PurCann Pharma Inc.

Canada

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        Patent 12
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        United States 5
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2023 2
2022 3
2021 10
2020 2
IPC Class
A61K 36/185 - Magnoliopsida (dicotyledons) 11
A61K 31/05 - Phenols 9
A61K 31/352 - Heterocyclic 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. cannabinols, methantheline 9
C07D 311/80 - DibenzopyransHydrogenated dibenzopyrans 9
C07C 39/23 - Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic, containing six-membered aromatic rings and other rings, with unsaturation outside the aromatic rings 6
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NICE Class
03 - Cosmetics and toiletries; cleaning, bleaching, polishing and abrasive preparations 5
05 - Pharmaceutical, veterinary and sanitary products 5
34 - Tobacco; smokers' articles 4
32 - Beers; non-alcoholic beverages 3
30 - Basic staples, tea, coffee, baked goods and confectionery 2
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Status
Pending 9
Registered / In Force 8

1.

METHOD FOR PRODUCING A PURIFIED CANNABINOID EXTRACT, AND A PURIFIED CANNABINOID EXTRACT OBTAINED THEREFROM

      
Application Number 18006463
Status Pending
Filing Date 2021-08-24
First Publication Date 2023-08-24
Owner PURCANN PHARMA INC. (Canada)
Inventor
  • Pigeon, Xavier
  • Carpentier, Claudia
  • Derrien, Maëlle
  • Bouchoucha, Meryem

Abstract

The present disclosure relates to a method for producing a purified cannabinoid extract comprising mixing a cannabaceae biomass extract comprising cannabinoid compounds in methanol to obtain a substantially homogeneous methanolic phase; mixing water and the methanolic-phase to obtain a hydro- methanolic-phase; performing a liquid-liquid extraction of the hydro-methanolic phase by using a non-polar solvent whereby cannabinoid compounds are extracted in the non-polar solvent; recovering a non-polar solvent phase comprising the cannabinoid compounds and a rafinate comprising the hydro-methanolic phase; and evaporating the non-polar solvent from the non-polar solvent phase comprising the cannabinoid to provide the purified cannabinoid extract.

IPC Classes  ?

  • C07D 311/80 - DibenzopyransHydrogenated dibenzopyrans
  • C07C 37/68 - SeparationPurificationStabilisationUse of additives
  • C07C 51/48 - SeparationPurificationStabilisationUse of additives by liquid-liquid treatment

2.

METHOD FOR PRODUCING A PURIFIED CANNABACEAE BIOMASS EXTRACT

      
Application Number 17996548
Status Pending
Filing Date 2021-04-13
First Publication Date 2023-07-13
Owner PurCann Pharma inc. (Canada)
Inventor
  • Pigeon, Xavier
  • Carpentier, Claudia
  • Derrien, Maëlle
  • Giret, Simon

Abstract

The present disclosure relates to a method for producing a purified cannabaceae biomass extract, wherein a crude alcoholic cannabaceae biomass extract comprising at least two cannabinoid compounds in an alcoholic solvent is circulating through a powdered layer of activated carbon and the purified cannabaceae biomass extract is recovered with a ratio of cannabinoid compounds in the purified cannabaceae biomass extract is higher than the ratio of the cannabinoid compounds in the crude alcoholic cannabaceae biomass extract.

IPC Classes  ?

  • A61K 36/185 - Magnoliopsida (dicotyledons)
  • A61K 31/05 - Phenols
  • A61K 31/352 - Heterocyclic 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. cannabinols, methantheline

3.

ORAL FORMULATIONS OF CANNABIS EXTRACTS AND METHODS OF MAKING SAME

      
Application Number 17633448
Status Pending
Filing Date 2020-08-07
First Publication Date 2022-09-15
Owner PURCANN PHARMA INC. (Canada)
Inventor
  • De Cicco, Michael
  • Harwood, Melody
  • Farokhi, Fereshteh
  • Wood, Graham
  • Brouillette, François-Karl

Abstract

The current application relates to a composition comprising a cannabis extract and a lipid-based carrier; wherein the lipid-based carrier comprises omega-3 fatty acids and at least one of monoacylglycerides, diacylglycerides, triglycerides or phospholipids. The composition can be formulated for oral or transmucosal administration and provides improved bioavailability of bioactive ingredients in the cannabis extract.

