US20160198759A1 - E-cigarette or vaping fluid - Google Patents

E-cigarette or vaping fluid Download PDF

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Publication number
US20160198759A1
US20160198759A1 US14/984,774 US201514984774A US2016198759A1 US 20160198759 A1 US20160198759 A1 US 20160198759A1 US 201514984774 A US201514984774 A US 201514984774A US 2016198759 A1 US2016198759 A1 US 2016198759A1
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United States
Prior art keywords
fluid
concentration
volume
cyclodextrin
ingredients
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Abandoned
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US14/984,774
Inventor
Shyam Kuntawala
Lawrence Moy
Ashish Patel
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Zip LLC
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Zip LLC
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Priority to US14/984,774 priority Critical patent/US20160198759A1/en
Priority to PCT/US2016/013248 priority patent/WO2016115250A1/en
Publication of US20160198759A1 publication Critical patent/US20160198759A1/en
Abandoned legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24BMANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
    • A24B15/00Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
    • A24B15/10Chemical features of tobacco products or tobacco substitutes
    • A24B15/16Chemical features of tobacco products or tobacco substitutes of tobacco substitutes
    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24BMANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
    • A24B15/00Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
    • A24B15/10Chemical features of tobacco products or tobacco substitutes
    • A24B15/16Chemical features of tobacco products or tobacco substitutes of tobacco substitutes
    • A24B15/167Chemical features of tobacco products or tobacco substitutes of tobacco substitutes in liquid or vaporisable form, e.g. liquid compositions for electronic cigarettes
    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24BMANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
    • A24B15/00Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
    • A24B15/18Treatment of tobacco products or tobacco substitutes
    • A24B15/28Treatment of tobacco products or tobacco substitutes by chemical substances
    • A24B15/281Treatment of tobacco products or tobacco substitutes by chemical substances the action of the chemical substances being delayed
    • A24B15/283Treatment of tobacco products or tobacco substitutes by chemical substances the action of the chemical substances being delayed by encapsulation of the chemical substances
    • A24B15/284Treatment of tobacco products or tobacco substitutes by chemical substances the action of the chemical substances being delayed by encapsulation of the chemical substances the additive being bound to a host by chemical, electrical or like forces, e.g. use of precursors, inclusion complexes
    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24BMANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
    • A24B15/00Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
    • A24B15/18Treatment of tobacco products or tobacco substitutes
    • A24B15/28Treatment of tobacco products or tobacco substitutes by chemical substances
    • A24B15/30Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
    • A24B15/308Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances vitamins
    • A24F47/008
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/465Nicotine; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/16Ginkgophyta, e.g. Ginkgoaceae (Ginkgo family)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/25Araliaceae (Ginseng family), e.g. ivy, aralia, schefflera or tetrapanax
    • A61K36/258Panax (ginseng)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/27Asclepiadaceae (Milkweed family), e.g. hoya
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/28Asteraceae or Compositae (Aster or Sunflower family), e.g. chamomile, feverfew, yarrow or echinacea
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/53Lamiaceae or Labiatae (Mint family), e.g. thyme, rosemary or lavender
    • A61K36/534Mentha (mint)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/77Sapindaceae (Soapberry family), e.g. lychee or soapberry
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/82Theaceae (Tea family), e.g. camellia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/84Valerianaceae (Valerian family), e.g. valerian
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
    • A61K47/40Cyclodextrins; Derivatives thereof
    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24FSMOKERS' REQUISITES; MATCH BOXES; SIMULATED SMOKING DEVICES
    • A24F40/00Electrically operated smoking devices; Component parts thereof; Manufacture thereof; Maintenance or testing thereof; Charging means specially adapted therefor
    • A24F40/10Devices using liquid inhalable precursors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/007Pulmonary tract; Aromatherapy

Definitions

  • the current invention is in the area of e-cigarettes and “vaping” and concerns an improved non-nicotine fluid for e-cigarette devices.
  • Smoking has a long history in human cultures. When plant materials are burned various organic chemicals that are constituents of the plant vaporize and attach themselves to the smoke particles. At the same time heat and combustion break down constituent organic chemicals and produce new chemicals all of which are present in the vapor state and/or attach themselves to the smoke particles. When the smoke is inhaled, the particles come into contact with the surface of lung cells and the chemicals absorbed to the particles transfer to the lung cells and eventually are transferred into the circulatory system. Because of the extremely large surface area of the lung, smoking is an extremely effective route for administering active compounds. Because plants contain a wide variety of secondary products inhaling the smoke delivers these products to the human body. The physiological results can be stimulation, depression or even hallucination depending on what type of plant is burned to produce the smoke.
  • tobacco smoking is highly addictive as in the case of nicotine in tobacco smoke.
  • tobacco smoking was once considered to be a benign or even healthful pastime, it is now considered to be a health hazard.
  • tobacco smoking is major cause of lung as well as other cancers in smokers as well as those exposed to “second hand” smoke.
  • tobacco smoking is major cause of lung as well as other cancers in smokers as well as those exposed to “second hand” smoke.
  • Electro cigarettes have been developed as a safer alternative to smoking tobacco.
  • a mechanism reduces a liquid (“e-cigarette fluid,” “e-fluid” or “vaping fluid”) into a smoke-like mixture of air and tiny droplets (an aerosol) which material is then inhaled. Any active constituents in the vaping fluid are then absorbed by the lungs like real smoke.
  • e-cigarettes do not produce smoke, other terms have been developed to describe using the devices.
  • vaping One such term that is gaining popularity is “vaping.”
  • one does not smoke an e-cigarette—one “vapes” it.
  • E-cigarettes are thought to be safer than smoking tobacco because nothing is actually burned in an e-cigarette.
  • the most common type of e-cigarette has a heating element which vaporizes the e-fluid to create an aerosol. Less commonly there is mechanical production of the aerosol. For example, some devices use a piezoelectric diaphragm which vibrates at ultrasonic speeds to directly form an aerosol from the e-fluid rather like a cool-mist humidifier.
  • e-fluids contain nicotine (approximately 0.04M-0.12M) so that vaping an e-cigarette can act as a substitute for smoking tobacco by delivering nicotine to the user.
  • nicotine e-cigarettes As smoking cessation devices. The idea is that the users transition to the e-cigarettes and then use e-fluids with diminishing levels of nicotine until the user's nicotine addiction is overcome.
