (en) 2017-02-27 2019-11-28 Third Pole, Inc. Systems and methods for ambulatory generation of nitric oxide
CA3058472C (en) 2017-03-31 2020-05-26 The General Hospital Corporation Systems and methods for a cooled nitric oxide generator
GB201707050D0 (en) * 2017-05-03 2017-06-14 British American Tobacco Investments Ltd Data communication
RU2766733C2 (ru) * 2017-08-09 2022-03-15 Твенти Сикстин (2016) Фарма Лимитед Устройство для пульмонального введения
GB201720338D0 (en) 2017-12-06 2018-01-17 British American Tobacco Investments Ltd Component for an aerosol-generating apparatus
GB201722278D0 (en) 2017-12-29 2018-02-14 British American Tobacco Investments Ltd Device identification and method
GB201722241D0 (en) 2017-12-29 2018-02-14 British American Tobacco Investments Ltd Data capture across devices
US11565059B2 (en) 2018-02-27 2023-01-31 Juul Labs, Inc. Mass output controlled vaporizer
US11986590B2 (en) 2018-06-26 2024-05-21 Juul Labs, Inc. Vaporizer wicking elements including a hollow core
US20200035118A1 (en) * 2018-07-27 2020-01-30 Joseph Pandolfino Methods and products to facilitate smokers switching to a tobacco heating product or e-cigarettes
US11413409B2 (en) 2018-09-12 2022-08-16 Juul Labs, Inc. Vaporizer including positive temperature coefficient of resistivity (PTCR) heating element
CN113164697B (zh) * 2018-10-28 2023-12-05 Syqe医药有限公司 送药盒单元配合件
CN113365518A (zh) * 2018-11-05 2021-09-07 尤尔实验室有限公司 用于蒸发器装置的料筒
TR201900204A2 (tr) * 2019-01-08 2019-02-21 Ali Raif Ilac Sanayi Ve Ticaret Anonim Sirketi İnhalasyon yolu i̇le pi̇rfeni̇don uygulanmasi
DE102019103990B4 (de) * 2019-02-18 2021-09-02 Hauni Maschinenbau Gmbh Verdampfereinsatz für einen Inhalator, insbesondere ein elektronisches Zigarettenprodukt, Verdampfer-Tank-Einheit und ein elektronisches Zigarettenprodukt
EP3711591A1 (en) * 2019-03-21 2020-09-23 Nerudia Limited Aerosol delivery system
JP2022533628A (ja) 2019-05-15 2022-07-25 サード ポール，インコーポレイテッド 一酸化窒素生成用電極
EP3969416A4 (en) 2019-05-15 2023-11-01 Third Pole, Inc. SYSTEMS AND METHODS FOR GENERATING NITRIC OXIDE
DE102019114473A1 (de) 2019-05-29 2020-12-03 Hauni Maschinenbau Gmbh Verdampfungsvorrichtung für einen elektrischen Inhalator
CN110169606B (zh) * 2019-05-31 2022-05-06 广州市澳键丰泽生物科技股份有限公司 一种加热不燃烧发烟颗粒及其制备方法和应用
KR102259895B1 (ko) * 2019-07-19 2021-06-02 주식회사 케이티앤지 에어로졸 생성 장치
US11020384B2 (en) 2019-08-01 2021-06-01 Incarda Therapeutics, Inc. Antiarrhythmic formulation
CN110367582A (zh) * 2019-08-30 2019-10-25 深圳雾芯科技有限公司 电子烟液
RU2717907C1 (ru) * 2019-09-16 2020-03-26 Федеральное государственное унитарное предприятие "Центральный аэрогидродинамический институт имени профессора Н.Е. Жуковского" (ФГУП "ЦАГИ") Дымогенератор
EP3795006A1 (en) * 2019-09-20 2021-03-24 Nerudia Limited Smoking substitute apparatus
EP3795005A1 (en) * 2019-09-20 2021-03-24 Nerudia Limited Smoking substitute apparatus
GB201914951D0 (en) * 2019-10-16 2019-11-27 Nicoventures Trading Ltd Aerosol provision system and method
KR102330310B1 (ko) * 2019-12-27 2021-11-24 주식회사 케이티앤지 모드에 따라 시각적으로 다른 증기를 배출하는 에어로졸 생성 장치
KR102437768B1 (ko) * 2019-12-27 2022-08-29 주식회사 케이티앤지 에어로졸 생성 장치
WO2021142472A1 (en) 2020-01-11 2021-07-15 Third Pole, Inc. Systems and methods for nitric oxide generation with humidity control
DE102020103417B4 (de) * 2020-02-11 2021-08-26 Hauni Maschinenbau Gmbh Flüssigkeitsbehälter für einen Inhalator
KR102427856B1 (ko) * 2020-04-13 2022-08-01 주식회사 케이티앤지 에어로졸 생성 장치 및 이를 제어하는 방법
US20210395905A1 (en) 2020-06-18 2021-12-23 Third Pole, Inc. Systems and methods for preventing and treating infections with nitric oxide
WO2022091316A1 (ja) * 2020-10-30 2022-05-05 日本たばこ産業株式会社 口腔内洗浄方法及び口腔内洗浄用エアロゾル発生装置
WO2022091317A1 (ja) * 2020-10-30 2022-05-05 日本たばこ産業株式会社 エアロゾルを用いて行う口腔内洗浄に使用される洗口液、カートリッジ、口腔内洗浄用エアロゾル発生装置、及び口腔内洗浄方法
CN112891545B (zh) * 2021-03-12 2022-06-07 中国药科大学 一种抗肝纤维化组合物及其应用
DE102021202546A1 (de) 2021-03-16 2022-09-22 Alveon GmbH Inhalator
WO2023049873A1 (en) 2021-09-23 2023-03-30 Third Pole, Inc. Systems and methods for delivering nitric oxide
US11957178B2 (en) 2021-11-15 2024-04-16 Apackaging Group Llc Aerosol actuator
CN114652734A (zh) * 2022-03-31 2022-06-24 李红梦 一种祛痘的药物组合物及其制备方法

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020168322A1 (en) * 1998-10-09 2002-11-14 Andrew Clark Flow resistance modulated aerosolized active agent delivery

Family Cites Families (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4243605A (en) 1976-05-17 1981-01-06 Union Carbide Corporation Novel isocyanates
US5015741A (en) 1989-10-03 1991-05-14 Philip Morris Incorporated Nicotine analogs
US5666977A (en) * 1993-06-10 1997-09-16 Philip Morris Incorporated Electrical smoking article using liquid tobacco flavor medium delivery system
PT706352E (pt) * 1993-06-29 2002-07-31 Ponwell Entpr Ltd Distribuidor
CN1259984C (zh) * 1993-06-29 2006-06-21 茵捷特数码浮质有限公司 利用吸入方式服用物质的方法和器具
US5743251A (en) * 1996-05-15 1998-04-28 Philip Morris Incorporated Aerosol and a method and apparatus for generating an aerosol
CN1106812C (zh) * 1996-06-17 2003-04-30 日本烟业产业株式会社 香味生成物品
US6234167B1 (en) * 1998-10-14 2001-05-22 Chrysalis Technologies, Incorporated Aerosol generator and methods of making and using an aerosol generator
US6196218B1 (en) * 1999-02-24 2001-03-06 Ponwell Enterprises Ltd Piezo inhaler
US6796956B2 (en) * 1999-04-30 2004-09-28 Medtronic, Inc. Method and apparatus to control drug therapy dosages in an implantable pump
