http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S63215621-A

Outgoing Links

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-62
filingDate 1987-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4640e4bb50458e53f99eb7b538b94ea
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_508112cbd6f8623ed673f6ea2fb891f3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_82858461a3b1fb26e65a1da03561cf57
publicationDate 1988-09-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S63215621-A
titleOfInvention Production of ethyl cellulose microcapsule preparation to contrive sustained release of oral antibiotic
abstract PURPOSE: To obtain the titled preparation having excellent sustained release and acting for a long time, by dispersing a solution containing ethyl cellulose and an antibiotic of core substance in an organic solvent into a dispersion medium containing a dispersing and separating agent and then evaporating the organic solvent. n CONSTITUTION: Ethyl cellulose is dissolved in an organic solvent comprising a lower alcohol and/or lower alkyl ketone, mixed with an oral antibiotic (e.g. cefalexin) as a core substance, well stirred and dispersed to prepared a primary emulsion. Then the primary emulsion is uniformly dispersed into a dispersion medium premixed with a dispersing and separating agent such as a surface active agent (e.g. sorbitan tristearate) having 2W3 HBL value and the organic solvent is evaporated to give microcapsules of matrix type. n COPYRIGHT: (C)1988,JPO&Japio
priorityDate 1987-03-03-04:00^^<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: 27.