  • many users alternate between “real” cigarettes and e-cigarettes so the usefulness of vaping e-cigarettes as an aid to smoking cessation is somewhat questionable. Certainly, the e-cigarette avoids the dangers of secondhand tobacco smoke.
  • vaping fluids can be obtained by combining a variety of active ingredients with the hydrophilic solvents typical of such fluids.
  • the active ingredients are chosen depending on the desired effects of using the fluid.
  • methylzanthines such as caffeine can be used to provide an energy boost product.
  • Energy boost formulae can also contain taurine, cyanocobalamin, carnitine, guarana, and ginseng.
  • Relaxation/sleep formulae can include chamomile, valerian, kava and other active ingredients.
  • Appetite suppressant formulae can contain hoodia, yerba mate, caralluma and lecithin.
  • scents/flavors and colors can also be included. It is preferred to used natural plant extracts to impart colors.
  • Cyclodextrin is included to enhance absorption of the active ingredients as well as to limit any tendency of the inhaled aerosol to cause irritation.
  • e-fluids contain water and one or more hydrophilic solvent such as glycerol, propylene glycol and/or polyethylene glycol.
  • the hydrophilic solvent is important for the production of aerosols by a heat source. When a water solution of these solvents contacts a heat source, the water rapidly vaporizes leaving behind an aerosol of hydrophilic solvent particles which contain the other ingredients that were dissolved in the original e-fluid and/or the other ingredients are present as tiny particles.
  • the “other ingredients” include flavors, scents and additives intended to enhance the efficacy of the other ingredients.
  • the ingredients must be carried into the user's lungs. This generally occurs because the ingredients are bound to or dissolved in the aerosol particles.
  • the aerosol particles may not always be of optimum size so that they are filtered out by lung structures before there is a chance for the active ingredients to be properly absorbed. In other cases the aerosol particles are somewhat irritating to the user's throat and other tissues.
  • cyclodextrins are useful for sequestering hydrophobic molecules and for forming droplets in a nebulizer.
  • cyclodextrins also promote aerosol formation with the heating elements of common e-cigarettes (as well as with the spray jets of nebulizers). More importantly, the addition of sufficient cyclodextrin to e-fluid enhances the absorption and bioavailability of any active ingredients while at the same time reducing any tendency towards irritation caused by the aerosol.
  • the cyclodextrin molecules form a somewhat conical structure—that is, a hollow cylinder having a smaller opening at one end than the other.
  • the cyclodextrin molecule in solution has an interior that is more hydrophobic than its exterior (i.e., the exterior is relatively hydrophilic).
  • the molecule to be sequestered must be at least partially hydrophobic and of dimensions to fit within the cyclodextrin ring.
  • Active ingredients such as methylxanthines and nicotine are of the right size for sequestration and are essentially hydrophobic at physiological and acid pHs.
  • cyclodextrin is affected by the active ingredient as well as the other ingredients in the e-fluid formula. Both ⁇ and ⁇ cyclodextrin have a water solubility that is approximately an order of magnitude higher than that of ⁇ cyclodextrin. Therefore, if it is desired to use a relatively high level of active ingredient, a and ⁇ cyclodextrin are preferred. Otherwise, ⁇ cyclodextrin operates adequately.
  • a methylxanthine alkaloid such as caffeine is combined with taurine which has beneficial biological as well as surfactant properties.
  • methylxanthine alkaloids improve energy and provide a feeling of well-being.
  • Taurine is a natural amino acid derivative that has an anti-anxiety effect as well as many health benefits.
  • taurine has surfactant properties and aids in the dispersion of insoluble ingredients.
  • Caffeine is effective in e-fluids of 0.01M to 0.15M. Much below this concentration range, there is little discernible effect whereas at much higher concentrations, the caffeine effect can be excessive. Currently, a concentration of 0.05M is preferred.
  • Taurine has a wide effective range of at least 0.01M to 0.1M; currently 0.015M is preferred.
  • cyanocobalamin vitamin B12
  • This water soluble vitamin is important for many cellular functions and seems to potentiate the effects of caffeine and taurine.
  • the cyanocobalamin has a red-magenta color and can be used as the sole coloring agent or other colors may be added as desired. This has been tested at concentrations between 0.01% and 0.1%; currently 0.083% (weight by volume) is preferred.
  • Other common methylxanthines such as theophylline or theobromine can be substituted or used in conjunction with caffeine.
  • Energy Boost ingredients can be used either alone or in conjunction with the methylxanthines.
  • green tea extracts can be employed not only as a source of caffeine and theophylline but also for beneficial antioxidants (and to impart a flavor).
  • Extracts of guarana can be used to supply caffeine as well as other beneficial natural ingredients.
  • Extracts of Ginkgo biloba can be used to supply antioxidants Extracts of ginseng ( Panax species) are also effective when combined with cyclodextrins.
  • carnitine is effective in energy formulae. These ingredients are generally used at concentration of about 0.5% by weight or less.
  • Caffeine, other methylxanthines and taurine can be stabilized as metal complexes (zinc, magnesium and/or sodium) and/or cyclodextrin complexes.
  • Metal complexes are formed by adding a molar excess of a water soluble salt of the desired metal. Cyclodextrin complexes form best with a molar excess of cyclodextrin. It has been found that a 2-3 fold molar excess works well although cyclodextrin is effective in the range of 0.5 to 5.0 molar ratio of cyclodextrin to active ingredient. Cyclodextrin is used preferable but can be used with the metal complex as well. That is, the required concentration of both metal and cyclodextrin can be used.
  • “Relaxation/sleep” formulae are also useful.
  • ingredients such as extracts of chamomile ( Matricaria chamomilla and/or Chamaemelum nobile ), extracts of kava ( Piper methysticum ), extracts of valerian ( Valeriana officinalis ), L-tryptophan and/or melatonin are used in place of the “energy” ingredients. Again these ingredients are used in the 0.5% by weight or lower concentration range.
