US2015165047A1PendingUtilityA1

Compositions and methods of delivery of pharmacological agents

Assignee: ABRAXIS BIOSCIENCE LLCPriority: Dec 9, 2002Filed: Feb 19, 2015Published: Jun 18, 2015
Est. expiryDec 9, 2022(expired)· nominal 20-yr term from priority
A61P 37/06A61P 43/00A61P 39/02A61P 9/00A61P 9/10A61P 9/04A61P 29/00A61P 31/04A61P 35/00A61P 23/00A61P 19/02A61K 31/337B82Y 5/00A61K 31/427A61K 31/16A61K 9/0078A61K 47/18Y10S977/911A61K 31/7048A61K 9/146A61K 9/1075A61K 47/42A61K 31/165A61K 47/32A61K 9/107A61K 31/436A61K 38/13A61K 31/00Y10S977/705A61K 31/343Y10S977/779Y10S977/773A61K 31/355A61K 31/164Y10S977/906A61K 31/198A61K 31/4745A61K 9/19A61K 9/0019A61K 31/24A61K 9/51A61K 31/05
60
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

The present invention relates to a pharmaceutical composition comprising a pharmaceutical agent and a pharmaceutically acceptable carrier, which carrier comprises a protein, for example, human serum albumin and/or deferoxamine. He human serum albumin is present in an amount effective to reduce one or more side effects associated with administration of the pharmaceutical composition. The inventor also provides methods for reducing on or more side effects of administration of the pharmaceutical composition, and methods for enhancing transport and binding of a pharmaceutical agent to a cell.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A pharmaceutical composition comprising a pharmaceutical agent and a pharmaceutically acceptable carrier, wherein the pharmaceutically acceptable carrier comprises albumin in an amount effective to reduce one or more side effects of administration of the pharmaceutical composition into a human, and wherein the pharmaceutically acceptable carrier comprises deferoxamine in an amount effective to inhibit microbial growth in the pharmaceutical composition. 
     
     
         2 . The pharmaceutical composition of  claim 1 , wherein the pharmaceutical agent is selected from the group consisting of anticancer agents, anesthetics, antimicrotubule agents, agents to treat cardiovascular disorders, antihypertensives, anti-inflammatory agents, anti-arthritic agents, antiasthmatics, analgesics, vasoactive agents, immunosuppressive agents, antifungal agents, antiarrhythmic agents, antibiotics, and hormones. 
     
     
         3 . The pharmaceutical composition of  claim 2 , wherein the pharmaceutical agent is selected from the group consisting of paclitaxel, docetaxel, taxanes, camptothecin, propofol, amiodarone, cyclosporine, rapamycin, amphotericin, liothyronine, epothilones, colchicines, thyroid hormones, vasoactive intestinal peptide, corticosteroids, melatonin, tacrolimus, mycophenolic acids, and derivatives thereof. 
     
     
         4 . The pharmaceutical composition of  claim 3 , wherein the pharmaceutical agent is propofol. 
     
     
         5 . The pharmaceutical composition of  claim 1 , wherein the pharmaceutical composition is a liquid and comprises from about 0.1% to about 25% by weight of albumin. 
     
     
         6 . The pharmaceutical composition of  claim 5 , wherein the pharmaceutical composition comprises about 0.5% to about 5% by weight of albumin. 
     
     
         7 . The pharmaceutical composition of  claim 5 , wherein the pharmaceutical composition is dehydrated. 
     
     
         8 . The pharmaceutical composition of  claim 6 , wherein the pharmaceutical composition is lyophilized. 
     
     
         9 . The pharmaceutical composition of  claim 1 , wherein the pharmaceutical composition comprises a mesylate salt of deferoxamine. 
     
     
         10 . The pharmaceutical composition of  claim 9 , wherein the pharmaceutical composition is a liquid and comprises from about 0.0001% to about 0.5% by weight of deferoxamine mesylate. 
     
     
         11 . The pharmaceutical composition of  claim 10 , wherein the pharmaceutical composition comprises about 0.1% by weight of deferoxamine mesylate. 
     
     
         12 . The pharmaceutical composition of  claim 10 , wherein the pharmaceutical composition is dehydrated. 
     
     
         13 . The pharmaceutical composition of  claim 12 , wherein the pharmaceutical composition is lyophilized. 
     
     
         14 . The pharmaceutical composition of  claim 1 , wherein the pharmaceutical composition is an oil-in-water emulsion. 
     
     
         15 . The pharmaceutical composition of  claim 5 , wherein the pharmaceutical agent is propofol. 
     
     
         16 . The pharmaceutical composition of  claim 10 , wherein the pharmaceutical agent is propofol. 
     
     
         17 . The pharmaceutical composition of  claim 9 , wherein the pharmaceutical agent is propofol, the propofol is present in an amount from about 0.1% to about 5% by weight, the albumin is present in an amount from about 0.1% to about 25% by weight, and the deferoxamine mesylate is present in an amount from about 0.0001% to about 0.5% by weight.

Join the waitlist — get patent alerts

Track US2015165047A1 — get alerts on status changes and closely related new filings.

We store only your email — no account needed. See our privacy policy.