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dc.contributor.authorMa, Gwo-Chinen_US
dc.contributor.authorLin, Wen-Hsiangen_US
dc.contributor.authorHuang, Chung-Eren_US
dc.contributor.authorChang, Ting-Yuen_US
dc.contributor.authorLiu, Jia-Yunen_US
dc.contributor.authorYang, Ya-Junen_US
dc.contributor.authorLee, Mei-Huien_US
dc.contributor.authorWu, Wan-Juen_US
dc.contributor.authorChang, Yun-Shiangen_US
dc.contributor.authorChen, Mingen_US
dc.date.accessioned2019-04-02T05:58:45Z-
dc.date.available2019-04-02T05:58:45Z-
dc.date.issued2019-02-01en_US
dc.identifier.issn2072-666Xen_US
dc.identifier.urihttp://dx.doi.org/10.3390/mi10020132en_US
dc.identifier.urihttp://hdl.handle.net/11536/148996-
dc.description.abstractCirculating fetal cells (CFCs) in maternal blood are rare but have a strong potential to be the target for noninvasive prenatal diagnosis (NIPD). Cell Reveal(TM) system is a silicon-based microfluidic platform capable to capture rare cell populations in human circulation. The platform is recently optimized to enhance the capture efficiency and system automation. In this study, spiking tests of SK-BR-3 breast cancer cells were used for the evaluation of capture efficiency. Then, peripheral bloods from 14 pregnant women whose fetuses have evidenced non-maternal genomic markers (e.g., de novo pathogenic copy number changes) were tested for the capture of circulating fetal nucleated red blood cells (fnRBCs). Captured cells were subjected to fluorescent in situ hybridization (FISH) on chip or recovered by an automated cell picker for molecular genetic analyses. The capture rate for the spiking tests is estimated as 88.1%. For the prenatal study, 2-71 fnRBCs were successfully captured from 2 mL of maternal blood in all pregnant women. The captured fnRBCs were verified to be from fetal origin. Our results demonstrated that the Cell Reveal(TM) system has a high capture efficiency and can be used for fnRBC capture that is feasible for the genetic diagnosis of fetuses without invasive procedures.en_US
dc.language.isoen_USen_US
dc.subjectcbNIPDen_US
dc.subjectfnRBCen_US
dc.subjectcapture efficiencyen_US
dc.subjectmicrofluidicsen_US
dc.subjectnanostructureen_US
dc.titleA Silicon-based Coral-like Nanostructured Microfluidics to Isolate Rare Cells in Human Circulation: Validation by SK-BR-3 Cancer Cell Line and Its Utility in Circulating Fetal Nucleated Red Blood Cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.3390/mi10020132en_US
dc.identifier.journalMICROMACHINESen_US
dc.citation.volume10en_US
dc.contributor.department國際半導體學院zh_TW
dc.contributor.departmentInternational College of Semiconductor Technologyen_US
dc.identifier.wosnumberWOS:000460798200057en_US
dc.citation.woscount0en_US
Appears in Collections:Articles