<mets:mets OBJID="oai:generic.eprints.org:70" LABEL="Eprints Item" xsi:schemaLocation="http://www.loc.gov/METS/ http://www.loc.gov/standards/mets/mets.xsd http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-0.xsd" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mets="http://www.loc.gov/METS/"><mets:metsHdr CREATEDATA="2012-02-08T19:08:24Z"><mets:agent TYPE="ORGANIZATION" ROLE="CUSTODIAN"><mets:name>The MIIS Eprints Archive</mets:name></mets:agent></mets:metsHdr><mets:dmdSec ID="DMD_oai:generic.eprints.org:70_mods"><mets:mdWrap MDTYPE="mods"><mets:xmlData><mods:titleInfo><mods:title>Capillary Agglutination Technology</mods:title></mods:titleInfo><mods:name type="personal"><mods:namePart type="given">Chris</mods:namePart><mods:namePart type="family">Breward</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">Giles</mods:namePart><mods:namePart type="family">Richardson</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:abstract>In medical diagnostic tests, including pregnancy testing and tests for typed red blood cells, a small fluid sample is placed at one end of a capillary channel, which has been lined with a dried reagent. If the sample contains the analyte (the substance being tested for) then an agglutination reaction occurs between it and the reagent in the channel, and the agglutinated complexes progressively slow the flow and may even block the channel, partially or completely, so that the flow only reaches the far end very slowly, or not at all. The aim is that this should give a reliable detection of quite low concentrations of analyte in the sample. Platform Diagnostics asked the Study Group to construct a mathematical model of the process, so that, for known binding forces in the agglutination complexes, we can design the channel size and shape, and the fluid viscosity, to maximize the reliable detection of low concentrations. A key question is how the flow time depends on channel size, fluid surface tension and viscosity, (a) in the absence of agglutination, and (b) in the presence of agglutination.</mods:abstract><mods:classification authority="lcc">Medical and pharmaceutical</mods:classification><mods:originInfo><mods:dateIssued encoding="iso8061">2006</mods:dateIssued></mods:originInfo><mods:genre>Study Group Report</mods:genre></mets:xmlData></mets:mdWrap></mets:dmdSec><mets:amdSec ID="TMD_oai:generic.eprints.org:70"><mets:rightsMD ID="rights_oai:generic.eprints.org:70_mods"><mets:mdWrap MDTYPE="mods"><mets:xmlData><mods:useAndReproduction>
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