http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20050121497-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e22d43b06453ae5bbc004fb2735d2508 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-2013 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-496 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-0053 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-496 |
| filingDate | 2004-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_869b1b52623d744d0397d421438a6214 |
| publicationDate | 2005-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-20050121497-A |
| titleOfInvention | Pharmaceutical compositions and the methods of an oral preparation of itraconazole |
| abstract | The present invention relates to a composition for oral administration of itraconazole, which improves the bioavailability by improving the solubility and dissolution rate of itraconazole, a poorly water-soluble drug, and is itraconazole, a physiologically acceptable organic acid, dimethylisosorbide and a pharmaceutical as a solubilizer. It relates to a composition for oral administration of itraconazole comprising an acceptable additive. The oral composition may be obtained by cooling after high temperature melting and dispersing it in a liquid state or in a dispersion carrier, or after dissolving in an organic solvent through a preparation method such as a dispersion carrier and spraying and drying. |
| priorityDate | 2004-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 89.