Compositions and methods for organ specific delivery of nucleic acids
View Patent ↗The present disclosure provides compositions which shown preferential targeting or delivery of a nucleic acid composition to a particular organ. In some embodiments, the composition comprises a steroid or sterol, an ionizable cationic lipid, a phospholipid, a PEG lipid, and a permanently cationic lipid which may be used to deliver a nucleic acid.
1. A method for targeted delivery of a gene or transcript editing composition to an organ or a cell therein, the method comprising: contacting said organ or said cell therein with said gene or transcript editing composition assembled with a selective organ targeting (SORT) lipid composition,
wherein said SORT lipid composition comprises: (1) an ionizable cationic lipid; and (2) a SORT lipid selected from the group consisting of a cationic SORT lipid, a zwitterionic SORT lipid, and an anionic SORT lipid;
thereby providing a modified expression profile of a target gene or transcript in said organ or said cell therein as compared to that achieved absent said SORT lipid.
2. The method of claim 1 , wherein said gene or transcript editing composition comprises a polynucleotide-guided nuclease.
3. The method of claim 2 , wherein said polynucleotide-guided nuclease is a clustered regularly interspaced short palindromic repeats (CRISPR)-associated (Cas) nuclease.
4. The method of claim 2 , wherein said gene or transcript editing composition further comprises a guide polynucleotide configured to complex with at least a portion of said target gene or transcript, or a polynucleotide comprising a sequence that encodes said guide polynucleotide.
5. The method of claim 1 , wherein said gene or transcript editing composition comprises a polynucleotide comprising a sequence encoding a polynucleotide-guided nuclease.
6. The method of claim 1 , wherein said gene or transcript editing composition comprises a messenger ribonucleic acid (mRNA) comprising a sequence encoding a polynucleotide-guided nuclease.
7. The method of claim 5 , wherein said gene or transcript editing composition further comprises a guide polynucleotide configured to complex with at least a portion of said target gene or transcript, or a polynucleotide comprising a sequence that encodes said guide polynucleotide.
8. The method of claim 1 , wherein said gene or transcript editing composition comprises a donor polynucleotide configured to repair a modified target gene or transcript.
9. The method of claim 1 , wherein said organ is liver.
10. The method of claim 1 , wherein said organ is a non-liver organ.
11. The method of claim 1 , wherein said contacting is in vivo or ex vivo.
12. The method of claim 1 , wherein said cationic SORT lipid is present in said SORT lipid composition at a molar percentage from about 5% to about 65%.
13. The method of claim 1 , wherein said cationic SORT lipid is a permanently cationic SORT lipid.
14. The method of claim 13 , wherein said permanently cationic SORT lipid comprises a quaternary ammonium ion.
15. The method of claim 13 , wherein said permanently cationic SORT lipid has a structure of Formula (I), Formula (II), or Formula (III), or a pharmaceutically acceptable salt, stereoisomer, tautomer thereof:
wherein, in Formula (I):
R 1 and R 2 are each independently alkyl (C8-C24) , alkenyl (C8-C24) , or a substituted version of either group;
R 3 , R 3 ′, and R 3 ″ are each independently alkyl (C≤6) or substituted alkyl (C≤6) ; and
X − is a monovalent anion;
wherein, in Formula (II):
R 4 and R 4 ′ are each independently alkyl (C6-C24) , alkenyl (C6-C24) , or a substituted version of either group;
R 4 ″ is alkyl (C≤24) , alkenyl (C≤24) , or a substituted version of either group;
R 4 ′″ is alkyl (C1-C8) , alkenyl (C2-C8) , or a substituted version of either group; and
X 2 − is a monovalent anion; and
wherein, in Formula (III):
R 1 and R 2 are each independently alkyl (C8-C24) , alkenyl (C8-C24) , or a substituted version of either group;
R 3 , R 3 ′, and R 3 ″ are each independently alkyl (C≤6) or substituted alkyl (C≤6) ;
R 4 is alkyl (C≤6) or substituted alkyl (C≤6) ; and
X − is a monovalent anion.
16. The method of claim 1 , wherein said cationic SORT lipid is an ionizable cationic SORT lipid.
17. The method of claim 16 , wherein said ionizable cationic SORT lipid is 1,2-dioleoyl-3-dimethylammonium-propane (DODAP).
18. The method of claim 1 , wherein said SORT lipid composition comprises said ionizable cationic lipid at a molar percentage from about 5% to about 30%.
19. The method of claim 1 , wherein said SORT lipid composition further comprises a phospholipid, a polymer-conjugated lipid, a steroid or steroid derivative, or any combination thereof.
20. The method of claim 19 , wherein said SORT lipid composition comprises said phospholipid at a molar percentage from about 8% to about 23%.
21. The method of claim 19 , wherein said SORT lipid composition comprises said polymer-conjugated lipid at a molar percentage from about 0.5% to about 10%.
22. The method of claim 19 , wherein said SORT lipid composition comprises said steroid or steroid derivative at a molar percentage from about 15% to about 46%.
23. The method of claim 1 , wherein said gene or transcript editing composition comprises a CRISPR-RNA (crRNA), a trans-activating CRISPR ribonucleic acid (tracrRNA), or a combination thereof.
24. The method of claim 4 , wherein said guide polynucleotide is a ribonucleic acid (RNA).
25. The method of claim 7 , wherein said guide polynucleotide is a ribonucleic acid (RNA).
26. The method of claim 1 , wherein the gene or transcript editing composition is formulated for administration: orally, intraadiposally, intraarterially, intraarticularly, intracranially, intradermally, intralesionally, intramuscularly, intranasally, intraocularly, intrapericardially, intraperitoneally, intrapleurally, intraprostatically, intrarectally, intrathecally, intratracheally, intratumorally, intraumbilically, intravaginally, intravenously, intravesicularlly, intravitreally, liposomally, locally, mucosally, parenterally, rectally, subconjunctival, subcutaneously, sublingually, topically, transbuccally, transdermally, vaginally, in crèmes, via a catheter, via a lavage, via continuous infusion, via infusion, via inhalation, via injection, via local delivery, or via localized perfusion.
27. The method of claim 10 , wherein said non-liver organ comprises a lung or spleen.
28. The method of claim 1 , where said organ or said cell therein exhibits an aberrant expression or activity of said target gene or transcript.
29. The method of claim 1 , wherein said contacting comprises administering the gene or transcript editing composition to a subject that comprises said organ or said cell therein.
30. The method of claim 29 , wherein said subject is a mammal or human.