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US20180007924A9 - Homogenous cannabis compositions and methods of making the same - Google Patents

Homogenous cannabis compositions and methods of making the same Download PDF

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Publication number
US20180007924A9
US20180007924A9 US15/084,954 US201615084954A US2018007924A9 US 20180007924 A9 US20180007924 A9 US 20180007924A9 US 201615084954 A US201615084954 A US 201615084954A US 2018007924 A9 US2018007924 A9 US 2018007924A9
Authority
US
United States
Prior art keywords
composition
oil
cannabis
cannabinoid
mixture
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US15/084,954
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English (en)
Other versions
US20170280740A1 (en
Inventor
Jeremy H. Goldstein
Justin Eric Singer
Adrian Verwolf
Garret Nicodemus
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
5071 Inc
Original Assignee
5071 Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to US15/084,954 priority Critical patent/US20180007924A9/en
Priority to CA2985332A priority patent/CA2985332C/fr
Priority to CA3176674A priority patent/CA3176674A1/fr
Priority to PCT/US2016/025044 priority patent/WO2016186735A1/fr
Assigned to 5071, INC. reassignment 5071, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: GOLDSTEIN, Jeremy H., SINGER, Justin Eric
Application filed by 5071 Inc filed Critical 5071 Inc
Assigned to 5071, INC. reassignment 5071, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: NICODEMUS, GARRET, VERWOLF, Adrian
Publication of US20170280740A1 publication Critical patent/US20170280740A1/en
Publication of US20180007924A9 publication Critical patent/US20180007924A9/en
Priority to US16/571,610 priority patent/US11980204B2/en
Priority to US18/340,572 priority patent/US12225913B2/en
Priority to US18/963,286 priority patent/US20250089735A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23FCOFFEE; TEA; THEIR SUBSTITUTES; MANUFACTURE, PREPARATION, OR INFUSION THEREOF
    • A23F3/00Tea; Tea substitutes; Preparations thereof
    • A23F3/06Treating tea before extraction; Preparations produced thereby
    • A23F3/14Tea preparations, e.g. using additives
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L2/00Non-alcoholic beverages; Dry compositions or concentrates therefor; Preparation or treatment thereof
    • A23L2/52Adding ingredients
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/105Plant extracts, their artificial duplicates or their derivatives
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/115Fatty acids or derivatives thereof; Fats or oils
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23PSHAPING OR WORKING OF FOODSTUFFS, NOT FULLY COVERED BY A SINGLE OTHER SUBCLASS
    • A23P10/00Shaping or working of foodstuffs characterised by the products
    • A23P10/40Shaping or working of foodstuffs characterised by the products free-flowing powder or instant powder, i.e. powder which is reconstituted rapidly when liquid is added
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/045Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
    • A61K31/05Phenols
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/658Medicinal preparations containing organic active ingredients o-phenolic cannabinoids, e.g. cannabidiol, cannabigerolic acid, cannabichromene or tetrahydrocannabinol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0087Galenical forms not covered by A61K9/02 - A61K9/7023
    • A61K9/0095Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1617Organic compounds, e.g. phospholipids, fats
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1617Organic compounds, e.g. phospholipids, fats
    • A61K9/1623Sugars or sugar alcohols, e.g. lactose; Derivatives thereof; Homeopathic globules
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1629Organic macromolecular compounds
    • A61K9/1658Proteins, e.g. albumin, gelatin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1664Compounds of unknown constitution, e.g. material from plants or animals
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00Food compositions, function of food ingredients or processes for food or foodstuffs