AU2001286875A1 (en) 2000-08-30 2002-03-13 University Of Kentucky Research Foundation Bridged nicotine compounds for use in the treatment of cns pathologies
US20030051728A1 (en) * 2001-06-05 2003-03-20 Lloyd Peter M. Method and device for delivering a physiologically active compound
WO2003094900A1 (en) * 2002-05-13 2003-11-20 Alexza Molecular Delivery Corporation Delivery of drug amines through an inhalation route
US7681572B2 (en) 2002-08-20 2010-03-23 Aga Ab Method and devices for administration of therapeutic gases
ATE491521T1 (de) * 2002-09-06 2011-01-15 Philip Morris Usa Inc Aerosolerzeugungsvorrichtungen und verfahren zur erzeugung von aerosolen mit gesteuerten teilchengrössen
US7913688B2 (en) * 2002-11-27 2011-03-29 Alexza Pharmaceuticals, Inc. Inhalation device for producing a drug aerosol
CN100381083C (zh) * 2003-04-29 2008-04-16 韩力 一种非可燃性电子喷雾香烟
US6995265B2 (en) 2003-08-26 2006-02-07 North Carolina State University Synthesis of nicotine derivatives from nicotine
ES2559410T3 (es) * 2004-04-23 2016-02-12 Philip Morris Products S.A. Generadores de aerosol y métodos para producir aerosoles
US9604016B2 (en) * 2006-01-31 2017-03-28 Philip Morris Usa Inc. Bent capillary tube aerosol generator
CN201067079Y (zh) * 2006-05-16 2008-06-04 韩力 仿真气溶胶吸入器
EP2218760B1 (en) * 2007-11-30 2015-09-02 Japan Tobacco Inc. Aerosol-generating solution for aerosol aspirator
CN201208444Y (zh) * 2008-06-06 2009-03-18 王京 新型雾化器
EP2319334A1 (en) * 2009-10-27 2011-05-11 Philip Morris Products S.A. A smoking system having a liquid storage portion
EP2555642A1 (en) * 2010-04-06 2013-02-13 Oglesby&Butler Research&Development Limited A portable handheld vaporising device
CN103209728B (zh) * 2010-09-24 2015-10-14 多诺万·B.·耶茨 紧凑、低流阻的气溶胶发生器及其操作方法
CN102160906B (zh) * 2010-11-01 2012-08-08 常州市富艾发进出口有限公司 口吸式便携雾化器
CN202014571U (zh) * 2011-03-30 2011-10-26 深圳市康泰尔电子有限公司 烟液可控式电子香烟

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020168322A1 (en) * 1998-10-09 2002-11-14 Andrew Clark Flow resistance modulated aerosolized active agent delivery

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Flow3d, Thermal bubble jets, downloaded online 1/5/2017. *

Cited By (316)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10244793B2 (en) 2005-07-19 2019-04-02 Juul Labs, Inc. Devices for vaporization of a substance
US11766399B2 (en) 2010-12-22 2023-09-26 Syqe Medical Ltd. Method and system for drug delivery
US11071712B2 (en) 2010-12-22 2021-07-27 Syqe Medical Ltd. Method and system for drug delivery
US20170360089A1 (en) 2010-12-22 2017-12-21 Syqe Medical Ltd. Method and system for drug delivery
US12023436B2 (en) 2011-10-28 2024-07-02 Evolv, Llc Electronic vaporizer that simulates smoking with power control
US10264820B2 (en) 2011-10-28 2019-04-23 Evolv, Llc Electronic vaporizer that simulates smoking with power control
US9795682B2 (en) * 2012-05-16 2017-10-24 Louise M Smith Beverages with compositions of vinegar
US20140255525A1 (en) * 2012-05-16 2014-09-11 Louise M Smith Beverages with compositions of vinegar
US10034988B2 (en) 2012-11-28 2018-07-31 Fontem Holdings I B.V. Methods and devices for compound delivery
US20150351457A1 (en) * 2013-01-05 2015-12-10 Qiuming Liu Electronic cigarette and method for adjusting flow rate of gas flow of electronic cigarette
US10306924B2 (en) 2013-03-14 2019-06-04 Rai Strategic Holdings, Inc. Atomizer for an aerosol delivery device formed from a continuously extending wire and related input, cartridge, and method
US10638792B2 (en) 2013-03-15 2020-05-05 Juul Labs, Inc. Securely attaching cartridges for vaporizer devices
US10279934B2 (en) 2013-03-15 2019-05-07 Juul Labs, Inc. Fillable vaporizer cartridge and method of filling
US20220273020A1 (en) * 2013-07-19 2022-09-01 Altria Client Services Llc Liquid aerosol formulation of an electronic smoking article
US10231487B2 (en) 2013-07-24 2019-03-19 Nu Mark Innovations Ltd. Solid core electronic cigarette
US20150027455A1 (en) * 2013-07-24 2015-01-29 Sis Resources, Ltd. Solid core electronic cigarette
US9955727B2 (en) * 2013-07-24 2018-05-01 Nu Mark Innovations Ltd. Solid core electronic cigarette
US10194693B2 (en) * 2013-09-20 2019-02-05 Fontem Holdings 1 B.V. Aerosol generating device
US20150196060A1 (en) * 2013-09-20 2015-07-16 E-Nicotine Technology, Inc. Devices and methods for modifying delivery devices
US11134719B2 (en) 2013-11-01 2021-10-05 Philter Labs, Inc. E-cigarette with valve allowing exhale filter
US20190082740A1 (en) * 2013-11-12 2019-03-21 VMR Products LLC. Vaporizer
US11134722B2 (en) * 2013-11-12 2021-10-05 Vmr Products Llc Vaporizer
US10653186B2 (en) 2013-11-12 2020-05-19 VMR Products, LLC Vaporizer, charger and methods of use
US10667561B2 (en) 2013-11-12 2020-06-02 Vmr Products Llc Vaporizer
US11606981B2 (en) 2013-11-12 2023-03-21 Vmr Products Llc Vaporizer
US10736360B2 (en) 2013-11-12 2020-08-11 Vmr Products Llc Vaporizer, charger and methods of use
US10980273B2 (en) 2013-11-12 2021-04-20 VMR Products, LLC Vaporizer, charger and methods of use
US11051557B2 (en) * 2013-11-12 2021-07-06 VMR Products, LLC Vaporizer
US11246337B2 (en) * 2013-12-05 2022-02-15 Philip Morris Products S.A. Heated aerosol generating article with air-flow barrier
US20160295917A1 (en) * 2013-12-05 2016-10-13 Philip Morris Products S.A. Heated aerosol generating article with air-flow barrier
US10701975B2 (en) 2013-12-23 2020-07-07 Juul Labs, Inc. Vaporization device systems and methods
