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dc.contributor.authorHou, Han Wei
dc.contributor.authorWarkiani, Majid Ebrahimi
dc.contributor.authorKhoo, Bee Luan
dc.contributor.authorLi, Zi Rui
dc.contributor.authorSoo, Ross A.
dc.contributor.authorTan, Daniel Shao-Weng
dc.contributor.authorLim, Wan-Teck
dc.contributor.authorHan, Jongyoon
dc.contributor.authorBhagat, Ali Asgar S.
dc.contributor.authorLim, Chwee Teck
dc.date.accessioned2014-05-15T14:44:44Z
dc.date.available2014-05-15T14:44:44Z
dc.date.issued2013-02
dc.date.submitted2012-10
dc.identifier.issn2045-2322
dc.identifier.urihttp://hdl.handle.net/1721.1/86978
dc.description.abstractPresence and frequency of rare circulating tumor cells (CTCs) in bloodstreams of cancer patients are pivotal to early cancer detection and treatment monitoring. Here, we use a spiral microchannel with inherent centrifugal forces for continuous, size-based separation of CTCs from blood (Dean Flow Fractionation (DFF)) which facilitates easy coupling with conventional downstream biological assays. Device performance was optimized using cancer cell lines (> 85% recovery), followed by clinical validation with positive CTCs enumeration in all samples from patients with metastatic lung cancer (n = 20; 5–88 CTCs per mL). The presence of CD133+ cells, a phenotypic marker characteristic of stem-like behavior in lung cancer cells was also identified in the isolated subpopulation of CTCs. The spiral biochip identifies and addresses key challenges of the next generation CTCs isolation assay including antibody independent isolation, high sensitivity and throughput (3 mL/hr); and single-step retrieval of viable CTCs.en_US
dc.description.sponsorshipSingapore. National Research Foundation (Singapore MIT Alliance for Research and Technology's BioSystems and Micromechanics Inter-Disciplinary Research programme)en_US
dc.description.sponsorshipSingapore. National Medical Research Council (grant NMRC 1225/2009)en_US
dc.language.isoen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/srep01259en_US
dc.rightsCreative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/en_US
dc.sourceScientific Reportsen_US
dc.titleIsolation and retrieval of circulating tumor cells using centrifugal forcesen_US
dc.typeArticleen_US
dc.identifier.citationHou, Han Wei, Majid Ebrahimi Warkiani, Bee Luan Khoo, Zi Rui Li, Ross A. Soo, Daniel Shao-Weng Tan, Wan-Teck Lim, Jongyoon Han, Ali Asgar S. Bhagat, and Chwee Teck Lim. “Isolation and Retrieval of Circulating Tumor Cells Using Centrifugal Forces.” Sci. Rep. 3 (February 12, 2013).en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.mitauthorHan, Jongyoonen_US
dc.contributor.mitauthorHou, Han Weien_US
dc.relation.journalScientific Reportsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsHou, Han Wei; Warkiani, Majid Ebrahimi; Khoo, Bee Luan; Li, Zi Rui; Soo, Ross A.; Tan, Daniel Shao-Weng; Lim, Wan-Teck; Han, Jongyoon; Bhagat, Ali Asgar S.; Lim, Chwee Tecken_US
dc.identifier.orcidhttps://orcid.org/0000-0001-7215-1439
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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