US2009181068A1PendingUtilityA1

Low Viscosity Liquid Polymeric Delivery System

Individually held — no corporate assignee on recordPriority: Jan 14, 2008Filed: Apr 10, 2008Published: Jul 16, 2009
Est. expiryJan 14, 2028(~1.5 yrs left)· nominal 20-yr term from priority
Inventors:Richard L. Dunn
A61P 35/00A61P 31/00A61P 25/18A61P 29/00A61L 31/16A61L 2300/604A61L 27/18A61L 31/14A61L 31/06A61L 27/54A61L 2300/43A61K 9/0024A61L 29/085A61K 31/485A61L 29/14A61L 27/58A61L 29/06A61L 2400/06A61L 29/16A61L 27/34A61K 31/445A61K 31/65A61L 31/10A61L 29/148A61L 31/148A61L 27/50A61L 2300/406A61L 2300/416A61K 33/243
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Claims

Abstract

Low viscosity biodegradable polymer solutions of a liquid biodegradable polymer and biocompatible solvent and methods of using the compositions to form a liquid polymer implant are provided.

Claims

exact text as granted — not AI-modified
1 . A liquid polymer composition, comprising:
 a biodegradable liquid polymer; and   a biocompatible organic solvent;   wherein the composition, when placed in contact with an aqueous medium or body fluid remains in a liquid form and does not form a solid in situ.   
     
     
         2 . The composition of  claim 1 , wherein the polymer is selected from the group consisting of polylactic acid, polyglycolic acid, polylactide, polyglycolide, polycaprolactones, polyanhydrides, polyamides, polyurethanes, polyesteramides, polyorthoesters, polydioxanones, polyacetals, polyketals, polycarbonates, polyphosphazenes, polyhydroxybutyrates, polyhydroxvalerates, polyalkylene oxalates, polyalkylene succinates, poly(malic acid), polyethylene glycol, hyaluronic acid, chitin, chitosan, and copolymers, terpolymers, and combinations or mixtures thereof. 
     
     
         3 . The composition of  claim 1 , wherein the polymer is a copolymer or terpolymer of any combination of lactide, glycolide, caprolactone, p-dioxanone, trimethylene carbonate, 1,5-dioxepan-2-one, 1,4-dioxepan-2-one, ethylene oxide, propylene oxide, sebacic anhydride, diketene acetals/diols, and lactic acid. 
     
     
         4 . The composition of  claim 1 , wherein the solvent is a hydrophilic organic solvent having a water solubility greater than 10% by weight of said solvent in water. 
     
     
         5 . The composition of  claim 4 , wherein the organic solvent is selected from the group consisting of N-methyl-2-pyrrolidone, 2-pyrrolidone, N-ethyl-2-pyrrolidone, N-cyclohexyl-2-pyrrolidone, N-hydroethyl-2-pyrrolidone, dimethyl acetamide, dimethyl formamide, acetic acid, lactic acid, ethanol, propanol, methyl lactate, ethyl lactate, methyl acetate, diethylene glycol monomethyl ether, glycofurol, glycerol formal, isopropylidene glycerol, dimethyl sulfoxide, ε-caprolactone, butyrolactone, propylene glycol, polyethylene glycol, glycerol, 1,3-butyleneglycol, methoxypolyethylene glycol, methoxypropylene glycol, acetone, methyl ethyl ketone, tetrahydrofuran, and combinations thereof. 
     
     
         6 . The composition of  claim 4 , wherein the solvent is selected from the group consisting of N-methyl-2-pyrrolidone, 2-pyrrolidone, dimethyl acetamide, dimethyl sulfoxide, ethyl lactate, glycofurol, glycerol formal, isopropylidene glycerol, propylene glycol, polyethylene glycol, methoxypolyethylene glycol, methoxypropylene glycol, and combinations thereof. 
     
     
         7 . The composition of  claim 1 , wherein the solvent is a lipophilic organic solvent having a water solubility less than 10% by weight of the solvent in water. 
     
     
         8 . The composition of  claim 7 , wherein the solvent is selected from the group consisting of ethyl acetate, ethyl butyrate, ethyl oleate, isopropyl palmitate, ethyl palmitate, methyl palmitate, isopropyl myristate, diethyl malonate, diethyl succinate, dimethyl adipate, dimethyl succinate, dibutyl sebacate, triacetin, triethyl citrate, tributyrin, acetyl triethyl citrate, acetyl tributyl citrate, acetyl trihexyl citrate, butyryl trihexyl citrate, tributyl citrate, caprylic/capric triglycerides, caprylic/capric/linoleic triglyceride, caprylic/capric/succinic triglyceride, propylene glycol dicaprylate/caprate, benzyl alcohol, ethyl benzoate, benzyl benzoate, propylene carbonate, dimethyl carbonate, N,N-diethyl-toluamide, N-dodecyl-2-pyrrolidone, N-octyl-2-pyrrolidone, N-methyl-2-caprolactam, N-dodecyl-caprolactam, heptanoic acid, oleic acid, sesame oil, peanut oil, castor oil, and combinations thereof. 
     