US10045567B2 (en) 2013-12-23 2018-08-14 Juul Labs, Inc. Vaporization device systems and methods
US10104915B2 (en) 2013-12-23 2018-10-23 Juul Labs, Inc. Securely attaching cartridges for vaporizer devices
US10993471B2 (en) 2013-12-23 2021-05-04 Juul Labs, Inc. Vaporization device systems and methods
US10986867B2 (en) 2013-12-23 2021-04-27 Juul Labs, Inc. Vaporization device systems and methods
US10117465B2 (en) 2013-12-23 2018-11-06 Juul Labs, Inc. Vaporization device systems and methods
US10912331B2 (en) 2013-12-23 2021-02-09 Juul Labs, Inc. Vaporization device systems and methods
US10117466B2 (en) * 2013-12-23 2018-11-06 Juul Labs, Inc. Vaporization device systems and methods
US10076139B2 (en) 2013-12-23 2018-09-18 Juul Labs, Inc. Vaporizer apparatus
US10070669B2 (en) 2013-12-23 2018-09-11 Juul Labs, Inc. Cartridge for use with a vaporizer device
US10159282B2 (en) 2013-12-23 2018-12-25 Juul Labs, Inc. Cartridge for use with a vaporizer device
US10111470B2 (en) 2013-12-23 2018-10-30 Juul Labs, Inc. Vaporizer apparatus
US10058129B2 (en) * 2013-12-23 2018-08-28 Juul Labs, Inc. Vaporization device systems and methods
US10667560B2 (en) 2013-12-23 2020-06-02 Juul Labs, Inc. Vaporizer apparatus
US20170095005A1 (en) * 2013-12-23 2017-04-06 James Monsees Vaporization device systems and methods
US10058130B2 (en) 2013-12-23 2018-08-28 Juul Labs, Inc. Cartridge for use with a vaporizer device
US10058124B2 (en) 2013-12-23 2018-08-28 Juul Labs, Inc. Vaporization device systems and methods
US10045568B2 (en) 2013-12-23 2018-08-14 Juul Labs, Inc. Vaporization device systems and methods
US10201190B2 (en) 2013-12-23 2019-02-12 Juul Labs, Inc. Cartridge for use with a vaporizer device
US11992044B2 (en) 2013-12-23 2024-05-28 Juul Labs, Inc. Vaporization device systems and methods
US11752283B2 (en) 2013-12-23 2023-09-12 Juul Labs, Inc. Vaporization device systems and methods
US10264823B2 (en) 2013-12-23 2019-04-23 Juul Labs, Inc. Vaporization device systems and methods
US9744320B2 (en) * 2014-02-04 2017-08-29 George Wakalopulos Electric wick and heater for portable vaporizer
US20150217068A1 (en) * 2014-02-04 2015-08-06 George Wakalopulos Electric wick and heater for portable vaporizer
US11452177B2 (en) 2014-02-06 2022-09-20 Juul Labs, Inc. Vaporization device systems and methods
US11019685B2 (en) 2014-02-06 2021-05-25 Juul Labs, Inc. Vaporization device systems and methods
US10709173B2 (en) 2014-02-06 2020-07-14 Juul Labs, Inc. Vaporizer apparatus
US10287155B2 (en) 2014-02-28 2019-05-14 Ayr Ltd. Electronic vaporizer system
US20190069603A1 (en) * 2014-02-28 2019-03-07 Beyond Twenty Ltd. E-cigarette personal vaporizer
US11085550B2 (en) 2014-02-28 2021-08-10 Ayr Ltd. Electronic vaporiser system
US10472226B2 (en) 2014-02-28 2019-11-12 Ayr Ltd. Electronic vaporiser system
US11571019B2 (en) 2014-02-28 2023-02-07 Ayr Ltd. Electronic vaporiser system
US10287154B2 (en) 2014-02-28 2019-05-14 Ayr Ltd. Electronic vaporiser system
US10266388B2 (en) 2014-02-28 2019-04-23 Beyond Twenty Ltd. Electronic vaporiser system
US10624394B2 (en) * 2014-02-28 2020-04-21 Ayr Ltd. E-cigarette personal vaporizer
US10588176B2 (en) 2014-02-28 2020-03-10 Ayr Ltd. Electronic vaporiser system
US9918495B2 (en) * 2014-02-28 2018-03-20 Rai Strategic Holdings, Inc. Atomizer for an aerosol delivery device and related input, aerosol production assembly, cartridge, and method
US10285430B2 (en) 2014-02-28 2019-05-14 Ayr Ltd. Electronic vaporiser system
US11083228B2 (en) 2014-02-28 2021-08-10 Ayr Ltd. E-cigarette personal vaporizer
US11234463B2 (en) 2014-02-28 2022-02-01 Rai Strategic Holdings, Inc. Atomizer for an aerosol delivery device and related input, aerosol production assembly, cartridge, and method
US20150245659A1 (en) * 2014-02-28 2015-09-03 R.J. Reynolds Tobacco Company Atomizer for an aerosol delivery device and related input, aerosol production assembly, cartridge, and method
US20150272216A1 (en) * 2014-03-31 2015-10-01 Westfield Limited (Ltd.) Personal vaporizer with liquid supply by suction
US9642397B2 (en) * 2014-03-31 2017-05-09 Westfield Limited (Ltd.) Personal vaporizer with liquid supply by suction
US11160309B2 (en) * 2014-05-21 2021-11-02 Philip Morris Products S.A. Aerosol-generating system comprising a cartridge with an internal air flow passage
US20170105452A1 (en) * 2014-05-21 2017-04-20 Philip Morris Products S.A. Aerosol-generating system comprising a cartridge with an internal air flow passage
US20150335074A1 (en) * 2014-05-22 2015-11-26 Nuryan Holdings Limited Handheld vaporizing device
US10334878B2 (en) * 2014-05-22 2019-07-02 Nuryan Holdings Limited Handheld vaporizing device
US10492531B2 (en) * 2014-05-28 2019-12-03 Huizhou Kimree Technology Co., Ltd., Shenzhen Branch Information pushing method and communication system
US11825565B2 (en) 2014-06-14 2023-11-21 Evolv, Llc Electronic vaporizer having temperature sensing and limit
US9886836B2 (en) * 2014-06-19 2018-02-06 Huizhou Kimree Technology Co., Ltd. Shenzhen Branch Data communication method and system
US20160284197A1 (en) * 2014-06-19 2016-09-29 Kimree Hi-Tech Inc. Data communication method and system
US20170135402A1 (en) * 2014-06-27 2017-05-18 Fontem Holdings 1 B.V. Electronic smoking device and capsule system
US10912335B2 (en) * 2014-06-27 2021-02-09 Fontem Holdings 1 B.V. Electronic smoking device and capsule system
US10080851B2 (en) 2014-06-30 2018-09-25 Syqe Medical Ltd. Method and device for vaporization and inhalation of isolated substances
