http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SE-540132-C2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d89ab39ebd50d413db55fd7e8fbac2d7
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-86
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-86
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-56
filingDate 2014-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_12baec074db765bd6ac02853b3620b8b
publicationDate 2018-04-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SE-540132-C2
titleOfInvention Method of analysis for the determination of anticoagulants in blood or blood plasma
abstract 22 ABSTRACT An assay to determine anticoagulants in a blood or blood plasmasample, wherein the assay comprises analyses with at least two wetchemistry prothrombine time (PT) methods. The assay comprises measuringPT in a first reaction mixture with a first PT method and measuring PT in asecond reaction mixture with a second PT method, wherein the concentrationof blood or blood plasma in the second reaction mixture differs from theconcentration of blood or blood plasma in the first reaction mixture. The PTmethods are calibrated to give the same or approximately the same PTresults for reference samples which lack anticoagulants of interest for theassay. Further, calculating a difference in PT from the measurements,wherein if the difference in PT is 1) significant, this is indicative of a presenceof anticoagulants in the sample, or 2) non-significant, this is indicative of anabsence of anti-coagulants above detectable level in the sample. Elected figure for publication: Fig. 1
priorityDate 2014-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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