Patent Application
20230329354
Aspects of the present disclosure relate generally to the field of medical devices, and more particularly to a device for delivering and related systems and methods, and more particularly a pressurized inhalation delivery device that eliminates a cartridge or reservoir or pod, the heating element and power source or battery.
The Center for Disease Control and Prevention (“CDC”) validates that smoking can cause cancer, most often lung cancer, and then block the human body from fighting the disease. It is well known in the art that the poisons in cigarette smoke can affectively weaken the body’s immune system, creating a greater challenge to kill cancer cells which grow and multiple over time. More specifically, the poisons in tobacco smoke can damage or change a cell’s DNA and once damaged, those cells can begin growing out of control and create a cancer tumor. In addition, vaping has become increasingly popular in recent years among teenagers and young adult populations, and the known additive nature of nicotine among youth and young adults has developed into a major health concern. These and related issues have become a considerable health risk, including for people who do not smoke or vape but are exposed to the second-hand smoke of another.
Vaping is a process of aerosolizing a solution and inhaling it into the lungs using an electronic cigarette (e-cigarettes) or other vaping device that serves as an alternative to conventional smoking. During the vaping process, e-cigarettes heat a liquid into an aerosol that the user inhales into their lungs, and commonly comprise a replaceable cartridge. A typical e-cigarette cartridge (also referred to as a reservoir or pod) contains four basic ingredients: water; nicotine; flavorings; and, a propylene or vegetable glycerin base commonly referred to as e-liquid. Consumers may choose from a wide variety of vapes and e-cigarette products that contain nicotine, flavorings, and other additives.
There are a variety of devices known in the art for vaping. For example, e-cigarettes or “e-cigs,” “cigalikes,” “e-hookahs,” “mods,” “vape pens,” “vapes,” and “tank systems” are vaping devices existing in the art today. By way of example, U.S. Pat. No. 8,511,318 describes an e-cigarette device that is comprised of a cylindrical shell containing an e-cigarette cell, a nicotine solution, a control circuit, and an electro-thermal vaporization nozzle. The device allows a person to suck air through an air suction fitting on one end of the shell, which the patent describes as beneficial as it eliminates tar from the nicotine solution and reduces the risk of fire between inhalations. Another example is provided in U.S. Pat. No. 9,737,093, which describes an e-cigarette device having a separate cartridge and vaporizer unit. The separate cartridge unit comprises a liquid with a seal that keeps the liquid safely within the cartridge tube, but may be pierced by a piercer prior to use. The piercer is described as part of the vaporizer unit, which further comprises a heater and an electronic circuit electrically connected to a battery. Notably, the prior art does not disclose a device for providing an aerosolized and/or micellized liquid nicotine formula. The prior art also fails to disclose an actuator that provides precise dosage such that a known amount of the liquid may be inhaled with each depression/activation. There are other problems with the prior art, including malfunctions with the electronic circuitry, battery failure, mechanical failure, leaking and/or harmful exposure to the liquid or other substance contained by the cartridge, and other problems addressed by the present disclosure.
Although numerous other prior art solutions have attempted to improve upon vaping and e-cigarette devices, none of the solutions effectively provides an aerosolized delivery device that is accurate, reproducible, that provides a known amount of liquid, including a dosage of micellized liquid nicotine formula, which may be inhaled with each depression/activation, that otherwise eliminates the varying dosing volumes created in prior art vaping and e-cigarettes. A number of other challenges and deficiencies in the art still persist or remained completely unsolved. It is with respect to these and other problems that the present disclosure is contemplated, as will be described in greater detail below.
Aspects of the present disclosure relate to an aerosol pressurized inhalation delivery device having an actuator, metered valve, receptacle housing and aluminum canister allowing a micellized liquid nicotine formula to be expelled through the actuator discharge nozzle by depressing the actuator discharge finger slide control and inhaling the formula into the lungs through the mouthpiece. Depressing the actuator discharge finger slide control delivers a known amount of total formula passing from the metered valve through the actuator discharge nozzle ensuring an accurate and known amount of micellized liquid nicotine formula is inhaled with each depression/activation eliminating the varying dosing volumes created in vapes and e-cigarettes. The aerosol pressurized inhalation delivery device eliminates the use of cartridges or reservoirs or pods, the heating element and power source or battery and addresses the deficiencies of inaccurate and inconsistent dosing with vaping by utilizing a microliter metered valve that dispenses a known volume of micellized liquid nicotine formula containing fractionally less nicotine while delivering an equivalent feeling of pleasure to the user.
