IP Library Granted Patent US 9,101,583
Granted Patent B2
US 9,101,583 · App. 14/228,020 · Granted Aug 11, 2015

Microparticles manufactured in an oil-in-water process comprising a prostamide

Inventors: James Chang (Newport Beach, CA); Patrick Hughes (Aliso Viejo, CA); Chin-Ming Chang (Tustin, CA)
Assignee: Allergan, Inc.
A61K31/165A61K9/0048A61K9/0051A61K9/107A61K9/146A61K9/1647A61K9/1694A61K31/5575A61K47/34B01J13/04B01J13/06
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Quick Facts
Patent No.
US 9,101,583
App. No.
14/228,020
Granted
Aug 11, 2015
Kind
B2
Abstract

Biocompatible microparticles include an ophthalmically active cyclic lipid component and a biodegradable polymer that is effective, when placed into the subconjunctival space, in facilitating release of the cyclic lipid component into the anterior and posterior segments of an eye for an extended period of time. The cyclic lipid component can be associated with a biodegradable polymer matrix, such as a matrix of a two biodegradable polymers. Or, the cyclic lipid component can be encapsulated by the polymeric component. The present microparticles include oil-in-water emulsified microparticles. The subconjunctivally administered microparticles can be used to treat or to reduce at least one symptom of an ocular condition, such as glaucoma or age related macular degeneration.

Claims (9)

1. A population of microparticles comprising a polymeric component encapsulating a prostamide component in the form of oil-in-water emulsified microparticles.

2. The population of claim 1 , wherein the polymeric component comprises a poly (lactide-co-glycolide) copolymer, and the prostamide component comprises at least one prostamide derivative selected from the group consisting of bimatoprost, salts thereof, and mixtures thereof.

3. The population of claim 1 which is terminally sterilized.

4. The population of claim 3 , wherein at least 80% of the prostamide component remains stable after the sterilization.

5. The population of claim 1 having a mean particle diameter from about 30 μm to about 50 μm.

6. The population of claim 1 , wherein the maximum particle diameter is less than about 200 μm.

7. The population of claim 1 , wherein the microparticles have a release rate of the prostamide component of about 0.7% per day in vitro.

8. The population of claim 1 , wherein the prostamide component comprises about 10% wt/wt of the microparticles.

9. The population of claim 1 , wherein the prostamide component comprises about 5% wt/wt of the microparticles.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2014
From: CHANG, JAMES; HUGHES, PATRICK; CHANG, CHIN-MING
To: ALLERGAN, INC.
Reel/Frame 032561/0281 →
Continuity (4)
Division 11371118 · Mar 8, 2006
Continuation In Part 11303462 · Dec 15, 2005
Continuation In Part 10837260 · Apr 30, 2004
Related Publication 20150004243A1 · Jan 1, 2015