US10118006B2 (en) * 2014-06-30 2018-11-06 Syqe Medical Ltd. Methods, devices and systems for pulmonary delivery of active agents
US10099020B2 (en) 2014-06-30 2018-10-16 Syqe Medical Ltd. Drug dose cartridge for an inhaler device
AU2015283590B2 (en) * 2014-06-30 2020-04-16 Syqe Medical Ltd. Methods, devices and systems for pulmonary delivery of active agents
US20170157343A1 (en) * 2014-06-30 2017-06-08 Syqe Medical Ltd. Methods, devices and systems for pulmonary delivery of active agents
US12016997B2 (en) 2014-06-30 2024-06-25 Syqe Medical Ltd. Flow regulating inhaler device
US11291781B2 (en) 2014-06-30 2022-04-05 Syqe Medical Ltd. Flow regulating inhaler device
US20220211958A1 (en) * 2014-06-30 2022-07-07 Syqe Medical Ltd. Methods, devices and systems for pulmonary delivery of active agents
US10166349B2 (en) 2014-06-30 2019-01-01 Syqe Medical Ltd. Flow regulating inhaler device
US9993602B2 (en) 2014-06-30 2018-06-12 Syqe Medical Ltd. Flow regulating inhaler device
US9839241B2 (en) 2014-06-30 2017-12-12 Syqe Medical Ltd. Methods, devices and systems for pulmonary delivery of active agents
US9802011B2 (en) 2014-06-30 2017-10-31 Syqe Medical Ltd. Drug dose cartridge for an inhaler device
US11160937B2 (en) 2014-06-30 2021-11-02 Syqe Medical Ltd. Drug dose cartridge for an inhaler device
US11298477B2 (en) * 2014-06-30 2022-04-12 Syqe Medical Ltd. Methods, devices and systems for pulmonary delivery of active agents
US10369304B2 (en) 2014-06-30 2019-08-06 Syqe Medical Ltd. Flow regulating inhaler device
US11311480B2 (en) 2014-06-30 2022-04-26 Syqe Medical Ltd. Method and device for vaporization and inhalation of isolated substances
WO2016019353A1 (en) * 2014-07-31 2016-02-04 MJAR Holdings, LLC Electronic cigarettes, cartridges, and inhalable formulations of medicinal cannabis compounds, and apparatuses and methods for making and using the same
US20160045685A1 (en) * 2014-08-13 2016-02-18 Elwha Llc Methods, systems, and devices related to a supplemental inhaler
US10987048B2 (en) 2014-08-13 2021-04-27 Elwha Llc Systems, methods, and devices to incentivize inhaler use
US10820855B2 (en) 2014-08-13 2020-11-03 Elwha Llc Systems, methods, and devices to incentivize inhaler use
US10765817B2 (en) 2014-08-13 2020-09-08 Elwha, Llc Methods, systems, and devices related to delivery of alcohol with an inhaler
US10245393B2 (en) * 2014-08-13 2019-04-02 Elwha Llc Methods, systems, and devices related to a supplemental inhaler
WO2016040575A1 (en) * 2014-09-10 2016-03-17 Fontem Holdings 1 B.V. Methods and devices for modulating air flow in delivery devices
CN107847696A (zh) * 2014-09-10 2018-03-27 方特慕控股第私人有限公司 用于调节递送装置中的气流的方法和装置
US10898660B2 (en) 2014-09-10 2021-01-26 Fontem Holdings 1 B.V. Methods and devices for modulating air flow in delivery devices
US20160270446A1 (en) * 2014-11-03 2016-09-22 Yuval Shenkal E-Cigarette with Valve Allowing Exhale Filter
US10617148B2 (en) * 2014-11-03 2020-04-14 Philter Labs Incorporated E-cigarette with valve allowing exhale filter
US20160136213A1 (en) * 2014-11-14 2016-05-19 Charles William Paul Process to suspend cannabis oil in glycerin
US10226076B2 (en) 2014-11-17 2019-03-12 Mcneil Ab Disposable cartridge for use in an electronic nicotine delivery system
US10542781B2 (en) 2014-11-17 2020-01-28 Mcneil Ab Electronic nicotine delivery system
US10531692B2 (en) 2014-11-17 2020-01-14 Mcneil Ab Disposable cartridge for use in an electronic nicotine delivery system
US10188148B2 (en) 2014-11-17 2019-01-29 Mcneil Ab Electronic nicotine delivery system
US10791768B2 (en) 2014-11-17 2020-10-06 Mcneil Ab Disposable cartridge for use in an electronic nicotine delivery system
US10842199B2 (en) 2014-11-17 2020-11-24 Mcneil Ab Electronic nicotine delivery system
US10512282B2 (en) 2014-12-05 2019-12-24 Juul Labs, Inc. Calibrated dose control
US10888121B2 (en) * 2014-12-15 2021-01-12 Philip Morris Products S.A. E-liquid collapsible cartridge
WO2016096762A1 (en) * 2014-12-15 2016-06-23 Philip Morris Products S.A. E-liquid collapsible cartridge
RU2688978C2 (ru) * 2014-12-15 2019-05-23 Филип Моррис Продактс С.А. Система, генерирующая аэрозоль, содержащая подвижный картридж
CN106998819A (zh) * 2014-12-15 2017-08-01 菲利普莫里斯生产公司 使用文丘里效应向加热元件传递基质的气溶胶生成系统
CN106998815A (zh) * 2014-12-15 2017-08-01 菲利普莫里斯生产公司 包括可移动筒的气溶胶生成系统
WO2016096728A1 (en) * 2014-12-15 2016-06-23 Philip Morris Products S.A. Aerosol-generating system comprising moveable cartridge
US20180035717A1 (en) * 2014-12-15 2018-02-08 Philip Morris Products S.A. E-liquid collapsible cartridge
KR20170094145A (ko) * 2014-12-15 2017-08-17 필립모리스 프로덕츠 에스.에이. E-액체 압출식 카트리지
KR20170094150A (ko) * 2014-12-15 2017-08-17 필립모리스 프로덕츠 에스.에이. 가열 요소로 기재를 전달하기 위하여 벤츄리 효과를 이용하는 에어로졸-발생 시스템
KR20170094151A (ko) * 2014-12-15 2017-08-17 필립모리스 프로덕츠 에스.에이. 이동식 카트리지를 포함하는 에어로졸 발생 시스템
EP3232834B1 (en) 2014-12-15 2019-04-17 Philip Morris Products S.a.s. An aerosol-generating system using the venturi effect to deliver substrate to a heating element
US20170360093A1 (en) * 2014-12-15 2017-12-21 Philip Morris Products S.A. Aerosol-generating system using the venturi effect to deliver substrate to a heating element
US10638793B2 (en) 2014-12-15 2020-05-05 Philip Morris Products S.A. Aerosol-generating system comprising moveable cartridge
KR102560299B1 (ko) 2014-12-15 2023-07-27 필립모리스 프로덕츠 에스.에이. 이동식 카트리지를 포함하는 에어로졸 발생 시스템
