IP Library › Granted Patent US 10,494,327
Granted Patent B2
US 10,494,327 · App. 15/698,852 · Granted Dec 3, 2019

Controlled release pharmaceutical formulations

Inventor: Peter Laing (Cambridge, GB)
Assignee: United Therapeutics Corporation
C07C69/708A61K31/558A61K31/5575C07C67/08C07C2603/14
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Quick Facts
Patent No.
US 10,494,327
App. No.
15/698,852
Granted
Dec 3, 2019
Kind
B2
Abstract

Disclosed herein are drug release polymer compounds and compositions comprising prostacyclin compounds of Formula (I), and methods of preparing the same. A preferred polymer has a repeating unit of the following structure:

Claims (25)

1. A method for producing a drug release polymer, comprising esterifying a drug moiety which comprises at least one carboxylic acid group and at least one hydroxyl group in the presence of a coupling agent and a catalyst to form a drug release polymer comprising a plurality of releasable drug moieties, wherein at least some drug moieties are covalently attached to each other via an ester bond formed by a previously present carboxylic acid group of one drug moiety and a previously present hydroxyl group of another drug moiety and wherein the drug moiety is a prostacyclin compound comprising at least one carboxylic acid group and at least one hydroxyl group.

2. The method of claim 1 , wherein the coupling agent is N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide or N,N′-Dicyclohexylcarbodiimide.

3. The method of claim 1 , wherein the catalyst is 4-(Dimethylamino)pyridine.

4. The method of claim 1 , wherein the drug moiety has at least two carboxylic acid groups and the method further comprises blocking one or more of the carboxylic acid groups of the drug moiety in excess of one carboxylic group, prior to esterification.

5. The method of claim 1 , wherein the drug moiety comprises at least two hydroxyl groups and the method further comprises blocking one or more of the hydroxyl groups of the drug moiety in excess of one hydroxyl group, prior to esterification.

6. The method of claim 5 , wherein the one or more hydroxyl groups are blocked using trimethylsilyl chloride or t-butyldimethylsilyl chloride.

7. The method of claim 1 , wherein the prostacyclin compound is selected from the group consisting of epoprostenol, treprostinil, beraprost, iloprost, cicaprost, and prostaglandin I2.

8. The method of claim 7 , wherein the prostacyclin compound is treprostinil.

9. The method of claim 1 , wherein the prostacyclin compound is a compound of Formula (I)

wherein

represents a single or a double bond;

Z 1 and Z 2 each independently represents an O or CH 2 ;

p=0 or 1;

m=1, 2, or 3;

R 1 represents a H or an acid protective group;

R 2 and R 3 each independently represents a H or a hydroxyl protective group;

R 4 represents H or a C 1-6 alkyl; and

R 5 represents a C 1-6 alkyl group or C 2-8 alkynylene group.

10. The method of claim 1 , wherein the polymer is at least a trimer.

11. The method of claim 1 , wherein the covalent attachment is an ester bond formed between said at least one hydroxyl group and said at least one carboxylic group.

12. The method of claim 1 , wherein the polymer further comprises a co-monomer covalently bonded to the carboxylic acid group of one drug moiety and the hydroxyl group of a second drug moiety.

13. The method of claim 12 , wherein the polymer is insoluble in water.

14. The method of claim 12 , wherein the polymer is soluble in water.

15. The method of claim 12 , wherein the co-monomer is selected from the group consisting of 6-hydroxyhexanoic acid, beta-hydroxybutyric acid, hydroxyl-polyethylene glycol-carboxylic acid, lactic acid, and glycolic acid.

16. The method of claim 1 , wherein the drug moieties that form the polymer have a structure selected from the group consisting of Formulae (IIa), (IIb), and (IIc):

Continuity (3)
Division 14264392 · Apr 29, 2014
Provisional Application 61817462 · Apr 30, 2013
Related Publication 20170369416A1 · Dec 28, 2017
Cited By (4)
US 12,390,475 US 12,697,315 US 12,734,143 US 12,740,954