US2009270317A1PendingUtilityA1

Pharmaceutical compositions comprising bioelastomer fusion proteins

Assignee: CHILKOTI ASHUTOSHPriority: Mar 19, 1999Filed: Sep 3, 2008Published: Oct 29, 2009
Est. expiryMar 19, 2019(expired)· nominal 20-yr term from priority
A61K 41/00C07K 16/1232B82Y 30/00A61K 47/58A61P 35/00
75
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Claims

Abstract

Bioelastomers are disclosed for use in methods of binding compounds including immunoassay methods, in biosensors and methods or regenerating biosensors, and in methods for targeting the delivery of a compound to a particular location within an animal subjects. In general, the bioelastomer is conjugated to a binding compound, which is in turn used to bind a compound of interest. For targeted compound delivery, the bioelastomer is conjugated to the compound to be delivered.

Claims

exact text as granted — not AI-modified
1 - 68 . (canceled) 
   
   
       69 . A pharmaceutical composition comprising a therapeutically effective amount of a fusion protein and a pharmaceutically acceptable carrier,
 the composition formulated for systemic administration by injection, and the fusion protein comprising a bioelastic protein and at least one therapeutic protein or peptide,   wherein the fusion protein is in soluble form at physiological conditions.   
   
   
       70 . The pharmaceutical composition of  claim 69 , wherein the bioelastic protein is fused to the C-terminus of the therapeutic protein or peptide. 
   
   
       71 . The pharmaceutical composition of  claim 69 , wherein the bioelastic protein has a molecular weight of from about 24.3 to about 71 kDa. 
   
   
       72 . The pharmaceutical composition of  claim 71 , wherein the bioelastic protein has a molecular weight of about 50 kDa. 
   
   
       73 . The pharmaceutical composition of  claim 69 , wherein the bioelastic protein has a transition temperature under physiological conditions of from about 37° C. to about 60° C. 
   
   
       74 . The pharmaceutical composition of  claim 69 , wherein the bioelastic protein has a transition temperature under physiological conditions of about 40 to 42° C. 
   
   
       75 . The pharmaceutical composition of  claim 69 , wherein the bioelastic protein forms a beta-spiral structure. 
   
   
       76 . The pharmaceutical composition of  claim 69 , wherein the bioelastic protein comprises repeats of the sequence Val-Pro-Gly-X-Gly, where each X is an independently selected amino acid. 
   
   
       77 . The pharmaceutical composition of  claim 76 , wherein X is independently selected from valine, alanine, and glycine. 
   
   
       78 . The pharmaceutical composition of  claim 76 , wherein the bioelastic protein has the formula (VPGXG) n , where n is greater than 100. 
   
   
       79 . The pharmaceutical composition of  claim 69 , wherein the therapeutic protein or peptide is an antibody or hormone sequence. 
   
   
       80 . The pharmaceutical composition of  claim 69 , wherein the composition is formulated for systemic administration by subcutaneous injection, intradermal injection, intravenous injection, or intramuscular injection. 
   
   
       81 . The pharmaceutical composition of  claim 69 , wherein the pharmaceutically acceptable carrier comprises a buffered aqueous solution. 
   
   
       82 . The pharmaceutical composition of  claim 69 , wherein the pharmaceutically acceptable carrier comprises a non-aqueous liquid. 
   
   
       83 . The pharmaceutical composition of  claim 69 , wherein the pharmaceutically acceptable carrier comprises a water-in-oil emulsion or an oil-in-water emulsion. 
   
   
       84 . The pharmaceutical composition of  claim 69 , wherein the composition is isotonic with human blood. 
   
   
       85 . A method for treating a patient comprising, administering the pharmaceutical composition of  claim 69  to a patient in need of said therapeutic protein or peptide.

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