CPC A61K 36/185 (2013.01) [A61K 9/0053 (2013.01); A61K 9/1075 (2013.01); A61K 31/05 (2013.01); A61K 31/352 (2013.01); A61P 25/20 (2018.01)] | 11 Claims |
1. A therapeutic preparation of full spectrum hemp oil formulated for oral administration to a human subject,
comprising 0.1% cannabinoids as a percent by weight of the preparation;
wherein at least 80% of the cannabinoids in the preparation are in the form of micelles suspended in an aqueous solvent;
wherein the cannabinoids comprise the following: at least 70% cannabidiol (CBD), at least 2% tetrahydrocannabivarin (THCV), at least 5% cannabidivarin (CBDV), and less than 1% Δ9-tetrahydrocannabinol (THC) as a percent by weight of the cannabinoids in the preparation;
wherein the micelles in the preparation have a median diameter between 10 and 100 nm;
wherein the micelles in the preparation are sized and formulated to promote intestinal absorption of the cannabinoids into the subject, whereby 25% to 50% or more of the cannabinoids from the preparation reach the circulation within 6 hours of oral administration.
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