http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2147130-C1

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Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7a6eeb51d9468e2289773fd659b5080c
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-72
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-569
filingDate 1998-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2000-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f5cfbde22d8f1ea6b492c08e8c9c0ded
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3de79ced398c7c9d8b34767d45dd57b3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_16d57d0641b3101eda0334fa314c5a15
publicationDate 2000-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2147130-C1
titleOfInvention Method for evaluating blood losses from the gastroenteric tract
abstract FIELD: medicine. SUBSTANCE: method involves setting coagglutination reaction using staphylococcus reagents of specific sensitivity for determining hemoglobin or human erythrocytes. Magnetic staphylococcus reagent is added to feces suspension and deposited in magnetic field. Double dilutions are carried out and coagglutination reaction is set on them using specific antihemoglobin and antierythrocyte reagents. The coagglutination reaction is described using four crosses system. Blood losses are calculated from formula Y Hb = X×4×6 mkg/cu.cm, where Y Hb is the hemoglobin quantity to be determined, X is the last blood double dilution denominator that was accounted as three crosses, 4 is the recalculation coefficient relative to the initial feces dilution degree, 6 mcg/cu.cm is the sensitivity index of the specific antihemoglobin reagent. Y Er = X×4×2,75×10 5 cells/cu.cm, where Y Er is the number of erythrocytes to be determined, X is the last blood double dilution denominator that was accounted as three crosses, 4 is the recalculation coefficient relative to the initial feces dilution, 2.75 mcg/2,75×10 5 cells/cu.cm is the sensitivity index of the specific antierythrocyte reagent. The difference between the facts that hemoglobin only is detected, or both hemoglobin and erythrocytes are detected, gives base for hemorrhage cause to be determined. EFFECT: enhanced accuracy in quantitative hemoglobin and erythrocytes determination using express-method.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2566730-C1
priorityDate 1998-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 19.