Suppositories comprising cannabinoids
This invention relates to a suppository composition comprising cannabinoids. The suppository composition is formulated for easy absorption through mucosal membrane. The suppository as provided herein is useful for administration of cannabinoids in patients with nausea, vomiting, other conditions preventing swallowing, or conditions wherein suppository administration is required. Methods to manufacture the suppository composition are provided. Methods to treat pain, nausea, post-operative ileus and/or inflammatory bowel diseases using the suppository according to this invention are also provided.
1. A method to treat intestinal inflammation, comprising:
administering 1-6 times per day to a mammal a suppository composition comprising:
at least one cannabinoid at 0.1% to 50% by weight of the total composition;
at least one sugar alcohol or sugar at 15% to 25% by weight of the total composition;
at least one fatty base suitable for suppository formulation selected from the group consisting of glycerol ricinoleate, hydrogenated coco-glycerin, and ceteareth-25 at 60% to 80% by weight of the total composition; and
at least one non-ionic surfactant selected from the group consisting of ceteareth-15 and ceteareth-17 at 2% to 10% by weight of the total composition,
wherein the at least one cannabinoid is nanoencapsulated into particles, and
wherein the composition is packaged in a suppository mold.
2. The method of claim 1 , wherein the cannabinoid is CBD, CBG, CBN, CBDV, or THCV.
3. The method of claim 1 , wherein the at least one cannabinoid is THC and wherein THC comprises 0.1% to 2% by weight of the total composition.
4. The method composition of claim 1 , wherein the at least one cannabinoid is from natural sources or synthetic.
5. The method of claim 1 , wherein the particles are of size 20-40 nm.
6. The method of claim 1 , wherein the at least one cannabinoid is encapsulated into hyaluronic acid derivative nanolattice, and wherein the hyaluronic acid derivative is sodium oleyl hyaluronate.
7. The method of claim 1 , wherein the at least one sugar is selected from the group consisting of dextrose, maltose, fructose, and sucrose.
8. The method of claim 1 , wherein the at least one sugar is provided in micronized form.
9. The method of claim 1 , wherein the at least one sugar alcohol is selected from the group consisting of isomalt, mannitol, sorbitol, xylitol, lactitol, maltitol, and erythritol.
10. The method of claim 1 , wherein the at least one sugar alcohol is provided in micronized form.
11. The method of claim 1 , wherein the intestinal inflammation is irritable bowel syndrome.
12. The method of claim 1 , wherein the intestinal inflammation is inflammatory bowel disease.