IP Library Granted Patent US 9,717,690
Granted Patent B2
US 9,717,690 · App. 14/124,615 · Granted Aug 1, 2017

Cleavable lipids

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Quick Facts
Patent No.
US 9,717,690
App. No.
14/124,615
Granted
Aug 1, 2017
Kind
B2
Abstract

Disclosed herein are novel compounds, pharmaceutical compositions comprising such compounds and related methods of their use. The compounds described herein are useful, e.g., as liposomal delivery vehicles to facilitate the delivery of encapsulated polynucleotides to target cells and subsequent transfection of said target cells, and in certain embodiments are characterized as having one or more properties that afford such compounds advantages relative to other similarly classified lipids.

Claims (47)

1. A nanoparticle comprising a compound of the structure:

and one or more polynucleotides; wherein

R 1 is selected from the group consisting of imidazole, guanidinium, imine, enamine, amino, and C 1 -C 6 alkyl amino;

R 2 is

R 3 and R 4 are each independently an optionally substituted, unsaturated C 6 -C 20 alkyl; and

n is zero or any positive integer.

2. The nanoparticle of claim 1 , wherein R 3 and R 4 are each an optionally substituted, polyunsaturated C 6 -C 20 alkyl.

3. The nanoparticle of claim 1 , wherein R 3 and R 4 are each an optionally substituted, polyunsaturated C 18 alkyl.

4. The nanoparticle of claim 1 , wherein R 3 and R 4 are each an unsubstituted polyunsaturated C 18 alkyl.

5. The nanoparticle of claim 1 , wherein R 1 is amino.

6. The nanoparticle of claim 5 , wherein R 3 and R 4 are each an unsubstituted, polyunsaturated C 18 alkyl.

7. The nanoparticle of claim 6 , wherein n is 1.

8. The nanoparticle of claim 1 , wherein R 1 is dimethylamino;

R 3 and R 4 are each an unsubstituted, polyunsaturated C 18 alkyl; and

n is 1.

9. The nanoparticle of claim 1 , wherein R 1 is imidazole.

10. The nanoparticle of claim 9 , wherein R 3 and R 4 are each an unsubstituted, polyunsaturated C 18 alkyl.

11. The nanoparticle of claim 10 , wherein n is 1.

12. The nanoparticle of claim 1 , wherein R 1 is imidazole;

R 3 and R 4 are each an unsubstituted, polyunsaturated C 18 alkyl; and

n is 1.

13. The nanoparticle of claim 1 , wherein R 1 is guanidinium.

14. The nanoparticle of claim 13 , wherein R 3 and R 4 are each an unsubstituted, polyunsaturated C 18 alkyl.

15. The nanoparticle of claim 14 , wherein n is 1.

16. The nanoparticle of claim 1 , wherein R 1 is guanidinium;

R 3 and R 4 are each an unsubstituted, polyunsaturated C 18 alkyl; and

n is 1.

17. The nanoparticle of claim 1 , comprising a compound of the structure:

18. The nanoparticle of claim 1 , comprising a compound of the structure:

19. The nanoparticle of claim 1 , comprising a compound of the structure:

20. The nanoparticle of claim 1 , further comprising one or more compounds selected from the group consisting of a cationic lipid, a PEG-modified lipid, a non-cationic lipid and a helper lipid.

21. The nanoparticle of claim 1 , wherein the one or more polynucleotides comprise RNA.

22. The nanoparticle of claim 1 , wherein the one or more polynucleotides comprise DNA.

23. The nanoparticle of claim 1 , wherein the one or more polynucleotides is selected from the group consisting of an antisense oligonucleotide, siRNA, miRNA, snRNA, snoRNA and combinations thereof.