  • the main vehicle is an approximately 50% aqueous solution of high boiling point hydrophilic solvent. It is not essential that the fluid be precisely 50% water. Typically either glycerol and/or propylene glycol are used as hydrophilic solvents. This translates to a 5.4M glycerol or a 6.6M propylene glycol solution. Tests suggest that a solution being at least about 2M of either of these solvents (or a combination thereof) is adequate. Using excess hydrophilic solvent increases both the cost and viscosity of the product. The hydrophilic solvents increase the solubility of the active ingredients and act as particle formers when the e-cigarette mechanism boils away much of the water. Without these solvents aerosol formation would be much less efficient.
  • the inactive ingredients include a variety of flavors and/or scents. Actually, these additives are primarily scents because the human sense of taste is primarily limited to sweet, salty, sour, bitter and umami. What we perceive of as “orange” flavor or taste is actually orange scent combined with a taste of sweet and sour.
  • the glycerol and propylene glycol components of the vehicle have an actual sweet taste that can be detected by most users. Depending on the pH of the vehicle there may also be a slight sour (low pH) taste. If active ingredients such as caffeine or nicotine are present at sufficiently high concentrations, there may also be an actual discernible bitter taste. Useful scents are practically unlimited. Traditionally, menthol and mint-related scents were used in tobacco cigarettes.
  • mint-related scents are useful in e-fluid.
  • fruit flavors i.e., orange and banana
  • scents such as vanilla.
  • the preferred “flavors” are green apple, vanilla cupcake, blueberry, and mango.
  • various herbal, musky and other scents may also be appropriate. Generally, these are used at very low concentrations. Generally, under 0.1% by volume. Many of the plant extracts mentioned above also provide a unique flavor/scent.
  • the ingredients are mixed, the pH adjusted to 6.5 and heated to 60° C. to ensure that the scent/flavor is properly dispersed.
  • the ingredients are mixed, the pH adjusted to 6.5 and heated to 60° C. to ensure that the scent/flavor is properly dispersed.
  • the ingredients are mixed, the pH adjusted to 6.5 and heated to 60° C. to ensure that the scent/flavor is properly dispersed.
  • the ingredients are mixed, the pH adjusted to 6.5 and heated to 60° C. to ensure that the scent/flavor is properly dispersed.
  • the ingredients are mixed, the pH adjusted to 6.5 and heated to 60° C. to ensure that the scent/flavor is properly dispersed.
  • the ingredients are mixed, the pH adjusted to 6.5 and heated to 60° C. to ensure that the scent/flavor is properly dispersed.
  • the ingredients are mixed, the pH adjusted to 6.5 and heated to 60° C. to ensure that the scent/flavor is properly dispersed.
  • the ingredients are mixed, the pH adjusted to 6.5 and heated to 60° C. to ensure that the scent/flavor is properly dispersed.

Abstract

Improved vaping fluids for energy boos, relaxation, appetite and other functions contain active ingredients combined with cyclodextrin to enhance absorption and avoid irritation. Active ingredients include caffeine, theophylline, yerba mate and valerian as well as taurine, carnitine and L-tryptophan. The active ingredients are combined with an aqueous solution of hydrophilic solvents (such as glycerin or propylene glycol) as well as traces of scents or flavors.

Description

    CROSS-REFERENCE TO PRIOR APPLICATIONS
  • This application is based on and claims the priority and benefit of U.S. Provisional Patent Application No. 62/102,894 which was filed on 13 Jan. 2015.
  • U.S. GOVERNMENT SUPPORT
  • Not applicable.
  • BACKGROUND OF THE INVENTION
  • 1. Area of the Art
  • The current invention is in the area of e-cigarettes and “vaping” and concerns an improved non-nicotine fluid for e-cigarette devices.
  • 2. Description of the Invention
  • Smoking has a long history in human cultures. When plant materials are burned various organic chemicals that are constituents of the plant vaporize and attach themselves to the smoke particles. At the same time heat and combustion break down constituent organic chemicals and produce new chemicals all of which are present in the vapor state and/or attach themselves to the smoke particles. When the smoke is inhaled, the particles come into contact with the surface of lung cells and the chemicals absorbed to the particles transfer to the lung cells and eventually are transferred into the circulatory system. Because of the extremely large surface area of the lung, smoking is an extremely effective route for administering active compounds. Because plants contain a wide variety of secondary products inhaling the smoke delivers these products to the human body. The physiological results can be stimulation, depression or even hallucination depending on what type of plant is burned to produce the smoke.
  • Of course, the active molecules delivered by the smoke can be highly addictive as in the case of nicotine in tobacco smoke. Probably because of its addictive nature tobacco has become the primary plant material that is smoke worldwide—to the point that “smoking” has become essentially synonymous with “tobacco smoking.” Whereas tobacco smoking was once considered to be a benign or even healthful pastime, it is now considered to be a health hazard. Over the last fifty years it has been shown that tobacco smoking is major cause of lung as well as other cancers in smokers as well as those exposed to “second hand” smoke. In addition, there is a correlation between smoking tobacco and heart as well as vascular disease.
  • It is true that because of the wide range of natural chemicals (“natural products”) in plants, smoke from burning many different plants shows at least some carcinogenic properties. However, for whatever reason it appears as if tobacco smoke may be more carcinogenic than other types of smoke. In addition, it also appears as if exposure to tobacco smoke results in more vascular damage than other smoke exposure. This may be because there are insufficient data on long term exposure to other types of smoke. Or perhaps chronic exposure to constituents of tobacco smoke results in vascular damage. In any case, there is a worldwide effort to reduce or eliminate tobacco smoking. Today smoking is prohibited on airlines, in most restaurants and buildings as well as a variety of other locales. Because nicotine is addictive, there is a major industry that attempts to help smokers stop smoking.
  • “Electronic cigarettes” (e-cigarettes) have been developed as a safer alternative to smoking tobacco. In an e-cigarette a mechanism reduces a liquid (“e-cigarette fluid,” “e-fluid” or “vaping fluid”) into a smoke-like mixture of air and tiny droplets (an aerosol) which material is then inhaled. Any active constituents in the vaping fluid are then absorbed by the lungs like real smoke. Because e-cigarettes do not produce smoke, other terms have been developed to describe using the devices. One such term that is gaining popularity is “vaping.” Thus, one does not smoke an e-cigarette—one “vapes” it. E-cigarettes are thought to be safer than smoking tobacco because nothing is actually burned in an e-cigarette. The most common type of e-cigarette has a heating element which vaporizes the e-fluid to create an aerosol. Less commonly there is mechanical production of the aerosol. For example, some devices use a piezoelectric diaphragm which vibrates at ultrasonic speeds to directly form an aerosol from the e-fluid rather like a cool-mist humidifier.
