http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0272045-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-08
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-38
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filingDate 1987-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1993-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_492e9a3cd58cf4365f237f292a57df44
publicationDate 1993-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0272045-B1
titleOfInvention Topical drug release system
abstract A pharmaceutical composition for topical administration consisting of two liquid phases designed to be admixed in situ or prior to use. The first phase contains a dissolved drug, and is preferably saturated in the drug, whilst the second phase is a chemically or physically different liquid from that in the first phase and contains no drug, but is miscible with the first phase. The two liquids are selected so that, on admixture of suitable volumes of the phases, the resultant drug concentration exceeds the saturated drug solubility in the resultant mixture. This produces a liquid mixture supersaturated in drug, which has been found to increase the rate of drug penetration into the skin. The two liquid phases may be gels, and the drug may be hydrocortisone. At least one phase contains an antinucleant to improve stability of the resulting supersaturated solution.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5993787-A
priorityDate 1986-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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