Lipids and compositions for the delivery of therapeutics
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:
1. A lipid having the structure of formula I
or a salt or isomer thereof, wherein:
R 1 and R 2 are each independently for each occurrence 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;
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, optionally substituted mPEG, optionally substituted heteroaryl, or optionally substituted heterocycle;
X and Y are each independently —O—, —S—, alkylene, —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 2 is independently for each occurrence O, S, N(Q)(Q), alkyl or alkoxy;
A 1 , and A 2 are each independently —O—, —S—, —CH 2 —, —CHR 5 —, —CR 5 R 5 —, —CHF— or —CF 2 —;
R 5 is H, halo, cyano, hydroxy, amino, optionally substituted alkyl, optionally substituted alkoxy, or optionally substituted cycloalkyl;
Z is N, or C(R 3 ); and
m and n are each independently 0 to 5, where m and n taken together result in a 3, 4, 5, 6, 7 or 8 member ring.
2. A lipid selected from the group consisting of:
and salts and isomers thereof.
3. A lipid particle comprising a lipid of claim 1 .
4. The lipid particle of claim 3 , further comprising a therapeutic agent.
5. The lipid particle of claim 4 , wherein the therapeutic agent is a nucleic acid.
6. The lipid particle of claim 5 , 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.
7. The lipid particle of claim 6 , wherein the nucleic acid is an siRNA.
8. A pharmaceutical composition comprising a lipid particle of claim 4 and a pharmaceutically acceptable excipient, carrier, or diluent.
9. The lipid particle of claim 5 , wherein the nucleic acid is mRNA.
10. The lipid of claim 1 , or a salt or isomer thereof, wherein X and Y are each independently —O—.
11. The lipid of claim 1 , or a salt or isomer thereof, wherein R 1 and R 2 are each independently for each occurrence 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.
12. The lipid of claim 11 , or a salt or isomer thereof, wherein R 1 and R 2 are each independently for each occurrence optionally substituted C 10 -C 30 alkenyl.
13. The lipid of claim 11 , or a salt or isomer thereof, wherein R 1 and R 2 are each independently for each occurrence optionally substituted C 10 -C 30 alkynyl.
14. The lipid of claim 1 , or a salt or isomer thereof, wherein A 1 , and A 2 are each independently —O—.
15. The lipid of claim 1 , or a salt or isomer thereof, wherein A 1 , and A 2 are each independently —CH 2 —.
16. The lipid of claim 1 , or a salt or isomer thereof, wherein Z is N.
17. The lipid of claim 1 , or a salt or isomer thereof, wherein Z is C(R 3 ).