  • Most e-fluids contain nicotine (approximately 0.04M-0.12M) so that vaping an e-cigarette can act as a substitute for smoking tobacco by delivering nicotine to the user. There is considerable use of such nicotine e-cigarettes as smoking cessation devices. The idea is that the users transition to the e-cigarettes and then use e-fluids with diminishing levels of nicotine until the user's nicotine addiction is overcome. However, many users alternate between “real” cigarettes and e-cigarettes so the usefulness of vaping e-cigarettes as an aid to smoking cessation is somewhat questionable. Certainly, the e-cigarette avoids the dangers of secondhand tobacco smoke.
  • There has been considerable development of e-fluid formulations with various flavors and scent ingredients being added to enhance the user's enjoyment. In addition, e-fluids without any nicotine have been marketed. The idea being that the user will sufficiently enjoy vaping so that nicotine becomes unnecessary. However, if the goal is to replace addictive nicotine, it is probably necessary to provide some other active component so that the user gets some sort of physiological result from the vaping process.
  • There is a very long history of humans ingesting various plant products for their physiological effects. Some plant products are intoxicating or even hallucinogenic. Generally, such materials are subject to strict legal controls. Other plant products are stimulants many of which are legal and widely used such as the methylxanthines: caffeine (coffee), theobromine (chocolate) and theophylline (tea). These agents improve energy and feeling of well-being. These stimulants are considered safe and many people enjoy their effects. The present inventor has considered substituting them for nicotine in e-fluid. It is believed that secondhand “smoke” from e-cigarettes containing methylxanthine derivatives would be free of the health concerns that attend secondhand e-cigarette nicotine “smoke.” There is a long history of inhaling strong preparations of theophylline and other methylxanthine derivatives as a bronchial dilator for the treatment of asthma and other obstructive lung conditions. Inhalation of these agents has not been associated with significant health problems. Therefore, use of much lower concentrations of methylxanthine derivatives in e-fluids is unlikely to have any negative health consequences. However, when inhaled, these agents will be systemically absorbed with general stimulant effects similar to consuming methylxanthine containing beverages. This will impart the physiological result to enhance the desirability of vaping.
  • SUMMARY OF THE INVENTION
  • The inventors have discovered that improved vaping fluids can be obtained by combining a variety of active ingredients with the hydrophilic solvents typical of such fluids. The active ingredients are chosen depending on the desired effects of using the fluid. For example, methylzanthines such as caffeine can be used to provide an energy boost product. Energy boost formulae can also contain taurine, cyanocobalamin, carnitine, guarana, and ginseng. Relaxation/sleep formulae can include chamomile, valerian, kava and other active ingredients. Appetite suppressant formulae can contain hoodia, yerba mate, caralluma and lecithin. Besides active ingredients a variety of scents/flavors and colors can also be included. It is preferred to used natural plant extracts to impart colors. Cyclodextrin is included to enhance absorption of the active ingredients as well as to limit any tendency of the inhaled aerosol to cause irritation. Detailed Description of the Invention
  • The following description is provided to enable any person skilled in the art to make and use the invention and sets forth the best modes contemplated by the inventor of carrying out his invention. Various modifications, however, will remain readily apparent to those skilled in the art, since the general principles of the present invention have been defined herein specifically to provide improved non-nicotine fluids for vaping.
  • Generally, e-fluids contain water and one or more hydrophilic solvent such as glycerol, propylene glycol and/or polyethylene glycol. The hydrophilic solvent is important for the production of aerosols by a heat source. When a water solution of these solvents contacts a heat source, the water rapidly vaporizes leaving behind an aerosol of hydrophilic solvent particles which contain the other ingredients that were dissolved in the original e-fluid and/or the other ingredients are present as tiny particles. The “other ingredients” (besides “active” ingredients such as nicotine, in traditional e-fluid, or methylxanthine or other active ingredients in the alternative e-fluid disclosed here) include flavors, scents and additives intended to enhance the efficacy of the other ingredients. To be effective the ingredients must be carried into the user's lungs. This generally occurs because the ingredients are bound to or dissolved in the aerosol particles. However, the aerosol particles may not always be of optimum size so that they are filtered out by lung structures before there is a chance for the active ingredients to be properly absorbed. In other cases the aerosol particles are somewhat irritating to the user's throat and other tissues.
  • The problem with the aerosol particles not being efficiently absorbed can be dealt with by increasing the concentration of the active ingredients. However, this may also increase the ability of the particles to cause irritation. Where the active ingredient is nicotine, it can be dangerous to increase the nicotine concentration too much since nicotine is extremely toxic. What is needed is a method to enhance the effectiveness of active ingredients while at the same time reducing any propensity for irritation. The present inventor has found that certain polysaccharides can serve this function. Addition of cyclodextrin to e-fluid enhances the absorbability of active ingredients while suppressing any irritating tendency of the aerosol. Cyclodextrin is a cyclic polysaccharide made of a 1, 4 linked glucose units. There are three common types: a cyclodextrin (6 glucose units), cyclodextrin (7 glucose units) and γ cyclodextrin (8 glucose units). It is known that cyclodextrins are useful for sequestering hydrophobic molecules and for forming droplets in a nebulizer. Until now it was not appreciated that cyclodextrins also promote aerosol formation with the heating elements of common e-cigarettes (as well as with the spray jets of nebulizers). More importantly, the addition of sufficient cyclodextrin to e-fluid enhances the absorption and bioavailability of any active ingredients while at the same time reducing any tendency towards irritation caused by the aerosol.
  • In solution the cyclodextrin molecules form a somewhat conical structure—that is, a hollow cylinder having a smaller opening at one end than the other. The cyclodextrin molecule in solution has an interior that is more hydrophobic than its exterior (i.e., the exterior is relatively hydrophilic). For the cyclodextrin to operate in the current invention, the molecule to be sequestered must be at least partially hydrophobic and of dimensions to fit within the cyclodextrin ring. Active ingredients such as methylxanthines and nicotine are of the right size for sequestration and are essentially hydrophobic at physiological and acid pHs. The choice of cyclodextrin is affected by the active ingredient as well as the other ingredients in the e-fluid formula. Both α and γ cyclodextrin have a water solubility that is approximately an order of magnitude higher than that of β cyclodextrin. Therefore, if it is desired to use a relatively high level of active ingredient, a and γ cyclodextrin are preferred. Otherwise, β cyclodextrin operates adequately.
