Please use this identifier to cite or link to this item: https://doi.org/10.1007/978-3-642-28160-0_5
DC FieldValue
dc.titleMicrofluidic technologies
dc.contributor.authorBhagat, A.A.S.
dc.contributor.authorLim, C.T.
dc.date.accessioned2014-06-17T09:45:06Z
dc.date.available2014-06-17T09:45:06Z
dc.date.issued2012
dc.identifier.citationBhagat, A.A.S.,Lim, C.T. (2012). Microfluidic technologies. Recent Results in Cancer Research 195 : 59-67. ScholarBank@NUS Repository. <a href="https://doi.org/10.1007/978-3-642-28160-0_5" target="_blank">https://doi.org/10.1007/978-3-642-28160-0_5</a>
dc.identifier.isbn9783642281594
dc.identifier.issn00800015
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/67156
dc.description.abstractPresence of circulating tumor cells (CTCs) in blood is an important intermediate step in cancer metastasis, a mortal consequence of cancer. However, CTCs are extremely rare in blood with highly heterogeneous morphologies and molecular signatures, thus making their isolation technically very challenging. In the past decade, a flurry of new microfluidic-based technologies has emerged to address this compelling problem. This chapter highlights the current state of the art in microfluidic systems developed for CTCs separation and isolation. The techniques presented are broadly classified as physical- or affinity-based isolation depending on the separation principle. The performance of these techniques is evaluated based on accepted separation metrics including sensitivity, purity and processing/analysis time. Finally, further insights associated with realizing an integrated microfluidic CTC lab-on-chip system as an onco-diagnostic tool will be discussed. © 2012 Springer-Verlag Berlin Heidelberg.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1007/978-3-642-28160-0_5
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentBIOENGINEERING
dc.description.doi10.1007/978-3-642-28160-0_5
dc.description.sourcetitleRecent Results in Cancer Research
dc.description.volume195
dc.description.page59-67
dc.description.codenRRCRB
dc.identifier.isiutNOT_IN_WOS
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