IP Library Patent Application 16699276
Patent Application
App. No. 16/699,276

COMPOSITIONS COMPRISING A CANNABINOID OR A CANNABIS-DERIVED COMPOUND, METHODS OF MAKING AND USE

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Patent No.
US None
App. No.
16/699,276
Abstract

Cannabis and cannabis-derived compositions, methods of making and methods of using the compositions in oral dosage forms, such as in beverage forms, are disclosed herein. The compositions comprise a cannabinoid or a cannabis-derived compound, inulin and pectin and may be in powder or liquid form.

Claims (42)

1 . A composition comprising a cannabinoid or a cannabis-derived compound, inulin and pectin.

2 . The composition of claim 1 , wherein the inulin and pectin are present in the composition in a ratio of inulin:pectin of between about 99%:1% w/w to about 60%:40% w/w.

3 - 5 . (canceled)

6 . The composition of claim 1 , wherein the pectin is a citrus pectin.

7 . The composition of claim 1 , wherein the pectin is a sugar beet pectin.

8 . The composition 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), trans-Δ10-tetrahydrocannabinol (trans-Δ10-THC), cis-Δ10-tetrahydrocannabinol (cis-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), Δ7-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, and Dodeca-2E,4E-dienoic acid isobutylamide, or any combination thereof.

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

10 . The composition of claim 1 , wherein the cannabis-derived compound is a terpene.

11 . (canceled)

12 . The composition of claim 1 , wherein the composition is a liquid formulation and further comprises a solvent.

13 . The composition of claim 12 , wherein the solvent is water and the liquid formulation is an emulsion.

14 . The composition of claim 1 , wherein the composition is a powder formulation.

15 - 16 . (canceled)

17 . The composition of claim 1 , comprising core-shell structures comprising a hydrophobic inner core comprising the cannabinoid or cannabis-derived compound and a hydrophilic outer shell comprising the inulin and pectin.

18 . The composition of claim 17 , comprising a ratio of hydrophilic outer shell:hydrophobic inner core of between about 90%:10% w/w to about 50%:50% w/w.

19 - 20 . (canceled)

21 . The composition of claim 17 , wherein the hydrophobic inner core further comprises a carrier solvent.

22 . (canceled)

23 . The composition of claim 21 , wherein the carrier solvent comprises coconut oil or medium-chain triglyceride (MCT) oil.

24 . The composition of claim 21 , comprising a weight ratio of cannabinoid:carrier solvent of between about 3:1 to about 1:3.

25 - 26 . (canceled)

27 . The composition according to claim 1 , comprising core-shell structures comprising a hydrophobic inner core comprising the cannabinoid and a hydrophilic outer shell comprising the inulin and pectin, wherein:

the inulin and pectin are present in a ratio of about 70%:30% w/w inulin:pectin;

the core-shell structures comprise a ratio of about 80%:20% w/w hydrophilic outer shell:hydrophobic inner core; and

the hydrophobic inner core further comprises a carrier solvent at a ratio of about 1:1 w/w cannabinoid:carrier solvent.

28 . (canceled)

29 . A method of preparing the composition of claim 1 , the method comprising: combining a cannabinoid or a cannabis-derived compound with inulin and pectin, and homogenizing the mixture with a solvent to form an emulsion.

30 . The method of claim 29 , which comprises:

combining the inulin and pectin in the solvent to form an inulin/pectin mixture;

combining the cannabinoid or the cannabis-derived compound with the inulin/pectin mixture; and

homogenizing the mixture to form an emulsion.

31 . The method according to claim 30 , further comprising mixing the cannabinoid or the cannabis-derived compound in a carrier solvent prior to combining the cannabinoid or the cannabis-derived compound with the inulin/pectin mixture.

32 . The method according to claim 31 , wherein the carrier solvent comprises coconut oil or medium-chain triglyceride (MCT) oil.

33 - 35 . (canceled)

36 . The method according to claim 29 , further comprising drying the emulsion to form a powder.

37 . (canceled)

38 . The method according to claim 36 , wherein the powder comprises core-shell structures comprising a hydrophobic inner core comprising the cannabinoid or cannabis-derived compound and a hydrophilic outer shell comprising the inulin and pectin.

39 . The method according to claim 38 , wherein at least 50% by weight of total the cannabinoid or cannabis-derived compound that was combined with the inulin and pectin is encapsulated in the hydrophobic inner core.

40 . (canceled)

41 . A composition prepared according to the method of claim 29 .

42 . A foodstuff comprising the composition of claim 1 .

43 . A beverage comprising the composition of claim 1 .

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: ADAIR, CHRIS; GEILING, BEN; MANJILI, MOHAMMADMEHDI HAGHDOOST; ZOLKIEWSKI, MARK
To: CANOPY GROWTH CORPORATION
Reel/Frame 051882/0398 →