IPC Classes  ?

  • A61K 31/352 - Heterocyclic 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. cannabinols, methantheline
  • A61K 31/05 - Phenols
  • A61K 36/185 - Magnoliopsida (dicotyledons)
  • A61K 47/44 - Oils, fats or waxes according to two or more groups of Natural or modified natural oils, fats or waxes, e.g. castor oil, polyethoxylated castor oil, montan wax, lignite, shellac, rosin, beeswax or lanolin
  • A61K 9/00 - Medicinal preparations characterised by special physical form
  • A61K 9/14 - Particulate form, e.g. powders

4.

METHOD FOR PRODUCING A PURIFIED CANNABINOID EXTRACT, AND A PURIFIED CANNABINOID EXTRACT OBTAINED THEREFROM

      
Document Number 03189932
Status Pending
Filing Date 2021-08-24
Open to Public Date 2022-03-10
Owner PURCANN PHARMA INC. (Canada)
Inventor
  • Bouchoucha, Meryem
  • Carpentier, Claudia
  • Pigeon, Xavier
  • Derrien, Maelle

Abstract

The present disclosure relates to a method for producing a purified cannabinoid extract comprising mixing a cannabaceae biomass extract comprising cannabinoid compounds in methanol to obtain a substantially homogeneous methanolic phase; mixing water and the methanolic-phase to obtain a hydro- methanolic-phase; performing a liquid-liquid extraction of the hydro-methanolic phase by using a non-polar solvent whereby cannabinoid compounds are extracted in the non-polar solvent; recovering a non-polar solvent phase comprising the cannabinoid compounds and a rafinate comprising the hydro-methanolic phase; and evaporating the non-polar solvent from the non-polar solvent phase comprising the cannabinoid to provide the purified cannabinoid extract.

IPC Classes  ?

  • A61K 31/05 - Phenols
  • A61K 31/192 - Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
  • A61K 31/352 - Heterocyclic 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. cannabinols, methantheline
  • A61K 36/185 - Magnoliopsida (dicotyledons)
  • C07C 39/23 - Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic, containing six-membered aromatic rings and other rings, with unsaturation outside the aromatic rings
  • C07C 65/19 - Compounds having carboxyl groups bound to carbon atoms of six-membered aromatic rings and containing any of the groups OH, O-metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups having unsaturation outside the aromatic ring
  • C07D 311/80 - DibenzopyransHydrogenated dibenzopyrans

5.

METHOD FOR PRODUCING A PURIFIED CANNABINOID EXTRACT, AND A PURIFIED CANNABINOID EXTRACT OBTAINED THEREFROM

      
Application Number CA2021051169
Publication Number 2022/047574
Status In Force
Filing Date 2021-08-24
Publication Date 2022-03-10
Owner PURCANN PHARMA INC. (Canada)
Inventor
  • Pigeon, Xavier
  • Carpentier, Claudia
  • Derrien, Maëlle
  • Bouchoucha, Meryem

Abstract

The present disclosure relates to a method for producing a purified cannabinoid extract comprising mixing a cannabaceae biomass extract comprising cannabinoid compounds in methanol to obtain a substantially homogeneous methanolic phase; mixing water and the methanolic-phase to obtain a hydro- methanolic-phase; performing a liquid-liquid extraction of the hydro-methanolic phase by using a non-polar solvent whereby cannabinoid compounds are extracted in the non-polar solvent; recovering a non-polar solvent phase comprising the cannabinoid compounds and a rafinate comprising the hydro-methanolic phase; and evaporating the non-polar solvent from the non-polar solvent phase comprising the cannabinoid to provide the purified cannabinoid extract.

IPC Classes  ?

