IP Library Granted Patent US 9,545,447
Granted Patent B2
US 9,545,447 · App. 14/043,456 · Granted Jan 17, 2017

Polymer-drug systems

Inventors: Karen Wooley (College Station, TX); Jiong Zou (College Station, TX); Mahmoud El Sabahy (College Station, TX); Shiyi Zhang (Bryan, TX); Fuwu Zhang (College Station, TX)
Assignee: The Texas A&M University System
A61K47/34A61K31/337A61K47/482A61K47/48192
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Quick Facts
Patent No.
US 9,545,447
App. No.
14/043,456
Granted
Jan 17, 2017
Kind
B2
Abstract

The present disclosure generally relates to polymer-drug systems, and more particularly to nanoscopic particles comprising amphiphilic block copolymers conjugated, physically encapsulated, or otherwise combined with chemotherapeutic agents along a selective region or regions of the backbone of the copolymer, so as to package the chemotherapeutic agent in selective domains within each nanoscopic particle, as well as to methods for making such particles, and applications and methods for using such particles, including in the formation of polymer micelles.

Claims (14)

1. A composition comprising:

an amphiphilic block copolymer derived from poly(ethylbutyl phospholane)-block-poly (butynyl phospholane) (PEBP-b-PBYP) by modifying from poly(ethylbutyl phospholane)-block-poly (butynyl phospholane) (PEBP-b-PBYP) with a functionality comprising an anionic, cationic, zwitterionic, or neutral moiety or a combination thereof, the amphiphilic block copolymer comprising a hydrophobic-functional AB diblock polyphosphoester comprising at least one degradable polyphosphoester block; and

a chemotherapeutic agent.

2. The composition of claim 1 , wherein the amphiphilic block copolymer comprises a polymer backbone and the chemotherapeutic agent is conjugated with the copolymer along a selective region of the polymer backbone.

3. The composition of claim 1 , further comprising a pendant compound selected from the following group: a dye, an imaging agent, and a hydrophilic polymer, wherein the pendant compound is chemically reacted with the polyphosphoester via the reactive side chain functionality of the polyphosphoester.

4. The composition of claim 1 , wherein the block copolymer encapsulates the chemotherapeutic agent.

5. The composition of claim 1 , wherein the chemotherapeutic agent comprises paclitaxel (PTX).

6. A composition of comprising:

a poly(ethylbutyl phospholane)-block-poly (butynyl phospholane)-graft-polyethylene glycol (PEBP-b-PBYP-g-PEG) amphiphilic block copolymer; and

a chemotherapeutic agent.

7. The composition of claim 6 , wherein the amphiphilic block copolymer comprises a polymer backbone and the chemotherapeutic agent is conjugated with the copolymer along a selective region of the polymer backbone.

8. The composition of claim 6 , wherein the block copolymer encapsulates the chemotherapeutic agent.

9. The composition of claim 6 , wherein the chemotherapeutic agent comprises paclitaxel (PTX).

10. The composition of claim 6 , further comprising a pendant compound selected from the following group: a dye, an imaging agent, and a hydrophilic polymer, wherein the pendant compound is chemically reacted with the polyphosphoester via the reactive side chain functionality of the polyphosphoester.

Assignments (2)
CONFIRMATORY LICENSE Recorded Dec 14, 2017
From: TEXAS A&M UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 044876/0561 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 24, 2015
From: WOOLEY, KAREN; ZOU, JIONG; EL SABAHY, MAHMOUD; ZHANG, SHIYI; ZHANG, FUWU
To: THE TEXAS A&M UNIVERSITY SYSTEM
Reel/Frame 035963/0600 →
Continuity (2)
Provisional Application 61708911 · Jan 4, 2013
Related Publication 20140193504A1 · Jul 10, 2014