US2013142939A1PendingUtilityA1

Methods of Forming Coatings with a Crystalline or Partially Crystalline Drug for Implantable Medical Devices using Sonocrystallization

Assignee: ADVANCED CARDIOVASCULAR SYSTEMPriority: Mar 22, 2004Filed: Dec 18, 2012Published: Jun 6, 2013
Est. expiryMar 22, 2024(expired)· nominal 20-yr term from priority
A61L 2420/08A61L 31/16A61L 2300/416A61L 2420/02A61L 2300/63B05D 5/00A61L 2300/606A61L 31/10A61F 2/82
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Claims

Abstract

Methods for making coatings on an implantable device such as a drug-eluting stent comprising a polymer and nano or microparticles of a drug in slow-dissolving polymorph, implantable devices produced by the methods and methods of using the coatings are provided.

Claims

exact text as granted — not AI-modified
1 . A method of forming a coating comprising nano-particles or microparticles of a drug in slow-dissolving polymorph on an implantable device, comprising:
 a) forming a coating on an implantable device comprising a drug and a polymeric material, and   b) inducing sonocrystallization of the drug by applying an ultrasound to the coating to form nano-particles or microparticles of the drug in slow-dissolving polymorph.   
     
     
         2 . The method of  claim 1 , wherein the polymeric material is selected from the group consisting of poly(ethylene glycol terephthalate)-co-poly(butylene terephthalate), hyaluronic acid, poly(ethylene glycol), phosphoryl choline, poly(amide ester), poly(D,L-lactide), polyhydroxyalkanoate, polycaprolactone, poly(vinylidene fluoride), poly(hexafluoro propylene), poly(ethylene vinyl alcohol), and combinations thereof. 
     
     
         3 . The method of  claim 2 , wherein the drug is selected from the group consisting of ABT-578™, paclitaxel, docetaxel, paclitaxel derivatives, tacrolimus, pimecrolimus, batimastat, mycophenolic acid, estradiol, clobetasol, dexamethasone, rapamycin, everolimus, 40-O-(3-hydroxy)propyl-rapamycin, 40-O-[2-(2-hydroxy)ethoxy]ethyl-rapamycin, 40-O-tetrazole-rapamycin, 4-amino-2,2,6,6-tetramethylpiperidine-1-oxyl (4-amino-TEMPO), and combinations thereof. 
     
     
         4 . The method of  claim 1 , wherein the crystallinity of the drug is selected from the group consisting of about 30%, about 40%, about 50%, about 60%, about 70%, about 75%, about 80%, about 90%, about 95%, about 99%, and about 100%. 
     
     
         5 . The method of  claim 1 , wherein the drug is everolimus and the polymer is poly(ethylene glycol terephthalate)-co-poly(butylene terephthalate). 
     
     
         6 . The method of  claim 1 , wherein the implantable medical device is a stent. 
     
     
         7 . The method of  claim 3 , wherein the implantable medical device is a stent. 
     
     
         8 . The method of  claim 5 , wherein the implantable medical device is a stent.

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