IP Library Patent Application 17124462
Patent Application
App. No. 17/124,462

LIPID NANOPARTICLE COMPOSITIONS FOR DELIVERY OF MRNA AND LONG NUCLEIC ACIDS

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Patent No.
US None
App. No.
17/124,462
Abstract

In some aspects, the present disclosure provides compositions of lipid nanoparticles useful for the delivery of large RNAs including mRNAs. These compositions may include a cationic ionizable lipid, a phospholipid, a PEGylated lipid, and a steroid including using less of a cationic ionizable lipid than compositions with shorter nucleic acids. These compositions may be used to treat a disease or disorder for which the delivery of an mRNA is therapeutically effective.

Claims (36)

1 .- 75 . (canceled)

76 . A method for delivering a messenger ribonucleic acid (mRNA) into a cell, the method comprising contacting said cell with a lipid composition coupled with said mRNA, which lipid composition comprises:

a cationic ionizable lipid at a molar percentage of less than about 30%; and

a phospholipid at a molar percentage of less than about 50%,

thereby delivering said mRNA into said cell.

77 . The method of claim 76 , wherein the lipid composition comprises said cationic ionizable lipid at a molar percentage from about 5% to about 30%.

78 . The method of claim 76 , wherein, prior to said contacting, said cell exhibits an aberrant expression or activity of a protein encoded by said mRNA.

79 . The method of claim 78 , wherein said aberrant expression or activity of said protein comprises an expression of a non-functional variant of said protein.

80 . The method of claim 78 , wherein said aberrant expression or activity of said protein is associated with a genetic disease or disorder.

81 . The method of claim 78 , wherein said mRNA is expressed in said cell, upon said contacting, to produce a functional variant of said protein.

82 . The method of claim 78 , wherein an expression of said mRNA in said cell increases an amount of a functional variant of said protein as compared to an amount of said functional variant of said protein generated in absence of said contacting.

83 . The method of claim 76 , wherein said contacting is in vivo.

84 . The method of claim 76 , wherein said cell is in a tissue or organ of a subject.

85 . The method of claim 84 , wherein said tissue or organ is a functionally compromised tissue or organ.

86 . The method of claim 84 , wherein said contacting comprises administering to said subject said lipid composition coupled with said mRNA.

87 . The method of claim 76 , further comprising repeating said contacting.

88 . The method of claim 76 , wherein said contacting comprises contacting a plurality of cells that comprises said cell.

89 . The method of claim 88 , wherein said messenger ribonucleic acid (mRNA) is expressed in at least 40% of said plurality of cells, upon said contacting, to produce a functional variant of a protein encoded by said mRNA.

90 . The method of claim 76 , wherein the lipid composition comprises said mRNA and said cationic ionizable lipid at a weight ratio from about 1:1 to about 1:100.

91 . The method of claim 76 , wherein said cationic ionizable lipid is a biodegradable cationic ionizable lipid.

92 . The method of claim 76 , wherein said cationic ionizable lipid comprises an amino group that is cationic at a physiological pH.

93 . The method of claim 92 , wherein said cationic ionizable lipid comprises two or more hydrophobic groups.

94 . The method of claim 76 , wherein said cationic ionizable lipid is a dendron or dendrimer.

95 . The method of claim 94 , wherein said dendron or dendrimer has a core structure that comprises monoamine or polyamine.

96 . The method of claim 94 , wherein said dendron or dendrimer has a terminating group that comprises a lipophilic group.

97 . The method of claim 76 , wherein the lipid composition comprises said phospholipid at a molar percentage from about 10% to about 50%.

98 . The method of claim 97 , wherein said phospholipid is a zwitterionic phospholipid.

99 . The method of claim 97 , wherein said phospholipid is 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC) or 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE).

100 . The method of claim 76 , wherein the lipid composition comprises a polymer-conjugated lipid at a molar percentage from about 0.25% to about 12.5%.

101 . The method of claim 100 , wherein said polymer-conjugated lipid is a polyethylene glycol (PEG)-conjugated lipid.

102 . The method of claim 76 , wherein the lipid composition comprises a steroid or a steroid derivative thereof at a molar percentage from about 15% to about 60%.

103 . The method of claim 102 , wherein said steroid or said steroid derivative comprises a cholesterol moiety.

104 . The method of claim 76 , wherein the 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.

105 . A composition comprising a lipid composition coupled with a messenger ribonucleic acid (mRNA), which lipid composition comprises:

a cationic ionizable lipid at a molar percentage of less than about 30%; and

a phospholipid at a molar percentage of less than about 50%.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 21, 2021
From: SIEGWART, DANIEL J.; CHENG, QIANG
To: THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 055661/0013 →