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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-49
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-36
filingDate 2014-08-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3c9f478d7334bd3de0f5713aab474bb2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10861f9fdfde27630ad7a6f02a879068
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7b006c5c382b9b26c193f19917056c91
publicationDate 2015-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2571288-C1
titleOfInvention Method for producing ex vivo soluble fibrinogen
abstract FIELD: medicine. n SUBSTANCE: fresh-frozen plasma is unfrozen and centrifuged; the produced cryoprecipitate is solubilised and treated with aluminium hydroxide; the produced suspension is centrifuged; the produced deposit containing non-target proteins are rejected; the supernatant is treated with polyethylene glycol; the suspension is centrifuged; the supernatant is rejected; the deposit is solubilised and subject to viral inactivation, cleaned from viral inactivation products by shaking with Vaseline oil and re-precipitating with glycerol; the deposit procedure is repeated twice; the produced fibrinogen solution is bottled and lyophilised. n EFFECT: producing fibrinogen, which possesses fast solubility. n 2 ex, 2 dwg, 3 tbl
priorityDate 2014-08-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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