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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P17-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-513
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-505
filingDate 1981-04-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1991-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3f8592d5d2713670d63c69e333ededa0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_92d24f8d54452b1c78482d385c9937ec
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publicationDate 1991-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1697814-A1
titleOfInvention Agent for basaliom treatment
abstract The invention relates to pharmaceutical compositions for the treatment of dermatoses associated with impaired keratonization and epidermosis, and relates to preparations for the treatment of basalitis, developing from a fine spot, nodule or limited hyperkeratosis. The aim of the invention is to increase specific activity and reduce toxicity. The tool is obtained as follows. 1.2 g of sodium hydroxide, 1.25 g of sodium carbonate, and 7.5 g of fluoro-fura are dissolved in 57.25 g of water. The resulting solution is heated to 80-85 ° C and a thin stream is poured with vigorous stirring into an alloy of fatty components consisting of 14.0 g of diethylene glycol stearate, 1.5 g of triethanolamine stearate, 5.0 g of stearin, 8.0 g olive oil, 0.1 g nipagina and 0.2 g nipazol. The emulsification is carried out at 70-75 ° C for 20 minutes, then continued at a gradually decreasing temperature, which after 35-40 minutes should be 18-20 ° C. Prepared ointment packaged in tubes. The use of the proposed remedy makes it possible to shorten the treatment time, ensures the absence of a general toxic effect, the normalization of the clinical and histological picture of hyperkeratosis, and the absence of relapses. fe
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type http://data.epo.org/linked-data/def/patent/Publication

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