http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6354323-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-59
filingDate 1986-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_843c54d61b0b19db5d4c2fd08571e979
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9674430cbc5b310b6176f13696812d00
publicationDate 1988-03-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6354323-A
titleOfInvention Composition for active type vitamin d3 preparation
abstract PURPOSE: To obtain the titled composition useful as a remedy for bone diseases and active type vitain D 3 preparation, having improved stability, by dissolving an active type vitamin D 3 in a propylene glycol fatty acid ester. n CONSTITUTION: An active type vitamin D 3 is dissolved in a propylene glycol fatty acid ester (A for short) to give a composition for active type vitamin D 3 prepartion. In this method, the active type vitamin D 3 extremely stable to light, heat, etc., can be pharmaceutically manufactured. 1α-Hydroxyvitamin D 3 , etc., may be cited as the active type vitamin D 3 . Propylene glycol dicaprylic acid, etc., are preferable as the component A. As the dissolution method, the active type vitamin D 3 is directly dissolved in the component B or the active type vitamin D 3 may be dissolved in ethanol, etc., and added to the component A and then the ethanol is removed by distillation. n COPYRIGHT: (C)1988,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H03272870-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H047160-A
priorityDate 1986-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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