IP Library › Granted Patent US 10,478,398
Granted Patent B2
US 10,478,398 · App. 15/872,895 · Granted Nov 19, 2019

Sol-gel phase-reversible hydrogel templates and uses thereof

Inventors: Kinam Park (West Lafayette, IN); Ghanashyam S. Acharya (West Lafayette, IN); Haesun Park (West Lafayette, IN)
Assignee: Akina, Inc.
A61K9/1682A61K9/1647A61K9/5031A61K9/5089A61K31/00Y10S977/773Y10S977/887Y10S977/89Y10S977/906
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Quick Facts
Patent No.
US 10,478,398
App. No.
15/872,895
Granted
Nov 19, 2019
Kind
B2
Abstract

Discrete microstructures of predefined size and shape are prepared using sol-gel phase-reversible hydrogel templates. An aqueous solution of hydrogel-forming material is covered onto a microfabricated silicon wafer master template having predefined microfeatures, such as pillars. A hydrogel template is formed, usually by lowering the temperature, and the formed hydrogel template is peeled away from the silicon master template. The wells of predefined size and shape on the hydrogel template are filled with a solution or a paste of a water-insoluble polymer, and the solvent is removed to form solid structures. The formed microstructures are released from the hydrogel template by simply melting the hydrogel template in water. The microstructures are collected by centrifugation. The microstructures fabricated by this method exhibit pre-defined size and shape that exactly correspond to the microwells of the hydrogel template. The method of preparing microstructures based on hydrogel templates is simple and can easily produce large quantities of the microstructures.

Claims (12)

1. A method of making drug-containing microparticles comprising:

(a) filling a plurality of wells provided in a preformed, dissolvable hydrogel mold with a non-aqueous composition comprising: at least one drug, a non-water soluble, biodegradable polymer comprising poly(lactic co-glycolic acid) polymer (PLGA) and non-aqueous solvent, which dissolvable hydrogel mold is formed of a sol-gel phase reversible hydrogel comprising gelatin;

(b) solidifying the composition in the plurality of wells by evaporating the non-aqueous solvent, thereby forming microparticles; and

(c) harvesting the microparticles from the preformed dissolvable hydrogel mold by dissolving the hydrogel mold in an aqueous solution.

2. The method of claim 1 , wherein the drug is present in the microparticles in the range of about 1-80% by weight.

3. The method of claim 1 , wherein the drug is present in the microparticles in the range of about 5-50% by weight.

4. The method of claim 1 , wherein the microparticles have a diameter in the range of about 0.5 μm to about 100 μm.

5. The method of claim 1 , wherein the microparticles have a diameter in the range of about 1 μm to about 50 μm.

6. The method of claim 1 , wherein the harvesting step further comprises filtering and/or centrifugation of the microparticles from the aqueous solution.

7. The method of claim 1 , wherein the harvested microparticles are of homogeneous size.

8. The method of claim 1 , wherein the harvested microparticles are of homogeneous shape.

9. The method of claim 1 , wherein the sol-gel phase reversible hydrogel comprises poly(vinyl alcohol).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 18, 2018
From: PARK, KINAM; ACHARYA, GHANASHYAM S.; PARK, HAESUN
To: AKINA, INC.
Reel/Frame 044656/0422 →
Continuity (5)
Continuation 14617804 · Feb 9, 2015
Continuation 12286147 · Sep 27, 2008
Provisional Application 61066376 · Feb 19, 2008
Provisional Application 60995693 · Sep 27, 2007
Related Publication 20180221281A1 · Aug 9, 2018
Cited By (2)
US 12,390,537 US 12,622,963