  • Active Ingredients
  • For an “Energy Boost” formulation a methylxanthine alkaloid such as caffeine is combined with taurine which has beneficial biological as well as surfactant properties. As already explained methylxanthine alkaloids improve energy and provide a feeling of well-being. Taurine is a natural amino acid derivative that has an anti-anxiety effect as well as many health benefits. In addition, taurine has surfactant properties and aids in the dispersion of insoluble ingredients. Caffeine is effective in e-fluids of 0.01M to 0.15M. Much below this concentration range, there is little discernible effect whereas at much higher concentrations, the caffeine effect can be excessive. Currently, a concentration of 0.05M is preferred. Taurine has a wide effective range of at least 0.01M to 0.1M; currently 0.015M is preferred. To these active ingredients can be added cyanocobalamin (vitamin B12). This water soluble vitamin is important for many cellular functions and seems to potentiate the effects of caffeine and taurine. The cyanocobalamin has a red-magenta color and can be used as the sole coloring agent or other colors may be added as desired. This has been tested at concentrations between 0.01% and 0.1%; currently 0.083% (weight by volume) is preferred. Other common methylxanthines such as theophylline or theobromine can be substituted or used in conjunction with caffeine.
  • Other “Energy Boost” ingredients can be used either alone or in conjunction with the methylxanthines. For example, green tea extracts can be employed not only as a source of caffeine and theophylline but also for beneficial antioxidants (and to impart a flavor). Extracts of guarana (Paullinia cupana) can be used to supply caffeine as well as other beneficial natural ingredients. Extracts of Ginkgo biloba can be used to supply antioxidants Extracts of ginseng (Panax species) are also effective when combined with cyclodextrins. Finally, carnitine is effective in energy formulae. These ingredients are generally used at concentration of about 0.5% by weight or less.
  • Caffeine, other methylxanthines and taurine can be stabilized as metal complexes (zinc, magnesium and/or sodium) and/or cyclodextrin complexes. Metal complexes are formed by adding a molar excess of a water soluble salt of the desired metal. Cyclodextrin complexes form best with a molar excess of cyclodextrin. It has been found that a 2-3 fold molar excess works well although cyclodextrin is effective in the range of 0.5 to 5.0 molar ratio of cyclodextrin to active ingredient. Cyclodextrin is used preferable but can be used with the metal complex as well. That is, the required concentration of both metal and cyclodextrin can be used.
  • Besides Energy formulae, “Relaxation/sleep” formulae are also useful. In these formulae ingredients such as extracts of chamomile (Matricaria chamomilla and/or Chamaemelum nobile), extracts of kava (Piper methysticum), extracts of valerian (Valeriana officinalis), L-tryptophan and/or melatonin are used in place of the “energy” ingredients. Again these ingredients are used in the 0.5% by weight or lower concentration range.
  • Finally, it is also possible to use safe appetite suppressants in place of the energy ingredients to yield a “weight loss” formula. Various plant extracts are useful—in particular extracts of yerba mate (Ilex paraguariensis), extracts of Hoodia gordonii and extracts of Carafluma fimbriata. In addition, certain compounds such as chromium chelate and lecithin are useful in these formulae. The chromium is used at a few parts per million (ppm) while the other ingredients are used up to 0.5% by weight.
  • Vehicle and Inactive Ingredients
  • The main vehicle is an approximately 50% aqueous solution of high boiling point hydrophilic solvent. It is not essential that the fluid be precisely 50% water. Typically either glycerol and/or propylene glycol are used as hydrophilic solvents. This translates to a 5.4M glycerol or a 6.6M propylene glycol solution. Tests suggest that a solution being at least about 2M of either of these solvents (or a combination thereof) is adequate. Using excess hydrophilic solvent increases both the cost and viscosity of the product. The hydrophilic solvents increase the solubility of the active ingredients and act as particle formers when the e-cigarette mechanism boils away much of the water. Without these solvents aerosol formation would be much less efficient.
  • Besides the vehicle, the inactive ingredients include a variety of flavors and/or scents. Actually, these additives are primarily scents because the human sense of taste is primarily limited to sweet, salty, sour, bitter and umami. What we perceive of as “orange” flavor or taste is actually orange scent combined with a taste of sweet and sour. The glycerol and propylene glycol components of the vehicle have an actual sweet taste that can be detected by most users. Depending on the pH of the vehicle there may also be a slight sour (low pH) taste. If active ingredients such as caffeine or nicotine are present at sufficiently high concentrations, there may also be an actual discernible bitter taste. Useful scents are practically unlimited. Traditionally, menthol and mint-related scents were used in tobacco cigarettes. Therefore, mint-related scents are useful in e-fluid. In addition, fruit flavors (i.e., orange and banana) are popular as are more floral or “perfumed” scents such as vanilla. Currently, the preferred “flavors” are green apple, vanilla cupcake, blueberry, and mango. However, various herbal, musky and other scents may also be appropriate. Generally, these are used at very low concentrations. Generally, under 0.1% by volume. Many of the plant extracts mentioned above also provide a unique flavor/scent.
  • Sample e-fluid formulae are given in the following tables.
  • Energy Boost (100 ml)
  • Ingredient Concentration
    Caffeine 0.05M
    Taurine 0.015M
    Magnesium Chloride 0.06M
    Cyanocobalamin 0.083% (weight by volume)
    Cyclodextrin 0.2M
    Scent/Flavor trace
    Vehicle To make 100 ml
  • The ingredients are mixed, the pH adjusted to 6.5 and heated to 60° C. to ensure that the scent/flavor is properly dispersed.
  • Focus Boost (100 ml)
  • Ingredient Concentration
    Ginkgo biloba extract 0.25% (volume by volume)
    Carnitine 0.1% (weight by volume)M
    Magnesium Chloride 0.06M
    Cyclodextrin 0.2M
    Scent/Flavor trace
    Vehicle To make 100 ml
  • The ingredients are mixed, the pH adjusted to 6.5 and heated to 60° C. to ensure that the scent/flavor is properly dispersed.