According to another aspect of the present disclosure, the invention relates to an aerosol pressurized inhalation delivery device having an actuator with a discharge finger slide control and mouthpiece, metered valve, receptacle housing, and aluminum canister containing a micellized liquid nicotine formula and a propellant such as pharma grade 1,3,3,3, -Tetrafluropropene, HFO 1234ze allowing the micellized liquid nicotine formula to be expelled as a nano mist and inhaled into the lungs with the depression of the actuator discharge finger slide control.
According to another aspect of the present disclosure, the device comprises an aluminum canister pressurized with a propellant, such as pharma grade 1,3,3,3, -Tetrafluropropene, HFO 1234ze, and may further comprise a crimped metered valve attached to the canister. In use, the canister may be inserted into a receptacle housing, which in turn allows an actuator to discharge a known dosage. The device and actuator may further comprise a childproof safety guard to be placed over the actuator. The receptacle housing may further comprise one or more finger slide control channels for providing a further safety feature with the device.
According to one specific aspect, the present disclosure relates to a An aerosol pressurized inhalation delivery device comprising: a metered valve crimped to an aluminum canister; an actuator having actuator discharge finger slide controls; an actuator positioned over a metered valve; a micellized liquid nicotine formula residing within the aluminum canister; a liquid propellant residing within the aluminum canister; an aluminum canister residing within a receptacle housing; and an actuator locked into a receptacle housing.
According to yet another specific aspect, the present disclosure relates to a method of delivering a nano mist micellized liquid formula comprising: coupling a metered valve on a canister containing micellized liquid formula; placing the canister and metered valve into a receptacle housing; positioning an actuator above the metered valve; activation the actuator by pressing actuator against the metered valve; piercing a diaphragm on the canister with a valve stem associated with the metered valve; delivering, under pressure, a volume of micellized liquid formula from the canister, through the metered valve, into an expansion chamber; delivering the volume of micellized liquid formula from the expansion chamber through a discharge nozzle.
According to one aspect, the invention comprises a non-combustible, smoke-free device for delivering a nano mist aerosolized nicotine (which according to one embodiment is 99.9% pure tobacco). In embodiments, the device has no heat, no battery, no oil and greatly reduced the risk of harm during use of the device. The device preferably comprises a proprietary water-soluble micellized liquid nicotine formula that reduces the nicotine content by up to 80% compared to electronic nicotine delivery systems (“ENDS”).
According to embodiments, the device may be manufactured utilizing a process or processes consistent with, or otherwise in observation of, Environmental Protection Agency and U.S. Food & Drug Administration regulatory guidelines. In embodiments, all ingredients of the micellized liquid nicotine formula are FDA and GRAS compliant, by the Natural & Non-Prescription Product Group. In embodiments, the invention is manufactured utilizing pharmaceutical grade equipment and components.
The devices and components described herein may comprise one or more of a polymeric material and a metallic material. More particularly, the present disclosure may be constructed of materials known to provide, or predictably manufactured to provide the various aspects of the present disclosure. These materials may include, for example, carbon fiber, ABS plastic, polyurethane, polyethylene, photo-polymers, resins, fiber-encased resinous materials, rubber, latex, synthetic rubber, synthetic materials, polymers, and natural materials. These materials may further include, for example, stainless steel, titanium alloy, aluminum alloy, chromium alloy, and other metals or metal alloys.
In one embodiment, at least a portion the delivery device described herein is reusable. Optionally, a portion of the delivery device is disposable, but in other embodiments the entire delivery device may be reusable or disposable after a set number of uses.
One having skill in the art will appreciate that embodiments of the present disclosure may have various sizes. The sizes of the various devices or their components may be sized based on various factors including, for example, the anatomy of the user, such as the height and weight of the person operating the device, or other physical features of replaceable or reusable components used with the devices described herein, including, for example, width, length and thickness, and the intended dosage(s) provided by the device.