24. The nanoparticle of claim 1 , wherein one or more of the polynucleotides comprises a chemical modification.

25. The nanoparticle of claim 21 , wherein the RNA comprises mRNA.

26. The nanoparticle of claim 25 , wherein the mRNA is modified to improve stability.

27. The nanoparticle of claim 21 , wherein the RNA encodes an enzyme.

28. The nanoparticle of claim 27 , wherein the enzyme is selected from the group consisting of agalsidase alfa, alpha-L-iduronidase, iduronate-2-sulfatase, N-acetylglucosamine-1-phosphate transferase, N-acetylglucosaminidase, alpha-glucosaminide acetyltransferase, N-acetylglucosamine 6-sulfatase, N-acetylgalactosamine-4-sulfatase, beta-glucosidase, galactose-6-sulfate sulfatase, beta-galactosidase, beta-glucuronidase, glucocerebrosidase, heparan sulfamidase, hyaluronidase, galactocerebrosidase, ornithine transcarbamylase, carbamoyl-phosphate synthetase 1, argininosuccinate synthetase, argininosuccinate lyase and arginase 1.

29. The nanoparticle of claim 20 , wherein the one or more cationic lipids are selected from the group consisting of amine 200-derived aminoalcohol lipidoid,1,2-dioleyl-3-trimethylammonium propane, 1,2-dioleyl-3-dimethylammonium propane, 1,2-di-O-octadecenyl-3-trimethylammonium propane, 1,2-dilinoleyloxy-N,N-dimethyl-3-aminopropane, 2-(2,2-di((9Z,12Z)-octadeca-9,12-dien-l-yl)-1,3-dioxolan-4-yl)-N,N-dimethylethanamine, 2-((2,3-Bis((9Z, 12Z)-octadeca-9, 12-dien-l-yloxy)propyl)disulfanyl)-N,N-dimethylethanamine, (15Z,18Z)-N,N-dimethyl-6-((9Z,12Z)-octadeca-9,12-dien-l-yl)tetracosa-4,l 5,18-trien-l-amine, and (3S, 10R, 13R, 17R)-10, 13-dimethyl- 17-((R)-6-methylheptan-2-yl)-2, 3, 4, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17-tetradecahydro-1 H-cyclopenta[a]phenanthren-3-yl 3-(l H-imidazol-4-yl)propanoate.

30. The nanoparticle of claim 20 , further comprising one or more PEG-modified lipids, wherein the one or more PEG-modified lipids comprise a polyethyleneglycol chain of up to 5kDa in length covalently attached to a lipid comprising one or more alkyl chains of C 6 -C 20 in length.

31. A pharmaceutical composition comprising the nanoparticle of claim 1 .

32. The pharmaceutical composition of claim 31 , wherein the nanoparticle comprises mRNA.

33. The pharmaceutical composition of claim 32 wherein upon reconstitution the nanoparticle has a Dv50 of less than 150 nm.

34. The pharmaceutical composition of claim 31 , wherein the nanoparticle comprises amine 200-derived aminoalcohol lipidoid, 1,2-dioleyl-sn-glycero-3-phosphoethanolamine, cholesterol and 1,2-dimyristoyl-sn-glycero-methoxypolyethylene Glycol 2000 MW.

35. The pharmaceutical composition of claim 31 , wherein the nanoparticle comprises 2-(2,2-di((9Z,12Z)-octadeca-9,12-dien-l-yl)-l,3-dioxolan-4-yl)-N,N-dimethylethanamine, 1,2-dioleyl-sn-glycero-3-phosphoethanolamine, cholesterol and 1,2-dimyristoyl-sn-glycero-methoxypolyethylene Glycol 2000 MW.

36. A method of transfecting one or more target cells with a polynucleotide, wherein the method comprises contacting the one or more target cells with the pharmaceutical composition of claim 31 such that the one or more target cells are transfected with the polynucleotide.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 10, 2021
From: GUILD, BRAYDON CHARLES; HEARTLEIN, MICHAEL; DEROSA, FRANK; ZHANG, JERRY CHI
To: SHIRE HUMAN GENETIC THERAPIES, INC.
Reel/Frame 055213/0294 →
CHANGE OF NAME Recorded Jul 20, 2017
From: RANA THERAPEUTICS, INC.
To: TRANSLATE BIO, INC.
Reel/Frame 043267/0165 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 6, 2017
From: SHIRE HUMAN GENETIC THERAPIES, INC.
To: RANA THERAPEUTICS, INC.
Reel/Frame 042177/0032 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2014
From: GUILD, BRAYDON CHARLES; HEARTLEIN, MICHAEL; DEROSA, FRANK; ZHANG, JERRY CHI
To: SHIRE HUMAN GENETIC THERAPIES, INC.
Reel/Frame 032551/0705 →