WO2016096497A1 (en) * 2014-12-15 2016-06-23 Philip Morris Products S.A. An aerosol-generating system using the venturi effect to deliver substrate to a heating element
KR102592719B1 (ko) * 2014-12-15 2023-10-23 필립모리스 프로덕츠 에스.에이. 가열 요소로 기재를 전달하기 위하여 벤츄리 효과를 이용하는 에어로졸-발생 시스템
RU2701846C2 (ru) * 2014-12-15 2019-10-01 Филип Моррис Продактс С.А. Образующая аэрозоль система, использующая эффект вентури для доставки субстрата к нагревательному элементу
US11478807B2 (en) * 2014-12-15 2022-10-25 Philip Morris Products S.A. Aerosol-generating system using the venturi effect to deliver substrate to a heating element
RU2703120C2 (ru) * 2014-12-15 2019-10-15 Филип Моррис Продактс С.А. Сжимаемый картридж для жидкости для электронных сигарет
KR102492954B1 (ko) 2014-12-15 2023-01-30 필립모리스 프로덕츠 에스.에이. E-액체 압출식 카트리지
EP3247235A4 (en) * 2015-01-22 2019-01-16 Fontem Holdings 1 B.V. ELECTRONIC EVAPORATOR DEVICES
US11089660B2 (en) 2015-01-22 2021-08-10 Fontem Holdings 1 B.V. Electronic vaporization devices
CN107995846A (zh) * 2015-01-22 2018-05-04 方特慕控股第私人有限公司 电子蒸发装置
US10660366B2 (en) * 2015-01-30 2020-05-26 Fontem Holdings 4 B.V. Wick-positioning cartomizer
US20160219936A1 (en) * 2015-01-30 2016-08-04 Fontem Holdings 2 B.V. Wick-positioning cartomizer
US20230112752A1 (en) * 2015-02-19 2023-04-13 Zorday IP, LLC Systems and methods for intelligent vaporizers
US20230063372A1 (en) * 2015-02-20 2023-03-02 Zorday IP, LLC Systems and methods for intelligent vaporizers
US10765151B2 (en) * 2015-03-04 2020-09-08 Altria Client Services Llc E-vaping cartridge
US20180271172A1 (en) * 2015-03-04 2018-09-27 Altria Client Services Llc E-vaping cartridge
US10645970B2 (en) 2015-03-13 2020-05-12 Fontem Holdings 1 B.V. Aerosol generating component for an electronic smoking device, electronic smoking device and method for generating an inhalant
EP3066941A1 (en) * 2015-03-13 2016-09-14 Fontem Holdings 1 B.V. Aerosol generating component for an electronic smoking device, electronic smoking device and method for generating an inhalant
US10520089B2 (en) * 2015-04-17 2019-12-31 Fontem Holdings 1 B.V. Liquid supply with spiral container
US11076641B2 (en) 2015-04-17 2021-08-03 Fontem Holdings 1 B.V. Liquid supply with sealing agent in a spiral container
US20180080559A1 (en) * 2015-04-17 2018-03-22 Fontem Holdings 1 B.V. Liquid supply with spiral container
CN111990695A (zh) * 2015-05-06 2020-11-27 奥驰亚客户服务有限责任公司 非燃烧吸烟装置及其元件
EP3292774A4 (en) * 2015-05-22 2019-01-16 Japan Tobacco Inc. MANUFACTURING METHOD OF DISPOSAL UNIT, DISINDER UNIT AND COMBUSTION FREE SCRUB PASTE
US10887949B2 (en) * 2015-05-22 2021-01-05 Japan Tobacco Inc. Method for manufacturing atomizing unit, atomizing unit, and non-combustion type flavor inhaler
US20180092402A1 (en) * 2015-05-22 2018-04-05 Japan Tobacco Inc. Method for manufacturing atomizing unit, atomizing unit, and non-combustion type flavor inhaler
WO2016200382A1 (en) * 2015-06-10 2016-12-15 Evolv, Llc Electronic vaporizer having reduced particle size
US10362803B2 (en) 2015-06-10 2019-07-30 Evolv, Llc Electronic vaporizer having reduced particle size
US10251425B2 (en) 2015-07-06 2019-04-09 Njoy, Llc Vaporizing device with power component
US10874139B2 (en) * 2015-07-07 2020-12-29 Altria Client Services Llc E-vapor device including capsule containing pre-vapor formulation
US20170006917A1 (en) * 2015-07-07 2017-01-12 Altria Client Services Inc. E-vapor device including capsule containing pre-vapor formulation
US10039323B2 (en) * 2015-07-16 2018-08-07 Njoy, Llc Vaporizer tank with atomizer
US20170013878A1 (en) * 2015-07-16 2017-01-19 Njoy, Inc. Vaporizer tank with atomizer
CN108024575A (zh) * 2015-08-25 2018-05-11 富特姆控股第有限公司 电子吸烟装置的液体供应器
US11083221B2 (en) 2015-08-25 2021-08-10 Fontem Holdings 1 B.V. Liquid supply for electronic smoking device
EP3340817A4 (en) * 2015-08-25 2018-09-05 Fontem Holdings 1 B.V. Liquid supply for electronic smoking device
US10285449B2 (en) 2015-09-01 2019-05-14 Ayr Ltd. Electronic vaporiser system
RU2722446C2 (ru) * 2015-09-16 2020-06-01 Филип Моррис Продактс С.А. Никотиновые составы и способы их получения и применения
WO2017048972A1 (en) * 2015-09-16 2017-03-23 Sansa Corporation (Barbados) Inc. Nicotine formulations and methods of making and using the same
US11224594B2 (en) 2015-09-16 2022-01-18 Philip Morris Products S.A. Nicotine formulations and methods of making and using the same
CN108024567A (zh) * 2015-09-18 2018-05-11 菲利普莫里斯生产公司 用于电子蒸汽烟装置的液体配制物
WO2017046400A1 (en) * 2015-09-18 2017-03-23 Philip Morris Products S.A. Liquid formulation of an electronic vapor device
WO2017059571A1 (en) 2015-10-08 2017-04-13 Fontem Holdings 1 B.V. Liquid supply for an electronic smoking device
EP3358972A4 (en) * 2015-10-08 2020-01-01 Fontem Holdings 1 B.V. LIQUID SUPPLY FOR ELECTRONIC SMOKING DEVICE
US10792685B2 (en) 2015-10-08 2020-10-06 Fontem Holdings 1 B.V. Liquid supply for an electronic smoking device
WO2017093535A1 (en) * 2015-12-03 2017-06-08 Jt International S.A. Heating system and method for an inhaler device
JP2020185006A (ja) * 2015-12-03 2020-11-19 ジェイティー インターナショナル エス．エイ． 吸入器デバイスのための加熱システムおよび加熱方法
JP2019503668A (ja) * 2015-12-03 2019-02-14 ジェイティー インターナショナル エス．エイ． 吸入器デバイスのための加熱システムおよび加熱方法
EA036457B1 (ru) * 2015-12-03 2020-11-12 Джт Интернэшнл С.А. Система и способ нагрева для ингаляционного устройства
EP3364797B1 (en) 2015-12-03 2019-08-28 JT International SA Heating system and method for an inhaler device
JP7059325B2 (ja) 2015-12-03 2022-04-25 ジェイティー インターナショナル エス．エイ． 吸入器デバイスのための加熱システムおよび加熱方法
