Water soluble compositions comprising purified cannabinoids

US12324801B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12324801-B2
Application numberUS-202117352071-A
CountryUS
Kind codeB2
Filing dateJun 18, 2021
Priority dateAug 29, 2016
Publication dateJun 10, 2025
Grant dateJun 10, 2025

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

This disclosure relates to new compositions and methods for making cannabinoid formulations. In one embodiment, this disclosure provides water soluble compositions comprising a first purified cannabinoid and Vitamin E TPGS. In one embodiment, the disclosure herein comprises a method of making powders comprising heatings material to a first temperature and a second temperature.

First claim

Opening claim text (preview).

What is claimed: 1. A liquid composition, comprising: one or more purified cannabinoids selected from the group consisting of D9-THC, D8-THC, THCA, THCV, D8-THCV, D9-THCV, THCVA, CBD, CBDA, CBDV, CBDVA, CBC, CBCA, CBCV, CBCVA, CBG, CBGA, CBGV, CBGVA, CBN, CBNA, CBNV, CBNVA, CBND, CBNDA, CBNDV, CBNDVA, CBE, CBEA, CBEV, CBEVA, CBL, CBLA, CBLV, and CBLVA; Vitamin E TPGS; and water, wherein the liquid composition comprises a ratio of total purified cannabinoid content to Vitamin E TPGS of about 1:1 to about 1:10 based on mass percent. 2. The liquid composition of claim 1 , wherein the liquid composition comprises a ratio of total purified cannabinoid content to Vitamin E TPGS of about 1:1 to about 1:8. 3. The liquid composition of claim 1 , wherein the liquid composition comprises a ratio of total purified cannabinoid content to Vitamin E TPGS of about 1:1 to about 1:6. 4. The liquid composition of claim 1 , wherein the liquid composition comprises a ratio of total purified cannabinoid content to Vitamin E TPGS of about 1:1 to about 1:4. 5. The liquid composition of claim 1 , wherein the liquid composition comprises a ratio of total purified cannabinoid content to Vitamin E TPGS of about 1:1 to about 1:2. 6. The liquid composition of claim 1 , wherein the one or more purified cannabinoids comprise THCA, CBC, THC, CBN, CBD, CBG, CBGA, CBDA, or a combination thereof. 7. The liquid composition of claim 1 , wherein the one or more purified cannabinoids comprise CBD, THC, or a combination thereof. 8. The liquid composition of claim 1 , wherein the one or more purified cannabinoids comprise a combination of THC and CBD. 9. The liquid composition of claim 1 , further comprising one or more purified terpenes. 10. The liquid composition of claim 9 , wherein the one or more purified terpenes is Alpha-terpineol, Bergamotene (a-cis-Bergamotene) (a-trans-Bergamotene), Bisabolol (13-Bisabolol), Borneol, Camphor, Capsaicin, Carvacrol, Caryophyllene (13-Caryophyllene), Caryophyllene oxide, Cineole, Cinnamaldehyde (a-amyl-Cinnamaldehyde) (a-hexyl-Cinnamaldehyde), Cinnamyl Alcohol, Citronella!, Citronellol, Ethyl, Cinnamate, Eucalyptol/1,8-Cineole, Farnesol, Fenchel (13-Fenchol), Geranyl acetate, Germacrene B, Guaiene (a-Guaiene), Humulene (a-Humulene) (13-Humulene), lonol (3-oxo-a-ionol) (13-lonol), lonone (a-lonone) (13-lonone), Isoamyl acetate, Isoprene, Kahweol, Laevo-Carvone, Lavandulol, Limonene, Linalool, Linalyl acetate, Luteolin, Lycopene, Menthol, Myrcene (13-Myrcene), Nerol, Nerolidol, Neryl acetate, P-cymene, Phytol, Pinene, Pristimerin, Retinol, Terpin hydrate, Terpineol, Terpinol-4-ol, Terpinolene, Thujone, Thymol, or Vanillin. 11. The liquid composition of claim 1 , wherein the liquid composition is a juice, a soft drink, a wine, a cocktail, a medicinal preparation, coffee, or tea. 12. A liquid composition, comprising: a first purified cannabinoid selected from the group consisting of D9-THC, D8-THC, THCA, THCV, D8-THCV, D9-THCV, THCVA, CBD, CBDA, CBDV, CBDVA, CBC, CBCA, CBCV, CBCVA, CBG, CBGA, CBGV, CBGVA, CBN, CBNA, CBNV, CBNVA, CBND, CBNDA, CBNDV, CBNDVA, CBE, CBEA, CBEV, CBEVA, CBL, CBLA, CBLV, and CBLVA; Vitamin E TPGS; and water, wherein the liquid composition comprises a ratio of the first purified cannabinoid content to Vitamin E TPGS of about 1:1 to about 1:10 based on mass percent. 