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filingDate 2002-05-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a4312a7b35719c8892121be20961aa1b
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publicationDate 2003-11-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2003207907-A1
titleOfInvention Delivery of microparticle-conjugated drugs for inhibition of stenosis
abstract Administration of a formulation comprising a antirestenotic compound conjugated to a microparticle carrier is effective to inhibit stenosis formation in a blood vessel. Such stenosis typically results, in the absence of treatment, from trauma to a vessel, such as an incision, excessive pressure, or an angioplasty procedure. The antirestenotic compound is typically an antiproliferative, immunosuppressive, or antiinflammatory drug, such as rapamycin, tacrolimus, paclitaxel, dexamethasone, or an active analog or derivative, or combinations thereof. The microparticle carrier comprises a suspension of gas-filled microbubbles or biocompatible polymeric microparticles, in a pharmaceutically acceptable liquid vehicle, and is effective to deliver the conjugated therapeutic to the site of vessel injury.
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID414396
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID433322218
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5472

Total number of triples: 308.