US20180369508A1 (en) * 2015-12-28 2018-12-27 Koninklijke Philips N.V. Air-flow in a nebulizer head
US11806331B2 (en) 2016-01-06 2023-11-07 Syqe Medical Ltd. Low dose therapeutic treatment
US20170208867A1 (en) * 2016-01-25 2017-07-27 Shenzhen First Union Technology Co., Ltd. Smart control method and control system for an electronic cigarette, and electronic cigarette
US10865001B2 (en) 2016-02-11 2020-12-15 Juul Labs, Inc. Fillable vaporizer cartridge and method of filling
US11751605B2 (en) 2016-02-11 2023-09-12 Juul Labs, Inc. Securely attaching cartridges for vaporizer devices
US10912333B2 (en) 2016-02-25 2021-02-09 Juul Labs, Inc. Vaporization device control systems and methods
US20170251723A1 (en) * 2016-03-03 2017-09-07 Altria Client Services Llc Methods to add menthol, botanic materials, and/or non-botanic materials to a cartridge, and/or an electronic vaping device including the cartridge
US10455863B2 (en) 2016-03-03 2019-10-29 Altria Client Services Llc Cartridge for electronic vaping device
US10433580B2 (en) * 2016-03-03 2019-10-08 Altria Client Services Llc Methods to add menthol, botanic materials, and/or non-botanic materials to a cartridge, and/or an electronic vaping device including the cartridge
US20170251722A1 (en) * 2016-03-03 2017-09-07 Altria Client Services Llc Flavor assembly for electronic vaping device
US20210219611A1 (en) 2016-03-08 2021-07-22 Altria Client Services Llc Combined cartridge for electronic vaping device
US10368580B2 (en) 2016-03-08 2019-08-06 Altria Client Services Llc Combined cartridge for electronic vaping device
US11871792B2 (en) 2016-03-10 2024-01-16 Altria Client Services Llc E-vaping cartridge and device
US10405582B2 (en) 2016-03-10 2019-09-10 Pax Labs, Inc. Vaporization device with lip sensing
US10258087B2 (en) 2016-03-10 2019-04-16 Altria Client Services Llc E-vaping cartridge and device
US11344065B2 (en) 2016-03-10 2022-05-31 Altria Client Services Llc E-vaping cartridge and device
US10357060B2 (en) 2016-03-11 2019-07-23 Altria Client Services Llc E-vaping device cartridge holder
US10368581B2 (en) 2016-03-11 2019-08-06 Altria Client Services Llc Multiple dispersion generator e-vaping device
US10244795B2 (en) 2016-03-31 2019-04-02 Altria Client Services Llc Vaporizing assembly comprising sheet heating element and liquid delivery device for an aerosol generating system
US11166491B2 (en) 2016-03-31 2021-11-09 Altria Client Services Llc Assembly comprising sheet heating element and delivery device
CN109069773A (zh) * 2016-03-31 2018-12-21 菲利普莫里斯生产公司 用于气溶胶生成系统的包括片状加热元件和液体递送装置的汽化组合件
WO2017167647A1 (en) * 2016-03-31 2017-10-05 Philip Morris Products S.A. Vaporizing assembly comprising sheet heating element and liquid delivery device for an aerosol generating system
US11857722B2 (en) 2016-03-31 2024-01-02 Altria Client Services Llc Assembly comprising sheet heating element and delivery device
US9962507B2 (en) * 2016-05-03 2018-05-08 Pneuma Respiratory, Inc. Droplet delivery device for delivery of fluids to the pulmonary system and methods of use
US11285274B2 (en) 2016-05-03 2022-03-29 Pneuma Respiratory, Inc. Methods for the systemic delivery of therapeutic agents to the pulmonary system using a droplet delivery device
US10525220B2 (en) 2016-05-03 2020-01-07 Pneuma Respiratory, Inc. Droplet delivery device for delivery of fluids to the pulmonary system and methods of use
US9956360B2 (en) * 2016-05-03 2018-05-01 Pneuma Respiratory, Inc. Methods for generating and delivering droplets to the pulmonary system using a droplet delivery device
US10898666B2 (en) 2016-05-03 2021-01-26 Pneuma Respiratory, Inc. Methods for generating and delivering droplets to the pulmonary system using a droplet delivery device
US20170319797A1 (en) * 2016-05-03 2017-11-09 Pneuma Respiratory, Inc. Droplet delivery device for delivery of fluids to the pulmonary system and methods of use
US11285283B2 (en) 2016-05-03 2022-03-29 Pneuma Respiratory, Inc. Methods for generating and delivering droplets to the pulmonary system using a droplet delivery device
US10449314B2 (en) 2016-05-03 2019-10-22 Pneuma Respiratory, Inc. Droplet delivery device for delivery of fluids to the pulmonary system and methods of use
US11285284B2 (en) 2016-05-03 2022-03-29 Pneuma Respiratory, Inc. Methods for treatment of pulmonary lung diseases with improved therapeutic efficacy and improved dose efficiency
US11285285B2 (en) 2016-05-03 2022-03-29 Pneuma Respiratory, Inc. Systems and methods comprising a droplet delivery device and a breathing assist device for therapeutic treatment
USD913583S1 (en) 2016-06-16 2021-03-16 Pax Labs, Inc. Vaporizer device
USD849996S1 (en) 2016-06-16 2019-05-28 Pax Labs, Inc. Vaporizer cartridge
USD929036S1 (en) 2016-06-16 2021-08-24 Pax Labs, Inc. Vaporizer cartridge and device assembly
USD848057S1 (en) 2016-06-23 2019-05-07 Pax Labs, Inc. Lid for a vaporizer
USD836541S1 (en) 2016-06-23 2018-12-25 Pax Labs, Inc. Charging device
USD851830S1 (en) 2016-06-23 2019-06-18 Pax Labs, Inc. Combined vaporizer tamp and pick tool
US11612185B2 (en) * 2016-06-29 2023-03-28 Nicoventures Trading Limited Article for use with apparatus for heating smokable material
RU2744863C2 (ru) * 2016-07-07 2021-03-16 Филип Моррис Продактс С.А. Расходная часть для доставки частиц никотина
RU2734847C2 (ru) * 2016-07-07 2020-10-23 Филип Моррис Продактс С.А. Ингаляционная система для никотина