  • A61K 36/185 - Magnoliopsida (dicotyledons)
  • A61K 31/05 - Phenols
  • A61K 31/192 - Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
  • A61K 31/352 - Heterocyclic 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. cannabinols, methantheline
  • C07C 39/23 - Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic, containing six-membered aromatic rings and other rings, with unsaturation outside the aromatic rings
  • C07C 65/19 - Compounds having carboxyl groups bound to carbon atoms of six-membered aromatic rings and containing any of the groups OH, O-metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups having unsaturation outside the aromatic ring
  • C07D 311/80 - DibenzopyransHydrogenated dibenzopyrans

6.

OOVIE

      
Serial Number 97133465
Status Pending
Filing Date 2021-11-19
Owner PurCann Pharma Inc. (Canada)
NICE Classes  ?
  • 03 - Cosmetics and toiletries; cleaning, bleaching, polishing and abrasive preparations
  • 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

Hemp oil for cosmetic purposes; Essential oils for use in aromatherapy; Cosmetic creams and lotions; Colognes, perfumes and cosmetics; Cosmetic hair care preparations; Cosmetic soaps; Cosmetics for personal use; Skin care cosmetics; Sunscreen for cosmetic purposes; all of the foregoing including hemp with a delta-9 tetrahydrocannabinol (THC) concentration of not more than 0.3 percent on a dry weight basis Hemp for medical and health use; Hemp for medical and health use; Medicinal herb extracts; Medicinal herbs in dried or preserved form; Hemp derivatives and hemp extracts for medical and health use; Dietary and nutritional supplements comprised of hemp, namely, extracts drops, flower essence, capsules, soft-gels, oils, gummies, mouth spray, ointments, powders, gels and tincture drops; Medicinal oils; Topical analgesic creams; Aromatherapy sprays and oils for relief of aches, pains, stress, and anxiety; all of the foregoing including hemp with a delta-9 tetrahydrocannabinol (THC) concentration of not more than 0.3 percent on a dry weight basis

7.

METHOD FOR PRODUCING A PURIFIED CANNABACEAE BIOMASS EXTRACT

      
Application Number CA2021050492
Publication Number 2021/217241
Status In Force
Filing Date 2021-04-13
Publication Date 2021-11-04
Owner PURCANN PHARMA INC. (Canada)
Inventor
  • Pigeon, Xavier
  • Carpentier, Claudia
  • Derrien, Maëlle
  • Giret, Simon

Abstract

The present disclosure relates to a method for producing a purified cannabaceae biomass extract, wherein a crude alcoholic cannabaceae biomass extract comprising at least two cannabinoid compounds in an alcoholic solvent is circulating through a powdered layer of activated carbon and the purified cannabaceae biomass extract is recovered with a ratio of cannabinoid compounds in the purified cannabaceae biomass extract is higher than the ratio of the cannabinoid compounds in the crude alcoholic cannabaceae biomass extract.

IPC Classes  ?

  • B01D 11/02 - Solvent extraction of solids
  • A23L 33/105 - Plant extracts, their artificial duplicates or their derivatives
  • A61K 31/05 - Phenols
  • A61K 31/192 - Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
  • A61K 31/352 - Heterocyclic 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. cannabinols, methantheline
  • A61K 36/185 - Magnoliopsida (dicotyledons)
  • C07C 39/23 - Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic, containing six-membered aromatic rings and other rings, with unsaturation outside the aromatic rings
  • C07C 65/19 - Compounds having carboxyl groups bound to carbon atoms of six-membered aromatic rings and containing any of the groups OH, O-metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups having unsaturation outside the aromatic ring
  • C07D 311/80 - DibenzopyransHydrogenated dibenzopyrans

8.

METHOD FOR PRODUCING A PURIFIED CANNABACEAE BIOMASS EXTRACT

      
Document Number 03180647
Status Pending
Filing Date 2021-04-13
Open to Public Date 2021-11-04
Owner PURCANN PHARMA INC. (Canada)
Inventor
  • Giret, Simon
  • Carpentier, Claudia
  • Pigeon, Xavier
  • Derrien, Maelle

Abstract

The present disclosure relates to a method for producing a purified cannabaceae biomass extract, wherein a crude alcoholic cannabaceae biomass extract comprising at least two cannabinoid compounds in an alcoholic solvent is circulating through a powdered layer of activated carbon and the purified cannabaceae biomass extract is recovered with a ratio of cannabinoid compounds in the purified cannabaceae biomass extract is higher than the ratio of the cannabinoid compounds in the crude alcoholic cannabaceae biomass extract.

