US2011293733A1PendingUtilityA1

Self-assembling nanoparticle drug delivery system

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Assignee: DE LOS RIOS MIGUEL APriority: May 25, 2004Filed: Apr 13, 2011Published: Dec 1, 2011
Est. expiryMay 25, 2024(expired)· nominal 20-yr term from priority
A61P 3/10A61P 31/12A61P 9/12A61P 7/02A61P 7/00A61P 7/04A61P 9/10A61P 3/06A61P 9/00A61P 37/02A61P 35/00A61P 9/06A61P 37/06A61P 3/08A61P 25/04A61P 31/00A61P 3/02A61P 25/08A61P 25/20A61P 25/18A61P 29/00A61P 25/24A61P 25/16A61P 31/04A61P 31/10A61P 25/00A61P 25/22A61P 25/06Y10S977/802A61P 11/08Y10S977/797A61P 19/02C07K 2319/00Y10S977/80C12N 2730/10122A61P 1/08A61P 11/00A61P 19/06C12N 7/00Y10S977/801A61K 9/5192A61P 1/04A61K 47/6901A61K 9/5184B82Y 5/00A61K 9/1277Y10S977/798C12N 2730/10123A61K 47/6913Y10S977/795A61P 11/06A61P 17/04C07K 14/005
51
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Claims

Abstract

A self-assembling nanoparticle drug delivery system for the delivery of drugs including peptides, proteins, nucleic acids or synthetic chemical drugs is provided. The self-assembling nanoparticle drug delivery system described herein includes viral capsid proteins, such as Hepatitis B Virus core protein, encapsulating the drug, a lipid bi-layer envelope and targeting or facilitating molecules anchored in the lipid bilayer. A method for construction of the self-assembling nanoparticle drug delivery system is also provided.

Claims

exact text as granted — not AI-modified
1 .- 13 . (canceled) 
     
     
         14 . A method for constructing a self-assembling nanoparticle drug delivery system comprising:
 mixing a drug with a hepatitis B virus (HBV) core protein to form a cage solution;   encapsulating said drug in a capsid comprised of HBV core protein by raising the ionic strength of said cage solution to form a nanoparticle; and   purifying said nanoparticles.   
     
     
         15 . The method of  claim 14  wherein said drug is selected from the group consisting of peptides, proteins, nucleic acids and small molecule synthetic chemical drugs. 
     
     
         16 . The method of  claim 30 , wherein said HBV core protein includes a protease recognition site replacing amino acids 79 and 80 of SEQ ID NO: 1 or SEQ ID NO: 2. 
     
     
         17 . The method of  claim 16  wherein said protease recognition site is a thrombin recognition site or a factor Xa recognition site. 
     
     
         18 . The method of  claim 30 , wherein said HBV core protein is mutated such that at least one amino acid of SEQ ID NO: 1 or SEQ ID NO: 2 selected from the group consisting of phenylalanine 23, aspartic acid 29, threonine 33, leucine 37, valine 120, valine 124, arginine 127, tyrosine 132, glutamic acid 77, aspartic acid 78 and alanine 80 is changed to a cysteine. 
     
     
         19 . The method of  claim 14  further comprising adding an envelopment guiding protein or peptide after said encapsulating step. 
     
     
         20 . The method of  claim 19  wherein said envelopment guiding protein is Hepatitis B Virus S-protein or the transmembrane engineered peptide of SEQ ID NO:5. 
     
     
         21 . The method of  claim 25 , wherein said phospholipid is selected from the group consisting of: phosphatidyl ethanolamine, phosphatidyl glycerol and hydrogenated soy phosphatidyl choline. 
     
     
         22 . The method of  claim 27 , said protein transduction domain comprises the Human Immunodeficiency Virus transactivator or polyarginine. 
     
     
         23 . The method of  claim 25 , further comprising inserting targeting antibodies into said lipid envelope. 
     
     
         24 . (canceled) 
     
     
         25 . The method of  claim 14 , further comprising adding phospholipid to said cage solution to form a lipid envelope surrounding the nanoparticle. 
     
     
         26 . The method of  claim 14 , further comprising adding a cholesterol-tagged polyethylene glycol to said cage solution. 
     
     
         27 . The method of  claim 25 , further comprising adding a cholesterol-tagged protein transduction domain to said cage solution. 
     
     
         28 . The method of  claim 14 , wherein the nanoparticle is purified by centrifugation. 
     
     
         29 . The method of  claim 14 , wherein the nanoparticle is purified by size exclusion chromatography. 
     
     
         30 . The method of  claim 14 , wherein the HBV core protein comprises the amino acid sequence of SEQ ID NO: 1 or SEQ ID NO: 2. 
     
     
         31 . The method of  claim 14 , wherein the HBV core protein is a modified HBV core protein. 
     
     
         32 . The method of  claim 30 , wherein the glutamic acid at amino acid 77 of SEQ ID NO: 1 or SEQ ID NO: 2 is changed to a cysteine. 
     
     
         33 . The method of  claim 25 , wherein the lipid envelope is covalently attached to said nanoparticle by a phosphatidyl-ethanolamine maleimide to the cysteine acid 77 of SEQ ID NO: 1 or SEQ ID NO: 2.

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