LIPID NANOPARTICLE COMPOSITIONS FOR DELIVERY OF MRNA AND LONG NUCLEIC ACIDS
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.
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%.