These and other features, utilities, and advantages of the various embodiments of the present invention will be apparent from the following more particular descriptions of the embodiments of the invention as illustrated in the accompanying drawings and defined in the appended claims.
Certain terms are used throughout the following description and claims to refer to a particular system or device components. As one skilled in the art will appreciate, companies may refer to a component by different names. This document does not intend to distinguish between components that differ in name but not function.
The phrases “at least one,” “one or more,” and “and/or,” as used herein, are open-ended expressions that are both conjunctive and disjunctive in operation. For example, each of the expressions “at least one of A, B and C,” “at least one of A, B, or C,” “one or more of A, B, and C,” “one or more of A, B, or C,” and “A, B, and/or C” means A alone, B alone, C alone, A and B together, A and C together, B and C together, or A, B and C together.
Unless otherwise indicated, all numbers expressing quantities, dimensions, conditions, and so forth used in the specification and claims are to be understood as being approximations which may be modified in all instances as required for a particular application of the novel apparatus described herein.
In the following disclosure, the use of “including,” “comprising,” or “having” and variations thereof herein is meant to encompass the items listed thereafter and equivalents thereof as well as additional items. Accordingly, the terms “including,” “comprising,” or “having” and variations thereof can be used interchangeably herein. In the claims, the terms “including” and “comprising” are used in an open-ended fashion, and thus should be interpreted to mean “including, but not limited to....”
The term “a” or “an” entity, as used herein, refers to one or more of that entity. As such, the terms “a” (or “an”), “one or more” and “at least one” can be used interchangeably herein.
The terms “determine,” “calculate,” and “compute,” and variations thereof, as used herein, are used interchangeably and include any type of methodology, process, mathematical operation, or technique.
The term “couple” or “couples” is intended to mean either an indirect or direct connection. When used in a mechanical context, if a first component couples or is coupled to a second component, the connection between the components may be through a direct engagement of the two components, or through an indirect connection that is accomplished via other intermediate components, devices and/or connections. In addition, when used in an electrical context, if a first device couples to a second device, that connection may be through a direct electrical connection, or through an indirect electrical connection via other devices and connections. Connections can occur in a unidirectional, bidirectional or variable directional manner over all known means of network connectivity.
By way of providing additional background, context, and to further satisfy the written description requirements of 35 U.S.C. § 112, the following are incorporated by reference in their entireties for the express purpose of explaining and further describing the various devices and apparatus that may be associated with aerosol and micellized nicotine delivery, in general: U.S. Pat. Nos. 8,511,318; 9,737,093; and, 11,172,704.
The Summary is neither intended nor should it be construed as being representative of the full extent and scope of the present disclosure. The present disclosure is set forth in various levels of detail in the Summary as well as in the attached drawings and the Detailed Description and no limitation as to the scope of the present disclosure is intended by either the inclusion or non-inclusion of elements, components, etc. in this Summary. Additional aspects of the present disclosure will become more readily apparent from the Detailed Description, particularly when taken together with the drawings.
The above-described benefits, embodiments, and/or characterizations are not necessarily complete or exhaustive, and in particular, as to the patentable subject matter disclosed herein. Other benefits, embodiments, and/or characterizations of the present disclosure are possible utilizing, alone or in combination, as set forth above and/or described in the accompanying figures and/or in the description herein below.
Many aspects of the disclosure can be better understood with reference to the following drawings. While several implementations are described in connection with these drawings, the disclosure is not limited to the implementations disclosed herein. On the contrary, the intent is to cover all alternatives, modifications, and equivalents.
In certain instances, details that are not necessary for an understanding of the disclosure or that render other details difficult to perceive may have been omitted. It should be understood, of course, that the disclosure is not necessarily limited to the particular embodiments illustrated in the following Figures. In the drawings:
It should be understood that the drawings are not meant to be and/or are not necessarily to scale.
For ease of reference, the following is a listing of components depicted in the drawing figures, some of which are described in greater detail herein:
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The following disclosure is directed to various embodiments, including those depicted in
The aerosol pressurized inhalation delivery device eliminates the use of a power source or battery which as used in prior art devices has been known to explode without warning and cause serious injuries including burns, broken bones or even death. The alternative use of a propellant, such as pharma grade 1,3,3,3, -Tetrafluropropene, HFO 1234ze, which is chlorofluorocarbon free and approved by the FDA for use in metered-dose inhalers for the treatment of asthma and other pulmonary obstructive diseases, eliminates the aforementioned safety concerns.
