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dc.contributor.authorChen, Hongmei
dc.contributor.authorZhang, