http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101323478-B1

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filingDate 2005-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2013-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-101323478-B1
titleOfInvention Water-Soluble Drug-Solid Formulations
abstract Even if various coatings were applied to release the drug from the lower part of the small intestine to the large intestine, bisacryl was poorly soluble so that it was difficult to obtain a sufficient effect, and it was necessary to mix more drugs. Conventionally, a technique for releasing bisacodeyl and dioctylsodium sulfosuccinate simultaneously from the lower part of the small intestine to the large intestine is not known. A solid preparation characterized in that the nucleus particles containing the poorly water-soluble drug and dioctylsodium sulfosuccinate are subjected to an enteric coating which releases the drug from the lower part of the small intestine to the large intestine.n n n n Bisacryl, Dioctylsodium sulfosuccinate, enteric coating, solid preparation
priorityDate 2004-03-10-04:00^^<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: 35.