IP Library Granted Patent US 9,399,704
Granted Patent B2
US 9,399,704 · App. 13/938,555 · Granted Jul 26, 2016

Method for generation of nanoparticles

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,399,704
App. No.
13/938,555
Granted
Jul 26, 2016
Kind
B2
Abstract

A discrete nanostructure formed by a method comprising providing an aliphatic multi-block copolymer. The aliphatic multi-block copolymer includes at least one polyester block and at least one functionalized polycarbonate block. The aliphatic multi-block copolymer, a deprotonating agent and water are mixed to form an aqueous mixture. The aqueous mixture is maintained at a reaction temperature suitable to result in self-assembly of the multi-block copolymer into nanoparticles.

Claims (36)

1. A method for self-assembly of a discrete nanostructure, the method comprising:

providing an aliphatic multi-block copolymer comprising at least one polyester block and at least one functionalized polycarbonate block, wherein the aliphatic multi-block copolymer is a polyester-polycarbonate-polyester tri-block copolymer having a compound of formula 1:

R 1 —O-A a B b C c —R 2

where:

A and C are polyester blocks;

B is the functionalized polycarbonate block;

a=20 to 40;

b=2 to 10;

c=20 to 40;

R 1 is a group formed from a catalyst initiator; and

R 2 is an end cap moiety formed from a cyclic monomer;

mixing the aliphatic multi-block copolymer, a deprotonating agent and water to form an aqueous mixture; and

maintaining the aqueous mixture at a reaction temperature suitable to result in self-assembly of the multi-block copolymer into nanoparticles.

2. The method of claim 1 , wherein the polycarbonate block of the tri-block copolymer is functionalized with a carboxylic acid or ester thereof.

3. The method of claim 2 , wherein the polycarbonate block of the tri-block copolymer is functionalized with a carboxylic acid ester comprising a benzyl protecting group, the method further comprising removing the benzyl protecting group prior to or during self-assembly.

4. The method of claim 1 , wherein the polyester-polycarbonate-polyester tri-block copolymer comprises a first polyester block of polycaprolactone and a second polyester block of polylactide.

5. The method of claim 1 , wherein A is a polyester formed by ring-opening polymerization of caprolactone monomers and C is a polyester formed by ring-opening polymerization of lactide monomers.

6. The method of claim 5 , wherein the polycarbonate block is functionalized with a plurality of carboxylic acid or carboxylic acid ester functionalities.

7. The method of claim 1 , wherein R 1 is selected from the group consisting of alkyl, aryl, arylalkyl, and alkylaryl.

8. The method of claim 1 , wherein the cyclic monomer is selected from the group consisting of cyclic anhydrides and aromatic monomers.

9. The method of claim 1 , wherein the reaction temperature ranges from about 75° C. to about 100° C.

10. The method of claim 1 , wherein the method is performed without high shear mixing.

11. A method for self-assembly of a discrete nanostructure, the method comprising:

providing an aliphatic multi-block copolymer comprising at least one polyester block and at least one functionalized polycarbonate block;

mixing the aliphatic multi-block copolymer, a deprotonatinq agent and water to form an aqueous mixture; and

maintaining the aqueous mixture at a reaction temperature suitable to result in self-assembly of the multi-block copolymer into nanoparticles,

wherein the method is performed in the absence of a solvent other than water.

12. A method for self-assembly of a discrete nanostructure, the method comprising:

providing an aliphatic multi-block copolymer comprising at least one polyester block and at least one functionalized polycarbonate block;

mixing the aliphatic multi-block copolymer, a deprotonatinq agent and water to form an aqueous mixture; and

maintaining the aqueous mixture at a reaction temperature suitable to result in self-assembly of the multi-block copolymer into nanoparticles,

wherein the deprotonating agent is a bicarbonate salt.

13. The method of claim 11 , wherein the reaction temperature ranges from about 75° C. to about 100° C.

14. The method of claim 11 , wherein the method is performed without high shear mixing.

15. The method of claim 12 , wherein the reaction temperature ranges from about 75° C. to about 100° C.

16. The method of claim 12 , wherein the method is performed without high shear mixing.

Assignments (11)
SECOND LIEN NOTES PATENT SECURITY AGREEMENT Recorded Jul 2, 2025
From: XEROX CORPORATION
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 071785/0550 →
FIRST LIEN NOTES PATENT SECURITY AGREEMENT Recorded Apr 11, 2025
From: XEROX CORPORATION
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 070824/0001 →
SECURITY INTEREST Recorded Feb 13, 2024
From: XEROX CORPORATION
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 066741/0001 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS RECORDED AT RF 064760/0389 Recorded Feb 13, 2024
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: XEROX CORPORATION
Reel/Frame 068261/0001 →
SECURITY INTEREST Recorded Nov 20, 2023
From: XEROX CORPORATION
To: JEFFERIES FINANCE LLC, AS COLLATERAL AGENT
Reel/Frame 065628/0019 →
SECURITY INTEREST Recorded Jun 22, 2023
From: XEROX CORPORATION
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 064760/0389 →
RELEASE OF SECURITY INTEREST IN PATENTS AT R/F 062740/0214 Recorded May 18, 2023
From: CITIBANK, N.A., AS AGENT
To: XEROX CORPORATION
Reel/Frame 063694/0122 →
SECURITY INTEREST Recorded Nov 10, 2022
From: XEROX CORPORATION
To: CITIBANK, N.A., AS AGENT
Reel/Frame 062740/0214 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 1, 2017
From: NATIONAL RESEARCH COUNCIL OF CANADA
To: XEROX CORPORATION
Reel/Frame 042195/0428 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 26, 2013
From: MYLES, ANDREW J
To: NATIONAL RESEARCH COUNCIL OF CANADA
Reel/Frame 031681/0635 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 26, 2013
From: MOFFAT, KAREN A.; FARRUGIA, VALERIE M.; WOSNICK, JORDAN H.
To: XEROX CORPORATION
Reel/Frame 031681/0557 →