Stereochemically enriched compositions for delivery of nucleic acids
Provided, in part, is a composition comprising one or more chemical entities of formula I, each of which is a compound of formula I: a pharmaceutically acceptable salt thereof, a solvate thereof, or a solvate of a pharmaceutically acceptable salt thereof, the composition characterized in that greater than a first threshold amount of the total amount of chemical entities of formula I in the composition: are chemical entities of formula I.a, wherein the first threshold amount is 50%; or are chemical entities of formula I.b.1, wherein the first threshold amount is 25%; or are chemical entities of formula I.b.2, wherein the first threshold amount is 25%, wherein the chemical entities of formula I.a, I.b.1, and I.b.2, are described herein, and methods of using such compositions, for example, for the delivery of a polynucleotide in vivo.
1. A lipid nanoparticle comprising:
a polynucleotide that is messenger RNA (mRNA);
one or more non-cationic lipids that are not a cholesterol-based lipid, one or more cholesterol-based lipids and/or one or more PEG-modified lipids;
and
one or more chemical entities of formula I, each of which is a compound of formula I:
or
a pharmaceutically acceptable salt thereof,
wherein 70% or more of the chemical entities of formula I have the structure set forth by formula I.a.i,
2. The lipid nanoparticle of claim 1 , wherein 80% or more of the chemical entities of formula I have the structure set forth by formula I.a.i.
3. The lipid nanoparticle of claim 1 , wherein 90% or more of the chemical entities of formula I have the structure set forth by formula I.a.i.
4. The lipid nanoparticle of claim 1 , wherein 95% or more of the chemical entities of formula I have the structure set forth by formula I.a.i.
5. A method of delivery of messenger RNA (mRNA) in vivo, comprising
administering to a subject in need of delivery the lipid nanoparticle of claim 1 , wherein administering of the lipid nanoparticle results in the expression of the protein encoded by the mRNA in vivo.
6. A method of treating a disease or disorder comprising the step of delivering an mRNA encoding a therapeutic protein using the lipid nanoparticle of claim 1 .
7. The lipid nanoparticle of claim 1 , wherein the one or more non-cationic lipids are selected from the group consisting of DSPC (1,2-distearoyl-sn-glycero-3-phosphocholine), DPPC (1,2-dipalmitoyl-sn-glycero-3-phosphocholine), DOPE (1,2-dioleyl-sn-glycero-3-phosphoethanolamine), DOPC (1,2-dioleyl-sn-glycero-3-phosphotidylcholine) DPPE (1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine), DMPE (1,2-dimyristoyl-sn-glycero-3-phosphoethanolamine), and DOPG (1,2-dioleoyl-sn-glycero-3-phospho-(1′-rac-glycerol)).
8. The lipid nanoparticle of claim 1 , wherein the one or more cholesterol-based lipids are cholesterol and/or PEGylated cholesterol.
9. The lipid nanoparticle of claim 1 , wherein the one or more PEG-modified lipids comprise a poly(ethylene) glycol chain of up to 5 kDa covalently attached to a lipid with alkyl chain(s) of C 6 -C 20 length.
10. A method of delivery of messenger RNA (mRNA) in vivo, comprising administering to a subject in need of delivery the lipid nanoparticle of claim 7 , wherein administering of the lipid nanoparticle results in the expression of the protein encoded by the mRNA in vivo.
11. A method of delivery of messenger RNA (mRNA) in vivo, comprising administering to a subject in need of delivery the lipid nanoparticle of claim 8 , wherein administering of the lipid nanoparticle results in the expression of the protein encoded by the mRNA in vivo.
12. A method of delivery of messenger RNA (mRNA) in vivo, comprising administering to a subject in need of delivery the lipid nanoparticle of claim 9 , wherein administering of the lipid nanoparticle results in the expression of the protein encoded by the mRNA in vivo.