Compounds and compositions for intracellular delivery of therapeutic agents

US12151995B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12151995-B2
Application numberUS-202318467190-A
CountryUS
Kind codeB2
Filing dateSep 14, 2023
Priority dateSep 17, 2015
Publication dateNov 26, 2024
Grant dateNov 26, 2024

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The disclosure features novel lipids and compositions involving the same. Nanoparticle compositions include a novel lipid as well as additional lipids such as phospholipids, structural lipids, and PEG lipids. Nanoparticle compositions further including therapeutic and/or prophylactics such as RNA are useful in the delivery of therapeutic and/or prophylactics to mammalian cells or organs to, for example, regulate polypeptide, protein, or gene expression.

First claim

Opening claim text (preview).

The invention claimed is: 1. A compound of Formula (I): or salts or isomers thereof, wherein: R 1 is —R″M′R′ or C 5-20 alkenyl; R 2 and R 3 are each independently selected from C 1-14 alkyl and C 2-14 alkenyl; R 4 is —(CH 2 ) n Q, wherein Q is OH and n is selected from 3, 4, and 5; M and M′ are each independently —C(O)O— or —OC(O)—; R 5 , R 6 , and R 7 are each H; R′ is a linear C 1-12 alkyl, or C 1-12 alkyl substituted with C 6-9 alkyl; R″ is C 3-14 alkyl; m is selected from 5, 6, 7, 8, 9, 10, 11, 12, and 13. 2. The compound of claim 1 , wherein n is 3 or 4. 3. The compound of claim 1 , wherein R 2 and R 3 are each independently C 6-8 alkyl. 4. The compound of claim 3 , wherein R 2 and R 3 are the same. 5. The compound of claim 3 , wherein R 2 and R 3 are different. 6. The compound of claim 1 , wherein R′ is C 6-9 alkyl substituted with C 6-9 alkyl. 7. The compound of claim 1 , wherein R′ is a linear C 6-9 alkyl. 8. The compound of claim 1 , wherein the compound is selected from: 9. A compound of Formula (I): or salts or isomers thereof, wherein: R 1 is —R″M′R′ or C 5-20 alkenyl; R 2 and R 3 are each independently selected from C 1-14 alkyl and C 2-14 alkenyl; R 4 is —(CH 2 ) n Q, wherein Q is OH and n is selected from 1, 2, 3, 4, and 5; M and M′ are each independently —C(O)O— or —OC(O)—; R 5 , R 6 , and R 7 are each H; R′ is a linear C 1-12 alkyl, or C 1-12 alkyl substituted with C 6-9 alkyl; R″ is C 6-14 alkyl; m is selected from 6, 7, 8, 9, 10, 11, 12, and 13. 10. The compound of claim 9 , wherein n is 2, 3, or 4. 11. The compound of claim 9 , wherein R″ is C 6-9 alkyl. 12. The compound of claim 9 , wherein m is selected from 6, 7, 8, and 9. 13. The compound of claim 9 , wherein R 2 and R 3 are each independently C 6-8 alkyl. 14. The compound of claim 13 , wherein R 2 and R 3 are the same. 15. The compound of claim 13 , wherein R 2 and R 3 are different. 16. The compound of claim 9 , wherein R′ is C 6-9 alkyl substituted with C 6-9 alkyl. 17. The compound of claim 9 , wherein R′ is a linear C 6-9 alkyl. 18. The compound of claim 9 , wherein the compound is selected from: 19. A compound of Formula (IA): or a salt or isomer thereof, wherein l is selected from 1, 2, 3, 4, and 5; m is selected from 5, 6, 7, 8, and 9; M 1 is a bond or M′; R 4 is unsubstituted C 1-3 alkyl, or —(CH 2 ) n Q, in which Q is OH, —NHC(S)N(R) 2 , —NHC(O)N(R) 2 , —N(R)C(O)R, —N(R)S(O) 2 R, —N(R)R 8 , —NHC(═NR 9 )N(R) 2 , —NHC(═CHR 9 )N(R) 2 , —OC(O)N(R) 2 , —N(R)C(O)OR, —N(OR)C(O)R, —N(OR)S(O) 2 R, —N(OR)C(O)OR, —N(OR)C(O)N(R) 2 , —N(OR)C(S)N(R) 2 , —N(OR)C(═NR 9 )N(R) 2 , —N(OR)C(═CHR 9 )N(R) 2 , or heteroaryl, and each n is selected from 1, 2, 3, 4, or 5; M and M′ are independently selected from —C(O)O—, —OC(O)—, —C(O)N(R′)-, —P(O)(OR′)O-, —S—S—, an aryl group, and a heteroaryl group; and R 2 and R 3 are both C 1-14 alkyl, or C 2-14 alkenyl; R 8 is selected from the group consisting of C 3-6 carbocycle and heterocycle; R 9 is selected from the group consisting of H, CN, NO 2 , C 1-6 alkyl, —OR, —S(O) 2 R, —S(O) 2 N(R) 2 , C 2-6 alkenyl, C 3-6 carbocycle and heterocycle; each R is independently selected from the group consisting of C 1-3 alkyl, C 2-3 alkenyl, and H; and R′ is a linear alkenyl. 20. A nanoparticle composition comprising a lipid component comprising a compound of claim 1 . 