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:
Mar. 14, 2017

Filed:

May. 22, 2012
Applicant:

Sankaran Thayumanavan, Amherst, MA (US);

Inventor:

Sankaran Thayumanavan, Amherst, MA (US);

Assignee:

University of Massachusetts, Boston, MA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61K 9/51 (2006.01); A61K 47/48 (2006.01); C08F 220/20 (2006.01); C08F 220/34 (2006.01); C08F 226/02 (2006.01); A61K 31/436 (2006.01); A61K 31/4745 (2006.01); C08F 8/00 (2006.01);
U.S. Cl.
CPC ...
A61K 47/48176 (2013.01); A61K 9/5138 (2013.01); A61K 31/436 (2013.01); A61K 31/4745 (2013.01); C08F 8/00 (2013.01); C08F 220/20 (2013.01); C08F 220/34 (2013.01); C08F 226/02 (2013.01); C08F 2810/20 (2013.01); Y10S 977/773 (2013.01); Y10S 977/906 (2013.01);
Abstract

The invention provides a novel system of nano-assemblies and related method for delivery of therapeutic, diagnostic or imaging agent to biological sites. The compositions and methods of the invention enable the syntheses of novel polymeric nano-assemblies (nanoparticles) under non-emulsion conditions with the incorporation of hydrophobic guest molecules. The versatilities and advantages of the polymer nanoparticles of the invention include: (i) the guest molecules (e.g., drug molecules) can be readily incorporated non-covalently within the nanoparticles; (ii) the surface of the nanoparticles are functionalizable; (iii) the non-covalently encapsulated guest molecule (payload) can be released in response to a biologically relevant stimulus at the target site; (iv) the payload is held by the polymeric nanoparticle before being internalized in cells and can be released within the cellular interiors; (v) encapsulating lipophilic small molecules within its crosslinked interiors and binding proteins on its surface through electrostatic interactions; (vi) facile synthetic methods for ligand functionalization that can be utilized to decorate nanogels with cell targeting ligands that facilitate receptor-dependent cellular uptake, and (vii) the payload release kinetics is tunable and controllable.


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