IP Library › Granted Patent US 8,471,044
Granted Patent B2
US 8,471,044 · App. 12/602,951 · Granted Jun 25, 2013

Epigallocatechin-3-gallate crystal compositions

Inventors: Michael Zaworotko (Tampa, FL); Sheshanka Kesani (Tampa, FL)
Assignee: University of South Florida
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Quick Facts
Patent No.
US 8,471,044
App. No.
12/602,951
Granted
Jun 25, 2013
Kind
B2
Abstract

Crystalline epigallocatechin-3-gallate compositions and methods of use.

Claims (17)

1. A composition comprising crystalline epigallocatechin-3-gallate wherein the crystalline epigallocatechin-3-gallate has an XRPD pattern exhibiting major peaks at about the following positions: 13.9, 17.2, 21.2, 23.6, 26.5, 29.0, and 31.5.

2. The composition of claim 1 wherein the crystalline epigallocatechin-3-gallate contains less than 1 wt. % non-aqueous, non-solvent, non-epicatechin gallate impurities.

3. A process for the preparation of a crystal form of epigallocatechin-3-gallate, wherein said process comprises: dissolving epigallocatechin-3-gallate in a solvent to form a solution, and precipitating crystalline epigallocatechin-3-gallate from the solution wherein the crystalline epigallocatechin-3-gallate consists essentially of epigallocatechin-3-gallate haying an XRPD pattern exhibiting major peaks at about the following positions: (i) 7.1, 7.8, 10.5, 13.0, 15.2, 20.3, 23.5, and 25.9, (ii) 13.4, 15.4, 19.4, 24.3, 27.8, 28.5, 31.3, and 37.5, or (iii) 13.9, 17.2, 21.2, 23.6, 26.5, 29.0, and 31.5.

4. The process of claim 3 wherein the solvent comprises acetonitrile.

5. The process of claim 3 wherein the precipitation of said crystal is initiated by adding a second solvent to the solution with or without seeding, evaporating the organic solvent from the solution, heating the solution, or cooling the solution.

6. The process of claim 5 wherein the second solvent is dichloromethane.

7. A pharmaceutical composition comprising crystalline epigallocatechin-3-gallate and a pharmaceutically acceptable excipient, wherein the crystalline epigallocatechin-3-gallate exhibits XRPD major peaks at about the following positions: (i) 13.9, 17.2, 21.2, 23.6, 26.5, 29.0, and 31.5, (ii) 7.1, 7.8, 10.5, 13.0, 15.2, 20.3, 23.5, and 25.9, or (iii) 13.4, 15.4, 19.4, 24.3, 27.8, 28.5, 31.3, and 37.5.

8. A foodstuff comprising crystalline epigallocatechin-3-gallate, wherein the crystalline epigallocatechin-3-gallate exhibits XRPD major peaks at about the following positions: (i) 13.9, 17.2, 21.2, 23.6, 26.5, 29.0, and 31.5, (ii) 7.1, 7.8, 10.5, 13.0, 15.2, 20.3, 23.5, and 25.9, or (iii) 13.4, 15.4, 19.4, 24.3, 27.8, 28.5, 31.3, and 37.5.

9. A process for treating a disease or condition resulting from oxidative stress, wherein said method comprises administering an effective amount of a composition comprising a crystal form of epigallocatechin-3-gallate to a person or animal having or predisposed to having a condition resulting from oxidative stress, wherein the crystalline epigallocatechin-3-gallate exhibits XRPD major peaks at about the following positions: (i) 13.9, 17.2, 21.2, 23.6, 26.5, 29.0, and 31.5, (ii) 7.1, 7.8, 10.5, 13.0, 15.2, 20.3, 23.5, and 25.9, or (iii) 13.4, 15.4, 19.4, 24.3, 27.8, 28.5, 31.3, and 37.5.

10. Crystalline epigallocatechin-3-gallate with less than a stoichiometric amount of water in isolated form, wherein the crystalline epigallocatechin-3-gallate exhibits XRPD major peaks at about the following positions: (i) 13.9, 17.2, 21.2, 23.6, 26.5, 29.0, and 31.5, (ii) 7.1, 7.8, 10.5, 13.0, 15.2, 20.3, 23.5, and 25.9, or (iii) 13.4, 15.4, 19.4, 24.3, 27.8, 28.5, 31.3, and 37.5.

11. The crystalline epigallocatechin-3-gallate of claim 10 wherein the crystal is solvated.

12. A process for improving animal health or nutrition, the process comprising administering to the animal a composition comprising crystalline epigallocatechin-3-gallate, wherein the crystalline epigallocatechin-3-gallate exhibits XRPD major peaks at about the following positions: (i) 13.9, 17.2, 21.2, 23.6, 26.5, 29.0, and 31.5, (ii) 7.1, 7.8, 10.5, 13.0, 15.2, 20.3, 23.5, and 25.9, or (iii) 13.4, 15.4, 19.4, 24.3, 27.8, 28.5, 31.3, and 37.5.

13. The composition of claim 1 wherein the crystalline epigallocatechin-3-gallate contains up to 20 mole % epicatechin gallate.

14. The composition of claim 10 wherein the crystalline epigallocatechin-3-gallate contains up to 20 mole % epicatechin gallate.

15. The composition of claim 11 wherein the crystalline epigallocatechin-3-gallate contains up to 20 mole % epicatechin gallate.

16. The crystalline epigallocatechin-3-gallate of claim 10 wherein the crystal is non-solvated.

17. The composition of claim 16 wherein the crystalline epigallocatechin-3-gallate contains up to 20 mole % epicatechin gallate.

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY NAME FROM "UNIVERSITY OF SOUTH FLORIDA OF TAMPA" TO "UNIVERSITY OF SOUTH FLORIDA" PREVIOUSLY RECORDED ON REEL 023693 FRAME 0882. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT OF ASSIGNOR'S INTEREST. Recorded Dec 31, 2009
From: ZAWOROTKO, MICHAEL; KESANI, SHESHANKA
To: UNIVERSITY OF SOUTH FLORIDA
Reel/Frame 023724/0750 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 23, 2009
From: ZAWOROTKO, MICHAEL; KESANI, SHESHANKA
To: UNIVERSITY OF SOUTH FLORIDA OF TAMPA
Reel/Frame 023693/0882 →
Continuity (2)
Provisional Application 60942355 · Jun 6, 2007
Related Publication 20100173984A1 · Jul 8, 2010