IP Library Patent Application 16699319
Patent Application
App. No. 16/699,319

WATER-SOLUBLE FORMULATIONS, METHODS OF MAKING AND USE

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Patent No.
US None
App. No.
16/699,319
Abstract

Water-soluble formulations including cannabinoids or a cannabis -derived compound for use in beverages and foods, methods of preparing the formulations, and methods of preparing beverages and foods including the formulations are disclosed herein. In other embodiments are provided water-soluble formulations that are physically and chemically stable, transparent or translucent in colour, calorie-free, and have minimal flavour.

Claims (45)

1 . A water-soluble formulation comprising a cannabinoid or a cannabis -derived compound; an emulsifier; and a glycerin-based carrier surfactant.

2 . The water-soluble formulation of claim 1 , further comprising a carrier oil.

3 . The water-soluble formulation of claim 2 , wherein the carrier oil is comprised of monoglycerides.

4 . The water-soluble formulation of claim 3 , wherein the monoglycerides comprise glyceryl monostearate, glyceryl hydroxystearate, glyceryl monoleate, winterized glyceryl monoleate, monolaurin, glyceryl monolinoleate, or any combination thereof.

5 . The water-soluble formulation of claim 2 , which comprises up to 10% by weight of the cannabinoid or cannabis -derived compound; up to 10% by weight of the carrier oil, and up to 10% by weight of the emulsifier.

6 . The water-soluble formulation of claim 2 , which comprises the cannabinoid or cannabis -derived compound; the carrier oil, and the emulsifier at an about equivalent amount by weight.

7 . The water-soluble formulation of claim 1 , which is an emulsion.

8 . The water-soluble formulation of claim 1 , wherein the cannabinoid is Cannabigerolic Acid (CBGA), Cannabigerolic Acid monomethylether (CBGAM), Cannabigerol (CBG), Cannabigerol monomethylether (CBGM), Cannabigerovarinic Acid (CBGVA), Cannabigerovarin (CBGV), Cannabichromenic Acid (CBCA), Cannabichromene (CBC), Cannabichromevarinic Acid (CBCVA), Cannabichromevarin (CBCV), Cannabidiolic Acid (CBDA), Cannabidiol (CBD), Δ6-Cannabidiol (Δ6-CBD), Cannabidiol monomethylether (CBDM), Cannabidiol-C4 (CBD-C4), Cannabidivarinic Acid (CBDVA), Cannabidivarin (CBDV), Cannabidiorcol (CBD-C1), Tetrahydrocannabinolic acid A (THCA-A), Tetrahydrocannabinolic acid B (THCA-B), Tetrahydrocannabinol (THC or Δ9-THC), Δ8-tetrahydrocannabinol (Δ8-THC), Δ10-tetrahydrocannabinol (Δ10-THC), Tetrahydrocannabinolic acid C4 (THCA-C4), Tetrahydrocannbinol C4 (THC C4), Tetrahydrocannabivarinic acid (THCVA), Tetrahydrocannabivarin (THCV), Δ8-Tetrahydrocannabivarin (Δ8-THCV), Δ9 Tetrahydrocannabivarin (Δ9-THCV), Tetrahydrocannabiorcolic acid (THCA-C1), Tetrahydrocannabiorcol (THC-C1), Delta 7 cis iso tetrahydrocannabivarin, Δ8 tetrahydrocannabinolic acid (Δ8-THCA), Δ9 tetrahydrocannabinolic acid (Δ9-THCA), Cannabicyclolic acid (CBLA), Cannabicyclol (CBL), Cannabicyclovarin (CBLV), Cannabielsoic acid A (CBEA-A), Cannabielsoic acid B (CBEA-B), Cannabielsoin (CBE), Cannabinolic acid (CBNA), Cannabinol (CBN), Cannabinol methylether (CBNM), Cannabinol-C4 (CBN-C4), Cannabivarin (CBV), Cannabino-C2 (CBN-C2), Cannabiorcol (CBN-C1), Cannabinodiol (CBND), Cannabinodivarin (CBDV), Cannabitriol (CBT), 11-hydroxy-Δ9-tetrahydrocannabinol (11-OH-THC), 11 nor 9-carboxy-Δ9-tetrahydrocannabinol, Ethoxy-cannabitriolvarin (CBTVE), 10 Ethoxy-9-hydroxy-Δ6a-tetrahydrocannabinol, Cannabitriolvarin (CBTV), 8,9 Dihydroxy-Δ6a(10a)-tetrahydrocannabinol (8,9-Di-OH-CBT-C5), Dehydrocannabifuran (DCBF), Cannbifuran (CBF), Cannabichromanon (CBCN), Cannabicitran (CBT), 10 Oxo-Δ6a(10a)-tetrahydrocannabinol (OTHC), Δ9-cis-tetrahydrocannabinol (cis-THC), Cannabiripsol (CBR), 3,4,5,6-tetrahydro-7-hydroxy-alpha-alpha-2-trimethyl-9-n-propyl-2,6-methano-2H-1-benzoxocin-5-methanol (OH-iso-HHCV), Trihydroxy-delta-9-tetrahydrocannabinol (triOH-THC), Yangonin, Epigallocatechin gallate, Dodeca-2E, 4E, 8Z, 10Z-tetraenoic acid isobutylamide, hexahydrocannibinol, Dodeca-2E,4E-dienoic acid isobutylamide, or any combination thereof.

