IP Library › Granted Patent US 12,280,117
Granted Patent B2
US 12,280,117 · App. 17/239,131 · Granted Apr 22, 2025

Lipid nanoparticle formulations for delivery of MRNA

Inventors: Frank DeRosa (Lexington, MA); Michael Heartlein (Lexington, MA); Shrirang Karve (Lexington, MA)
Assignee: TRANSLATE BIO, INC.
A61K47/554A61K9/0078A61K9/1272A61K38/1709A61K47/28A61K47/543A61K47/60A61K47/6911A61K48/0008A61K48/0033A61K48/0041A61K48/0066A61K48/0075A61P11/12
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Quick Facts
Patent No.
US 12,280,117
App. No.
17/239,131
Granted
Apr 22, 2025
Kind
B2
Abstract

The present invention provides, among other things, compositions and methods of formulating nucleic acid-containing nanoparticles comprising no more than three distinct lipids components, one distinct lipid component being a sterol-based cationic lipid. In some embodiments, the present invention provides compositions and methods in which the lipid nanoparticles further comprise helper lipids and PEG-modified lipids. The resulting formulation comprises a high encapsulation percentage for nucleic acids.

Claims (34)

1. A method of delivering messenger RNAs (mRNAs) encoding a protein or a peptide in vivo comprising administering by pulmonary delivery to a subject in need of delivery a composition comprising:

the mRNAs; and

lipid nanoparticles encapsulating the mRNAs, wherein each individual lipid nanoparticle comprises no more than three distinct lipid components, wherein the three lipid components are a non-cationic lipid, a PEG-modified lipid, and a sterol-based cationic lipid, wherein the sterol-based cationic lipid has a structure according to Formula (A),

B-L 1 -S  (Formula A),

or a protonated form thereof, wherein:

B is a basic functional group selected from

dialkylamino and guanidine;

L 1 is an optionally substituted linker group; and

S is a sterol.

2. The method of claim 1 , wherein the mRNAs are codon-optimized and/or comprise one or more modified nucleotides.

3. The method of claim 1 , wherein the lipid nanoparticles have a size less than about 100 nm.

4. The method of claim 1 , wherein the lipid nanoparticles have a lipid/mRNA (N/P) ratio of 2 or 4.

5. The method of claim 1 , wherein the molar percentage of the PEG-modified lipid in the lipid nanoparticles is no more than 5%.

6. The method of claim 1 , wherein the molar percentage of the sterol-based cationic lipid in the lipid nanoparticles is no more than 70%.

7. The method of claim 1 , wherein the molar percentage of the sterol-based cationic lipid in the lipid nanoparticles is at least 40%.

8. A composition comprising:

messenger RNAs (mRNAs) encoding a protein or a peptide; and

lipid nanoparticles encapsulating the mRNAs, wherein each individual lipid nanoparticle comprises no more than three distinct lipid components, wherein the three lipid components are a non-cationic lipid, a PEG-modified lipid, and a sterol-based cationic lipid, wherein the sterol-based cationic lipid has a structure according to Formula (A),

B-L 1 -S  (Formula A),

or a protonated form thereof, wherein:

B is a basic functional group selected from

dialkylamino and guanidine;

L 1 is an optionally substituted linker group; and

S is a sterol, and

further wherein the lipid nanoparticles have an encapsulation percentage for mRNAs of at least 70%.

9. The composition of claim 8 , wherein the sterol-based cationic lipid constitutes no more than 70% of the total lipids.

10. The composition of claim 8 , wherein L′ is an optionally substituted linker group that is a C 1 -C 20 alkylene or a 2- to 20-membered heteroalkylene.

11. The composition of claim 8 , wherein L′ does not comprise substituents having the structure-N(R′) 2 , or a positively charged form thereof, wherein each R′ is independently hydrogen or optionally substituted C 1 -C 20 alkyl.

12. The composition of claim 8 , wherein S is a sterol selected from a zoosterol, or an oxidized or reduced form thereof, a phytosterol, or an oxidized or reduced form thereof, a synthetic sterol, or an oxidized or reduced form thereof, cholesterol, an oxidized form of cholesterol, a reduced form of cholesterol, alkyl lithocholate, stigmasterol, stigmastanol, campesterol, ergosterol, and sitosterol.

13. The composition of claim 8 , wherein the mRNAs are codon-optimized and/or comprise one or more modified nucleotides.

14. The composition of claim 8 , wherein the lipid nanoparticles have a lipid/mRNA (N/P) ratio of 2 or 4.

15. The composition of claim 8 , wherein the molar percentage of the PEG-modified lipid in the lipid nanoparticles is no more than 5%.

16. The composition of claim 8 , wherein the molar percentage of the sterol-based cationic lipid in the lipid nanoparticles is no more than 70%.

17. The composition of claim 8 , wherein the molar percentage of the sterol-based cationic lipid in the lipid nanoparticles is at least 40%.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 15, 2022
From: DEROSA, FRANK; HEARTLEIN, MICHAEL; KARVE, SHRIRANG
To: TRANSLATE BIO MA, INC.
Reel/Frame 059272/0422 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 15, 2022
From: TRANSLATE BIO MA, INC.
To: TRANSLATE BIO, INC.
Reel/Frame 059272/0433 →
Continuity (9)
Division 16599928 · Oct 11, 2019
Division 15809605 · Nov 10, 2017
Provisional Application 62420421 · Nov 10, 2016
Provisional Application 62420428 · Nov 10, 2016
Provisional Application 62421021 · Nov 11, 2016
Provisional Application 62421007 · Nov 11, 2016
Provisional Application 62464327 · Feb 27, 2017
Provisional Application 62464330 · Feb 27, 2017
Related Publication 20210353761A1 · Nov 18, 2021
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