IP Library Granted Patent US 9,150,748
Granted Patent B1
US 9,150,748 · App. 13/772,595 · Granted Oct 6, 2015

Polyethylene glycol based oligomers for coating nanoparticles, nanoparticles coated therewith, and related methods

Inventors: Hedi Mattoussi (Tallahassee, FL); Goutam Palui (Tallahassee, FL); Hyon Bin Na (Tallahassee, FL)
Assignee: The Florida State University Research Foundation, Inc.
C09D133/02C08F20/06C08F22/00C08K5/00C08K5/13C08L33/00C08L71/08C08F220/26
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Quick Facts
Patent No.
US 9,150,748
App. No.
13/772,595
Granted
Oct 6, 2015
Kind
B1
Abstract

In a composition aspect of the invention, a nanoparticle coating comprises repeating polyacrylic acid monomers covalently bound together to form an aliphatic chain having a plurality of carboxylic acid functional groups and modified carboxylic acid functional groups extending therefrom. A first portion of the modified carboxylic acid functional groups are modified by a PEG oligomer having a terminal methoxy functional group and a second portion of the modified carboxylic acid functional groups are modified by a PEG oligomer having at least one terminal sulfur moiety.

Claims (16)

1. A composition comprising repeating polyacrylic acid monomer units covalently bound together in an aliphatic chain having a plurality of carboxylic acid functional groups and modified carboxylic acid functional groups extending therefrom, wherein a first portion of the modified carboxylic acid functional groups are modified by a PEG oligomer having a terminal methoxy functional group and a second portion of the modified carboxylic acid functional groups are modified by a PEG oligomer having at least one terminal sulfur moiety.

2. The composition of claim 1 , wherein the at least one terminal sulfur moiety is formed from thioctic acid.

3. The composition of claim 1 , wherein the at least one terminal sulfur moiety is formed from dihydrolipoic acid.

4. The composition of claim 1 , wherein the PEG oligomer having a terminal methoxy functional group is formed from a Compound 2 having a structure:

wherein n has a value such that an average molecular weight of the PEG oligomer is about 750.

5. The composition of claim 1 , wherein the PEG oligomer having at least one terminal sulfur moiety is formed from a Compound 1 having a structure:

wherein n has a value such that an average molecular weight of the PEG oligomer is about 600.

6. The composition of claim 1 , wherein the PEG oligomer having a terminal methoxy functional group is formed from a Compound 2 and the PEG oligomer having at least one terminal sulfur moiety is formed from a Compound 1; wherein the Compound 2 and the Compound 1 have the following structures:

wherein n has a value such that an average molecular weight of the PEG oligomer is about 750; and

wherein n has a value such that an average molecular weight of the PEG oligomer is about 600.

7. The composition of claim 1 , wherein the PEG oligomer having at least one terminal sulfur moiety is formed from dihydrolipoic acid.

8. The composition of claim 1 , further comprising a third portion of the modified carboxylic acid functional groups, wherein the third portion of the modified carboxylic acid functional groups are modified by a PEG oligomer having a terminal azide functional group.

9. The composition of claim 8 , wherein the PEG oligomer having at least one terminal sulfur moiety is formed from a Compound 1 having a structure:

wherein n has a value such that an average molecular weight of the PEG oligomer is about 600.

10. The composition of claim 1 , further comprising a third portion of the modified carboxylic acid functional groups, wherein the third portion of the modified carboxylic acid functional groups are modified by a PEG oligomer having a terminal amine functional group.

11. The composition of claim 10 , wherein the PEG oligomer having at least one terminal sulfur moiety is formed from dihydrolipoic acid.

Assignments (3)
CONFIRMATORY LICENSE Recorded Apr 11, 2016
From: FLORIDA STATE UNIVERSITY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 038401/0473 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNORS LAST NAME MISSPELLED PREVIOUSLY RECORDED ON REEL 031581 FRAME 0153. ASSIGNOR(S) HEREBY CONFIRMS THE MATTOUSI SHOULD BE SPELLED MATTOUSSI AND PAULI SHOULD BE SPELLED PALUI. Recorded Jul 7, 2015
From: MATTOUSSI, HEDI; PALUI, GOUTAM; NA, HYON BIN
To: THE FLORIDA STATE UNIVERSITY RESEARCH FOUNDATION, INC.
Reel/Frame 036073/0918 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 12, 2013
From: MATTOUSI, HEDI; NA, HYON BIN; PAULI, GOUTAM
To: THE FLORIDA STATE UNIVERSITY RESEARCH FOUNDATION, INC.
Reel/Frame 031581/0153 →
Continuity (2)
Continuation In Part 13608119 · Sep 10, 2012
Provisional Application 61532756 · Sep 9, 2011