Elemene compositions containing liquid oil
The present invention provides injectable water-in-oil emulsions that comprise elemenes (preferably, bete-elemene), liquid oil, an emulsifier (optionally) and a pharmaceutically acceptable aqueous phase. The present invention also provides methods for making and using such emulsions.
1 . An injectable oil-in-water emulsion comprising a therapeutically effective concentration of elemene(s), at least one liquid oil, and water.
2 . The emulsion according to claim 1 wherein the liquid oil is selected from the group consisting of a triglyceride, a diglyceride, a monoglyceride, a mixture of diglyceride and monoglyceride, vitamin E, and a derivative of vitamin E.
3 . The emulsion according to claim 1 additionally comprising an emulsifier.
4 . The emulsion according to claim 3 wherein the emulsifier is an egg or soy phospholipid.
5 . The emulsion according to claim 2 wherein the triglyceride oil is an oil ester of C6 to C22 aliphatic fatty acids.
6 . The emulsion according to claim 2 wherein the monoglyceride or diglyceride is an ester of C6 to C12 saturated fatty acid or C16 to C18 unsaturated fatty acid.
7 . The emulsion according to claim 2 wherein the vitamin E or the derivative thereof is selected from alpha tocopherol and alpha tocopherol acetate.
8 . The emulsion according to claim 1 wherein the elemene(s) contain greater than 50% beta-elemene based on the weight of all elemene isomers present, and wherein betal-elemene has the structure:
9 . The emulsion according to claim 8 wherein the elemene(s) contain greater than 80% beta-elemene based on the weight of all elemene isomers present.
10 . The emulsion according to claim 8 wherein the elemene(s) contain greater than 90% beta-elemene based on the weight of all elemene isomers present.
11 . The emulsion according to claim 1 wherein the therapeutically effective concentration of elemene(s) is from about 0.5 mg/ml to about 50 mg/ml.
12 . The emulsion according to claim 1 wherein the therapeutically effective concentration of elemene(s) is about 5 mg/ml.
13 . The emulsion according to claim 1 additionally comprising a tonicity-adjusting agent.
14 . The emulsion according to claim 13 wherein the tonicity-adjusting agent is selected from the group consisting of propylene glycol, glycerol, mannitol, sorbitol, xylitol, sucrose, glucose, fructose, trehalose, lactose, glycine, dextrin, sodium chloride and a mixture thereof.
15 . The emulsion according to claim 1 additionally comprising disodium edetate.
16 . The emulsion according to claim 1 wherein the liquid oil is a mixture of long chain triglyceride and medium chain triglyceride, and wherein the emulsion further comprises phospholipid.
17 . The emulsion of claim 16 further comprising a tonicity-adjusting agent, disodium edetate, or both a tonicity-adjusting agent and disodium edetate.
18 . An injectable oil-in-water emulsion comprising about 0.5% (w/w) elemene(s), about 5% (w/w) vegetable oil, about 5% (w/w) medium chain triglyceride, about 1% (w/w) to 3% (w/w) phospholipid, about 1% (w/w) glycine, about 2% (w/w) glycerol, and water.
19 . A method of reducing neoplasm in mammals comprising administering to a mammal in need thereof a therapeutically effective amount of elemene(s) in the emulsion according to claim 1 .
20 . The method according to claim 19 wherein the neoplasm is selected from the group consisting of leukemias, sarcomas, carcinomas, and myelomas.