21. The nanoparticle composition of claim 20 , wherein the lipid component further comprises a phospholipid, wherein the phospholipid is selected from the group consisting of 1,2-dilinoleoyl-sn-glycero-3-phosphocholine (DLPC), 1,2-dimyristoyl-sn-glycero-phosphocholine (DMPC), 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC), 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC), 1,2-diundecanoyl-sn-glycero-phosphocholine (DUPC), 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC), 1,2-di-O-octadecenyl-sn-glycero-3-phosphocholine (18:0 Diether PC), 1-oleoyl-2-cholesterylhemisuccinoyl-sn-glycero-3-phosphocholine (OChemsPC), 1-hexadecyl-sn-glycero-3-phosphocholine (C16 Lyso PC), 1,2-dilinolenoyl-sn-glycero-3-phosphocholine, 1,2-diarachidonoyl-sn-glycero-3-phosphocholine, 1,2-didocosahexaenoyl-sn-glycero-3-phosphocholine,1,2-dioleoyl-sn-glycero-3-phosphoethanola mine (DOPE), 1,2-diphytanoyl-sn-glycero-3-phosphoethanolamine (ME 16.0 PE), 1,2-distearoyl-sn-glycero-3-phosphoethanolamine, 1,2-dilinoleoyl-sn-glycero-3-phosphoethanolamine, 1,2-dilinolenoyl-sn-glycero-3-phosphoethanolamine, 1,2-diarachidonoyl-sn-glycero-3-phosphoethanolamine, 1,2-didocosahexaenoyl-sn-glycero-3-phosphoethanolamine, 1,2-dioleoyl-sn-glycero-3-phospho-rac-(1-glycerol) sodium salt (DOPG), dipalmitoylphosphatidylglycerol (DPPG), palmitoyloleoylphosphatidylethanolamine (POPE), distearoyl-phosphatidyl-ethanolamine (DSPE), dipalmitoyl phosphatidyl ethanolamine (DPPE), dimyristoylphosphoethanolamine (DMPE), 1-stearoyl-2-oleoyl-phosphatidyethanolamine (SOPE), 1-stearoyl-2-oleoyl-phosphatidylcholine (SOPC), sphingomyelin, phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine, phosphatidylinositol, phosphatidic acid, palmitoyloleoyl phosphatidylcholine, lysophosphatidylcholine, lysophosphatidylethanolamine (LPE), and mixtures thereof. 22. The nanoparticle composition of claim 20 , wherein the lipid component further comprises a structural lipid, wherein the structural lipid is selected from the group consisting of cholesterol, fecosterol, sitosterol, ergosterol, campesterol, stigmasterol, brassicasterol, tomatidine, ursolic acid, alpha-tocopherol, and mixtures thereof. 23. The nanoparticle composition of claim 20 , wherein the lipid component further comprises a PEG lipid, wherein the PEG lipid is selected from the group consisting of a PEG-modified phosphatidylethanolamine, a PEG-modified phosphatidic acid, a PEG-modified ceramide, a PEG-modified dialkylamine, a PEG-modified diacylglycerol, a PEG-modified dialkylglycerol, and mixtures thereof. 24. The nanoparticle composition of claim 20 , further comprising a therapeutic and/or prophylactic agent. 25. The nanoparticle composition of claim 24 , wherein the therapeutic and/or prophylactic agent is a nucleic acid. 26. A nanoparticle composition comprising a lipid component

Assignees

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Classifications

  • by reactions involving amino or carboxyl groups, e.g. hydrolysis of esters or amides, by formation of halides, salts or esters · CPC title

  • the non-active part being non-polymeric · CPC title

  • Complement proteins, e.g. anaphylatoxin, C3a or C5a · CPC title

  • Natural ribonucleic acids, i.e. containing only riboses attached to adenine, guanine, cytosine or uracil and having 3'-5' phosphodiester links · CPC title

  • obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyamines, polyanhydrides · CPC title

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What does patent US12151995B2 cover?
The disclosure features novel lipids and compositions involving the same. Nanoparticle compositions include a novel lipid as well as additional lipids such as phospholipids, structural lipids, and PEG lipids. Nanoparticle compositions further including therapeutic and/or prophylactics such as RNA are useful in the delivery of therapeutic and/or prophylactics to mammalian cells or organs to, for…
Who is the assignee on this patent?
Modernatx Inc
What technology area does this patent fall under?
Primary CPC classification C07C229/12. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Nov 26 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).