IP Library Granted Patent US 11,510,880
Granted Patent B2
US 11,510,880 · App. 17/711,911 · Granted Nov 29, 2022

Compositions and methods for organ specific delivery of nucleic acids

Inventors: Qiang Cheng (Dallas, TX); Tuo Wei (Dallas, TX); Daniel J. Siegwart (Dallas, TX)
Assignee: The Board of Regents of The University of Texas System
A61K9/5123A61K48/0033C12N9/22C12N15/11C12N15/111C12N15/113C12N2310/20C12N2320/32
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Quick Facts
Patent No.
US 11,510,880
App. No.
17/711,911
Granted
Nov 29, 2022
Kind
B2
Abstract

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.

Claims (47)

1. A composition comprising a lipid composition assembled with a therapeutic agent, which lipid composition comprises:

an ionizable cationic lipid; and

a cationic selective organ targeting (SORT) lipid separate from said ionizable cationic lipid,

which lipid composition comprises said cationic SORT lipid in an amount sufficient to yield an apparent pKa of said lipid composition outside a range of about 6 to about 7, wherein said apparent pKa is determined by a 2-(p-toluidino)-6-naphthalenesulfonic acid titration assay.

2. The composition of claim 1 , wherein said apparent pKa is of about 8 or higher.

3. The composition of claim 1 , wherein said apparent pKa is of about 6 or lower.

4. The composition of claim 1 , wherein said cationic SORT lipid is present in said lipid composition at a molar percentage from about 5% to about 65%, wherein the molar percentage is determined based on total lipids present in the lipid composition.

5. The composition of claim 1 , wherein said cationic SORT lipid is a permanently cationic SORT lipid.

6. The composition of claim 5 , wherein said permanently cationic SORT lipid comprises a quaternary ammonium ion.

7. The composition of claim 5 , wherein said permanently cationic SORT lipid has a structure of Formula (I), Formula (II), or Formula (III), or a pharmaceutically acceptable salt, stereoisomer, or 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; or

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; or

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.

8. The composition of claim 1 , wherein said cationic SORT lipid is an ionizable cationic SORT lipid.

9. The composition of claim 8 , wherein said ionizable cationic SORT lipid is 1,2-dioleoyl-3-dimethylammonium-propane (DODAP).

10. The composition of claim 1 , wherein said lipid composition comprises said ionizable cationic lipid at a molar percentage from about 5% to about 30%, wherein the molar percentage is determined based on total lipids present in the lipid composition.

11. The composition of claim 1 , wherein said lipid composition further comprises a zwitterionic lipid.

12. The composition of claim 11 , wherein said zwitterionic lipid is a zwitterionic phospholipid.

13. The composition of claim 11 , wherein said lipid composition comprises said zwitterionic lipid at a molar percentage from about 8% to about 23%, wherein the molar percentage is determined based on total lipids present in the lipid composition.

14. The composition of claim 1 , wherein said lipid composition further comprises a polymer-conjugated lipid.

15. The composition of claim 14 , wherein said lipid composition comprises said polymer-conjugated lipid at a molar percentage from about 0.5% to about 10%, wherein the molar percentage is determined based on total lipids present in the lipid composition.

16. The composition of claim 14 , wherein said polymer-conjugated lipid is a poly(ethylene glycol) (PEG)-conjugated lipid.

17. The composition of claim 1 , wherein said lipid composition further comprises a steroid or steroid derivative.

18. The composition of claim 17 , wherein said lipid composition comprises said steroid or steroid derivative at a molar percentage from about 15% to about 46%, wherein the molar percentage is determined based on total lipids present in the lipid composition.

19. The composition of claim 1 , wherein said therapeutic agent comprises one or more members selected from a small interfering ribonucleic acid (siRNA), a micro-ribonucleic acid (miRNA), a primary micro-ribonucleic acid (pri-miRNA), a messenger ribonucleic acid (mRNA), a clustered regularly interspaced short palindromic repeats (CRISPR) related nucleic acid, a CRISPR-RNA (crRNA), a single guide ribonucleic acid (sgRNA), a trans-activating CRISPR ribonucleic acid (tracrRNA), a plasmid deoxyribonucleic acid (pDNA), a transfer ribonucleic acid (tRNA), an antisense oligonucleotide (ASO), a guide ribonucleic acid, a double stranded deoxyribonucleic acid (dsDNA), a single stranded deoxyribonucleic acid (ssDNA), a single stranded ribonucleic acid (ssRNA), a double stranded ribonucleic acid (dsRNA), a protein, and a CRSIPR-associated (Cas) protein.

20. The composition of claim 1 , wherein said therapeutic agent comprises a messenger ribonucleic acid (mRNA).

21. The composition of claim 20 , wherein said mRNA encodes a Cas protein.

22. The composition of claim 20 , wherein said therapeutic agent further comprises a CRISPR-RNA (crRNA), a single guide ribonucleic acid (sgRNA), a trans-activating CRISPR ribonucleic acid (tracrRNA), or a combination thereof.

23. The composition of claim 20 , wherein said therapeutic agent further comprises a single guide polynucleotide.

24. The composition of claim 20 , wherein said therapeutic agent further comprises a double stranded deoxyribonucleic acid (dsDNA), a single stranded deoxyribonucleic acid (ssDNA), or a combination thereof.

25. The composition of claim 1 , wherein said therapeutic agent comprises a protein.

26. The composition of claim 25 , wherein said protein is a CRSIPR-associated (Cas) protein.

27. The composition of claim 25 , wherein said therapeutic agent further comprises a CRISPR-RNA (crRNA), a single guide ribonucleic acid (sgRNA), a trans-activating CRISPR ribonucleic acid (tracrRNA), or a combination thereof.

28. The composition of claim 25 , wherein said therapeutic agent further comprises a single guide polynucleotide.

29. The composition of claim 25 , wherein said therapeutic agent further comprises a double stranded deoxyribonucleic acid (dsDNA), a single stranded deoxyribonucleic acid (ssDNA), or a combination thereof.

30. The composition of claim 1 , wherein said therapeutic agent is present in a ratio of said lipid composition to said therapeutic agent from about 1:1 to about 1:100.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 6, 2023
From: CHENG, QIANG; WEI, TUO; SIEGWART, DANIEL J.
To: THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 063864/0828 →
Continuity (6)
Continuation 17572615 · Jan 10, 2022
Continuation 17473863 · Sep 13, 2021
Continuation 17191895 · Mar 4, 2021
Continuation PCTUS2019049565 · Sep 4, 2019
Provisional Application 62726741 · Sep 4, 2018
Related Publication 20220233460A1 · Jul 28, 2022
Cited By (1)
US 12,357,580