Transdermal cannabinoid formulations
The present invention includes a transdermal composition which contains a pharmaceutically effective amount of a cannabinoid for delivery of the cannabinoid to the bloodstream of a user. The composition may comprise the following components: a surfactant-lecithin organogel; and a cannabinoid. The composition may also comprise an exogenous terpene. The cannabinoid is capable of diffusing from the composition into the bloodstream of the user, and may be used in methods for treating a patient suffering from a condition such as pain, nausea and emesis, convulsions, muscle spasm, inflammation, depression, and cachexia.
1. A transdermal composition comprising a pharmaceutically effective amount of a cannabinoid for delivery of the cannabinoid to the bloodstream of a user, said composition comprising:
a) a surfactant-lecithin organogel comprising a mixture of: water, high molecular weight acrylic acid polymers, PPG-2 myristyl ether propionate, at least one exogenous terpene or terpenoid, and oleic acid; and
b) at least one cannabinoid;
wherein the cannabinoid is capable of diffusing from the composition into the bloodstream of the user.
2. The composition of claim 1 , wherein the surfactant-lecithin organogel is present in an amount of between about between about 95% and about 98% w/w.
3. The composition of claim 1 , wherein the terpene or terpenoid comprises myrcene or menthol.
4. The composition of claim 1 , wherein the composition further comprises isopropyl myristate.
5. The composition of claim 1 , wherein the cannabinoid comprises THC.
6. The composition of claim 5 , wherein the THC is in an amount between about 0.1% and about 3%.
7. The composition of claim 1 , wherein the cannabinoid comprises THCa.
8. The composition of claim 7 , wherein the THCa is in an amount between about 0.1% and about 3%.
9. The composition of claim 1 , wherein the cannabinoid comprises CBD.
10. The composition of claim 9 , wherein the CBD is in an amount between about 0.1% and about 3%.
11. The composition of claim 1 , wherein the cannabinoid comprises CBDa.
12. The composition of claim 11 , wherein the CBDa is in an amount between 0.1% and about 3%.
13. The composition of claim 1 , wherein the cannabinoid comprises CBN in an amount of between 0.1% and about 3%.
14. The composition of claim 1 , wherein the cannabinoid comprises CBC in an amount of 0.1% and about 3%.
15. The composition of claim 1 , wherein the cannabinoid comprises THCv in an amount of between about 0.1% and about 3%.
16. The composition of claim 1 , wherein the cannabinoid comprises CBC in an amount of between about 0.1% and about 3%.
17. A method for treating a patient suffering from a condition selected from the group consisting of pain, nausea and emesis, convulsions, muscle spasm, inflammation, depression, and cachexia comprising administering the composition of claim 1 .
18. The composition of claim 1 , wherein water is present in an amount between about 1% to 30%.
19. The composition of claim 1 , wherein water is present in an amount between about 4% to 20%.
20. The composition of claim 1 , wherein water is present in an amount between about 8% to 12%.