Please use this identifier to cite or link to this item: https://doi.org/10.1039/c0lc00579g
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dc.titleHigh-throughput cell cycle synchronization using inertial forces in spiral microchannels
dc.contributor.authorLee, W.C.
dc.contributor.authorBhagat, A.A.S.
dc.contributor.authorHuang, S.
dc.contributor.authorVan Vliet, K.J.
dc.contributor.authorHan, J.
dc.contributor.authorLim, C.T.
dc.date.accessioned2014-10-08T09:44:12Z
dc.date.available2014-10-08T09:44:12Z
dc.date.issued2011-04-07
dc.identifier.citationLee, W.C., Bhagat, A.A.S., Huang, S., Van Vliet, K.J., Han, J., Lim, C.T. (2011-04-07). High-throughput cell cycle synchronization using inertial forces in spiral microchannels. Lab on a Chip - Miniaturisation for Chemistry and Biology 11 (7) : 1359-1367. ScholarBank@NUS Repository. https://doi.org/10.1039/c0lc00579g
dc.identifier.issn14730197
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/87819
dc.description.abstractEfficient synchronization and selection of cells at different stages of the cell replication cycle facilitates both fundamental research and development of cell cycle-targeted therapies. Current chemical-based synchronization methods are unfavorable as these can disrupt cell physiology and metabolism. Microfluidic systems developed for physical cell separation offer a potential alternative over conventional cell synchronization approaches. Here we introduce a spiral microfluidic device for cell cycle synchronization, using the combined effects of inertial forces and Dean drag force. By exploiting the relationship between cell diameter and cell cycle (DNA content/ploidy), we have successfully fractionated several asynchronous mammalian cell lines, as well as primary cells comprising bone marrow-derived human mesenchymal stem cells (hMSCs), into enriched subpopulations of G0/G1 (>85%), S, and G2/M phases. This level of cell cycle enrichment is comparable to existing microfluidic systems, but the throughput (∼15 × 106 cells per h) and viability (∼95%) of cells thus synchronized are significantly greater. Further, this platform provides rapid collection of synchronized cells or of diameter-sorted cells post-separation, to enable diverse applications in the study and manipulation of cell proliferation. © The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c0lc00579g
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentBIOENGINEERING
dc.description.doi10.1039/c0lc00579g
dc.description.sourcetitleLab on a Chip - Miniaturisation for Chemistry and Biology
dc.description.volume11
dc.description.issue7
dc.description.page1359-1367
dc.description.codenLCAHA
dc.identifier.isiut000288455100024
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