IP Library Patent Application 13481397
Patent Application
App. No. 13/481,397

Methods of preparing progesterone pharmaceutical compositions

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 None
App. No.
13/481,397
Abstract

The invention provides a method of preparing a pharmaceutical composition comprising: (a) combining progesterone particles with a liquid carrier to provide a mixture; (b) wet-milling the mixture to provide a wet-milled progesterone composition; and (c) processing the wet-milled progesterone composition to provide a pharmaceutical composition. Pharmaceutical compositions prepared by the method are also provided.

Claims (53)

1 . A method of preparing a pharmaceutical composition comprising:

(a) combining progesterone particles with a liquid carrier to provide a mixture;

(b) wet-milling the mixture to provide a wet-milled progesterone composition; and

(c) processing the wet-milled progesterone composition to provide a pharmaceutical composition.

2 . A method of preparing a pharmaceutical composition comprising wet-milling progesterone particles in a liquid carrier to provide a wet-milled progesterone composition and processing the wet-milled progesterone composition to provide a pharmaceutical composition.

3 . The method of claim 1 , wherein the pharmaceutical composition is an oral pharmaceutical composition.

4 . The method of claim 1 , wherein the pharmaceutical composition is a capsule.

5 . The method of claim 1 , wherein the pharmaceutical composition is a soft-shelled capsule.

6 . The method of claim 1 , wherein the pharmaceutical composition is a hard-shelled capsule.

7 . The method of claim 1 , wherein processing the wet-milled progesterone composition comprises encapsulating the wet-milled progesterone composition to provide a capsule.

8 . The method of claim 1 , wherein wet-milling provides progesterone particles having a cumulative size distribution D 90 from about 10 μm to about 70 μm.

9 . The method of claim 1 , wherein wet-milling provides progesterone particles having a cumulative size distribution D 50 from about 5 μm to about 30 μm.

10 . The method of claim 1 , wherein wet-milling provides progesterone particles having a cumulative size distribution D 10 from about 2 μm to about 15 μm.

11 . The method of claim 1 , wherein the liquid carrier comprises any one or more of a long-chain glyceride, a free fatty acid, a fatty acid ester, and a medium-chain glyceride.

12 . The method of claim 11 , wherein the liquid carrier comprises at least one long-chain glyceride, and the at least one long-chain glyceride is selected from the group consisting of any one or more of peanut oil, soybean oil, sunflower oil, olive oil, sesame oil, colza oil, almond oil, safflower oil, corn oil, linseed oil, rapeseed oil, evening primrose oil, grape seed oil, cottonseed oil, flaxseed oil, and menhaden oil.

13 . The method of claim 11 , wherein the liquid carrier comprises at least one fatty acid ester, and the at least one fatty acid ester is selected from the group consisting of glycerol mono-, di, or tri-esters of a long or medium chain fatty acid.

14 . The method of claim 11 , wherein the liquid carrier comprises at least one fatty acid ester, and the at least one fatty acid ester is selected from the group consisting of propylene glycol mono- and di-esters of a long or medium chain fatty acid.

15 . The method of claim 1 , wherein the liquid carrier comprises at least one phospholipid.

16 . The method of claim 15 , wherein the phospholipid is lecithin.

17 . The method of claim 1 , wherein the liquid carrier comprises at least one lipophilic surfactant.

18 . The method of claim 1 , wherein the mixture comprises from about 4% to about 80% progesterone by weight of the mixture.

19 . The method of claim 1 , wherein the mixture comprises from about 10% to about 70% progesterone by weight of the mixture.

20 . The method of claim 1 , wherein the mixture comprises from about 20% to about 60% progesterone by weight of the mixture.

21 . The method of claim 1 , wherein the mixture comprises from about 40% to about 50% progesterone by weight of the mixture.

22 . The method of claim 1 , wherein the mixture comprises from about 20% to about 96% liquid carrier by weight of the mixture.

23 . The method of claim 1 , wherein the mixture comprises from, about 30% to about 90% liquid carrier by weight of the mixture.

24 . The method of claim 1 , wherein the mixture comprises from about 40% to about 80% liquid carrier by weight of the mixture.

25 . The method of claim 1 , wherein the mixture comprises from about 50% to about 60% liquid carrier by weight of the mixture.

