http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6456618-A

Outgoing Links

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filingDate 1987-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ab9f13e639eaff24af890fea32b3cd03
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publicationDate 1989-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6456618-A
titleOfInvention Sustained release steroidal rectal administration pharmaceutical
abstract PURPOSE:To obtain the titled readily producible pharmaceutical, having a delayed elution rate of an active ingredient and long duration of sustained blood level without any side effects, by blending a fatty and oily base with prednisolone acetate which is a synthetic adrenocortical hormone having anti- inflammatory action. CONSTITUTION:A sustained release steroidal rectal administration pharmaceutical obtained by blending a fatty and oily base selected from the group consisting of animal and vegetable fats and oils, mineral oils and glycerol esters of fatty acids with prednisolone acetate. The amount thereof blended is preferably within the range of 0.1-20wt.%, especially 0.2-10wt.% in the rectal administration pharmaceutical, which is prepared by blending and dispersing the prednisolone acetate with the fatty and oily base according to a conventional method and forming a solid suppository having 30-37 deg.C melting point or filling the blend or dispersion in an injection type rectal administration tube. Furthermore, the aforementioned fatty and oily base is preferably a solid at ordinary temperature and has 26-37 deg.C, especially 30-37 deg.C melting point.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0511310-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H04346916-A
priorityDate 1987-08-28-04:00^^<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: 26.