http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2003138496-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-145
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-26
filingDate 2002-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_69b6f8b30aeba84d09fcb8902aa30b24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_711f81ec5ce09bb1264a0fa0ae9fa18a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a32d35914af3cd49913202edbaa6938a
publicationDate 2003-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2003138496-A1
titleOfInvention Drug delivery system for enhanced bioavailability of hydrophobic active ingredients
abstract The present invention provides a drug delivery system for the oral administration of a hydrophobic active ingredient. The active ingredient's post-ingestion dissolution rate and its corresponding bioavailability can be optimized by intimately mixing a micronized hydrophobic drug with suitably sized inert particles to a dispersion that will facilitate desired bioavailability. In a particular embodiment, the hydrophobic active ingredient is fenofibrate. Suitably sized inert particles include microcrystalline cellulose and lactose. Dispersion may be monitored by microscopic visualization.
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type http://data.epo.org/linked-data/def/patent/Publication

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