  • Focus Boost II (100 ml)
  • Ingredient Concentration
    Taurine 0.015M
    Sodium Chloride 0.06M
    Cyanocobalamin 0.083% (weight by volume)
    Cyclodextrin 0.05M
    Scent/Flavor trace
    Vehicle To make 100 ml
  • The ingredients are mixed, the pH adjusted to 6.5 and heated to 60° C. to ensure that the scent/flavor is properly dispersed.
  • Sleep (100 ml)
  • Ingredient Concentration
    Valerian extract 0.5% (volume by volume)
    Chamomile extract 0.25% (volume by volume
    Sodium Chloride 0.06M
    Cyclodextrin 0.05M
    Scent/Flavor trace
    Vehicle To make 100 ml
  • The ingredients are mixed, the pH adjusted to 6.5 and heated to 60° C. to ensure that the scent/flavor is properly dispersed.
  • Appetite suppressant (100 ml)
  • Ingredient Concentration
    Yerba mate extract 0.5% (volume by volume)
    Lecithin 0.5% (weight by volume)
    Cyclodextrin 0.05M
    Scent/Flavor trace
    Vehicle To make 100 ml
  • The ingredients are mixed, the pH adjusted to 6.5 and heated to 60° C. to ensure that the scent/flavor is properly dispersed.
  • Flavor only (100 ml)
  • Ingredient Concentration
    Cyclodextrin 0.01M
    Scent/Flavor trace
    Vehicle To make 100 ml
  • The ingredients are mixed, the pH adjusted to 6.5 and heated to 60° C. to ensure that the scent/flavor is properly dispersed.
  • Enhanced Traditional (nicotine containing) (100 ml)
  • Ingredient Concentration
    Nicotine 0.08M
    Taurine 0.015M
    Sodium Chloride 0.015M
    Cyanocobalamin 0.083% (weight by volume)
    Cyclodextrin 0.2M
    Scent/Flavor trace
    Vehicle To make 100 ml
  • The ingredients are mixed, the pH adjusted to 6.5 and heated to 60° C. to ensure that the scent/flavor is properly dispersed.
  • Improved Traditional (nicotine containing) (100 ml)
  • Ingredient Concentration
    Nicotine 0.08M
    Cyclodextrin 0.1M
    Scent/Flavor trace
    Vehicle To make 100 ml
  • The ingredients are mixed, the pH adjusted to 6.5 and heated to 60° C. to ensure that the scent/flavor is properly dispersed.
  • The following claims are thus to be understood to include what is specifically illustrated and described above, what is conceptually equivalent, what can be obviously substituted and also what essentially incorporates the essential idea of the invention. Those skilled in the art will appreciate that various adaptations and modifications of the just-described preferred embodiment can be configured without departing from the scope of the invention. The illustrated embodiment has been set forth only for the purposes of example and that should not be taken as limiting the invention. Therefore, it is to be understood that, within the scope of the appended claims, the invention may be practiced other than as specifically described herein.

Claims (14)

What is claimed is:
1. An e-fluid for use in an e-cigarette or similar device comprising:
caffeine at a concentration of between about 0.01M to about 0.15M;
cyclodextrin at a concentration having a molar ratio with the caffeine concentration of 0.5 to 5.0; and
an aqueous solution of hydrophilic solvent being between about 2M and 10M hydrophilic solvent.
2. The e-fluid of claim 1 wherein the hydrophilic solvent is selected from the group consisting of glycerol and propylene glycol.
3. The e-fluid of claim 1 further comprising carnitine at a concentration of about 0.01% and about 0.5% volume by volume.
4. The e-fluid of claim 1 further comprising taurine at a concentration of between about 0.01M and about 0.1M.
5. The e-fluid of claim 1 further comprising cyanocobalamin at a concentration of between about 0.01% weight by volume and 0.1% weight by volume.
6. An e-fluid for use in an e-cigarette or similar device comprising:
valerian extract at a concentration of between about 0.01% and about 0.5% volume by volume;
cyclodextrin at a concentration having a molar ratio with the valerian extract concentration of 0.5 to 5.0; and
an aqueous solution of hydrophilic solvent being between about 2M and 10M hydrophilic solvent.
7. The e-fluid of claim 6 wherein the hydrophilic solvent is selected from the group consisting of glycerol and propylene glycol.
8. The e-fluid of claim 6 further comprising L-tryptophan at a concentration of about 0.01% and about 0.5% weight by volume.
9. The e-fluid of claim 6 further comprising extract of chamomile at a concentration of about 0.01% and about 0.5% volume by volume.
10. The e-fluid of claim 6 further comprising cyanocobalamin at a concentration of between about 0.01% weight by volume and 0.1% weight by volume.
11. An e-fluid for use in an e-cigarette or similar device comprising:
nicotine at a concentration of between about 0.01 M to about 0.2M;
cyclodextrin at a concentration having a molar ratio with the nicotine concentration of 0.5 to 5.0; and
an aqueous solution of hydrophilic solvent being between about 2M and 10M hydrophilic solvent.
12. The e-fluid of claim 11 wherein the hydrophilic solvent is selected from the group consisting of glycerol and propylene glycol.
13. The e-fluid of claim 11 further comprising taurine at a concentration of between about 0.01M to about 0.1M.
14. The e-fluid of claim 11 further comprising cyanocobalamin at a concentration of between about 0.01% weight by volume and 0.1% weight by volume.