26 . The method of claim 1 , wherein the mixture comprises from about 0.05% to about 5% phospholipid and/or lipophilic surfactant by weight of the mixture.

27 . A pharmaceutical composition prepared according to the method of claim 1 .

28 . A method of preparing a wet-milled progesterone composition comprising:

(a) combining progesterone particles with a liquid carrier, optionally with at least one phospholipid and/or at least one lipophilic surfactant, to provide a mixture; and

(b) wet-milling the mixture to provide a wet-milled progesterone composition.

29 . The method of claim 28 , wherein wet-milling provides progesterone particles having a cumulative size distribution D 90 from about 10 μm to about 70 μm.

30 . The method of claim 28 , wherein wet-milling provides progesterone particles having a cumulative size distribution D 50 from about 5 μm to about 30 μm.

31 . The method of claim 28 , wherein wet-milling provides progesterone particles having a cumulative size distribution D 10 from about 2 μm to about 15 μm.

32 . The method of claim 28 , wherein the liquid carrier comprises any one or more of a long-chain glyceride, a free fatty acid, a fatty acid ester, and a medium-chain glyceride.

33 . The method of claim 32 , wherein the liquid carrier comprises at least one long-chain glyceride, and the at least one long-chain glyceride is selected from the group consisting of any one or more of peanut oil, soybean oil, sunflower oil, olive oil, sesame oil, colza oil, almond oil, safflower oil, corn oil, linseed, oil, rapeseed oil, evening primrose oil, grape seed oil, cottonseed oil, flaxseed oil, and menhaden oil.

34 . The method of claim 33 , wherein the liquid carrier comprises at least one fatty acid ester, and the at least one fatty acid ester is selected from the group consisting of glycerol mono-, di, or tri-esters of a long or medium chain fatty acid.

35 . The method of claim 33 , wherein the liquid carrier comprises at least one fatty acid ester, and the at least one fatty acid ester is selected from the group consisting of propylene glycol mono- and di-esters of a long or medium chain fatty acid.

36 . The method of claim 28 , wherein the liquid carrier comprises at least one phospholipid.

37 . The method of claim 36 , wherein the phospholipid is lecithin.

38 . The method of claim 2 , wherein the liquid carrier comprises at least one lipophilic surfactant.

39 . The method of claim 2 , wherein the mixture comprises from about 4% to about 80% progesterone by weight of the mixture.

40 . The method of claim 2 , wherein the mixture comprises from about 10% to about 70% progesterone by weight of the mixture.

41 . The method of claim 2 , wherein the mixture comprises from about 20% to about 60% progesterone by weight of the mixture.

42 . The method of claim 2 , wherein the mixture comprises from about 40% to about 50% progesterone by weight of the mixture.

43 . The method of claim 2 , wherein the mixture comprises from about 20% to about 96% liquid carrier by weight of the mixture.

44 . The method of claim 2 , wherein the mixture comprises from about 30% to about 90% liquid carrier by weight of the mixture.

45 . The method of claim 2 , wherein the mixture comprises from about 40% to about 80% liquid carrier by weight of the mixture.

46 . The method of claim 2 , wherein the mixture comprises from about 50% to about 60% liquid carrier by weight of the mixture.

47 . The method of claim 2 , wherein the mixture comprises from about 0.05% to about 5% phospholipid and/or lipophilic surfactant by weight of the mixture.

48 . A wet-milled progesterone composition prepared according to the method of claim 28 .

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Nov 18, 2021
From: ATHYRIUM OPPORTUNITIES II ACQUISITION LP
To: PHARMACEUTICS INTERNATIONAL, INC.
Reel/Frame 058155/0054 →
SECURITY INTEREST Recorded Aug 31, 2016
From: PHARMACEUTICS INTERNATIONAL, INC.
To: ATHYRIUM OPPORTUNITIES II ACQUISITION LP
Reel/Frame 039885/0722 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 9, 2012
From: ABIDI, SYED E.; COUTINHO, ERIC R.; GUMUDAVELLI, SRIDHAR; AGRAWAL, SWATI; GULLAPALLI, RAMPURNA
To: PHARMACEUTICS INTERNATIONAL, INC.
Reel/Frame 028515/0891 →