Definitions

  • This disclosure relates to the cannabis industry.
  • the disclosure relates to cannabis compositions for use in the making beverages, methods of making beverages, and beverages.
  • Cannabis has a long history of being consumed for many purposes and in many forms.
  • the psychoactive effects of cannabis are well known, however the medical benefits are just as useful. Treating glaucoma, pain management, appetite stimulation and easing anxiety are just a few of the potential benefits.
  • the source of these effects are in the cannabinoids, a class of compounds found exclusively in the cannabis plant.
  • cannabinoids a class of compounds found exclusively in the cannabis plant.
  • THC tetrahydrocannabniol
  • CBD cannabidiol
  • CBD is also another major cannabinoid comprising up to 40% of cannabis extract and could have as many health benefits as THC.
  • a common method is alcohol extraction. Using a solvent to extract the cannabinoids and then evaporating the alcohol leaving a resin. Further extraction and evaporation can yield a product that is closer to a solid.
  • Another common method for the purposes of making edibles is placing the cannabis leaves in butter, heavy cream, oil, etc and then heating to extract the cannabinoids. The end product is then used as an ingredient in baking or cooking which usually results in a high caloric food due to the fat needed to extract the cannabinoids.
  • Cannabinoids are soluble in fats and alcohols. Which is why when making cannabis tea the cannabinoids have to be already extracted. Just placing cannabis leaves in hot water will not effectively extract any of the vital cannabinoids.
  • the cannabis arts do not have homogenous cannabis beverages.
  • Existing cannabis beverages include large amounts of caloric material.
  • Existing cannabis beverages are not capable of providing consistent cannabinoid concentrations, especially at low cannabinoid concentrations.
  • these new cannabis compositions are beverages, such as tea.
  • these new cannabis compositions are dehydrated beverages, such as powders or crystalline forms, which can be mixed with other components, like tea, and added to water.
  • the disclosed cannabis compositions are homogenous. In one embodiment, the disclosed cannabis compositions include a surfactant and a carrier oil. In one embodiment, the disclosed cannabis compositions are consistent with respect to cannabinoid amount. In one embodiment, the disclosed cannabis compositions are low-calorie cannabis beverages, such as low calorie cannabis teas.
  • compositions comprising:
  • cannabinoid refers to a compound that acts on the cannabinoid receptor.
  • the compositions are low does compositions having 0.1 to 10 mg of cannabinoid. In some embodiments, the composition comprises between 0.5 to 5 mg.
  • cannabinoid can be used, such as more than 10 mg, for example 20-500 mg or 50-200 mg.
  • cannabinoids are tetrahydrocannabinol, cannabidiol, cannabigerol, cannabichromene, cannabicyclol, cannabivarin, cannabielsoin, cannabicitran, cannabigerolic acid, cannabigerolic acid monomethylether, cannabigerol monomethylether, cannabigerovarinic acid, cannabigerovarin, cannabichromenic acid, cannabichromevarinic acid, cannabichromevarin, cannabidolic acid, cannabidiol monomethylether, cannabidiol-C 4 , cannabidivarinic acid, cannabidiorcol, delta-9-tetrahydrocannabinolic acid A, delta-9-tetrahydrocannabinolic
  • THC tetrahydrocannabinol
  • CBD canbidiol
  • surfactant refers to a compound that lowers the surface tension between two liquids or between a liquid and solid.
  • Surfactants can be anionic, cationic, non-ionic and amphoteric.
  • Examples of surfactants are ammonium lauryl sulfate, dioctyl sodium sulfosuccinate, perflurooctanoic acid, potassium lauryl sulfate, soap, sodium dodecyl sulfate, sodium dodecylbenzenesulfonate, sodium laureth sulfate, sodium lauroyl sarcosinate, sodium myreth sulfate, sodium pareth sulfate, sodium stearate, perflurobutanesulfonic acid, perfluorononanoic acid, perlurooactanesulfonic acid, benzalkonium chloride, benzethonium chloride, bronidox, dimethyldioctade
  • polysorbate 80 refers to a compound having the following structure:
  • glycol monostearate refers to a compound having the following structure:
  • carrier oil refers to an oil that can be used to form a homogenized mixture with cannabis oil. Examples include coconut oil, palm oil, palm kernel oil, hemp oil, caproic acid and caprylic acid.
  • carrier oils within the context of this disclosure is medium chain triglycerides.
  • coconut oil is another example of a carrier oil within the context of this disclosure.
  • hemp oil is another example of a carrier oil within the context of this disclosure.
  • coconut oil means oil extracted from the kernel or meat of coconuts.
  • coconut is the fruit of the coconut palm.
  • coconut oil is noted for it's high saturated content. Examples include lauric acid, myristic acid, palmitic acid, and decanoic acid.
  • hemp oil refers to oil obtained from hemp seeds. Hemp seeds come from a variety of the Cannabis sativa plant that does not contain a high amount of tetrahydrocannabinol.
  • the oil is about 80% essential fatty acids. Examples include linolenic acid, omega-6, alpha-linolenic acid, and omega-3.
  • the composition comprises a cannabinoid, a surfactant, a carrier oil, and a sugar alcohol.
  • sugar alcohol refers to alcohols prepared from sugars with the general chemical formula HOCH 2 (CHOH) n CH 2 OH.
