IP Library Granted Patent US 9,458,090
Granted Patent B2
US 9,458,090 · App. 14/682,494 · Granted Oct 4, 2016

Low molecular weight cationic lipids for oligonucleotide delivery

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Quick Facts
Patent No.
US 9,458,090
App. No.
14/682,494
Granted
Oct 4, 2016
Kind
B2
Abstract

The instant invention provides for novel cationic lipids that can be used in combination with other lipid components such as cholesterol and PEG-lipids to form lipid nanoparticles with oligonucleotides. It is an object of the instant invention to provide a cationic lipid scaffold that demonstrates enhanced efficacy along with lower liver toxicity as a result of lower lipid levels in the liver. The present invention employs low molecular weight cationic lipids comprising at least one short lipid chain to enhance the efficiency and tolerability of in vivo delivery of siRNA.

Claims (37)

1. A lipid nanoparticle comprising an oligonucleotide and a lipid of Formula A:

wherein:

R 1 and R 2 are independently selected from H, (C 1 -C 6 )alkyl, heterocyclyl, and polyamine, wherein said alkyl, heterocyclyl and polyamine are optionally substituted with one to three substituents selected from R′, or R 1 and R 2 can be taken together with the nitrogen to which they are attached to form a monocyclic heterocycle with 4-7 members optionally containing, in addition to the nitrogen, one or two additional heteroatoms selected from N, O and S, said monocyclic heterocycle is optionally substituted with one to three substituents selected from R′;

R 3 is selected from H and (C 1 -C 6 )alkyl, said alkyl optionally substituted with one to three substituents selected from R′;

R′ is independently selected from halogen, R″, OR″, SR″, CN, CO 2 R″ or CON(R″) 2 ;

R″ is independently selected from H and (C 1 -C 6 )alkyl, alkyl is optionally substituted with halogen and OH;

n is 0, 1, 2, 3, 4 or 5;

X is selected from O, NR″, (C═O)O, NR″(C═O), O(C═O)O, NR″(C═O)NR″, O(C═O)NR″, and NR″(C═O)O;

L 1 is selected from C 4 -C 24 alkyl and C 4 -C 24 alkenyl, said alkyl and alkenyl are optionally substituted with one or more substituents selected from R′; and

L 2 is selected from unsubstituted C 9 alkyl and unsubstituted C 9 alkenyl;

or any pharmaceutically acceptable salt or stereoisomer thereof.

2. The lipid nanoparticle of claim 1 , wherein in the lipid of Formula A

R 1 and R 2 are each methyl;

R 3 is H;

n is 3;

X is (C═O)O;

L 1 is selected from C 4 -C 24 alkyl and C 4 -C 24 alkenyl; and

L 2 is selected from C 3 -C 9 alkyl and C 3 -C 9 alkenyl;

or any pharmaceutically acceptable salt or stereoisomer thereof.

3. The lipid nanoparticle of claim 1 , wherein the lipid is:

(20Z,23Z)-nonacosa-20,23-dien-10-yl 4-(dimethylamino)butanoate (Compound 1); and

(18Z)-heptacos-18-en-10-yl4-(dimethylamino)butanoate (Compound 2);

or any pharmaceutically acceptable salt or stereoisomer thereof.

4. The lipid nanoparticle according to claim 1 , wherein the oligonucleotide is siRNA or miRNA.

5. The lipid nanoparticle according to claim 1 , wherein the oligonucleotide is siRNA.

6. The lipid nanoparticle of claim 1 , wherein L 1 is C 4 -C 24 alkenyl.

7. The lipid nanoparticle of claim 6 , wherein L 1 is C 12 -C 24 alkenyl.

8. The lipid nanoparticle of claim 7 , wherein L 1 is C 19 alkenyl.

9. The lipid nanoparticle of claim 7 , wherein L 1 is

10. The lipid nanoparticle of claim 1 , wherein R 1 and R 2 are independently selected from H, methyl, ethyl and propyl.

11. The lipid nanoparticle of claim 10 , wherein R 1 and R 2 each are methyl.

12. The lipid nanoparticle of claim 1 , wherein R 3 is H or methyl.

13. The lipid nanoparticle of claim 12 , wherein R 3 is H.

14. The lipid nanoparticle of claim 1 , wherein n is 2, 3 or 4.

15. The lipid nanoparticle of claim 14 , wherein n is 3.

16. The lipid nanoparticle of claim 1 , wherein X is O, NR″, (C═O)O, NR″(C═O), O(C═O)O, NR″(C═O)NR″, O(C═O)NR″ or NR″C(C═O)O.

17. The lipid nanoparticle of claim 16 , wherein X is (C═O)O.

Assignments (3)
SECURITY INTEREST Recorded Oct 1, 2025
From: ALNYLAM PHARMACEUTICALS, INC.; SIRNA THERAPEUTICS, INC.
To: BANK OF AMERICA, N.A.
Reel/Frame 072996/0337 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 8, 2016
From: COLLETTI, STEVEN L.; STANTON, MATTHEW G.
To: MERCK SHARP & DOHME CORP.
Reel/Frame 038842/0432 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 8, 2016
From: MERCK SHARP & DOHME CORP.
To: SIRNA THERAPEUTICS, INC.
Reel/Frame 038842/0446 →