IP Library Granted Patent US 9,505,867
Granted Patent B2
US 9,505,867 · App. 11/916,252 · Granted Nov 29, 2016

Triblock copolymers for cytoplasmic delivery of gene-based drugs

Inventors: Tatiana Segura (Los Angeles, CA); Jeffrey A. Hubbell (Lausanne, CH)
Assignee: Ecole Polytechmique Fédérale De Lausanne
C08F297/02A61L31/048C08L53/00C08L53/005
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Quick Facts
Patent No.
US 9,505,867
App. No.
11/916,252
Granted
Nov 29, 2016
Kind
B2
Abstract

The invention features a triblock copolymer including a hydrophilic block; a hydrophobic block; and a positively charged block capable of reversibly complexing a negatively charged molecule, e.g., a nucleic acid, wherein the hydrophobic block is disposed between the hydrophilic block and the positively charged block. Desirably, the triblock copolymer is capable of self-assembling into a supramolecular structure, such as a micelle or vesicle. The invention further features methods of delivering negatively charged molecules and methods of treating a disease or condition using the polymers of the invention.

Claims (43)

1. A triblock copolymer comprising:

(i) a hydrophilic block comprising poly(ethylene glycol) (PEG), poly(ethylene oxide)-co-poly(propylene oxide) di- or multiblock copolymer, poly(ethylene oxide), poly(vinvl alcohol), poly(ethylene-co-vinyl alcohol), poly(N-vinyl pyrrolidone), poly(acrvlic acid), poly(ethyloxazoline), poly(alkylacrylates), poly(acrvlamide), poly(N-alkylacrylamides), polysaccharide, poly(N,N-dialkylacrylamides), hyaluronic acid, or poly(N-acryloylmorpholine);

(ii) a hydrophobic block comprising a polymer selected from the group consisting of poly(propylene sulfide) (PPS), poly(propylene glycol), and esterified poly(acrylic acid); and

(iii) a positively charged block capable of reversibly complexing a negatively charged molecule, wherein said hydrophobic block is disposed between said hydrophilic block and said positively charged block, wherein said hydrophobic block and said positively charged block are bonded to each other through a bond that is labile in an endosome.

2. The triblock copolymer of claim 1 , wherein said triblock copolymer is capable of self-assembling into a supramolecular structure.

3. The triblock copolymer of claim 2 , wherein said supramolecular structure is a micelle or vesicle.

4. The triblock copolymer of claim 1 , wherein said bond comprises a disulfide bond, vinyl ether, orthoester, acyl hydrazone, or a —N—PO 3 — group.

5. The triblock copolymer of claim 1 , wherein said hydrophilic block comprises poly(ethylene glycol).

6. The triblock copolymer of claim 1 , wherein said hydrophobic block comprises poly(propylene sulfide) or poly(propylene glycol.

7. The triblock copolymer of claim 1 , wherein said positively charged block comprises a polypeptide, poly(ethyleneimine), or poly(amidoamine).

8. The triblock copolymer of claim 7 , wherein said polypeptide comprises SEQ ID NO: 1, 2, 4, or 5 or an Arg-Lys copolymer.

9. The triblock copolymer of claim 1 , wherein said hydrophilic block is PEG, said hydrophobic block is PPS, and said positively charged block is a polypeptide.

10. The triblock copolymer of claim 9 , wherein said triblock copolymer comprises PEG 45 , PPS 5 or PPS 10 , and SEQ ID NO: 1 or SEQ ID NO: 2.

11. The triblock copolymer of claim 1 , further comprising an internalization agent.

12. The triblock copolymer of claim 11 , wherein said internalization agent comprises transferrin, folate, a lectin, a growth factor, an RGD peptide, or a mannose-containing glycopeptide.

13. The triblock copolymer of claim 1 , further comprising a negatively charged molecule complexed to said positively charged block.

14. The triblock copolymer of claim 13 , wherein said negatively charged molecule comprises a nucleic acid.

15. The triblock copolymer of claim 14 , wherein said nucleic acid is an siRNA, an olioodeoxynucleotide (ODN), or a plasmid.

