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AssigneeNorthwestern University
InventorsC. Shad Thaxton, Chad A. Mirkin, Kaylin McMahon, Sushant Tripathy, Raja Kannan Mutharasan, David M. Leander, Andrea J. Luthi
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Articles, compositions, kits, and methods relating to nanostructures, including synthetic nanostructures, are provided. Certain embodiments described herein include structures having a core-shell type arrangement; for instance, a nanostructure core may be surrounded by a shell including a material, such as a lipid bilayer, and may include other components such as oligonucleotides. In some embodiments, the structures, when introduced into a subject, can be used to deliver nucleic acids and/or can regulate gene expression. Accordingly, the structures described herein may be used to diagnose, prevent, treat or manage certain diseases or bodily conditions. In some cases, the structures are both a therapeutic agent and a diagnostic agent.
A structure comprising:
A structure comprising:
A structure comprising:
A nanostructure comprising an oligonucleotide adapted to regulate gene expression, a lipid, and an apolipoprotein.
A nanostructure comprising an oligonucleotide adapted to regulate gene expression and apolipoprotein A1.
A method comprising:
A pharmaceutical composition, comprising:
A kit for diagnosing, preventing, treating or managing a disease or bodily condition comprising:
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the structure has a binding constant to cholesterol, Ka, of less than or equal to about 10 mM.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the oligonucleotide is able to regulate gene expression.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the shell substantially surrounds the nanostructure core.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the shell comprises a lipid.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the shell comprises a phospholipid.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the shell comprises a lipid monolayer.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the shell comprises a lipid bilayer.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the lipid bilayer comprises a phospholipid.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the lipid bilayer comprises 50-200 phospholipids.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the phospholipid comprises:
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the phospholipid comprises:
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein at least a portion of the lipid bilayer is covalently bound to the core.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein at least a portion of the lipid bilayer is physisorbed to the core.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the lipid bilayer comprises a plurality of hydrophilic groups pointing towards the core and a plurality of hydrophobic groups extending away from the core.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the lipid bilayer is attached to the nanostructure core through a thiol-metal bond.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the lipid bilayer is attached to the nanostructure core through an amino group.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, comprising a protein associated with at least a portion of the structure.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, comprising a protein associated with at least the outer surface of the shell.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the shell comprises a lipoprotein structure.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the shell comprises an apolipoprotein.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the shell comprises an apolipoprotein from a subject.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the apolipoprotein is apolipoprotein A-I, apolipoprotein A-II, or apolipoprotein E.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the structure has 1-6 apolipoproteins.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the structure comprises a density of Apo A-1 that is within 10% of the density of Apo A-1 on endogenous HDL.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the shell includes a first layer and second layer, and at least a portion of the apolipoprotein is positioned between the first and second layers.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the shell comprises a self-assembled monolayer of components.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the shell comprises a mixed layer of components.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the shell comprises a mixed layer of components comprising a thiol end-group.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the shell is substantially formed from components having a molecular weight of less than about 1,000 g/mol.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the shell is substantially formed from non-polymeric components.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the shell is substantially formed from components that are uncharged.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the shell comprises at least three layers.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the structure exhibits a binding affinity to macrophages and hepatocytes substantially equal to the binding affinity of endogenous HDL.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the structure has a largest cross-sectional dimension of less than or equal to about 50 nm.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the structure has a largest cross-sectional dimension of less than or equal to about 35 nm.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the structure has a largest cross-sectional dimension of less than or equal to about 30 nm.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the structure comprises a core that is hollow or at least partially hollow.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the core has a largest cross-sectional dimension of less than or equal to about 50 nm.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the core has a largest cross-sectional dimension of less than or equal to about 30 nm.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the core has a largest cross-sectional dimension of less than or equal to about 25 nm.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the core has a largest cross-sectional dimension of less than or equal to about 20 nm.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the core has a largest cross-sectional dimension of less than or equal to about 15 nm, less than or equal to about 10 nm, or less than or equal to about 5 nm.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the nanostructure core is an inorganic nanostructure.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the nanostructure core comprises an inorganic material.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the nanostructure core comprises a metal, or is substantially formed from a metal.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the nanostructure core comprises gold.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the nanostructure core comprises a semiconductor, or is substantially formed from a semiconductor.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the nanostructure comprises a polymer, or is substantially formed from a polymer.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the nanostructure core comprises a quantum dot.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the nanostructure is substantially spherical.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the nanostructure core is non-spherical.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the nanostructure is disk-shaped.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the nanostructure core is a nanotube.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the nanostructure core is a nanorod.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, further comprising a bioactive agent associated with the structure.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the bioactive agent includes one or more of an anti-inflammatory, a nucleic acid species, a chemotherapeutic, and a cholesterol agent.
A mixture of a plurality of structures as in any one of the preceding claims, the plurality of structures having a distribution of cross-sectional dimensions such that no more than about 20% of the structures have a cross-sectional dimension greater than about 20% of the average cross-sectional dimension.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the structure is adapted to sequester at least 5 molecules of cholesterol during use.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the cholesterol is esterified cholesterol.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the cholesterol is free cholesterol.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the structure comprises a contrast agent.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the shell comprises a contrast agent.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the nanostructure core comprises a contrast agent.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the structure comprises an enzyme.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the structure comprises lecithin-cholesterol acyltransferase.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the disease or bodily condition is associated with a cancer.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the disease or bodily condition is associated with inflammation.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the disease or bodily condition is associated with prostate cancer.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the disease or bodily condition comprises atherosclerosis.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the disease or bodily condition comprises hyperlipidemia.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the disease or bodily condition comprises a protein storage disease.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the disease or bodily condition comprises a disease of hemostasis.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the disease or bodily condition comprises a rheumatic disease.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the disease or bodily condition comprises a neurologic disease.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the composition is administered in a single or divided dose according to a dosing schedule.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, comprising a nucleic acid or oligonucleotide having a length of about 8 to about 500 nucleotides or base pairs in length, between about 10 to about 200 nucleotides or base pairs in length, about 10 to about 150 nucleotides or base pairs in length, about 10 to about 100 nucleotides or base pairs in length, about 10 to about 75 nucleotides or base pairs in length, or about 10 to about 50 nucleotides or base pairs in length.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the oligonucleotide is single stranded.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the oligonucleotide is double stranded.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the oligonucleotide comprises antisense DNA, siRNA, or microRNA.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, further comprising releasing at least a portion of the oligonucleotide from the structure.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the oligonucleotide is covalently or near-covalently bonded to the nanostructure core or to the shell.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the oligonucleotide is physisorbed onto a portion of the shell.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the oligonucleotide is covalently attached to cholesterol.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the oligonucleotide is modified with a lipid.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the oligonucleotide is cholesterylated.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the oligonucleotide comprises 5′-cholesteryl DNA or 3′-cholesteryl DNA.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the oligonucleotide, prior to attachment, has an end modified to include an alkylthiol.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the oligonucleotide is adapted and arranged to modulate expression of a target by at least about 50%, at least about 60%, at least about 70%, at least about 80%, or at least about 90% when contacted with a biological sample or patient under physiological conditions and at a concentration where a nonsense or sense control has little or no effect.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the structure is both a therapeutic and a diagnostic agent.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the structure is adapted to deliver therapeutic oligonucleotides and/or is adapted to be used as an intracellular diagnostic sensor.
A structure, pharmaceutical composition, kit, or method as in any one of the preceding claims, wherein the oligonucleotide comprises a fluorophore that is adapted to change in fluorescence intensity upon binding to a target protein or a small molecule.
Dependencies are inferred from the claim text.