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Cited By (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9770055B2 (en) 2015-05-15 2017-09-26 Lunatech, Llc Vaporizable material handling for electronic vapor device
US9888723B2 (en) 2015-05-15 2018-02-13 Lunatech, Llc Hybrid vapor delivery system utilizing nebulized and non-nebulized elements
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US9936737B2 (en) 2015-10-28 2018-04-10 Lunatech, Llc Methods and systems for a dual function vapor device
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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
US10045568B2 (en) 2013-12-23 2018-08-14 Juul Labs, Inc. Vaporization device systems and methods
US10060639B2 (en) 2015-06-11 2018-08-28 Lunatech, Llc Air analyzer and treatment apparatus
US10058130B2 (en) 2013-12-23 2018-08-28 Juul Labs, Inc. Cartridge for use with a vaporizer device
US10065138B2 (en) 2015-06-17 2018-09-04 Lunatech, Llc Remote controllable air treatment apparatus
US10076139B2 (en) 2013-12-23 2018-09-18 Juul Labs, Inc. Vaporizer apparatus
US10088463B2 (en) 2015-06-11 2018-10-02 Lunatech, Llc Calibrating electronic vapor device
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
US20180338905A1 (en) * 2017-05-26 2018-11-29 Inhale Health, LLC Bioavailable aerosolized supplement formulations
USD836541S1 (en) 2016-06-23 2018-12-25 Pax Labs, Inc. Charging device
US10215430B2 (en) 2015-06-15 2019-02-26 Lunatech, Llc Electronic vapor and analysis with HVAC integration
US10215429B2 (en) 2015-06-15 2019-02-26 Lunatech, Llc Localized air sensing and treatment
USD842536S1 (en) 2016-07-28 2019-03-05 Juul Labs, Inc. Vaporizer cartridge
US10244793B2 (en) 2005-07-19 2019-04-02 Juul Labs, Inc. Devices for vaporization of a substance
US10279934B2 (en) 2013-03-15 2019-05-07 Juul Labs, Inc. Fillable vaporizer cartridge and method of filling
WO2019086857A1 (en) * 2017-11-01 2019-05-09 Nicoventures Holdings Limited Flavoured vaporisable formulation
WO2019086858A1 (en) * 2017-11-01 2019-05-09 British American Tobacco (Investments) Limited Aerosolisable formulation
USD849996S1 (en) 2016-06-16 2019-05-28 Pax Labs, Inc. Vaporizer cartridge
USD851830S1 (en) 2016-06-23 2019-06-18 Pax Labs, Inc. Combined vaporizer tamp and pick tool
US10405582B2 (en) 2016-03-10 2019-09-10 Pax Labs, Inc. Vaporization device with lip sensing
US10512282B2 (en) 2014-12-05 2019-12-24 Juul Labs, Inc. Calibrated dose control
WO2020089638A1 (en) * 2018-11-01 2020-05-07 Nicoventures Trading Limited Aerosolised formulation
WO2020089634A1 (en) * 2018-11-01 2020-05-07 Nicoventures Trading Limited Aerosolisable formulation
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WO2020089641A1 (en) * 2018-11-01 2020-05-07 Nicoventures Trading Limited Aerosolisable formulation
USD887632S1 (en) 2017-09-14 2020-06-16 Pax Labs, Inc. Vaporizer cartridge
WO2020205676A1 (en) * 2019-03-29 2020-10-08 V Rush Vapes LLC Composition of athletic and fitness supplements, method for production and method for pulmonary administration of same
US10865001B2 (en) 2016-02-11 2020-12-15 Juul Labs, Inc. Fillable vaporizer cartridge and method of filling
WO2021042269A1 (en) * 2019-09-03 2021-03-11 深圳雾芯科技有限公司 E-cigarette liquid
CN112911950A (en) * 2018-11-01 2021-06-04 尼科创业贸易有限公司 Aerosol formulation
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WO2022049512A1 (en) * 2020-09-03 2022-03-10 Rai Strategic Holdings, Inc. Aerosolisable formulation
CN114299688A (en) * 2021-12-29 2022-04-08 张璇燕 Tobacco tar component identification method and system based on electronic smoke detection
RU2785541C2 (en) * 2018-11-01 2022-12-08 Никовенчерс Трейдинг Лимитед Aerosolised composition
US11553734B2 (en) 2018-11-08 2023-01-17 Juul Labs, Inc. Cartridges for vaporizer devices

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110558605B (en) * 2019-09-27 2021-07-06 深圳雾芯科技有限公司 Electronic cigarette liquid
GB2586301B (en) 2020-04-07 2021-08-25 Splash Tm Gmbh Stable-Foam inhalation Device and Cartridge

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030159702A1 (en) * 2002-01-21 2003-08-28 Lindell Katarina E.A. Formulation and use manufacture thereof
US20030171408A1 (en) * 2002-03-11 2003-09-11 Caplan Jay L. Therapeutic method of delivering a medicament to avoid irritating effects on membranes of user
JP2012505878A (en) * 2008-10-14 2012-03-08 マクニール アーベー Multiple partial oral dosage forms and uses thereof

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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
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
US10104915B2 (en) 2013-12-23 2018-10-23 Juul Labs, Inc. Securely attaching cartridges for vaporizer devices
US10912331B2 (en) 2013-12-23 2021-02-09 Juul Labs, Inc. Vaporization device systems and methods
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US10111470B2 (en) 2013-12-23 2018-10-30 Juul Labs, Inc. Vaporizer apparatus
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US10045567B2 (en) 2013-12-23 2018-08-14 Juul Labs, Inc. Vaporization device systems and methods
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US10058130B2 (en) 2013-12-23 2018-08-28 Juul Labs, Inc. Cartridge for use with a vaporizer device
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US10117466B2 (en) 2013-12-23 2018-11-06 Juul Labs, Inc. Vaporization device systems and methods
US10159282B2 (en) 2013-12-23 2018-12-25 Juul Labs, Inc. Cartridge for use with a vaporizer device