16. The triblock copolymer of claim 15 , wherein said nucleic acid is an siRNA that targets HIF-1α or PAI-1.

17. A pharmaceutical composition comprising (i) a triblock copolymer of claim 1 , (ii) a nucleic acid complexed to said triblock copolymer, and (iii) a pharmaceutically acceptable diluent.

18. A triblock copolymer comprising:

(i) a hydrophilic block comprising poly(ethylene glycol) (PEG), poly(ethylene oxide)-co-poly(propylene oxide) di- or multiblock copolymers, poly(ethylene oxide), poly(vinvl alcohol), poly(ethylene-co-vinyl alcohol), poly(N-vinyl pyrrolidone), poly(acrylic acid), poly(ethyloxazoline), poly(alkylacrylates), poly(acrvlamide), poly(N-alkylacrylamides), polysaccharide, poly(N,N-dialkylacrylamides), hyaluronic acid, or poly (N-acryloylmorpholine);

(ii) a hydrophobic block comprising a poly(propylene sulfide) (PPS) or poly(propylene glycol); and

(iii) a positively charged block capable of reversibly complexing a negatively charged molecule, said positively charged block having between 5 and 20 positive charges;

wherein said hydrophobic block is disposed between said hydrophilic block and said positively charged block.

19. The triblock copolymer of claim 18 , wherein said triblock copolymer is capable of self-assembling into a supramolecular structure.

20. The triblock copolymer of claim 19 , wherein said supramolecular structure is a micelle or vesicle.

21. The triblock copolymer of claim 18 , wherein said hydrophobic block and said positively charged block are bonded to each other through a bond that is labile in an endosome.

22. The triblock copolymer of claim 21 , wherein said bond comprises a disulfide bond, vinyl ether, orthoester, acyl hydrazone, or a —N—PO 3 — group.

23. The triblock copolymer of claim 18 , wherein said hydrophilic block comprises poly(ethylene glycol) (PEG).

24. The triblock copolymer of claim 18 , wherein said hydrophobic block comprises poly(propylene sulfide).

25. The triblock copolymer of claim 18 , wherein said positively charged block comprises a polypeptide, poly(ethyleneimine), or poly(amidoamine).

26. The triblock copolymer of claim 25 , wherein said polypeptide comprises (SEQ ID NO: 1 2, 4, or 5 or an Arg-Lys copolymer.

27. The triblock copolymer of claim 18 , wherein said hydrophilic block is PEG, said hydrophobic block is PPS, and said positively charged block is a polypeptide.

28. The triblock copolymer of claim 27 , wherein said triblock copolymer comprises PEG 45 , PPS 5 or PPS 10 , and SEQ ID NO: 1 or SEQ ID NO: 2.

29. The triblock copolymer of claim 18 , further comprising an internalization agent.

30. The triblock copolymer of claim 29 , wherein said internalization agent comprises transferrin, folate, a lectin, a growth factor, an RGD peptide, or a mannose-containing glycopeptide.

31. The triblock copolymer of claim 18 , further comprising a negatively charged molecule complexed to said positively charged block.

32. The triblock copolymer of claim 31 , wherein said negatively charged molecule comprises a nucleic acid.

33. The triblock copolymer of claim 32 , wherein said nucleic acid is an siRNA, an oliaodeoxynucleotide (ODN), or a plasmid.

34. The triblock copolymer of claim 33 , wherein said nucleic acid is an siRNA that targets HIF-1α or PAI-1.

35. A pharmaceutical composition comprising (i) a triblock copolymer of claim 18 , (ii) a nucleic acid complexed to said triblock copolymer, and (iii) a pharmaceutically acceptable diluent.

36. The triblock copolymer of claim 1 , wherein said hydrophobic block is poly(propylene sulfide).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 21, 2010
From: SEGURA, TATIANA; HUBBELL, JEFFREY A.
To: ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE
Reel/Frame 024422/0225 →
Continuity (2)
Provisional Application 61686188 · May 31, 2005
Related Publication 20100222407A1 · Sep 2, 2010