     
         9 . The composition of  claim 7 , wherein the solvent is selected from the group consisting of ethyl acetate, ethyl oleate, isopropyl myristate, triacetin, triethyl citrate, acetyl tributyl citrate, ethyl benzoate, benzyl benzoate, sesame oil, and combinations thereof. 
     
     
         10 . The composition of  claim 1 , wherein the solvent is a combination of a hydrophilic solvent and a lipophilic solvent. 
     
     
         11 . A composition, comprising:
 a pharmaceutically acceptable, biodegradable liquid polymer; and   a biocompatible organic solvent that is dissolvable or dispersible in situ in a body fluid;   wherein the composition when placed in a body forms a polymeric material having a liquid consistency which does not form into a solid in situ.   
     
     
         12 . The composition of  claim 11 , further comprising a therapeutically effective amount of a biologically active agent. 
     
     
         13 . The composition of  claim 12  wherein the biologically active agent is selected from the group consisting of cisplatin, carboplatin, anastozole, fulvestrant, exemestane, estradiol, testosterone, misoprostol, follicle-stimulating hormone, dustasteride, doxycycline, ciprofloxacin, quinolone, ivermectin, haloperidol, diazepam, risperidone, olanzapine, naltrexone, fentanyl, buprenorphine, butorphanol, loperamide, nafarelin, buserelin, histrelin, deslorelin, leuprolide, goserelin, triptorelin, ganirelix, abarelix, cetrorelix, teverelix, octreotide, lanreotide, human growth hormone, interferon-alpha, interferon-beta, interferon-gamma, interleukin, calcitonin, growth hormone releasing peptides, glucagon-like peptides, granulocyte-colony stimulating factor, nerve growth factor, platelet-derived growth factor, insulin-like growth factor, vascular endothelial growth factor, fibroblast growth factor, bone morphogenic protein, erythropoietin, and salts, complexes, prodrugs, and analogs thereof. 
     
     
         14 . The composition of  claim 11 , wherein the polymer is a liquid at 25° C. up to 37° C. 
     
     
         15 - 23 . (canceled) 
     
     
         24 . A kit comprising in association:
 a container of a pharmaceutically acceptable, biodegradable liquid polymer; and   a container of a biocompatible organic solvent that is dissolvable or dispersible in situ in a body fluid;   wherein the liquid polymer and the organic solvent when combined, will form a liquid composition which, when placed in contact with a body fluid, will form a polymeric implant having a liquid consistency which does not form into a solid in situ; and   directions for preparation and administration of the liquid composition to form the polymeric implant.   
     
     
         25 . The kit of  claim 24 , further comprising a container of a therapeutically effective amount of a biologically active agent;
 wherein the biologically active agent, when combined in the liquid composition and placed in contact with the body fluid will be released into the body as the polymeric implant biodegrades within the body.   
     
     
         26 . The kit of  claim 24 , further comprising a container of a therapeutically effective amount of a biologically active agent in a pharmaceutically acceptable carrier or diluent;
 wherein the biologically active agent, when combined in the liquid composition and placed in contact with body fluid will be released into the body as the polymeric implant biodegrades within the body.   
     
     
         27 . A kit comprising in association:
 a container of a liquid composition comprising a pharmaceutically acceptable, biodegradable liquid polymer dissolved in a biocompatible organic solvent that is dissolvable or dispersible in situ in a body fluid;   wherein the liquid composition, when placed in contact with body fluid, will form a polymeric implant having a liquid consistency which does not form into a solid in situ; and   directions for administration of the liquid composition to form the polymeric implant.   
     
     
         28 . The kit of  claim 27 , further comprising a container of a therapeutically effective amount of a biologically active agent;
 wherein the biologically active agent, when combined in the liquid composition and placed in contact with body fluid will be released as the polymeric implant biodegrades within the body.   
     
     
         29 . A kit comprising in association:
 a container of a liquid composition comprising a pharmaceutically acceptable, biodegradable liquid polymer dissolved in a biocompatible organic solvent that is dissolvable or dispersible in situ in a body fluid, and a biologically active agent;   wherein the liquid composition, when placed in contact with body fluid, will form a polymeric implant having a liquid consistency which does not form into a solid in situ; and the biologically active agent will be released into the body as the polymeric implant biodegrades within the body; and   directions for administration of the liquid composition to form the polymeric implant.   
     
     
         30 . The composition of  claim 12 , wherein the biologically active agent is released from the polymeric material as the polymeric material biodegrades.

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