The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Nov. 10, 2015

Filed:

Dec. 21, 2012
Applicant:

The Regents of the University of Colorado, a Body Corporate, Boulder, CO (US);

Inventors:

Kristi S. Anseth, Boulder, CO (US);

Andrea M. Kasko, Boulder, CO (US);

Mark W. Tibbitt, Boulder, CO (US);

April M. Kloxin, Newark, DE (US);

Balaji Sridhar, Denver, CO (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C08F 20/34 (2006.01); C08F 220/34 (2006.01); C08G 75/00 (2006.01); A61K 47/34 (2006.01); A61K 38/38 (2006.01); G03F 7/00 (2006.01); A61K 41/00 (2006.01); A61K 38/18 (2006.01); A61K 38/36 (2006.01);
U.S. Cl.
CPC ...
A61K 47/34 (2013.01); A61K 38/1841 (2013.01); A61K 38/36 (2013.01); A61K 38/385 (2013.01); A61K 41/0042 (2013.01); C08F 20/34 (2013.01); C08F 220/34 (2013.01); C08G 75/00 (2013.01); G03F 7/0037 (2013.01);
Abstract

Here, we present a photodegradable microparticle system that can be employed to entrap and deliver bioactive proteins to cells during culture. By using a photosensitive delivery system, experimenters can achieve a wide variety of spatiotemporally regulated release profiles with a single microparticle formulation, thereby enabling one to probe many questions as to how protein presentation can be manipulated to regulate cell function. Photodegradable microparticles were synthesized via inverse suspension polymerization with a mean diameter of 22 μm, and degradation was demonstrated upon exposure to several irradiation conditions. The protein-loaded depots were incorporated into cell cultures and release of bioactive protein was quantified during the photodegradation process. This phototriggered release allowed for the delivery of TGF-β1 to stimulate PE25 cells and for the delivery of fluorescently labeled Annexin V to assay apoptotic 3T3 fibroblasts during culture. By incorporating these photoresponsive protein delivery depots into cell culture, new types of experiments are now possible to test hypotheses about how individual or multiple soluble factors might affect cell function when presented in a uniform, temporally varying, or gradient manner.


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