WO2018007887A1 (en) * 2016-07-07 2018-01-11 Philip Morris Products S.A. Nicotine particle delivery consumable
US20220232897A1 (en) * 2016-07-07 2022-07-28 Altria Client Services Llc Additive assembly for electronic vaping device
US11317654B2 (en) * 2016-07-07 2022-05-03 Altria Client Services Llc Additive assembly for electronic vaping device
US11849768B2 (en) * 2016-07-07 2023-12-26 Altria Client Services Llc Additive assembly for electronic vaping device
WO2018007886A1 (en) * 2016-07-07 2018-01-11 Philip Morris Products S.A. Nicotine inhaler system
CN109328083A (zh) * 2016-07-07 2019-02-12 菲利普莫里斯生产公司 尼古丁吸入器系统
US11273268B2 (en) 2016-07-07 2022-03-15 Philip Morris Products S.A. Nicotine inhaler system
US10945460B2 (en) 2016-07-07 2021-03-16 Philip Morris Products S.A. Nicotine particle delivery consumable
US10231485B2 (en) * 2016-07-08 2019-03-19 Rai Strategic Holdings, Inc. Radio frequency to direct current converter for an aerosol delivery device
US20180007969A1 (en) * 2016-07-08 2018-01-11 Rai Strategic Holdings, Inc. Radio frequency to direct current converter for an aerosol delivery device
US11980228B2 (en) * 2016-07-25 2024-05-14 Altria Client Services Llc Manufacturing a fluid permeable heater assembly with cap
US20220295905A1 (en) * 2016-07-25 2022-09-22 Altria Client Services Llc Manufacturing a fluid permeable heater assembly with cap
US20170318863A1 (en) * 2016-07-27 2017-11-09 Shenzhen First Union Technology Co., Ltd. Electronic cigarette, control method and control system having same
USD825102S1 (en) 2016-07-28 2018-08-07 Juul Labs, Inc. Vaporizer device with cartridge
USD842536S1 (en) 2016-07-28 2019-03-05 Juul Labs, Inc. Vaporizer cartridge
US11351314B2 (en) * 2016-08-09 2022-06-07 Hauni Maschinenbau Gmbh Inhaler and fluid reservoir for an inhaler
EP3519026A4 (en) * 2016-10-03 2020-05-27 Neto, Jorge Neval Moll DEVICES, SYSTEMS AND METHODS FOR THE DELIVERY OF VOLATILE MATERIAL FROM COFFEE
US11771864B2 (en) 2016-10-03 2023-10-03 Jorge Neval Moll Neto Devices, systems and methods for delivering coffee-derived volatiles
WO2018067579A1 (en) 2016-10-03 2018-04-12 Neto Jorge Neval Moll Devices, systems and methods for delivering coffee-derived volatiles
CN110022922A (zh) * 2016-10-03 2019-07-16 乔吉·内瓦尔·莫尔·内托 递送咖啡衍生挥发物的装置、系统和方法
US20180110939A1 (en) * 2016-10-21 2018-04-26 Somniferum Labs LLC Method, system and apparatus for controlled delivery of opioid and other medications
US20180110725A1 (en) * 2016-10-21 2018-04-26 Somniferum Labs LLC Compositions, methods and kits for the safe inhaled delivery of targeted opioids for the treatment of pain and addiction
US10736359B2 (en) 2016-12-02 2020-08-11 VMR Products, LLC Cartridge-based vaporizers
US11425795B2 (en) 2016-12-19 2022-08-23 Altria Client Services Llc Vapor-generating system having an external cartridge
CN110022703A (zh) * 2016-12-19 2019-07-16 菲利普莫里斯生产公司 具有外部筒的气溶胶生成系统
US10834963B2 (en) 2017-01-31 2020-11-17 Philter Labs, Inc. Low emissions electronic smoking device and emissions filtering device
US10588344B2 (en) 2017-01-31 2020-03-17 Philter Labs, Inc. Low emissions electronic smoking device and emissions filtering device
US10687561B2 (en) 2017-01-31 2020-06-23 Philter Labs, Inc. Low emissions electronic smoking device and emissions filtering device
US10945458B2 (en) 2017-01-31 2021-03-16 Philter Labs, Inc. Low emissions electronic smoking device and emissions filtering device
US11529476B2 (en) 2017-05-19 2022-12-20 Pneuma Respiratory, Inc. Dry powder delivery device and methods of use
US11589621B2 (en) 2017-05-23 2023-02-28 Rai Strategic Holdings, Inc. Heart rate monitor for an aerosol delivery device
US11992061B2 (en) 2017-05-23 2024-05-28 Rai Strategic Holdings, Inc. Heart rate monitor for an aerosol delivery device
CN111372511A (zh) * 2017-05-23 2020-07-03 莱战略控股公司 用于气溶胶递送设备的心率监测器
US11026451B2 (en) 2017-06-01 2021-06-08 Fontem Holdings 1 B.V. Electronic cigarette fluid pump
US11692102B2 (en) 2017-06-12 2023-07-04 Altria Client Services Llc Corrosion-resistant reservoir for an e-vaping device and method of manufacturing thereof
US11053395B2 (en) 2017-06-12 2021-07-06 Altria Client Services Llc Corrosion-resistant reservoir for an e-vaping device and method of manufacturing thereof
USD927061S1 (en) 2017-09-14 2021-08-03 Pax Labs, Inc. Vaporizer cartridge
USD887632S1 (en) 2017-09-14 2020-06-16 Pax Labs, Inc. Vaporizer cartridge
US11738158B2 (en) 2017-10-04 2023-08-29 Pneuma Respiratory, Inc. Electronic breath actuated in-line droplet delivery device and methods of use
US11458267B2 (en) 2017-10-17 2022-10-04 Pneuma Respiratory, Inc. Nasal drug delivery apparatus and methods of use
US11771852B2 (en) 2017-11-08 2023-10-03 Pneuma Respiratory, Inc. Electronic breath actuated in-line droplet delivery device with small volume ampoule and methods of use
CN111670027A (zh) * 2018-02-01 2020-09-15 赛德玛公司 环肽在美容中的用途
US10449310B2 (en) 2018-02-08 2019-10-22 Optimist Inhaler LLC Security features for an electronic metered-dose inhaler system
US11241044B2 (en) 2018-07-23 2022-02-08 Juul Labs, Inc. Airflow management for vaporizer device
US11464082B2 (en) 2018-07-31 2022-10-04 Juul Labs, Inc. Cartridge-based heat not burn vaporizer
US11033049B2 (en) 2018-08-01 2021-06-15 R.J. Reynolds Tobacco Company Apparatus for recovering tobacco material and related method
US11771130B2 (en) 2018-08-01 2023-10-03 R.J. Reynolds Tobacco Company Apparatus for recovering tobacco material and related method
