http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20150096460-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-70
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filingDate 2013-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1229204194dce1238e61f431002158ec
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d2994b905012de132ac1fb1e70eeb29d
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publicationDate 2015-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20150096460-A
titleOfInvention Transdermal delivery system
abstract The present invention relates to a method for treating a patient's pain by applying a buprenorphine transdermal therapeutic system for percutaneous administration to the skin of a patient for 7 days, A) a buprenorphine-impermeable backing layer, B) a) polymer base, b) buprenorphine, and c) the buprenorphine is solubilized internally to form a mixture, and wherein the carboxylic acid buprenorphine mixture is selected from the group consisting of oleic acid, linoleic acid, linolenic acid, levulic acid, and linoleic acid in an amount sufficient to form a deposit, Carboxy &lt; / RTI &gt; acid &lt; RTI ID = 0.0 &gt; A buprenorphine-containing matrix layer on said buprenorphine-impermeable backing layer, and C) a skin contact layer on said buprenorphine-containing matrix layer comprising a polymer- Comprising a buprenorphine-containing self-adhesive layer structure, Optionally, the buprenorphine-containing self-adhesive layer structure contains the buprenorphine in an amount of less than 0.8 mg / cm2 of buprenorphine base or an equimolar amount of a pharmaceutically acceptable salt thereof.
priorityDate 2012-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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