IP Library Granted Patent US 9,271,933
Granted Patent B2
US 9,271,933 · App. 13/828,105 · Granted Mar 1, 2016

Graft copolymer polyelectrolyte complexes for drug delivery

Inventors: David Devore (Fort Sam Houston, TX); Charles Roth (Princeton, NJ)
Assignees: RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY; US ARMY, SECRETARY OF THE ARMY
A61K9/1272A61K9/1271A61K47/32C12N15/111C12N15/1135C12N2310/14C12N2320/32
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Quick Facts
Patent No.
US 9,271,933
App. No.
13/828,105
Granted
Mar 1, 2016
Kind
B2
Abstract

Graft copolymer polyelectrolyte complexes are disclosed for the efficient delivery of anionic, cationic or polyelectrolyte therapeutic agents into biological cells, and for maintaining the biological activity of these molecules while in serum and other aqueous environments are provided. Such complexes comprise (1) an anionic graft copolymer containing an anionic polymer backbone, with pendent carboxylic acid groups and pendant chains containing amphipathic or hydrophilic polymers covalently bonded to a portion of the pendant carboxylic acid groups, (2) one or more anionic, cationic or polyelectrolyte therapeutic agents, and (3) optionally a liposome optionally containing an additional therapeutic agent. Also disclosed are functional nanoparticles containing the complexes.

Claims (37)

1. A graft copolymer polyelectrolyte complex comprising:

(1) an anionic graft copolymer comprising:

(i) a backbone comprising a poly(alkylacrylic acid); and

(ii) one or more polyetheramine pendent chains covalently attached to said copolymer backbone as amides of acrylic acid groups, wherein said pendent chains predominantly comprise ethylene oxide repeating units;

wherein said copolymer has a graft density between about 0.1 and about 25 mole percent;

(2) one or more anionic, cationic or polyelectrolyte therapeutic agents; and

(3) optionally, a liposome which optionally comprises a further therapeutic agent;

wherein when said anionic, cationic or polyelectrolyte therapeutic agent is a polynucleotide molecule, said liposome, optionally comprising said further therapeutic agent, is also present; and wherein said pendent chains further comprise one or more ligands that target a microbial biofilm or a planktonic microbe; or said pendent chains further comprise one or more ligands which comprise a phosphonate molecule that targets bone tissue.

2. The complex of claim 1 , wherein the copolymer backbone comprises poly(propyl acrylic acid) or poly(methacrylic acid).

3. The complex of claim 1 , wherein said copolymer has a graft density between about 0.5 and about 5 mole percent.

4. The complex of claim 1 , wherein said liposome is present.

5. The complex of claim 1 , wherein said anionic, cationic or polyelectrolyte therapeutic agent is stabilized toward biological degradation in vivo.

6. A functional nanoparticle comprising the complex of claim 1 , wherein said nanoparticle provides in vivo delivery of the anionic, cationic or polyelectrolyte therapeutic agent.

7. A method of treating a patient in need thereof with a polyelectrolyte therapeutic agent comprising the steps of:

(1) formulating the complex of claim 1 with one or more pharmaceutically acceptable carriers to provide a pharmaceutical composition; and

(2) administering said pharmaceutical composition to said patient in an amount effective to treat said patient.

8. The method of claim 7 , wherein said anionic, cationic or polyelectrolyte therapeutic agent is selected from the group consisting of antibacterial agents, anticancer agents, wound treatment agents and tissue regeneration agents.

9. The method of claim 7 , wherein the administration is via oral, enteral, parenteral or topical delivery.

10. The method of claim 7 , wherein said pharmaceutical composition is selected from the group consisting of injectable aqueous solutions, injectable aqueous dispersions, emulsions, gels, pastes, aerosols, sprays, coatings, hydrogels, topical creams, topical ointments, natural and synthetic polymeric fibers, porous ceramics, polymeric and ceramic composites, and wound treatment compositions.

11. A method of preparing a graft copolymer-polyelectrolyte complex of claim 1 , comprising the steps of:

(1) providing an aqueous mixture of an anionic graft copolymer comprising:

(i) a backbone comprising a poly(alkyl acrylic acid); and

(ii) one or more polyetheramine pendent chains covalently attached to said copolymer backbone as amides of acrylic acid groups, wherein said pendent chains predominantly comprise ethylene oxide repeating units;

wherein said copolymer has a graft density between about 0.1 and about 25 mole percent;

(2) adding one or more polyelectrolytes to form a polyelectrolyte-copolymer mixture;

(3) optionally adding an aqueous mixture containing a liposome which optionally comprises a further therapeutic agent, to form a liposome-containing polyelectrolyte-copolymer mixture; and

(4) allowing said polyelectrolyte-copolymer mixture or said liposome-containing polyelectrolyte-copolymer mixture to self-assemble in the aqueous medium to form said complex, which further forms nanoparticles.

12. A graft copolymer polyelectrolyte complex comprising:

(1) an anionic graft copolymer comprising:

(i) a backbone comprising a poly(alkylacrylic acid); and

(ii) one or more polyetheramine pendent chains covalently attached to said copolymer backbone as amides of acrylic acid groups, wherein said pendent chains predominantly comprise ethylene oxide repeating units;

wherein said copolymer has a graft density between about 0.1 and about 25 mole percent;

(2) one or more anionic, cationic or polyelectrolyte therapeutic agents; and

(3) optionally, a liposome which optionally comprises a further therapeutic agent;

wherein said anionic, cationic or polyelectrolyte therapeutic agent is selected from the group consisting of vancomycin, telavancin, daptomicin, mepivacaine, lidocaine, bupivacaine, benzocaine and procaine.

13. The complex of claim 12 , wherein said anionic, cationic or polyelectrolyte therapeutic agent is daptomicin.

14. The complex of claim 12 , wherein said anionic, cationic or polyelectrolyte therapeutic agent is selected from the group consisting of mepivacaine, lidocaine, bupivacaine, benzocaine and procaine.

Assignments (5)
CORRECTIVE ASSIGNMENT TO CORRECT THE NAME OF THE RECEIVING PARTY PREVIOUSLY RECORDED ON REEL 036584 FRAME 0921. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded May 10, 2018
From: DEVORE, DAVID I
To: THE GOVERNMENT OF THE UNITED STATES, AS REPRESENTED BY THE SECRETARY OF THE ARMY
Reel/Frame 046124/0832 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 10, 2015
From: DEVORE, DAVID I.
To: US ARMY, SECRETARY OF THE ARMY
Reel/Frame 036534/0765 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 10, 2015
From: DEVORE, DAVID I
To: USA AS REPRESENTED BY THE SECRETARY OF THE ARMY ON BEHALF OF USAMRMC
Reel/Frame 036584/0921 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 23, 2014
From: ROTH, CHARLES
To: RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY
Reel/Frame 034580/0017 →
CONFIRMATORY LICENSE Recorded Dec 3, 2013
From: RUTGERS THE STATE UNIVERSITY NEW BRUNSWICK
To: US ARMY, SECRETARY OF THE ARMY
Reel/Frame 031753/0615 →
Continuity (4)
Continuation In Part 12744824
Provisional Application 61619234 · Apr 2, 2012
Provisional Application 60990606 · Nov 27, 2007
Related Publication 20130183379A1 · Jul 18, 2013