EP3607985A1 (en) 2018-08-09 2020-02-12 GSW Creative Corporation A vaporization device
CN112512347A (zh) * 2018-08-21 2021-03-16 菲利普莫里斯生产公司 用于气溶胶生成装置的消耗品以及填充和制造用于气溶胶生成装置的消耗品的方法
WO2020058881A1 (en) * 2018-09-20 2020-03-26 Rai Strategic Holdings, Inc. Flavorants for smoking articles
CN113226073A (zh) * 2018-10-15 2021-08-06 尤尔实验室有限公司 用于蒸发器装置的料盒
WO2020081527A1 (en) * 2018-10-15 2020-04-23 Juul Labs, Inc. Cartridges for vaporized devices
US11911557B2 (en) 2018-10-15 2024-02-27 Juul Labs, Inc. Heating element
US11684080B2 (en) * 2018-10-24 2023-06-27 Zanoprima Lifesciences Limited Electronic cigarette compositions, devices, and related methods
US11690396B2 (en) 2018-10-24 2023-07-04 Zanoprima Lifesciences Limited Electronic cigarette compositions, devices, and related methods
US11464921B2 (en) 2018-11-05 2022-10-11 Juul Labs, Inc. Cartridges for vaporizer devices
US11564287B2 (en) 2018-11-05 2023-01-24 Juul Labs, Inc. Cartridges with vaporizable material including at least one ionic component
US11838997B2 (en) 2018-11-05 2023-12-05 Juul Labs, Inc. Cartridges for vaporizer devices
US11300114B2 (en) * 2018-12-24 2022-04-12 Zhenjiang Chen Automatic e-liquid transportation system and method of electronic cigarette as well as peristaltic pump
US20220125109A1 (en) * 2019-01-15 2022-04-28 Philip Morris Products S.A. Aerosol-generating device with movable top cover
US12016388B2 (en) * 2019-01-15 2024-06-25 Philip Morris Products S.A. Aerosol-generating device with movable top cover
US11253001B2 (en) 2019-02-28 2022-02-22 Juul Labs, Inc. Vaporizer device with vaporizer cartridge
EP3711802A1 (en) * 2019-03-21 2020-09-23 Nerudia Limited Aerosol delivery system
EP3711800A1 (en) * 2019-03-21 2020-09-23 Nerudia Limited Aerosol delivery system
WO2020187945A1 (en) * 2019-03-21 2020-09-24 Nerudia Limited Aerosol delivery system
WO2020187937A1 (en) * 2019-03-21 2020-09-24 Nerudia Limited Aerosol delivery system
EP3711799A1 (en) * 2019-03-21 2020-09-23 Nerudia Limited Aerosol delivery system
EP3711798A1 (en) * 2019-03-21 2020-09-23 Nerudia Limited Aerosol delivery system
EP3711598A1 (en) * 2019-03-21 2020-09-23 Nerudia Limited Aerosol delivery system
WO2020187940A1 (en) * 2019-03-21 2020-09-24 Nerudia Limited Aerosol delivery system
EP3711593A1 (en) * 2019-03-21 2020-09-23 Nerudia Limited Aerosol delivery system
US20200315253A1 (en) * 2019-04-02 2020-10-08 Juul Labs, Inc. Fixed dose cartridge for vaporizer device
CN113840547A (zh) * 2019-05-06 2021-12-24 进立有限公司 用于微型蒸发器的平板加热元件
CN111920096A (zh) * 2019-05-13 2020-11-13 西姆雷尔收藏有限责任公司 具有混合室的汽化器冷却系统
US11998681B2 (en) 2019-07-03 2024-06-04 Airja, Inc. Aerosol delivery devices and methods of using same
US20220295896A1 (en) * 2019-07-03 2022-09-22 Airja, Inc. Aerosol delivery devices and methods of using same
US20220202097A1 (en) * 2019-09-20 2022-06-30 Nerudia Limited Smoking substitute apparatus
US20220256919A1 (en) * 2019-09-20 2022-08-18 Nerudia Limited Smoking substitute apparatus
US20240114949A1 (en) * 2019-10-09 2024-04-11 Nicoventures Trading Limited Aerosolizable material
IT201900018632A1 (it) * 2019-10-11 2021-04-11 Matteo Ratti Composizione per trattare le corde vocali di un soggetto
USD920570S1 (en) 2019-11-13 2021-05-25 Canopy Growth Corporation Vaporizer cartridge
USD920571S1 (en) 2019-11-20 2021-05-25 Canopy Growth Corporation Vaporizer cartridge
US11446244B2 (en) * 2020-01-17 2022-09-20 Matthew McLeay Compositions containing verteporfin, ribavirin, gemcitabine, or combinations thereof and methods of use for treating COVID-19, cancer, or non cancer diseases
US11918598B2 (en) 2020-01-17 2024-03-05 Matthew McLeay Compositions containing Verteporfin, Ribavirin, Gemcitabine, or combinations thereof and methods of use for treating COVID-19, cancer, or non cancer diseases
US11819604B2 (en) * 2020-03-31 2023-11-21 Pu Yuan Biotech Co., Ltd. Breathing airflow detecting device for a nebulizing device
US20210299366A1 (en) * 2020-03-31 2021-09-30 Pu Yuan Biotech Co., Ltd. Breathing airflow detecting device for a nebulizing device
US20210338948A1 (en) * 2020-04-30 2021-11-04 Mcneil Ab Biomarker Based Nicotine Replacement Therapy
CN113208148A (zh) * 2021-05-12 2021-08-06 云南中烟工业有限责任公司 一种协同释放尼古丁和致香成分的超分子凝胶
US11793945B2 (en) 2021-06-22 2023-10-24 Pneuma Respiratory, Inc. Droplet delivery device with push ejection
IT202100021824A1 (it) * 2021-08-12 2023-02-12 E Liquid Labs S R L Formulazione liquida aromatizzata per sigaretta elettronica
WO2023039266A1 (en) * 2021-09-12 2023-03-16 Niconox Llc Delivery devices and compositions
WO2023052097A1 (en) * 2021-09-28 2023-04-06 Nerudia Limited Smoking substitute apparatus
RU213319U1 (ru) * 2022-02-21 2022-09-06 Общество с ограниченной ответственностью "Небулайзер" Портативный компрессорный ингалятор с подогревом аэрозоля

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KR20150095709A (ko) 2015-08-21
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JP6429788B6 (ja) 2019-01-30
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CN104955508A (zh) 2015-09-30
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EP2925395A1 (en) 2015-10-07
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CA2890204C (en) 2022-04-05
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GB2508520A (en) 2014-06-04
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CN204147375U (zh) 2015-02-11
JP2016501588A (ja) 2016-01-21

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