  • examples include glycerol, erythritol, threitol, arabitol, xylitol, mannitol, ribitol, mannitol, galacitol, fucitol, inositol, volemitol, maltitol, lacitol, malootetraitol, polyglycitol, sorbitol, iditol, isomalt, and maltotriitol.
  • sugar alcohols within the context of this disclosure include glycerol/glycerin or sorbitol.
  • glycol refers to a compound having the following structure:
  • sorbitol refers to a compound having the following structure:
  • the composition disclosed herein comprises a cannabinoid, a surfactant, a carrier oil, and a gelling agent.
  • gelling agent means a substance that dissolves in the liquid phase and forms a weak cohesive internal structure. Examples include natural gums, starches, pectins, agar-agar, and gelatin.
  • gelatin refers to a gelling agent derived from the collagen of various all byproducts.
  • the composition comprises a cannabinoid, a surfactant, a carrier oil, and has less than 10 mass % water. In one embodiment, the composition is a solid. In one embodiment, the composition is a granual.
  • the term “less than 10 mass % water” means less than 10% of water, by mass, of the composition.
  • the composition comprises a cannabinoid, a surfactant, a carrier oil, and has more than 95 mass % water.
  • the term “more than 95 mass % water” means less than 95% of water, by mass, of the composition.
  • the composition comprises a cannabinoid, a surfactant, a carrier oil, and a flavoring agent.
  • flavoring agent means a compound that adds a flavor to a composition.
  • flavoring agents include amyl acetate, benzaldehyde, ethyl butyrate, methyl anthranilate, methyl salicylate, fumaric acid, diacetyl, cinnamaldehyde, ethyl propionate, limonene, ethyl decadienoate, allyl hexanoate, ethyl maltol, ethylvanillin, and methyl salicylate.
  • the composition comprises a coloring agent.
  • coloring agent means any substance that adds or changes the color of the substance to which the coloring agent is added.
  • examples of the term coloring agent include any dye, pigment or substance that imparts color when it is added to food or drink.
  • the coloring agent can be natural or non-natural. Such agents come in many forms, including liquids, powders, gels, dyes, lakes, and pastes.
  • one or more coloring agents can be added to the compositions of this disclosure to match the coloring between two ingredients.
  • brownish color is added to a compositions comprising a cannabinoid, a surfactant, and a carrier oil in order to make the said compositions take on the color of natural tea.
  • the composition comprises a cannabinoid, a surfactant, a carrier oil, and tea.
  • tea are tea leaves.
  • tea is meant to include any composition that is similar or labeled as tea, either natural or synthetic. Tea refers to both artificially flavored and/or artificially colored compositions in addition to all forms of natural tea leaves.
  • the cannabis compositions are brown granules.
  • leaf refers to forms of the plant Camellia sinensis.
  • the composition comprises less than 4 grams of caloric mass. In one embodiment the caloric mass is less than 2 grams.
  • caloric mass means mass metabolized by humans to generate energy. Examples include carbohydrates and proteins which give 4 cal/gram and fats which give 9 cal/gram.
  • the composition comprises 0.5 to 5 mg of the cannabinoid is present in a consistent amount, having less than 0.2 mg of deviation across sample portions of the composition.
  • the term“consistent amount” means a collection of samples would all have relatively similar amounts of the cannabinoid. Similar means limited amount of deviation in the mass of the cannabinoid. For example, if a collection of compositions were analyzed to determine the mass of cannabinoid present, each sample in that collection would have a similar mass of cannabinoid present in relation to the total amount of each composition.
  • the composition comprises:
  • the gram amounts of ingredients depend on the batch size. Gram amounts for batches can be determined by following the mixing guidelines below.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Polymers & Plastics (AREA)
  • Food Science & Technology (AREA)
  • Nutrition Science (AREA)
  • Botany (AREA)
  • Mycology (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Zoology (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Medicines Containing Plant Substances (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)
US15/084,954 2015-05-18 2016-03-30 Homogenous cannabis compositions and methods of making the same Abandoned US20180007924A9 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
US15/084,954 US20180007924A9 (en) 2015-05-18 2016-03-30 Homogenous cannabis compositions and methods of making the same
CA2985332A CA2985332C (fr) 2015-05-18 2016-03-30 Compositions de cannabis homogenes et methodes de preparation
CA3176674A CA3176674A1 (fr) 2015-05-18 2016-03-30 Compositions de cannabis homogenes et methodes de preparation
PCT/US2016/025044 WO2016186735A1 (fr) 2015-05-18 2016-03-30 Compositions de cannabis homogènes et leurs procédés de production
US16/571,610 US11980204B2 (en) 2015-05-18 2019-09-16 Cannabis compositions and methods of making the same
US18/340,572 US12225913B2 (en) 2015-05-18 2023-06-23 Cannabis compositions and methods of making the same
US18/963,286 US20250089735A1 (en) 2015-05-18 2024-11-27 Cannabis compositions and methods of making the same