IPC Classes  ?

  • A23L 33/105 - Plant extracts, their artificial duplicates or their derivatives
  • A61K 31/05 - Phenols
  • A61K 31/192 - Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
  • A61K 31/352 - Heterocyclic 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. cannabinols, methantheline
  • A61K 36/185 - Magnoliopsida (dicotyledons)
  • B01D 11/02 - Solvent extraction of solids
  • C07C 39/23 - Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic, containing six-membered aromatic rings and other rings, with unsaturation outside the aromatic rings
  • C07C 65/19 - Compounds having carboxyl groups bound to carbon atoms of six-membered aromatic rings and containing any of the groups OH, O-metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups having unsaturation outside the aromatic ring
  • C07D 311/80 - DibenzopyransHydrogenated dibenzopyrans

9.

METHOD FOR PREVENTING OR REDUCING CANNABACEAE BIOMASS DECOMPOSITION

      
Application Number CA2021050093
Publication Number 2021/151198
Status In Force
Filing Date 2021-01-29
Publication Date 2021-08-05
Owner PURCANN PHARMA INC. (Canada)
Inventor
  • Giret, Simon
  • Gosselin, André
  • Mellon, Christophe

Abstract

The present disclosure relates to a method for preventing or reducing cannabaceae biomass decomposition during storage by packaging an amount of the biomass in a flexible film of gas impervious material to provide a cannabaceae biomass package which is impermeable to gases.

IPC Classes  ?

  • B65B 29/00 - Packaging of materials presenting special problems
  • A01N 3/00 - Preservation of plants or parts thereof, e.g. inhibiting evaporation, improvement of the appearance of leavesGrafting wax
  • A61K 36/185 - Magnoliopsida (dicotyledons)
  • B65B 31/04 - Evacuating, pressurising or gasifying filled containers or wrappers by means of nozzles through which air or other gas, e.g. an inert gas, is withdrawn or supplied
  • B65D 81/20 - Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents providing specific environment for contents, e.g. temperature above or below ambient under vacuum or superatmospheric pressure, or in a special atmosphere, e.g. of inert gas
  • C07C 65/19 - Compounds having carboxyl groups bound to carbon atoms of six-membered aromatic rings and containing any of the groups OH, O-metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups having unsaturation outside the aromatic ring
  • C07D 311/80 - DibenzopyransHydrogenated dibenzopyrans

10.

METHOD FOR PREVENTING OR REDUCING CANNABACEAE BIOMASS DECOMPOSITION

      
Document Number 03168632
Status Pending
Filing Date 2021-01-29
Open to Public Date 2021-08-05
Owner PURCANN PHARMA INC. (Canada)
Inventor
  • Gosselin, Andre
  • Giret, Simon
  • Mellon, Christophe

Abstract

The present disclosure relates to a method for preventing or reducing cannabaceae biomass decomposition during storage by packaging an amount of the biomass in a flexible film of gas impervious material to provide a cannabaceae biomass package which is impermeable to gases.

IPC Classes  ?

  • A01N 3/00 - Preservation of plants or parts thereof, e.g. inhibiting evaporation, improvement of the appearance of leavesGrafting wax
  • A61K 36/185 - Magnoliopsida (dicotyledons)
  • B65B 29/00 - Packaging of materials presenting special problems
  • B65B 31/04 - Evacuating, pressurising or gasifying filled containers or wrappers by means of nozzles through which air or other gas, e.g. an inert gas, is withdrawn or supplied
  • B65D 81/20 - Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents providing specific environment for contents, e.g. temperature above or below ambient under vacuum or superatmospheric pressure, or in a special atmosphere, e.g. of inert gas
  • C07C 65/19 - Compounds having carboxyl groups bound to carbon atoms of six-membered aromatic rings and containing any of the groups OH, O-metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups having unsaturation outside the aromatic ring
  • C07D 311/80 - DibenzopyransHydrogenated dibenzopyrans

11.