9 . The water-soluble formulation of claim 1 , wherein the cannabinoid is cannabidiol (CBD), tetrahydrocannabinol (THC), or a combination thereof.

10 . (canceled)

11 . The water-soluble formulation of claim 1 , wherein the emulsifier comprises a soy lecithin.

12 . The water-soluble formulation of claim 1 , wherein the emulsifier comprises a sucrose monoester.

13 . The water-soluble formulation of claim 1 , wherein the emulsifier comprises a soy lecithin and a sucrose monoester.

14 . The water-soluble formulation of claim 13 , wherein the sucrose monoester is sucrose monopalmitate, sucrose monolaurate, sucrose monostearate, or any combination thereof.

15 . The water-soluble formulation of claim 13 , wherein the sucrose monoester is sucrose monopalmitate.

16 . The water-soluble formulation of claim 13 , which comprises an about equivalent amount by weight of the soy lecithin and the sucrose monoester.

17 . The water-soluble formulation of claim 1 , wherein the glycerin-based carrier surfactant is a vegetable glycerin.

18 . The water-soluble formulation of claim 1 , which comprises between about 60% and about 97% by weight of the glycerin-based carrier surfactant.

19 - 21 . (canceled)

22 . A powder formulation prepared by drying the water-soluble formulation of claim 1 .

23 . A product comprising the water-soluble formulation of claim 1 .

24 . The product of claim 23 , which is a beverage and further comprises an aqueous solution.

25 . The product of claim 23 , further comprising a stabilizer.

26 . The product of claim 25 , wherein the stabilizer is a chelating agent.

27 . The product of claim 26 , wherein the chelating agent is calcium disodium EDTA.

28 . The product of claim 23 , which comprises between about 0.5% and about 25% by weight of the water-soluble formulation.

29 - 31 . (canceled)

32 . A method for preparing the water-soluble formulation of claim 1 , the method comprising mixing, in any order, a cannabinoid or a cannabis -derived compound with a glycerin-based carrier surfactant and an emulsifier to prepare the water-soluble formulation.

33 . The method according to claim 32 , comprising:

mixing the cannabinoid or the cannabis -derived compound with a carrier oil until a homogenous mixture is formed; and

mixing the glycerin-based carrier surfactant and the emulsifier into the homogenous mixture to prepare the water-soluble formulation.

34 - 35 . (canceled)

36 . The method according to claim 33 , further comprising mixing a sucrose monoester into the homogenous mixture.

37 . The method according to claim 32 , further comprising microfluidizing the water-soluble formulation to obtain a particle size of between about 30 nm and about 100 nm.

38 . (canceled)

39 . A method for preparing a product comprising the water-soluble formulation of claim 1 , the method comprising: mixing, in any order, a cannabinoid or a cannabis -derived compound with a glycerin-based carrier surfactant and an emulsifier to prepare the water-soluble formulation; and mixing the water-soluble formulation with an aqueous solution.

40 . The method according to claim 39 , comprising:

mixing the cannabinoid or the cannabis -derived compound and a carrier oil until a homogenous mixture is formed;

mixing the glycerin-based carrier surfactant and the emulsifier into the homogenous mixture to prepare the water-soluble formulation; and

mixing the water-soluble formulation with the aqueous solution.

41 . The method according to claim 40 , further comprising mixing a sucrose monoester into the homogenous mixture.

42 . (canceled)

43 . The method according to claim 39 , further comprising adding a chelating agent to the aqueous solution.

44 . The method according to claim 43 , wherein the chelating agent is calcium disodium EDTA.

45 . The water-soluble formulation of claim 1 , which comprises a cannabinoid distillate or a cannabinoid isolate, monoglycerides, a soy lecithin, and a sucrose monoester, in a vegetable glycerin.

Assignments (2)
NOTICE OF GRANT OF SECURITY INTEREST IN PATENTS Recorded Mar 22, 2021
From: CANOPY GROWTH CORPORATION
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 055683/0826 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 20, 2020
From: GEILING, BEN; HAJIRAHIMKHAN, SOHEIL; JACKOWETZ, JOHN NICHOLAS; PASQUARIELLO, BRANDON; YOUNG, SCOTT
To: CANOPY GROWTH CORPORATION
Reel/Frame 051882/0433 →