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201562163316P 2015-05-18 2015-05-18
US15/084,954 US20180007924A9 (en) 2015-05-18 2016-03-30 Homogenous cannabis compositions and methods of making the same

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US16/571,610 Continuation US11980204B2 (en) 2015-05-18 2019-09-16 Cannabis compositions and methods of making the same

Publications (2)

Publication Number Publication Date
US20170280740A1 US20170280740A1 (en) 2017-10-05
US20180007924A9 true US20180007924A9 (en) 2018-01-11

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Family Applications (4)

Application Number Title Priority Date Filing Date
US15/084,954 Abandoned US20180007924A9 (en) 2015-05-18 2016-03-30 Homogenous cannabis compositions and methods of making the same
US16/571,610 Active US11980204B2 (en) 2015-05-18 2019-09-16 Cannabis compositions and methods of making the same
US18/340,572 Active US12225913B2 (en) 2015-05-18 2023-06-23 Cannabis compositions and methods of making the same
US18/963,286 Pending US20250089735A1 (en) 2015-05-18 2024-11-27 Cannabis compositions and methods of making the same

Family Applications After (3)

Application Number Title Priority Date Filing Date
US16/571,610 Active US11980204B2 (en) 2015-05-18 2019-09-16 Cannabis compositions and methods of making the same
US18/340,572 Active US12225913B2 (en) 2015-05-18 2023-06-23 Cannabis compositions and methods of making the same
US18/963,286 Pending US20250089735A1 (en) 2015-05-18 2024-11-27 Cannabis compositions and methods of making the same

Country Status (3)

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US (4) US20180007924A9 (fr)
CA (2) CA2985332C (fr)
WO (1) WO2016186735A1 (fr)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020073032A1 (fr) * 2018-10-06 2020-04-09 Capaldi Francesco Systèmes et procédés permettant de combiner des cannabinoïdes et une solution à base de sucre, et de créer des comprimés à dissolution buccale
WO2020176806A1 (fr) * 2019-02-27 2020-09-03 3-Delta, Inc. Compositions qui contiennent une matière végétale lipophile et un tensioactif, et procédés associés
US11980204B2 (en) 2015-05-18 2024-05-14 5071, Inc. Cannabis compositions and methods of making the same
US12264296B2 (en) 2020-09-02 2025-04-01 Michael V. Zumpano Compositions that contain lipophilic plant material and surfactant, and related methods

