IP Library › Granted Patent US 7,981,445
Granted Patent B2
US 7,981,445 · App. 12/402,358 · Granted Jul 19, 2011

Compositions and methods for preparation of poorly water soluble drugs with increased stability

Assignee: Abraxis Bioscience, LLC
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,981,445
App. No.
12/402,358
Granted
Jul 19, 2011
Kind
B2
Abstract

The present invention provides stable pharmaceutical compositions of poorly water soluble pharmaceutical agents and stabilizing agents which function to increase stability of the compositions. The use of stabilizing agents provide extended stability of nanoparticle suspensions and other formulations of poorly water soluble pharmaceutical agents such as docetaxel under certain conditions, for example upon dilution for administration.

Claims (14)

1. A composition comprising 1) nanoparticles comprising docetaxel coated with a carrier protein, wherein said carrier protein is albumin and 2) a citrate selected from the group consisting of citric acid and sodium citrate, wherein stability of the composition is enhanced as compared to that of a composition without citric acid or sodium citrate.

2. The composition according to claim 1 , wherein the ratio of albumin to docetaxel is about 18:1 or less.

3. The composition according to claim 1 , wherein the nanoparticles in the composition have an average or mean particle size of no greater than about 200 nm.

4. The composition according to claim 1 , wherein the composition is a liquid suspension of docetaxel at a concentration of at least about 1 mg/ml.

5. The composition according to claim 1 , wherein the composition is a dry composition that can be reconstituted to a liquid suspension with at least about 1 mg/ml docetaxel.

6. The composition according to claim 1 , wherein the composition further comprises sodium chloride.

7. The composition according to claim 6 , wherein the composition comprises about 200 mM sodium citrate and about 300 mM sodium chloride.

8. The composition according to claim 1 , wherein the albumin is human serum albumin.

9. The composition according to claim 1 , wherein the citrate is sodium citrate.

10. The composition according to claim 1 , wherein the pH of the composition is no less than about 6.

11. The composition according to claim 1 , wherein the composition is stable for at least about 24 hours following reconstitution or rehydration.

12. The composition according to claim 8 , wherein the composition further comprises sodium chloride.

13. The composition according to claim 8 , wherein the citrate is sodium citrate.

14. The composition according to claim 13 , further comprising sodium chloride.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 28, 2009
From: DE, TAPAS; DESAI, NEIL P.; YANG, ANDREW; YIM, ZACHARY; SOON-SHIONG, PATRICK
To: ABRAXIS BIOSCIENCE, INC.
Reel/Frame 023017/0648 →
MERGER Recorded Jul 28, 2009
From: ABRAXIS BIOSCIENCE, INC.
To: ABRAXIS BIOSCIENCE, LLC
Reel/Frame 023017/0669 →
Continuity (5)
Continuation 11513756 · Aug 30, 2006
Provisional Application 60712865 · Aug 31, 2005
Provisional Application 60736962 · Nov 14, 2005
Provisional Application 60736931 · Nov 14, 2005
Related Publication 20090196933A1 · Aug 6, 2009