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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d57693244195a4ac180f18e9e037919c
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-483
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N24-00
filingDate 1994-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1998-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b8ed14d4234ade9f0cfaff146a471292
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e9c398f6fead3acec89748e9f7d42ac5
publicationDate 1998-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2114435-C1
titleOfInvention Method of determining nitrate-reduction capacity of biological fluid
abstract FIELD: clinical biochemistry. SUBSTANCE: method includes sampling, dividing sample into test and reference portions, adding sodium nitrate to the test portion, incubation, adding reagents to the two portions, and determining nitrite content by reference to calibration curve and subsequently comparing data from the test and reference portions of sample. As reagent, crystalline sodium thiosulfate, ferric sulfate, and sodium ascorbate are used, and reaction mixtures obtained are frozen under liquid nitrogen. To determine nitrite concentration, EPR spectroscopy is involved. EFFECT: increased accuracy and reduced determination time.
priorityDate 1994-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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