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3344066A4 (fr) * 2015-12-09 2019-11-13 Poviva Tea, LLC Compositions de boissons stables prêtes à boire comprenant des agents actifs lipophiles
AU2018283411B2 (en) * 2017-06-16 2021-04-29 Sorse Technology Corporation Preparing stable liquid emulsion forms of plant extract
EP3651738B1 (fr) * 2017-07-14 2024-04-03 5071, Inc. Compositions comprenant des cannabinoïdes et leurs production
WO2019018705A1 (fr) * 2017-07-21 2019-01-24 Masaya World, Llc Acide caprylique enrichi en cannabidiol
NZ764977A (en) 2017-10-30 2023-01-27 Whistler Tech Corp Terpene enrichment methods and systems
CA3128712A1 (fr) * 2018-11-30 2020-06-04 Canopy Growth Corporation Formulations hydrosolubles, methodes de fabrication et utilisation
US20200352191A1 (en) * 2019-05-06 2020-11-12 Karl Lonsbery Edible formulations and uses thereof
US10919828B1 (en) * 2020-02-14 2021-02-16 Aicardo Roa-Espinosa Process for manufacturing cannabidiol
US11311559B2 (en) 2020-04-20 2022-04-26 Poviva Corp. Compositions and methods for enhanced delivery of antiviral agents
US20210329938A1 (en) * 2020-04-27 2021-10-28 Mikki West Cannabis beverage compositions
AU2021293266A1 (en) * 2020-06-19 2023-02-02 NuRevelation, LLC Nanoparticle-encapsulated cannabinoids and methods for making and using same
US20210393540A1 (en) * 2020-06-19 2021-12-23 NuRevelation, LLC Nanoparticle-encapsulated cannabinoids and methods for making and using same