Placing the aluminum canister into the receptacle housing protects the aluminum canister from impact and allows the actuator to be positioned over the receptacle housing and locked into a secure position via the actuator receptacle locking clip and receptacle actuator locking edge.
An actuator discharge finger slide control child proof safety guard can be snapped into position over the receptacle housing finger slide control channels eliminating the ability to depress the actuator discharge finger slide control downward providing a child proof aerosol pressurized inhaler deliver device.
The metered valve is preferably crimped onto the aluminum canister with, for example, a metal crimping collette, which couples the metered valve mounting cup of the metered valve against the rim of the aluminum canister. The crimp or an equivalent connector securely holds the metered valve onto the aluminum canister which once gassed can maintain, by way of example but not limitation, approximately 75 psi (pounds per square inch) pressure inside the aluminum canister.
The actuator is preferably made from high quality plastic or resinous material and contains a discharge finger slide control that once depressed activates the metered valve and delivers an exact volume of micellized liquid nicotine formula to the user through the mouthpiece. The actuator, once fully depressed downward on the metered valve, allows the metered valve’s valve stem to be pushed downward into the canister. The micellized liquid nicotine formula is thereby forced, under approximately 72 psi, through the metering chamber and into the expansion chamber. Once the volume of micellized liquid nicotine formula is passed into the expansion chamber, the volume is delivered through the nano mist discharge nozzle.
The volume of liquid micellized formulation delivered with each activation of the actuator is preferably within the range of 50 to 100 microliters. In one embodiment, the volume is precisely controlled at 100 microliters by utilizing a metered valve configured to release 100 microliters. In another embodiment, the volume is precisely controlled at 65 microliters. According to one particular aspect, the method of delivering a known volume of micellized liquid nicotine formula is as follows: once the valve stem has been fully depressed, a valve stem side piercing passes through a diaphragm. The volume of micellized liquid nicotine formula enters into the metering chamber, which includes a precise, controlled volume of micellized liquid nicotine formula and propellant based on the configuration of metered valve.
From the first actuation until the last actuation, the pressure in the cannister remains constant allowing a controlled, consistent and precise dose of liquid micellized formula and propellant to be expelled through the actuators discharge nozzle.
In one aspect, the combination of the micellized liquid nicotine formula and propellant, which in one embodiment may be a propellant known commercially as HFA 134a, becomes miscible, visibly clear, having a viscosity similar to water, homogenous mixture, which makes it easier to deliver a precise metered dose of the combined micellized liquid nicotine formula and propellant through the actuator discharge nozzle.
In embodiments, the nicotine formula is preferably micellized, a phase separation of water from oil. This process, referred to herein as micellization, converts an otherwise oil-based product and their ingredients and making them bio-absorbable or “bio available” to the body, without changing their molecular form and structure.
Through research and experimentation, the applicant has found that micelles formulated, full spectrum hemp oil (“FSHO”) has demonstrated significantly more bioavailability than non-micelles, unformulated hemp-based oils. This means that the FSHO, using micelle technology is more effective, delivering better than 85% absorption to the body, GI tract and/or skin, with a quicker onset than that of traditional, lower dose, FSHO based, or Cannabidiol based products. The same will apply to Tetrahydrocannabinol oil based micellized formulas.
The spirit of this disclosure, in one particular aspect, is to eliminate the use of cartridges or reservoirs or pods, heating elements and power sources or batteries in prior art devices, such as vape units, and to replace the corresponding formulas containing nicotine, flavorings, and propylene glycol with a safer known dispensed micellized liquid nicotine formula that dramatically decreases the nicotine percentage oral uptake, delivers better absorption to the body, and helps minimize the known threats of cancer to the user.
E-cigarette’s use of a battery, the most common called “18650” batteries, heat up the nicotine formula, flavorings and other chemicals and turn them into a vapor the user can breathe. This vapor can contain formaldehyde, heavy metals and other particles that can cause cancer and loge themselves in the users’ deepest parts of the lungs. The present disclosure eliminates the battery or power supply required by e-cigarettes and vaping devices.
