Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/73310
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dc.titleDeformability based cell margination for malarial infected red blood cell enrichment
dc.contributor.authorHou, H.W.
dc.contributor.authorAsgar, A.
dc.contributor.authorBhagat, S.
dc.contributor.authorMao, P.
dc.contributor.authorHan, J.
dc.contributor.authorLim, C.T.
dc.date.accessioned2014-06-19T05:33:37Z
dc.date.available2014-06-19T05:33:37Z
dc.date.issued2010
dc.identifier.citationHou, H.W.,Asgar, A.,Bhagat, S.,Mao, P.,Han, J.,Lim, C.T. (2010). Deformability based cell margination for malarial infected red blood cell enrichment. 14th International Conference on Miniaturized Systems for Chemistry and Life Sciences 2010, MicroTAS 2010 2 : 1370-1372. ScholarBank@NUS Repository.
dc.identifier.isbn9781618390622
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/73310
dc.description.abstractIn this work, the physiological phenomenon of leukocyte margination is mimicked in microfluidic systems for biological separation of malarial infected RBCs (iRBCs) from blood. Change in cell stiffness is a characteristic of iRBCs which can act as an intrinsic biomarker for separation. Tests were conducted using early ring stage and late trophozoite/schizont stage iRBCs which vary significantly in their deformability. Filtration efficiency was quantified by analyzing the dispersion of iRBCs across the microchannel width at the outlet. Flow cytometry analysis was conducted on the outlet samples indicating filtration efficiency of ∼80% for early stage iRBCs and >90% for late stage iRBCs. This is the first demonstration applying this unique biomimetic separation technique to iRBCs filtration for disease diagnostic application.
dc.sourceScopus
dc.subjectCell separation
dc.subjectDeformability
dc.subjectMalaria
dc.subjectMargination
dc.subjectRed blood cells
dc.typeConference Paper
dc.contributor.departmentMECHANICAL ENGINEERING
dc.description.sourcetitle14th International Conference on Miniaturized Systems for Chemistry and Life Sciences 2010, MicroTAS 2010
dc.description.volume2
dc.description.page1370-1372
dc.identifier.isiutNOT_IN_WOS
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