IP Library Granted Patent US 9,764,036
Granted Patent B2
US 9,764,036 · App. 14/953,677 · Granted Sep 19, 2017

Lipids and compositions for the delivery of therapeutics

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Quick Facts
Patent No.
US 9,764,036
App. No.
14/953,677
Granted
Sep 19, 2017
Kind
B2
Abstract

The present invention provides lipids that are advantageously used in lipid particles for the in vivo delivery of therapeutic agents to cells. In particular, the invention provides lipids having the following structures:

Claims (35)

1. A lipid having the structure of formula XXXV

or a salt or isomer thereof, wherein:

R 1 and R 2 are each independently for each occurrence substituted C 10 -C 30 alkyl, optionally substituted C 10 -C 30 alkoxy, optionally substituted C 10 -C 30 alkenyl, optionally substituted C 10 -C 30 alkenyloxy, optionally substituted C 10 -C 30 alkynyl, optionally substituted C 10 -C 30 alkynyloxy, or optionally substituted C 10 -C 30 acyl, or linker-ligand;

R 3 is independently for each occurrence H, optionally substituted C 1 -C 10 alkyl, optionally substituted C 2 -C 10 alkenyl, optionally substituted C 2 -C 10 alkynyl, optionally substituted alkylheterocycle, optionally substituted heterocyclealkyl, optionally substituted alkylphosphate, optionally substituted phosphoalkyl, optionally substituted alkylphosphorothioate, optionally substituted phosphorothioalkyl, optionally substituted alkylphosphorodithioate, optionally substituted phosphorodithioalkyl, optionally substituted alkylphosphonate, optionally substituted phosphonoalkyl, optionally substituted amino, optionally substituted alkylamino, optionally substituted di(alkyl)amino, optionally substituted aminoalkyl, optionally substituted alkylaminoalkyl, optionally substituted di(alkyl)aminoalkyl, optionally substituted hydroxyalkyl, optionally substituted polyethylene glycol (PEG), optionally substituted mPEG, optionally substituted heteroaryl, or optionally substituted heterocycle, or linker-ligand; or,

each R 3 taken together with the atom to which they are attached are a 3-8 membered optionally substituted cycloalkyl group or a 3-8 membered optionally substituted heterocycle group;

X and Y are each independently —O—, —S—, —N(Q)-, —C(O)—, —O(CO)—, —OC(O)N(Q)-, —N(Q)C(O)O—, —C(O)O, —OC(O)O—, —OS(O)(Q 2 )O—, or —OP(O)(Q 2 )O—;

Q is H, alkyl, ω-aminoalkyl, ω-(substituted)aminoalkyl, ω-phosphoalkyl, or ω-thiophosphoalkyl;

Q 1 is independently for each occurrence O or S; and,

Q 2 is independently for each occurrence O, S, N(Q)(Q), alkyl or alkoxy.

2. A lipid, or a salt or isomer thereof, selected from the group consisting of:

3. A lipid particle comprising a lipid of claim 1 .

4. The lipid particle of claim 3 , wherein the particle further comprises a neutral lipid and a lipid capable of reducing aggregation.

5. The lipid particle of claim 4 , wherein the lipid particle consists essentially of

a. a lipid of claim 3 ;

b. a neutral lipid selected from DSPC, DPPC, POPC, DOPE and SM;

c. a sterol; and

d. PEG-DMG,

in a molar ratio of about 20-60% lipid of claim 1 :5-25% neutral lipid:25-55% sterol:0.5-15% PEG-DMG.

6. The lipid particle of claim 3 , further comprising a therapeutic agent.

7. The lipid particle of claim 6 , wherein the therapeutic agent is a nucleic acid.

8. The lipid particle of claim 7 , wherein the nucleic acid is a plasmid.

9. The lipid particle of claim 7 , wherein the nucleic acid is an immunostimulatory oligonucleotide.

10. The lipid particle of claim 7 , wherein the nucleic acid is selected from the group consisting of an siRNA, an antisense oligonucleotide, a microRNA, an antagomir, an aptamer, and a ribozyme.

11. The lipid particle of claim 10 , wherein the nucleic acid is an siRNA.

12. A pharmaceutical composition comprising a lipid particle of claim 6 and a pharmaceutically acceptable excipient, carrier, or diluent.

13. A method of modulating the expression of a target gene in a cell, comprising providing to a cell the lipid particle of claim 6 .

14. The method of claim 13 , wherein the therapeutic agent is selected from an siRNA, an antagomir, an antisense oligonucleotide, and a plasmid capable of expressing an siRNA, a ribozyme, an aptamer or an antisense oligonucleotide.

15. A method of treating a disease or disorder characterized by overexpression of a polypeptide in a subject, comprising providing to the subject the pharmaceutical composition of claim 12 , wherein the therapeutic agent is selected from an siRNA, a microRNA, an antisense oligonucleotide, and a plasmid capable of expressing an siRNA, a microRNA, or an antisense oligonucleotide, and wherein the siRNA, microRNA, or antisense RNA comprises a polynucleotide that specifically binds to a polynucleotide that encodes the polypeptide, or a complement thereof.

16. A method of treating a disease or disorder characterized by underexpression of a polypeptide in a subject, comprising providing to the subject the pharmaceutical composition of claim 12 , wherein the therapeutic agent is a plasmid that encodes the polypeptide or a functional variant or fragment thereof.

17. A method of inducing an immune response in a subject, comprising providing to the subject the pharmaceutical composition of claim 12 , wherein the therapeutic agent is an immunostimulatory oligonucleotide.

18. The lipid of claim 1 , wherein the PEG has a molecular weight range from 100 to 40,000.

19. The lipid of claim 1 , wherein the mPEG has a molecular weight range from 120 to 40,000.

20. The lipid of claim 1 , wherein R 1 and R 2 are each independently C 10 -C 30 alkenyl.

21. The lipid of claim 1 , wherein X and Y are each independently —O—.

22. A lipid particle comprising a lipid of claim 2 .

Assignments (4)
MERGER AND CHANGE OF NAME Recorded Jul 27, 2018
From: PROTIVA BIOTHERAPEUTICS INC.; ARBUTUS BIOPHARMA CORPORATION
To: ARBUTUS BIOPHARMA CORPORATION
Reel/Frame 046640/0764 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 17, 2017
From: MANOHARAN, MUTHIAH; RAJEEV, KALLANTHOTTATHIL G.; BUTLER, DAVID; NARAYANANNAIR, JAYAPRAKASH K.; JAYARAMAN, MUTHUSAMY; ELTEPU, LAXMAN
To: ALNYLAM PHARMACEUTICALS, INC.
Reel/Frame 041625/0478 →
CHANGE OF NAME Recorded Mar 17, 2017
From: TEKMIRA PHARMACEUTICALS CORPORATION
To: ARBUTUS BIOPHARMA CORPORATION
Reel/Frame 041625/0491 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 17, 2017
From: ALNYLAM PHARMACEUTICALS, INC.
To: TEKMIRA PHARMACEUTICALS CORPORATION
Reel/Frame 041625/0493 →