Family Cites Families (84)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US28919A (en) * 1860-06-26 Improvement in plows
US3506457A (en) 1965-02-25 1970-04-14 Pillsbury Co Agglomerated sugar products and method
DE3702029A1 (de) 1987-01-24 1988-08-04 Basf Ag Waessriges oder pulverfoermiges, wasserdispergierbares praeparat eines in wasser schwerloeslichen pharmazeutischen wirkstoffs und verfahren zu seiner herstellung
US4830862A (en) 1987-07-31 1989-05-16 The Procter & Gamble Company Calcium-supplemented beverages and beverage concentrates containing low levels of sulfate
US5284674A (en) 1992-05-11 1994-02-08 Fazio Susan C Powdered dairy creamer
US6197356B1 (en) 1993-08-03 2001-03-06 Immunopath Profile, Inc. Process for preparing hypoallergenic foods
US5554400A (en) 1994-08-25 1996-09-10 The Procter & Gamble Company Infusion beverage product comprising co-agglomerated creamer and sweetener suitable for bag and filter pack brewing
GB9625589D0 (en) 1996-12-10 1997-01-29 Boots Co Plc Therapeutic agents
GB9726916D0 (en) 1997-12-19 1998-02-18 Danbiosyst Uk Nasal formulation
US6440449B1 (en) * 1998-01-15 2002-08-27 Edward Hirschberg Methods of infusing phytochemicals, nutraceuticals, and other compositions into food products
ZA200003120B (en) 1999-06-30 2001-01-02 Givaudan Roure Int Encapsulation of active ingredients.
ES2228357T3 (es) 1999-07-06 2005-04-16 Dsm Ip Assets B.V. Composiciones que contienen substancias solubles en grasas en una matriz de hidrato de carbono.
GB0015417D0 (en) 2000-06-24 2000-08-16 Cerestar Holding Bv Agglomerated starch-based product for food preparation
US6365176B1 (en) 2000-08-08 2002-04-02 Functional Foods, Inc. Nutritional supplement for patients with type 2 diabetes mellitus for lipodystrophy
US20020188024A1 (en) 2000-08-23 2002-12-12 Chilton Floyd H. Fatty acid-containing emulsion with increased bioavailability
US6887493B2 (en) 2000-10-25 2005-05-03 Adi Shefer Multi component controlled release system for oral care, food products, nutraceutical, and beverages
US6730330B2 (en) * 2001-02-14 2004-05-04 Gw Pharma Limited Pharmaceutical formulations
US20040234579A1 (en) 2003-05-22 2004-11-25 Mark D. Finke, Inc. Dietary supplements and methods of preparing and administering dietary supplements
US7713440B2 (en) * 2003-10-08 2010-05-11 Lyotropic Therapeutics, Inc. Stabilized uncoated particles of reversed liquid crystalline phase materials
US20080064679A1 (en) * 2004-06-24 2008-03-13 Martin Billy R Water Soluble Cannabinoids
JP5322643B2 (ja) 2005-08-30 2013-10-23 フイルメニツヒ ソシエテ アノニム カプセル化された活性成分、カプセル化された活性成分の製造方法および使用
MY147363A (en) 2005-09-20 2012-11-30 Nestec Sa Water dispersible composition and method for preparing same
US20140357708A1 (en) * 2005-11-07 2014-12-04 Murty Pharmaceuticals, Inc. Oral dosage form of tetrahydrocannabinol and a method of avoiding and/or suppressing hepatic first pass metabolism via targeted chylomicron/lipoprotein delivery
AU2006311818B9 (en) 2005-11-07 2013-05-16 Murty Pharmaceuticals, Inc Improved delivery of tetrahydrocannabinol
US9265724B2 (en) * 2005-11-07 2016-02-23 Ram B. Murty Oral dosage form of tetrahydrocannabinol and a method of avoiding and/or suppressing hepatic first pass metabolism via targeted chylomicron/lipoprotein delivery
US20070213298A1 (en) 2006-02-07 2007-09-13 Universitetet I Oslo Omega 3
EP2048965B1 (fr) 2006-06-28 2015-02-11 Voyava Republic LLC Procédé d'infusion a froid destiné à l'enrichissement des grains de café
ATE516796T1 (de) 2006-09-15 2011-08-15 Echo Pharmaceuticals Bv Granulat mit einem pharmazeutischen wirkstoff und einem emulgator und herstellungsverfahren dafür
US20090095164A1 (en) * 2007-05-17 2009-04-16 Salvatore Albert Celeste Method of enhancing beverages by means of a unique microencapsulated delivery system
US20090162524A1 (en) 2007-12-21 2009-06-25 Tropicana Products, Inc. Food product including one or more omega-3 fatty acids and one or more fruit flavors
