US2021322573A1PendingUtilityA1
Use of liposomes in a carrier comprising a continuous hydrophobic phase for delivery of polynucleotides in vivo
Assignee: IMMUNOVACCINE TECHNOLOGIES INCPriority: Sep 27, 2007Filed: May 7, 2021Published: Oct 21, 2021
Est. expirySep 27, 2027(~1.2 yrs left)· nominal 20-yr term from priority
A61K 9/127A61K 9/107A61K 31/7088A61K 38/208A61P 37/08A61P 43/00A61P 31/00A61P 37/02C12N 2310/14A61K 48/0008C12N 2320/32A61P 25/00C12N 15/1136A61P 9/10A61K 48/005C12N 15/88A61K 2039/55566A61P 35/00A61K 38/2013A61K 39/39
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Claims
Abstract
The invention provides compositions comprising a carrier comprising a continuous phase of a hydrophobic substance, liposomes, and a polynucleotide, and methods for using such compositions for delivering a polynucleotide to a subject.
Claims
exact text as granted — not AI-modified1 - 26 . (canceled)
27 . An injectable composition comprising:
a carrier comprising a continuous phase of oil; liposomes comprising a saturated or unsaturated phospholipid; and a polynucleotide encapsulated within said liposomes, said polynucleotide encoding a polypeptide and capable of being expressed in mammalian cells.
28 . The composition according to claim 27 , wherein the composition is a water-in-oil emulsion.
29 . The composition according to claim 27 , wherein said carrier is free of water.
30 . The composition according to claim 27 , wherein said oil comprises a natural oil, a synthetic oil or a combination thereof.
31 . The composition according to claim 27 , wherein said liposomes comprise cholesterol, dioleoyl phosphatidylcholine (DOPC), phosphoglycerol, phosphoethanolamine, phosphoserine, phosphocholine, phosphoinositol, phosphatidylcholine, lecithin, phosphatidylcholine and ascorbyl palmitate, 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP),1-[2-(oleoyloxy)ethyl]-2-oleyl-3-(2-hydroxyethyl)imidazolinium chloride (DOTIM), or combinations thereof.
32 . The composition according to claim 27 , further comprising an emulsifier.
33 . The composition according to claim 32 , wherein said emulsifier comprises mannide oleate, mannide monooleate, lecithin, polysorbate 80, sorbitan laurate, sorbitan monooleate, sorbitan sesquioleate, sorbitan trioleate, or combinations thereof.
34 . The composition according to claim 27 , further comprising an adjuvant.
35 . The composition according to claim 27 , wherein said polynucleotide is inserted in an expression plasmid or is contained in a bacterial or viral vector.
36 . The composition according to claim 27 , wherein said polynucleotide is present both encapsulated within said liposomes and exterior to said liposomes.
37 . The composition according to claim 34 , wherein said adjuvant is present: (a) within said liposomes; (b) exterior to said liposomes; or (c) both within said liposomes and exterior to said liposomes.
38 . The composition according to claim 27 , wherein said polypeptide is an antigen, an antibody or antibody fragment, an enzyme, a cytokine, a therapeutic protein, a chemokine, a regulatory protein, a structural protein, a chimeric protein, a nuclear protein, a transcription factor, a viral protein, a TLR protein, an interferon regulatory factor, an angiostatic or angiogenic protein, an apoptotic protein, an Fc gamma receptor, a hematopoietic protein, a tumor suppressor, a cytokine receptor, or a chemokine receptor.
39 . A method for delivering a polynucleotide to a subject, comprising administering the composition of claim 27 to said subject.
40 . The method according to claim 39 , wherein said subject is a human.
41 . A method for making a composition comprising:
(a) providing a polynucleotide that encodes a polypeptide and that is capable of being expressed in mammalian cells; (b) encapsulating said polynucleotide in liposomes comprising a saturated or unsaturated phospholipid; and (c) combining said liposomes with a carrier comprising a continuous phase of oil.
42 . The method according to claim 41 , wherein said liposomes are dehydrated before they are combined with said carrier.
43 . The method according to claim 41 , wherein said carrier is a water-in-oil emulsion.
44 . The method according to claim 41 , wherein said carrier is free of water.
45 . The method according to claim 41 , wherein said oil comprises a natural oil, a synthetic oil, or a combination thereof.
46 . The method according to claim 41 wherein said liposomes comprise cholesterol, dioleoyl phosphatidylcholine (DOPC), phosphoglycerol, phosphoethanolamine, phosphoserine, phosphocholine, phosphoinositol, phosphatidylcholine, lecithin, phosphatidylcholine and ascorbyl palmitate, 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP),1-[2-(oleoyloxy)ethyl]-2-oleyl-3-(2-hydroxyethyl)imidazolinium chloride (DOTIM), or combinations thereof.
47 . The method according to claim 41 , wherein said carrier comprises an emulsifier.
48 . The method according to claim 47 , wherein said emulsifier comprises mannide oleate, mannide monooleate, lecithin, polysorbate 80, sorbitan laurate, sorbitan monooleate, sorbitan sesquioleate, sorbitan trioleate, or combinations thereof.
49 . The method according to claim 41 , further comprising combining an adjuvant with said polynucleotides, said liposomes, or said carrier.
50 . The method according to claim 41 , wherein said polypeptide is an antigen, an antibody or antibody fragment, an enzyme, a cytokine, a therapeutic protein, a chemokine, a regulatory protein, a structural protein, a chimeric protein, a nuclear protein, a transcription factor, a viral protein, a TLR protein, an interferon regulatory factor, an angiostatic or angiogenic protein, an apoptotic protein, an Fc gamma receptor, a hematopoietic protein, a tumor suppressor, a cytokine receptor, or a chemokine receptor.
51 . A composition produced by the method according to claim 41 .
52 . The composition according to claim 27 , wherein said oil comprises, a vegetable oil, mineral oil, a nut oil, soybean oil, or combinations thereof.
53 . The method according to claim 41 , wherein said oil comprises, a vegetable oil, mineral oil, a nut oil, soybean oil, or combinations thereof.Cited by (0)
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