The invention describes alpha lipoic acid complexes, that can be oligomeric, polymeric, monomeric and mixtures thereof. The complexes can be salts, chelates, etc. of the oligomers, polymers, or monomeric alpha lipoic acid.
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1. A composition comprising: a stable complex of oligomeric lipoic acid and a counterion, wherein the average degree of oligomerization is between 2 and about 7 and has a melting point above that of monomeric lipoic acid and the counterion is a basic amino acid. 2. The composition of claim 1, wherei
1. A composition comprising: a stable complex of oligomeric lipoic acid and a counterion, wherein the average degree of oligomerization is between 2 and about 7 and has a melting point above that of monomeric lipoic acid and the counterion is a basic amino acid. 2. The composition of claim 1, wherein the basic amino acid is ornithine, arginine, lysine or mixtures thereof. 3. A composition comprising: a stable oligomeric lipoic acid complex and a counterion comprising formula (I): wherein each R+ independently denote a counterion, andn is a value between about 2 and about 50 and has a melting point above that of monomeric lipoic acid and the counterion is a basic amino acid. 4. The composition of claim 3 wherein the basic amino acid is ornithine, arginine, lysine or mixtures thereof. 5. A stable oligomeric lipoic acid complex and a basic amino acid counterion prepared by the process of: a) reacting a basic amino acid with lipoic acid in an aqueous solution;b) maintaining the solution at an elevated temperature for a period of between about 1 to about 5 hours; andc) precipitating a complex of the oligomeric lipoic acid and basic amino acid counterion from the aqueous solution by addition of a non-solvent wherein the degree of oligomerization is between 2 and about 50 and has a melting point above that of monomeric lipoic acid. 6. The oligomeric lipoic acid complex of the process of claim 5, further comprising the step of: d) collecting the precipitated complex. 7. The oligomeric lipoic acid complex of claim 5, wherein the temperature of the reaction is between about 30° C. and about 50° C. 8. The oligomeric lipoic acid complex of claim 5, wherein the solution was maintained at the elevated temperature for about 3 hours. 9. The oligomeric lipoic acid complex of claim 5, wherein the non-solvent is an alcohol, a chlorinated hydrocarbon, an aliphatic ketone, an aliphatic ether, an alkyl hydrocarbon, an aromatic hydrocarbon or mixtures thereof. 10. The oligomeric lipoic acid complex of claim 9, wherein the non-solvent is one of acetonitrile, dichloromethane, acetone, 2-propanol, diethyl ether, hexane, octane, toluene, petroleum ether, tetrahydrofuran, octanol, benzene, dioxane or mixtures thereof. 11. The oligomeric lipoic acid complex of claim 5, wherein the amino acid is ornithine, arginine, lysine or mixtures thereof. 12. A composition comprising: a stable mixed oligomeric alpha lipoic acid complex and a counterion comprising formula (II): wherein n is a value between about 2 and about 7 and has a melting point above that of monomeric lipoic acid; andeach R1 independently is a hydrogen atom or counterion provided at least one R1 is a counterion and the counterion is a basic amino acid. 13. A pharmaceutical composition comprising the composition of claim 1 and a pharmaceutically acceptable carrier. 14. A pharmaceutical composition comprising the composition of claim 3 and a pharmaceutically acceptable carrier. 15. A pharmaceutical composition comprising the composition of claim 5 and a pharmaceutically acceptable carrier. 16. A pharmaceutical composition comprising the composition of claim 12 and a pharmaceutically acceptable carrier. 17. A composition comprising: an isolated complex of oligomeric lipoic acid and a counterion, wherein the degree of oligomerization is between 2 and about 7 and has a melting point above that of monomeric lipoic acid and the counterion is a basic amino acid. 18. The composition of claim 17, wherein the basic amino acid is ornithine, arginine, lysine or mixtures thereof. 19. A composition comprising: an isolated oligomeric lipoic acid complex and a counterion comprising formula (I): wherein each R+ independently denote a counterion, andn is a value between about 2 and about 7 and has a melting point above that of monomeric lipoic acid and the counterion is a basic amino acid. 20. The composition of claim 19, wherein the basic amino acid is ornithine, arginine, lysine or mixtures thereof. 21. A composition comprising: an isolated mixed oligomeric alpha lipoic acid complex and a counterion comprising formula (II): wherein n is a value between about 2 and about 7 and has a melting point above that of monomeric lipoic acid; andeach R1 independently is a hydrogen atom or counterion provided at least one R1 is a counterion and the counterion is a basic amino acid. 22. A pharmaceutical composition comprising the composition of claim 17 and a pharmaceutically acceptable carrier. 23. A pharmaceutical composition comprising the composition of claim 19 and a pharmaceutically acceptable carrier. 24. A pharmaceutical composition comprising the composition of claim 21 and a pharmaceutically acceptable carrier. 25. The composition of claim 1, wherein the complex has a melting point up to between about 165° C. and 170° C. 26. The composition of claim 3, wherein the complex has a melting point between about 165° C. and 170° C. 27. The composition of claim 5, wherein the complex has a melting point between about 165° C. and 170° C. 28. The composition of claim 12, wherein the complex has a melting point between about 165° C. and 170° C. 29. The composition of claim 17, wherein the complex has a melting point between about 165° C. and 170° C. 30. The composition of claim 19, wherein the complex has a melting point between about 165° C. and 170° C. 31. The composition of claim 21, wherein the complex has a melting point between about 165° C. and 170° C.
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이 특허에 인용된 특허 (14)
Helmut Hettche DE; Matthias Rischer DE; Werner Sarlikiotis DE, Dosage forms containing thioctic acid or solid salts of thioctic acid with improved release and bioavailability.
Hettche Helmut,DEX ; Rischer Matthias,DEX ; Sarlikiotis Werner,DEX, Dosage forms containing thioctic acid or solid salts of thioctic acid with improved release and bioavailability.
Tucker Mark J. (Round Steps ; High Street Stow-on-the-Wold ; Gloucester GL54 1DL GBX) Tucker Mark R. (P.O. Box 23530 Bahrain BHX), Occlusive body for administering a physiologically active substance.
Farhadieh Bahram (Libertyville IL) Gokhale Rajeev D. (Vernon Hills IL) Berger Hana (Lincolnshire IL) Vallner Joseph (Mountainview CA), Single layer transdermal drug administration system.
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