OOVIE

      
Application Number 211092200
Status Registered
Filing Date 2021-06-01
Registration Date 2024-04-04
Owner PurCann Pharma Inc. (Canada)
NICE Classes  ?
  • 03 - Cosmetics and toiletries; cleaning, bleaching, polishing and abrasive preparations
  • 05 - Pharmaceutical, veterinary and sanitary products
  • 34 - Tobacco; smokers' articles

Goods & Services

(1) Cannabis and hemp oil for cosmetic purposes; Essential oils for use in aromatherapy; Cannabis infused cosmetic creams and lotions; Cannabis infused cosmetic hair care preparations; Cannabis infused cosmetic soaps; Cannabis infused cosmetics for personal use; Cannabis infused skin care cosmetics; Cannabis infused sunscreen for cosmetic purposes. (2) Cannabis and hemp for medical and health use; Medicinal herbs in dried or preserved form; Cannabis and hemp extracts for medical and health use; Dietary and nutritional supplements comprised of cannabis and hemp namely, extracts drops, flower essence, capsules, soft-gels, oils, gummies, mouth spray, ointments, powders, gels and tincture drops; Medicinal oils; Topical analgesic creams; Aromatherapy sprays and oils for relief of aches, pains, stress, and anxiety. (3) Oral vaporizers for smoking purposes; Cannabis oil for electronic cigarettes liquid and for oral vaporizers for smoking; Dried cannabis for smoking.

12.

MOONKEY

      
Application Number 210704000
Status Registered
Filing Date 2021-05-13
Registration Date 2024-01-26
Owner PurCann Pharma Inc. (Canada)
NICE Classes  ?
  • 03 - Cosmetics and toiletries; cleaning, bleaching, polishing and abrasive preparations
  • 05 - Pharmaceutical, veterinary and sanitary products
  • 30 - Basic staples, tea, coffee, baked goods and confectionery
  • 32 - Beers; non-alcoholic beverages
  • 34 - Tobacco; smokers' articles

Goods & Services

(1) Cannabis and hemp oil for cosmetic purposes; Essential oils for use in aromatherapy; Cannabis infused cosmetic creams and lotions; Cannabis infused Colognes, perfumes and cosmetics; Cannabis infused cosmetic hair care preparations; Cannabis infused cosmetic soaps; Cannabis infused cosmetics for personal use; Cannabis infused skin care cosmetics; Cannabis infused sunscreen for cosmetic purposes. (2) Cannabis and hemp for medical and health use; Medicinal herb extracts for general health and well being; Medicinal herbs in dried or preserved form; Cannabis and hemp extracts for medical and health use; Dietary and nutritional supplements comprised of cannabis and hemp namely, extracts drops, flower essence, capsules, soft-gels, oils, gummies, mouth spray, ointments, powders, gels and tincture drops; Medicinal oils; Topical analgesic creams; Aromatherapy sprays and oils for relief of aches, pains, stress, and anxiety. (3) Food products containing cannabis and hemp and cannabis and hemp extracts namely: biscuits, breakfast cereals, brownies, cakes, candy, cereal bars, chewing gum, chocolate bars, coffee-based snack foods, cupcakes, energy bars, grain-based snack foods, granola-based snack foods, muffins, sugar confectionery, teas and wheat-based snack foods. (4) Non-alcoholic beverages made from, containing or infused with cannabis and hemp, cannabis and hemp derivatives, cannabis and hemp extracts. (5) Oral vaporizers for smoking purposes; Cannabis oil for electronic cigarettes liquid and for oral vaporizers for smoking; Dried cannabis for smoking.

13.