US10701975B2 (en) 2013-12-23 2020-07-07 Juul Labs, Inc. Vaporization device systems and methods
US10076139B2 (en) 2013-12-23 2018-09-18 Juul Labs, Inc. Vaporizer apparatus
US10058129B2 (en) 2013-12-23 2018-08-28 Juul Labs, Inc. Vaporization device systems and methods
US10512282B2 (en) 2014-12-05 2019-12-24 Juul Labs, Inc. Calibrated dose control
US10039320B2 (en) 2015-05-14 2018-08-07 Lunatech, Llc Multi-chambered vaporizer and blend control
US9888723B2 (en) 2015-05-15 2018-02-13 Lunatech, Llc Hybrid vapor delivery system utilizing nebulized and non-nebulized elements
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US10865001B2 (en) 2016-02-11 2020-12-15 Juul Labs, Inc. Fillable vaporizer cartridge and method of filling
US10405582B2 (en) 2016-03-10 2019-09-10 Pax Labs, Inc. Vaporization device with lip sensing
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EP3630119A4 (en) * 2017-05-26 2020-12-30 Inhale Health LLC Bioavailable aerosolized supplement formulations and methods thereof
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KR20200060478A (en) * 2017-11-01 2020-05-29 니코벤처스 트레이딩 리미티드 Flavorable vaporizing agent
CN111542233A (en) * 2017-11-01 2020-08-14 尼科创业贸易有限公司 Aerosol formulation
CN111629607A (en) * 2017-11-01 2020-09-04 尼科创业贸易有限公司 Flavored vaporizable formulations
KR102559988B1 (en) * 2017-11-01 2023-07-25 니코벤처스 트레이딩 리미티드 Aerosolizable formulations
US20210177040A1 (en) * 2017-11-01 2021-06-17 Nicoventures Trading Limited Aerosolizable formulation
KR102444095B1 (en) * 2017-11-01 2022-09-15 니코벤처스 트레이딩 리미티드 Flavored Vaporizing Agents
WO2019086857A1 (en) * 2017-11-01 2019-05-09 Nicoventures Holdings Limited Flavoured vaporisable formulation
JP2021500888A (en) * 2017-11-01 2021-01-14 ニコベンチャーズ トレーディング リミテッド Aerosolizable formulations
JP2021500890A (en) * 2017-11-01 2021-01-14 ニコベンチャーズ トレーディング リミテッド Fragrant vaporizable formulation
JP7041261B2 (en) 2017-11-01 2022-03-23 ニコベンチャーズ トレーディング リミテッド Fragrant vaporizable formulation
WO2019086858A1 (en) * 2017-11-01 2019-05-09 British American Tobacco (Investments) Limited Aerosolisable formulation
KR20200056459A (en) 2017-11-01 2020-05-22 니코벤처스 트레이딩 리미티드 Aerosolizable formulations
RU2745353C1 (en) * 2017-11-01 2021-03-24 Никовенчерс Трейдинг Лимитед Flavored vaporable composition
AU2019372223B2 (en) * 2018-11-01 2022-07-14 Nicoventures Trading Limited Aerosolised formulation
JP2022506067A (en) * 2018-11-01 2022-01-17 ニコベンチャーズ トレーディング リミテッド Aerosolizable formulations
CN113038842A (en) * 2018-11-01 2021-06-25 尼科创业贸易有限公司 Aerosol formulation
CN113056208A (en) * 2018-11-01 2021-06-29 尼科创业贸易有限公司 Aerosol formulation
KR20210080406A (en) * 2018-11-01 2021-06-30 니코벤처스 트레이딩 리미티드 Aerosolizable formulations
CN113163841A (en) * 2018-11-01 2021-07-23 尼科创业贸易有限公司 Aerosol formulation
CN113163840A (en) * 2018-11-01 2021-07-23 尼科创业贸易有限公司 Aerosol formulation
CN113163842A (en) * 2018-11-01 2021-07-23 尼科创业贸易有限公司 Aerosol formulation
WO2020089638A1 (en) * 2018-11-01 2020-05-07 Nicoventures Trading Limited Aerosolised formulation
CN113226067A (en) * 2018-11-01 2021-08-06 尼科创业贸易有限公司 Aerosol formulation
EP4324341A3 (en) * 2018-11-01 2024-04-17 Nicoventures Trading Limited Aerosolisable formulation
US20210368852A1 (en) * 2018-11-01 2021-12-02 Nicoventures Trading Limited Aerosolised formulation
US20210386111A1 (en) * 2018-11-01 2021-12-16 Nicoventures Trading Limited Aerosolisable formulation
JP2022505851A (en) * 2018-11-01 2022-01-14 ニコベンチャーズ トレーディング リミテッド Aerosolizable formulations
RU2764202C1 (en) * 2018-11-01 2022-01-14 Никовенчерс Трейдинг Лимитед Composition turned to aerosol
JP2022506076A (en) * 2018-11-01 2022-01-17 ニコベンチャーズ トレーディング リミテッド Aerosolized formulation
JP2022506107A (en) * 2018-11-01 2022-01-17 ニコベンチャーズ トレーディング リミテッド Aerosolizable formulations
CN112911950A (en) * 2018-11-01 2021-06-04 尼科创业贸易有限公司 Aerosol formulation
KR102652876B1 (en) 2018-11-01 2024-03-28 니코벤처스 트레이딩 리미티드 Aerosolizable Formulations
WO2020089634A1 (en) * 2018-11-01 2020-05-07 Nicoventures Trading Limited Aerosolisable formulation
RU2806111C2 (en) * 2018-11-01 2023-10-26 Никовенчерс Трейдинг Лимитед Aerosol creating composition
WO2020089639A1 (en) * 2018-11-01 2020-05-07 Nicoventures Trading Limited Aerosolised formulation
AU2019371080B2 (en) * 2018-11-01 2022-07-14 Nicoventures Trading Limited Aerosolisable formulation
WO2020089635A1 (en) * 2018-11-01 2020-05-07 Nicoventures Trading Limited Aerosolisable formulation
AU2019370810B2 (en) * 2018-11-01 2022-11-10 Nicoventures Trading Limited Aerosolised formulation
AU2019370809B2 (en) * 2018-11-01 2022-12-01 Nicoventures Trading Limited Aerosolisable formulation
RU2785541C2 (en) * 2018-11-01 2022-12-08 Никовенчерс Трейдинг Лимитед Aerosolised composition
RU2785974C2 (en) * 2018-11-01 2022-12-15 Никовенчерс Трейдинг Лимитед Aerosolising composition
WO2020089641A1 (en) * 2018-11-01 2020-05-07 Nicoventures Trading Limited Aerosolisable formulation
US11553734B2 (en) 2018-11-08 2023-01-17 Juul Labs, Inc. Cartridges for vaporizer devices
WO2020205676A1 (en) * 2019-03-29 2020-10-08 V Rush Vapes LLC Composition of athletic and fitness supplements, method for production and method for pulmonary administration of same
WO2021042269A1 (en) * 2019-09-03 2021-03-11 深圳雾芯科技有限公司 E-cigarette liquid
WO2022049512A1 (en) * 2020-09-03 2022-03-10 Rai Strategic Holdings, Inc. Aerosolisable formulation
CN114299688A (en) * 2021-12-29 2022-04-08 张璇燕 Tobacco tar component identification method and system based on electronic smoke detection

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