US20090264475A1 (en) 2008-01-24 2009-10-22 Schwartz Daniel M Methods and compositions for altering dietary behavior
HUE032158T2 (en) 2008-10-31 2017-09-28 Univ Mississippi Process for the preparation of delta9-THC amino acid esters
AR081323A1 (es) 2010-03-31 2012-08-08 Fonterra Co Operative Group Produccion de composiciones de grasa de leche concentrada y composicio-nes unificadas de alta densidad
CN101904401A (zh) 2010-07-09 2010-12-08 云南龙润茶业集团有限公司 一种茶凝胶软糖
US20120043242A1 (en) 2010-08-19 2012-02-23 Andrew David Hospodor Medicinal cannabis fatty foodstuff
US20120095087A1 (en) 2010-10-15 2012-04-19 Keith Hyatt Enhanced products by sustainable processes for medicinal use
US20120231083A1 (en) * 2010-11-18 2012-09-13 The Board Of Trustees Of The University Of Illinois Sustained release cannabinoid medicaments
US20130309291A1 (en) 2011-02-03 2013-11-21 Snap Infusion Llc Confection composition
WO2012130278A1 (fr) 2011-03-28 2012-10-04 Les Chocolats De L'iris S.A. Infusion de pelures de feves de cacao et procede d'obtention
WO2013009928A1 (fr) 2011-07-11 2013-01-17 Organic Medical Research Formulations de cannabinoïdes
CA2848214A1 (fr) 2011-09-08 2013-03-14 Rutgers, The State University Of New Jersey Obtention de produits enrichis
US20130164412A1 (en) 2011-12-23 2013-06-27 Udi Amrani Modified or infused cinnamon sticks for beverage and food use
US20130196022A1 (en) 2012-01-31 2013-08-01 Raisio Plc Milk and a process for its preparation
CN104302193A (zh) 2012-03-16 2015-01-21 詹尼弗·赖特 基于大麻的婴儿配方食品和制备其的方法
CN104619318A (zh) * 2012-05-03 2015-05-13 回音制药公司 含有δ9-四氢大麻酚的大麻植物分离物及其制备方法
US8741341B2 (en) 2012-05-07 2014-06-03 Insys Therapeutics, Inc. Manufacturing and packaging room temperature stable dronabinol capsules
US20130337113A1 (en) 2012-06-18 2013-12-19 George H. Clark Carbonated dairy nutrient beverage and method of making a carbonated dairy nutrient beverage to supply the same qualitative nutrition contained in skim milk to the human diet
US9345771B2 (en) * 2012-10-04 2016-05-24 Insys Development Company, Inc. Oral cannabinoid formulations
ES2856727T3 (es) 2013-02-28 2021-09-28 Swm Luxembourg Sarl Composición para preparar una bebida de té o caldos de hierbas y de verdura
CN103110582A (zh) 2013-03-04 2013-05-22 上海医药工业研究院 大麻酚类化合物微乳剂及其制备方法
US20140370181A1 (en) 2013-03-15 2014-12-18 The Folger Coffee Company Coffee composition for use with a beverage unit and methods of using the same
WO2014186896A1 (fr) 2013-05-22 2014-11-27 Earth's Own Food Company Inc Boisson aux fruits à coque et aux produits laitiers
US20150035204A1 (en) * 2013-08-01 2015-02-05 Intertape Polymer Corp. Silicone adhesive tapes and method of masking using same
US9693574B2 (en) 2013-08-08 2017-07-04 Virun, Inc. Compositions containing water-soluble derivatives of vitamin E mixtures and modified food starch
WO2015024055A1 (fr) 2013-08-20 2015-02-26 Deakin University Séparation d'acides gras oméga-3
US9326967B2 (en) 2013-08-22 2016-05-03 Stephen C. Perry Vaporizable cannabinoid compositions
CA2931039C (fr) 2013-11-20 2022-07-12 Mary Lynch Compositions et methodes de traitement de l'inflammation oculaire et de la douleur
US9259449B2 (en) * 2014-01-07 2016-02-16 Joshua Michael Raderman Method for modifying THC content in a lipid-based extract of cannabis
US10071053B2 (en) * 2014-01-31 2018-09-11 Pocket Tea, Llc Tea composition for oral administration
US20170340562A9 (en) * 2014-05-12 2017-11-30 Hddc Holdings Llc Cannabinoid caffeinated drinks, powder, beans, and cannabinoid loose tea leaf
US9480647B2 (en) * 2014-06-06 2016-11-01 CannTrust Inc. Single serve beverage pod containing cannabis
JP6920197B2 (ja) 2014-06-11 2021-08-18 ポビバ コーポレーションPoviva Corp. 親油性活性剤を注入された飲食料品組成物とその使用方法
US10307397B2 (en) 2014-07-28 2019-06-04 Concept Matrix Solutions Oral dissolvable film that includes plant extract
US20160058866A1 (en) * 2014-09-02 2016-03-03 Ronald D. Sekura Alternative solutions for the administration of cannabis derived botanical products
US10016363B2 (en) 2014-09-18 2018-07-10 Virun, Inc. Pre-spray emulsions and powders containing non-polar compounds