OLLOPA

      
Application Number 210704100
Status Registered
Filing Date 2021-05-13
Registration Date 2024-01-26
Owner PurCann Pharma Inc. (Canada)
NICE Classes  ?
  • 03 - Cosmetics and toiletries; cleaning, bleaching, polishing and abrasive preparations
  • 05 - Pharmaceutical, veterinary and sanitary products
  • 30 - Basic staples, tea, coffee, baked goods and confectionery
  • 32 - Beers; non-alcoholic beverages
  • 34 - Tobacco; smokers' articles

Goods & Services

(1) Cannabis and hemp oil for cosmetic purposes; Essential oils for use in aromatherapy; Cannabis infused cosmetic creams and lotions; Cannabis infused Colognes, perfumes and cosmetics; Cannabis infused cosmetic hair care preparations; Cannabis infused cosmetic soaps; Cannabis infused cosmetics for personal use; Cannabis infused skin care cosmetics; Cannabis infused sunscreen for cosmetic purposes. (2) Cannabis and hemp for medical and health use; Medicinal herb extracts for general health and well being; Medicinal herbs in dried or preserved form; Cannabis and hemp extracts for medical and health use; Dietary and nutritional supplements comprised of cannabis and hemp namely, extracts drops, flower essence, capsules, soft-gels, oils, gummies, mouth spray, ointments, powders, gels and tincture drops; Medicinal oils; Topical analgesic creams; Aromatherapy sprays and oils for relief of aches, pains, stress, and anxiety. (3) Food products containing cannabis and hemp and cannabis and hemp extracts namely: biscuits, breakfast cereals, brownies, cakes, candy, cereal bars, chewing gum, chocolate bars, coffee-based snack foods, cupcakes, energy bars, grain-based snack foods, granola-based snack foods, muffins, sugar confectionery, teas and wheat-based snack foods. (4) Non-alcoholic beverages made from, containing or infused with cannabis and hemp, cannabis and hemp derivatives, cannabis and hemp extracts. (5) Oral vaporizers for smoking purposes; Cannabis oil for electronic cigarettes liquid and for oral vaporizers for smoking; Dried cannabis for smoking.

14.

ORAL FORMULATIONS OF CANNABIS EXTRACTS AND METHODS OF MAKING SAME

      
Document Number 03149652
Status Pending
Filing Date 2020-08-07
Open to Public Date 2021-02-11
Owner PURCANN PHARMA INC. (Canada)
Inventor
  • De Cicco, Michael
  • Harwood, Melody
  • Farokhi, Fereshteh
  • Wood, Graham
  • Brouillette, Francois-Karl

Abstract

The current application relates to a composition comprising a cannabis extract and a lipid-based carrier; wherein the lipid-based carrier comprises omega-3 fatty acids and at least one of monoacylglycerides, diacylglycerides, triglycerides or phospholipids. The composition can be formulated for oral or transmucosal administration and provides improved bioavailability of bioactive ingredients in the cannabis extract.

IPC Classes  ?

  • A61K 31/05 - Phenols
  • A61K 31/352 - Heterocyclic 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. cannabinols, methantheline
  • A61K 36/185 - Magnoliopsida (dicotyledons)
  • A61K 47/12 - Carboxylic acidsSalts or anhydrides thereof
  • A61K 47/14 - Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
  • A61K 47/22 - Heterocyclic compounds, e.g. ascorbic acid, tocopherol or pyrrolidones
  • A61K 47/24 - Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing atoms other than carbon, hydrogen, oxygen, halogen, nitrogen or sulfur, e.g. cyclomethicone or phospholipids
  • A61K 47/44 - Oils, fats or waxes according to two or more groups of Natural or modified natural oils, fats or waxes, e.g. castor oil, polyethoxylated castor oil, montan wax, lignite, shellac, rosin, beeswax or lanolin
  • A61K 47/46 - Ingredients of undetermined constitution or reaction products thereof, e.g. skin, bone, milk, cotton fibre, eggshell, oxgall or plant extracts
  • C07C 39/23 - Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic, containing six-membered aromatic rings and other rings, with unsaturation outside the aromatic rings
  • C07D 311/80 - DibenzopyransHydrogenated dibenzopyrans

15.

