US2008038361A1PendingUtilityA1

Water-Soluble Nanoparticles Stabilized with Multi-Functional Group Ligands and Method of Preparation Thereof

Assignee: UNIV YONSEI SEOULPriority: Sep 3, 2004Filed: Sep 30, 2004Published: Feb 14, 2008
Est. expirySep 3, 2024(expired)· nominal 20-yr term from priority
A61P 43/00A61P 35/00Y10S977/795A61K 49/1836A61K 49/1875Y10S977/896B82Y 5/00A61K 47/6923Y10S977/81A61K 49/1839A61K 49/1866A61K 47/6929Y10S977/773Y10S977/811B82B 3/00B82Y 30/00
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Claims

Abstract

Disclosed are water-soluble nanoparticles. The water-soluble nanoparticles are each surrounded by a multifunctional group ligand including an adhesive region, a cross linking region, and a reactive region. In the water-soluble nanoparticles, the cross-linking region of the multifunctional group ligand is cross-linked with another cross-linking region of a neighboring multifunctional group ligand. Furthermore, the present invention provides a method of producing water-soluble nanoparticles, which includes (1) synthesizing water-insoluble nanoparticles in an organic solvent, (2) dissolving the water insoluble nanoparticles in a first solvent and dissolving water-soluble multifunctional group ligands in a second solvent, (3) mixing the two solutions from the step (2) to substitute surfaces of the water-insoluble nanoparticles with the multifunctional group ligands and dissolving a mixture in an aqueous solution to conduct a separation process, and (4) cross-linking the substituted multifunctional group ligands with each other.

Claims

exact text as granted — not AI-modified
1 . Water-soluble nanoparticles, which are each surrounded by a multifunctional group ligand (L I -L II -L III ) including an adhesive region (L I ), a cross-linking region (L II ), and a reactive region (L III ), and in which the cross-linking region of the multifunctional group ligand is cross-linked with another cross-linking region of a neighboring multifunctional group ligand.  
     
     
         2 . The water-soluble nanoparticles as set forth in  claim 1 , wherein each of the nanoparticles includes a metal, a metal chalcogenide, a magnetic material, a magnetic alloy, a semiconductor material, or a multicomponent mixed structure, and each of them has a diameter of 1-1000 nm.  
     
     
         3 . The water-soluble nanoparticles as set forth in  claim 2 , wherein the metal is selected from the group consisting of Pt, Pd, Ag, Cu, Ru, Rh, Os and Au.  
     
     
         4 . The water-soluble nanoparticles as set forth in  claim 2 , wherein the metal chalcogenide is selected from the group consisting of M x E y  (M=Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zr, Mo, Ru, Rh, Ag, W, Re, Ta, Zn; E=O, S, Se, 0<x≦3, 0<y≦5), BaSr x Ti 1-x O 3 , PbZr x Ti 1-x O 3  (0≦x≦1), and SiO 2 .  
     
     
         5 . The water-soluble nanoparticles as set forth in  claim 2 , wherein the magnetic material is selected from the group consisting of Co, Mn, Fe, Ni, Gd, MM′ 2 O 4 , M x O y  (M or M′=Co, Fe, Ni, Mn, Zn, Gd, Cr, 0<x≦3, 0<y≦5).  
     
     
         6 . The water-soluble nanoparticles as set forth in  claim 2 , wherein the magnetic alloy is selected from the group consisting of CoCu, CoPt, FePt, CoSm, CoAu, CoAg, CoPtAu, CoPtAg, NiFe and NiFeCo.  
     
     
         7 . The water-soluble nanoparticles as set forth in  claim 2 , wherein the semiconductor material is a first semiconductor material consisting of an element selected from a group II and an element selected from a group VI, a second semiconductor material consisting of an element selected from a group III and an element selected from a group V, a third semiconductor material consisting of a group IV, a fourth semiconductor material consisting of an element selected from the group IV and an element selected from the group VI, or a fifth semiconductor material consisting of an element selected from the group V and an element selected from the group VI.  
     
     
         8 . The water-soluble nanoparticles as set forth in  claim 2 , wherein the multicomponent mixed structure includes two or more components selected from the group consisting of the metal, the metal chalcogenide, the magnetic material, the magnetic alloy, and the semiconductor according to selected from the group of Pt, Pd, Ag, Cu, Ru, Rh, Os, and Au, and has a core-shell or bar code shape.  
     
     
         9 . The water-soluble nanoparticles as set forth in  claim 1 , wherein the adhesive region (L I ) includes a functional group selected from the group consisting of —COOH, —NH 2 , —SH, —CONH 2 , —PO 3 H, —PO 4 H, —SO 3 H, —SO 4 H, and —OH.  
     
     
         10 . The water-soluble nanoparticles as set forth in  claim 1 , wherein the cross-linking region (L II ) includes a functional group selected from the group consisting of —SH, —NH 2 , —COOH, —OH, epoxy, -ethylene, and -acetylene.  
     
     
         11 . The water-soluble nanoparticles as set forth in  claim 1 , wherein the reactive region (L III ) includes a functional group selected from the group consisting of —SH, —COOH, —NH 2 , —OH, —NR 4   + X − , -sulfonate, -nitrate, and phosphonate.  
     
