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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c902faf6ae746c51fc8010672fc22894
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4433
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-366
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-107
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-48
filingDate 1998-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_84116af137f4c5de71f0906ba774b73a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1bede2f5d82175d4a7f82882f291ec29
publicationDate 2000-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CZ-2000158-A3
titleOfInvention Pharmaceutical compositions in the form of a self-emulsifying formulation for lipophilic compounds
abstract Pharmaceutical composition based on the use of certain oilyna phase that contains pyranone compounds asna pharmaceutically active substance, a mixture of diglyceride andnmonoglyceride in a ratio of from about 9: 1 to about 6: 4n(diglyceride: monoglyceride), wherein the diglyceride is amonoglyceridenare unsaturated fatty acid mono- or di-esters andnglycerol of sixteen to twenty-two carbon atomsnin the chain, one or more pharmaceutically acceptablena solvent and one or more pharmaceutically acceptablena surfactant. Composition in the formna self-emulsifying formulation that ensures highnconcentration and high oral bioavailability fornlipophilic pyran compounds having an inhibitory effect onnretroviral proteases are useful in the treatment of AIDS.
priorityDate 1998-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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