In the “News in Health” article presented by the NIH, National Institute of Health, https://newsinhealth.nih.gov/2020/05/risks-vaping, the risk of vaping is described and acknowledgment is made that “Studies suggest nicotine vaping may be less harmful than traditional cigarettes when people who regularly smoke switch to them as a complete replacement. But nicotine vaping could still damage your health, according to the NIH, because a person must necessarily inhale propylene glycol, vegetable glycerin, and flavorants that were meant to be eaten but not inhaled, not to mention nicotine. When vaping, all of those chemicals are heated up by the power supply and reactor, which may cause those components to turn into other potentially dangerous chemicals.
An object of this disclosure, in another aspect, is to create a safer aerosol pressurized inhalation delivery device compared to smoking or vaping using similar components to those employed in pressurized metered dose inhalers, pMDI’s, and having a micellized liquid nicotine formula that once inhaled into the lungs delivers greater absorption to the body and significantly lowers the percentage of nicotine inhaled while providing a similar feeling of pleasure for the user.
Various aspects of the present disclosure are shown in
With respect to the embodiments described above, it is expressly understood that such embodiments may be incorporated for use in practicing the novel methods described herein. In certain embodiments, those methods may comprise greater or fewer steps than as described above. By way of example, but not limitation, one step for use with the various embodiments described above may comprise the step of removing and replacing the canister or securing a safety guard, with different steps included in the method of operation provided accordingly. Thus, variations on this and other steps, and the inclusion or exclusion of additional steps described herein, are expressly contemplated by the present disclosure.
It is expressly understood that where the term “consumer” has been used to describe the various embodiments of the disclosure, the term should not be construed as limiting in any way. For instance, a consumer could be a human user or, in a veterinary application, an animal. Therefore, it is intended that the device and methods described herein apply equally to veterinary science as they would if practiced on a human being. The apparatus and methods described herein therefore have application beyond controlled dosage of nicotine, by way of example.
The foregoing discussion of the disclosure has been presented for purposes of illustration and description. The foregoing is not intended to limit the disclosure to the form or forms disclosed herein. In the foregoing Detailed Description for example, various features of the disclosure are grouped together in one or more embodiments for the purpose of streamlining the disclosure. This method of disclosure is not to be interpreted as reflecting an intention that the claimed disclosure requires more features than are expressly recited in each claim. Rather, as the following claims reflect, inventive aspects lie in less than all features of a single foregoing disclosed embodiment. Thus, the following claims are hereby incorporated into this Detailed Description, with each claim standing on its own as a separate preferred embodiment of the disclosure.
The present inventions, in various embodiments, include components, methods, processes, systems and/or apparatuses substantially as depicted and described herein, including various embodiments, subcombinations, and subsets thereof. Those of skill in the art will understand how to make and use the present inventions after understanding the present disclosure. The present inventions, in various embodiments, include providing devices and processes in the absence of items not depicted and/or described herein or in various embodiments hereof, including in the absence of such items as may have been used in previous devices or processes, e.g., for improving performance, achieving ease and\or reducing cost of implementation.
Moreover, though the present disclosure has included description of one or more embodiments and certain variations and modifications, other variations and modifications are within the scope of the disclosure, e.g., as may be within the skill and knowledge of those in the art, after understanding the present disclosure. For further illustration, the information and materials supplied with the provisional application from which this application claims priority is expressly made a part of this disclosure and incorporated by reference herein in their entirety. This form of disclosure, therefore, is intended to obtain rights which include alternative embodiments to the extent permitted, including alternate, interchangeable and/or equivalent structures, functions, ranges or steps to those claimed, whether or not such alternate, interchangeable and/or equivalent structures, functions, ranges or steps are disclosed herein, and without intending to publicly dedicate any patentable subject matter.
The present application claims priority under 35 U.S.C. §119(e) to U.S. Provisional Patent Application Serial No. 63/331,497, filed Apr. 15, 2022, the entirety of which is incorporated herein.
| Number | Date | Country | |
|---|---|---|---|
| 63331497 | Apr 2022 | US |