PanHash

      
Application Number 207716200
Status Registered
Filing Date 2021-01-13
Registration Date 2023-06-21
Owner PurCann Pharma Inc. (Canada)
NICE Classes  ?
  • 03 - Cosmetics and toiletries; cleaning, bleaching, polishing and abrasive preparations
  • 05 - Pharmaceutical, veterinary and sanitary products
  • 29 - Meat, dairy products, prepared or preserved foods
  • 32 - Beers; non-alcoholic beverages
  • 34 - Tobacco; smokers' articles
  • 35 - Advertising and business services

Goods & Services

(1) Cosmetics; cosmetic preparations for humans and animals, namely, cosmetics for pets and livestock, cosmetic preparations for skincare; cosmetic preparations for topical use on skin, hair, and lips, namely, skin and body topical lotions, creams and oils for cosmetic use, cosmetic hair care preparations, lip care preparations; cosmetics made from the hemp plant and extracted hemp oil, namely bar and liquid soaps, oils for cosmetic purposes, hair oils, cosmetic creams; hemp extracts for cosmetic purposes; cosmetics made from tetrahydrocannabinols (THC) concentrates, namely bar and liquid soaps, oils for cosmetic purposes, hair oils, cosmetic creams; tetrahydrocannabinols (THC) concentrates for cosmetic purposes; cosmetics made from cannabinols (CBD) concentrates, namely bar and liquid soaps, oils for cosmetic purposes, hair oils, cosmetic creams; cannabinols (CBD) concentrates for cosmetic purposes; cosmetic preparations containing cannabis, namely, cannabis-based cosmetic preparations for skin care; cosmetic preparations containing cannabis, cannabinols (CBD) concentrates, tetrahydrocannabinols (THC) concentrates and hemp extracts for topical use, namely, skin and body topical lotions, creams and oils for cosmetic use. (2) Dietary supplements for humans and animals containing cannabis and cannabis derivatives for medicinal purposes; herbal tinctures, capsules and concentrates for general health and well-being; tinctures and capsules containing, hemp extracts, cannabinols (CBD), tetrahydrocannabinols (THC) for general health and well-being; hemp extracts, cannabinols (CBD) concentrates, tetrahydrocannabinols (THC) concentrates for general health and well-being; cannabis extracts namely capsules, tinctures and concentrates for general health and well-being; cannabidiol (CBD) oil for medicinal purposes; tetrahydrocannabinol [THC] oil for medical purposes; hemp oil for medicinal purposes. (3) Cannabis oil for food; hemp oil for food; edible cannabis oil, cannabis extracts namely, cannabis-based concentrates and pastes for culinary purposes, cannabidiol [CBD] oil for food, tetrahydrocannabinol [THC] oil for food. (4) Fruit beverages and juices; non-alcoholic carbonated beverages; vegetable-based beverages; wine flavoured beverages infused with cannabis; non-alcoholic beverages containing cannabis, cannabinols (CBD) concentrates, tetrahydrocannabinols (THC) concentrates, hemp extracts, Cannabis oil, cannabis extracts, cannabidiol [CBD] oil, tetrahydrocannabinol [THC] oil. (5) Cannabidiol (CBD) derived from hemp for smoking purposes; tetrahydrocannabinol [THC] oil for electronic cigarettes; cannabis oil for electronic cigarettes; cannabis extracts, namely, cannabis-derived resins for recreational use, for smoking; cannabidiol [CBD] oil for smoking purposes; tetrahydrocannabinol [THC] oil for smoking purposes; cannabis for smoking, dried cannabis, cannabis cigarettes. (1) Online sale, retail sale and distribution of cosmetics, cosmetic preparations for humans and animals, cosmetic preparations for topical use on skin, hair, and lips, cosmetics made from the hemp plant or extracted hemp oil, namely soaps, oils, creams, hemp extracts for cosmetic purposes, cosmetics made from tetrahydrocannabinols (THC) concentrates, namely soaps, oils, creams, tetrahydrocannabinols (THC) concentrates for cosmetic purposes, cosmetics made from cannabinols (CBD) concentrates, namely soaps, oils, creams, cannabinols (CBD) concentrates for cosmetic purposes, cosmetic preparations containing cannabis, cosmetic preparations containing cannabis, cannabinols (CBD) concentrates, tetrahydrocannabinols (THC) concentrates or hemp extracts for topical use, dietary supplements for humans and animals, herbal tinctures, capsules and concentrates for general health and well-being, tinctures and capsules containing, hemp extracts, cannabinols (CBD), tetrahydrocannabinols (THC) for general health and well-being, hemp extracts, cannabinols (CBD) concentrates, tetrahydrocannabinols (THC) concentrates for general health and well-being, cannabis extracts namely capsules, tinctures and concentrates for general health and well-being, cannabidiol (CBD) oil for medicinal purposes, tetrahydrocannabinol [THC] oil for medical purposes, hemp oil for medicinal purposes, cannabis oil for food, hemp oil for food, edible cannabis oil, cannabis extracts, cannabidiol [CBD] oil, tetrahydrocannabinol [THC] oil, cannabidiol (CBD) derived from hemp for smoking purposes, tetrahydrocannabinol [THC] oil for electronic cigarettes, cannabis oil, cannabis extracts, cannabidiol [CBD] oil, tetrahydrocannabinol [THC] oil, beverages, beverages containing cannabis, cannabinols (CBD) concentrates, tetrahydrocannabinols (THC) concentrates, hemp extracts, Cannabis oil, cannabis extracts, cannabidiol [CBD] oil, tetrahydrocannabinol [THC] oil, cannabis for smoking, dried cannabis, cannabis cigarettes.

