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:
May. 09, 2017

Filed:

Jan. 10, 2011
Applicants:

Jean M. J. Frechet, Oakland, CA (US);

Eric M. Bachelder, Dublin, OH (US);

Tristan T. Beaudette, San Francisco, CA (US);

Kyle E. Broaders, Berkeley, CA (US);

Inventors:

Jean M. J. Frechet, Oakland, CA (US);

Eric M. Bachelder, Dublin, OH (US);

Tristan T. Beaudette, San Francisco, CA (US);

Kyle E. Broaders, Berkeley, CA (US);

Assignee:
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61F 2/00 (2006.01); C08B 37/00 (2006.01); A61K 9/16 (2006.01); A61L 17/10 (2006.01); A61L 17/14 (2006.01); A61L 27/14 (2006.01); A61L 27/34 (2006.01); A61L 27/58 (2006.01); A61L 31/10 (2006.01); A61L 31/14 (2006.01); C08B 30/18 (2006.01); C08B 37/02 (2006.01); C08L 1/02 (2006.01); C08L 1/08 (2006.01); C08L 3/02 (2006.01); C08L 5/00 (2006.01); C08L 5/02 (2006.01); C08L 5/06 (2006.01);
U.S. Cl.
CPC ...
C08B 37/0006 (2013.01); A61K 9/1652 (2013.01); A61L 17/10 (2013.01); A61L 17/145 (2013.01); A61L 27/14 (2013.01); A61L 27/34 (2013.01); A61L 27/58 (2013.01); A61L 31/10 (2013.01); A61L 31/148 (2013.01); C08B 30/18 (2013.01); C08B 37/0021 (2013.01); C08L 1/02 (2013.01); C08L 1/08 (2013.01); C08L 3/02 (2013.01); C08L 5/00 (2013.01); C08L 5/02 (2013.01); C08L 5/06 (2013.01);
Abstract

Compositions and methods of making a modified polyhydroxylated polymer comprising a polyhydroxylated polymer having reversibly modified hydroxyl groups, whereby the hydroxyl groups are modified by an acid-catalyzed reaction between a polydroxylated polymer and a reagent such as acetals, aldehydes, vinyl ethers and ketones such that the modified polyhydroxylated polymers become insoluble in water but freely soluble in common organic solvents allowing for the facile preparation of acid-sensitive materials. Materials made from these polymers can be made to degrade in a pH-dependent manner. Both hydrophobic and hydrophilic cargoes were successfully loaded into particles made from the present polymers using single and double emulsion techniques, respectively. Due to its ease of preparation, processability, pH-sensitivity, and biocompatibility, of the present modified polyhydroxylated polymers should find use in numerous drug delivery applications.


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