http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100288890-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K47-34
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-495
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-10
filingDate 1998-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2001-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_49721db4a69bc2544a1c62fe65ef2d7b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_32d7ec35115f2d4c8a5cb9d0c3f3fe0c
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publicationDate 2001-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100288890-B1
titleOfInvention Itraconazole oral preparation and preparation method thereof
abstract The present invention was prepared by dissolving, dispersing and spray-drying 0.5 to 5.0 parts by weight of pH-dependent and inert water-soluble polymer in one or more solvents selected from methylene chloride, chloroform, ethanol and methanol in 1 part of itraconazole to form a solid dispersion. The present invention relates to an itraconazole oral preparation having improved bioavailability. In other words, in the present invention, in the preparation of oral dosage form of poorly soluble itraconazole in water, the pharmaceutical composition is dispersed and spray-dried using a pH-dependent water-soluble polymer that has a characteristic of rapidly dissolving at a low pH and eluting in a short time. The present invention relates to an itraconazole oral preparation and a method for preparing the same, which greatly improve solubility and elute rapidly regardless of food intake, thereby improving the bioavailability of itraconazole.
priorityDate 1997-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 39.