16.

Cold extraction method for cannabinoids and terpenes from cannabis by organic solvents

      
Application Number 16999846
Grant Number 11110372
Status In Force
Filing Date 2020-08-21
First Publication Date 2020-12-24
Grant Date 2021-09-07
Owner PURCANN PHARMA INC. (Canada)
Inventor
  • Farokhi, Fereshteh
  • St-Jean, Pierre
  • Villeneuve, Etienne

Abstract

cannabis plant material, where the extracts comprise cannabinoids and terpenes. The methods comprise extracting fresh or dried plant material with a cold organic solvent. The methods allow for the extraction of cannabinoids and terpenes, while leaving behind impurities such as waxes and chlorophyll that are commonly found in extractions with room temperature (RT) or warm solvent extraction methods. The methods can produce extracts having more than 90% cannabinoids.

IPC Classes  ?

  • A61K 36/185 - Magnoliopsida (dicotyledons)
  • B01D 11/02 - Solvent extraction of solids
  • A61K 31/05 - Phenols
  • A61K 31/352 - Heterocyclic 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. cannabinols, methantheline

17.

COLD EXTRACTION METHOD FOR CANNABINOIDS AND TERPENES FROM CANNABIS BY POLYUNSATURATED LIPID-BASED SOLVENTS

      
Document Number 03107888
Status Pending
Filing Date 2019-08-08
Open to Public Date 2020-02-13
Owner PURCANN PHARMA INC. (Canada)
Inventor
  • Farokhi, Fereshteh
  • St-Jean, Pierre
  • Villeneuve, Etienne

Abstract

The invention relates to methods for producing botanical extracts comprising cannabinoids and terpenes using cold extraction with highly polyunsaturated lipid solvents. These methods allow for the extraction of cannabinoids and terpenes while leaving behind impurities that are commonly found in organic solvent extraction methods.

IPC Classes  ?

  • A23G 3/48 - Sweetmeats, confectionery or marzipanProcesses for the preparation thereof characterised by the composition containing plants or parts thereof, e.g. fruits, seeds, extracts
  • A23G 4/06 - Chewing gum characterised by the composition
  • A23L 2/52 - Adding ingredients
  • A23L 33/105 - Plant extracts, their artificial duplicates or their derivatives
  • A61K 31/05 - Phenols
  • A61K 31/352 - Heterocyclic 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. cannabinols, methantheline
  • A61K 36/185 - Magnoliopsida (dicotyledons)
  • B01D 11/02 - Solvent extraction of solids
  • C07C 39/23 - Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic, containing six-membered aromatic rings and other rings, with unsaturation outside the aromatic rings
  • C07D 311/80 - DibenzopyransHydrogenated dibenzopyrans