US20160143972A1 (en) 2014-11-21 2016-05-26 Cannamark Inc. Method and apparatus for preparing a solid form of cannabinoid
EP3229789A4 (fr) 2014-12-12 2018-08-08 Ojai Energetics PBC Compositions de cannabinoïdes microencapsulées
US10238745B2 (en) * 2015-01-31 2019-03-26 Constance Therapeutics, Inc. Cannabinoid composition and products including α-tocopherol
US9629886B2 (en) 2015-02-24 2017-04-25 Ers Holdings, Llc Method for conducing concentrated cannabis oil to be stable, emulsifiable and flavorless for use in hot beverages and resulting powderized cannabis oil
EP3268043A4 (fr) * 2015-03-10 2018-12-19 Nanosphere Health Sciences, LLC Compositions et méthodes à base de nanoparticules lipidiques en tant que support de cannabinoïdes sous des formes posologiques dosées avec précision
US20180007924A9 (en) 2015-05-18 2018-01-11 5071, Inc. Homogenous cannabis compositions and methods of making the same
EP3368014B1 (fr) 2015-10-26 2023-10-04 Yissum Research Development Company of the Hebrew University of Jerusalem Ltd Nouvelles formulations de cannabinoïdes
US9937147B2 (en) 2015-10-29 2018-04-10 NBDD, Inc. Edible base product composition
CA2952335A1 (fr) 2015-12-19 2017-06-19 Delta 9 Gardening B.V. Formulations d'administration therapeutique et systemes renfermant des cannabinoides et des terpenes
US20180206518A1 (en) 2016-04-15 2018-07-26 Ronald Silver Method of making cannabis oil hydrophilic using emulsifiers and related cannabinoid compositions
US11529329B2 (en) 2016-05-27 2022-12-20 Nordiccan A/S Powdered composition comprising a complex between a cannabinoid and a basic ion exchange resin
IL246790A0 (en) 2016-07-14 2016-09-29 Friedman Doron Self-emulsifying compositions of cannabinoids
EP3644986A4 (fr) 2017-05-01 2021-01-06 MJ Wooly Corporation Méthodologie et formulation pour créer une poudre d'un composant encapsulé à base de cannabis incorporé dans une matrice polymère
AU2018283411B2 (en) 2017-06-16 2021-04-29 Sorse Technology Corporation Preparing stable liquid emulsion forms of plant extract
EP3651738B1 (fr) 2017-07-14 2024-04-03 5071, Inc. Compositions comprenant des cannabinoïdes et leurs production
US20190240148A1 (en) 2018-02-07 2019-08-08 Tarukino Holdings, Inc. Lubricant composition and method for preparing the composition
US11192870B2 (en) 2018-03-07 2021-12-07 Socati Technologies—Oregon, Llc Continuous isolation of cannabidiol and conversion of cannabidiol to delta 8-tetrahydrocannabinol and delta 9-tetrahydrocannabinol
US10413845B1 (en) 2018-12-14 2019-09-17 Socati Technologies Processes for solvent extraction of cannabinoids, terpenes and flavonoids from biomass
US10414709B1 (en) 2018-12-14 2019-09-17 Socati Technologies Processes for solvent extraction of cannabinoids, terpenes and flavonoids from biomass

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11980204B2 (en) 2015-05-18 2024-05-14 5071, Inc. Cannabis compositions and methods of making the same
US12225913B2 (en) 2015-05-18 2025-02-18 5071, Inc. Cannabis compositions and methods of making the same
WO2020073032A1 (fr) * 2018-10-06 2020-04-09 Capaldi Francesco Systèmes et procédés permettant de combiner des cannabinoïdes et une solution à base de sucre, et de créer des comprimés à dissolution buccale
WO2020176806A1 (fr) * 2019-02-27 2020-09-03 3-Delta, Inc. Compositions qui contiennent une matière végétale lipophile et un tensioactif, et procédés associés
US12415145B2 (en) 2019-02-27 2025-09-16 Michael V. Zumpano Compositions that contain lipophilic plant material and surfactant, and related methods
US12264296B2 (en) 2020-09-02 2025-04-01 Michael V. Zumpano Compositions that contain lipophilic plant material and surfactant, and related methods

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US20170280740A1 (en) 2017-10-05
US11980204B2 (en) 2024-05-14
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US20200008441A1 (en) 2020-01-09
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