13. A liquid composition, comprising: one or more purified cannabinoids; Vitamin E TPGS; and water, wherein the liquid composition comprises a ratio of total purified cannabinoid content to Vitamin E TPGS of about 1:1 to about 1:10 based on mass percent and the liquid composition does not comprise a TPGS coprecipitate. 14. The liquid composition of claim 13 , wherein the liquid composition comprises a ratio of total purified cannabinoid content to Vitamin E TPGS of about 1:1 to about 1:8. 15. The liquid composition of claim 13 , wherein the liquid composition comprises a ratio of total purified cannabinoid content to Vitamin E TPGS of about 1:1 to about 1:6. 16. The liquid composition of claim 13 , wherein the liquid composition comprises a ratio of total purified cannabinoid content to Vitamin E TPGS of about 1:1 to about 1:4. 17. The liquid composition of claim 13 , wherein the liquid composition comprises a ratio of total purified cannabinoid content to Vitamin E TPGS of about 1:1 to about 1:2. 18. The liquid composition of claim 13 , wherein the one or more purified cannabinoids comprise THCA, CBC, THC, CBN, CBD, CBG, CBGA, CBDA, or a combination thereof. 19. The liquid composition of claim 13 , wherein the one or more purified cannabinoids comprise CBD, THC, or a combination thereof. 20. The liquid composition of claim 13 , wherein the one or more purified cannabinoids comprise a combination of THC and CBD. 21. The liquid composition of claim 13 , further comprising one or more purified terpenes. 22. The liquid composition of claim 21 , wherein the one or more purified terpenes is Alpha-terpineol, Bergamotene (a-cis-Bergamotene) (a-trans-Bergamotene), Bisabolol (13-Bisabolol), Borneol, Camphor, Capsaicin, Carvacrol, Caryophyllene (13-Caryophyllene), Caryophyllene oxide, Cineole, Cinnamaldehyde (a-amyl-Cinnamaldehyde) (a-hexyl-Cinnamaldehyde), Cinnamyl Alcohol, Citronella!, Citronellol, Ethyl, Cinnamate, Eucalyptol/1,8-Cineole, Farnesol, Fenchel (13-Fenchol), Geranyl acetate, Germacrene B, Guaiene (a-Guaiene), Humulene (a-Humulene) (13-Humulene), lonol (3-oxo-a-ionol) (13-lonol), lonone (a-lonone) (13-lonone), Isoamyl acetate, Isoprene, Kahweol, Laevo-Carvone, Lavandulol, Limonene, Linalool, Linalyl acetate, Luteolin, Lycopene, Menthol, Myrcene (13-Myrcene), Nerol, Nerolidol, Neryl acetate, P-cymene, Phytol, Pinene, Pristimerin, Retinol, Terpin hydrate, Terpineol, Terpinol-4-ol, Terpinolene, Thujone, Thymol, or Vanillin. 23. The liquid composition of claim 13 , wherein the liquid composition is a juice, a soft drink, a wine, a cocktail, a medicinal preparation, coffee, or tea.

Assignees

Inventors

Classifications

  • Cannabis · CPC title

  • o-phenolic cannabinoids, e.g. cannabidiol, cannabigerolic acid, cannabichromene or tetrahydrocannabinol · CPC title

  • Tocopherols, e.g. vitamin E · CPC title

  • Diphenyl-substituted acyclic alcohols · CPC title

  • Persulfides (thiuram disulfides A61K31/145; thiosulfonic acids A61K31/185) · CPC title

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What does patent US12324801B2 cover?
This disclosure relates to new compositions and methods for making cannabinoid formulations. In one embodiment, this disclosure provides water soluble compositions comprising a first purified cannabinoid and Vitamin E TPGS. In one embodiment, the disclosure herein comprises a method of making powders comprising heatings material to a first temperature and a second temperature.
Who is the assignee on this patent?
Canopy Growth Corp
What technology area does this patent fall under?
Primary CPC classification A61K31/353. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Jun 10 2025 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 7 related publications on this page (citations in our corpus or others sharing the same primary CPC).