     
         12 . The water-soluble nanoparticles as set forth in  claim 1 , wherein the active component is selected from the group consisting of a bioactive component, a polymer, and an inorganic supporter.  
     
     
         13 . The water-soluble nanoparticles as set forth in  claim 12 , wherein the bioactive component is selected from the group consisting of an antigen, an antibody, RNA, DNA, hapten, avidin, streptavidin, protein A, protein G, lectin, selectin, an anticancer drug, an antibiotic drug, a hormone, a hormone antagonist, interleukin, interferon, a growth factor, a tumor necrosis factor, endotoxin, lymphotoxin, urokinase, streptokinase, a tissue plasminogen activator, a protease inhibitor, alkyl phosphocholine, a component indicated by a radioactive isotope, a surfactant, a cardiovascular pharmaceutical, a gastrointestinal pharmaceutical, and a neuro pharmaceutical.  
     
     
         14 . The water-soluble nanoparticles as set forth in  claim 12 , wherein the polymer is selected from the group consisting of polyphosphazene, polylactide, polylactide-co-glycolide, polycaprolactone, polyanhydride, polymaleic acid and derivatives thereof, polyalkylcyanoacrylate, polyhydroxybutylate, polycarbonate, polyorthoester, polyethylene glycol, poly-L-lycine, polyglycolide, polymethylmethacrylate, and polyvinylpyrrolidone.  
     
     
         15 . The water-soluble nanoparticles as set forth in  claim 12 , wherein the inorganic supporter is selected from the group consisting of silica (SiO 2 ), titania (TiO 2 ), indium tin oxide (ITO), a carbon material, a semiconductor substrate, and a metal substrate.  
     
     
         16 . The water-soluble nanoparticles as set forth in  claim 1 , wherein the multifunctional group ligand is a peptide containing at least one amino acid having —SH, —COOH, —NH 2 , or —OH as a branched chain.  
     
     
         17 . The water-soluble nanoparticles as set forth in  claim 16 , wherein the peptide contains any one of amino acid sequences described in SEQ ID Nos. 1 to 3.  
     
     
         18 . The water-soluble nanoparticles as set forth in  claim 1 , wherein the multifunctional group ligand is a compound, which includes —COOH as a functional group of the adhesive region (L I ), —SH as a functional group of the cross-linking region (L II ), and —COOH or —SH as a functional group of the reactive region (L III ).  
     
     
         19 . The water-soluble nanoparticles as set forth in  claim 18 , wherein the compound is selected from the group consisting of dimercaptosuccinic acid, dimercaptomaleic acid, and dimercaptopentadionic acid.  
     
     
         20 . The water-soluble nanoparticles as set forth in  claim 1 , wherein the multifunctional group ligand is combined with a biodegradable polymer.  
     
     
         21 . The water-soluble nanoparticles as set forth in  claim 20 , wherein the biodegradable polymer is selected from the group consisting of polyphosphazene, polylactide, polylactide-co-glycolide, polycaprolactone, polyanhydride, polymaleic acid and derivatives thereof, polyalkylcyanoacrylate, polyhydroxybutylate, polycarbonate, polyorthoester, polyethylene glycol, poly-L-lycine, polyglycolide, polymethylmethacrylate, and polyvinylpyrrolidone.  
     
     
         22 . A method of producing water-soluble nanoparticles, comprising: 
 (1) synthesizing water-insoluble nanoparticles in an organic solvent;    (2) dissolving the water-insoluble nanoparticles in a first solvent and dissolving water-soluble multifunctional group ligands in a second solvent;    (3) mixing two solutions in the step (2) to substitute surfaces of the water-insoluble nanoparticles with the multifunctional group ligands and dissolving a mixture in an aqueous solution to conduct a separation process; and    (4) cross-linking the substituted multifunctional group ligands with each other.    
     
     
         23 . The method as set forth in  claim 22 , wherein the water-insoluble nanoparticles of the step (1) are produced through a chemical reaction of a nanoparticle precursor in an organic solvent containing a surface stabilizer.  
     
     
         24 . The method as set forth in  claim 23 , wherein the water-insoluble nanoparticles are produced according to a process which comprises adding the nanoparticle precursor to the organic solvent containing the surface stabilizer at 10-600° C., maintaining the resulting solvent under temperature and time conditions suitable for making the desired water-insoluble nanoparticles to chemically react the nanoparticle precursor and thus grow the nanoparticles, and separating and purifying the nanoparticles.  
     
     
         25 . The method as set forth in  claim 22 , wherein the organic solvent is selected from the group consisting of a benzene-based solvent, a hydrocarbon solvent, an ether-based solvent, and a polymer solvent.  
     
     
         26 . The method as set forth in  claim 22 , wherein the first solvent in the step (2) is selected from the group consisting of a benzene-based solvent, a hydrocarbon solvent, an ether-based solvent, halohydrocarbon, alcohol, a sulfoxide-based solvent, and an amide-based solvent.  
     
     
         27 . The method as set forth in  claim 22 , wherein the second solvent in the step (2) is selected from the group consisting of a benzene-based solvent, a hydrocarbon solvent, an ether-based solvent, halohydrocarbon, alcohol, a sulfoxide-based solvent, an amide-based solvent, and water.

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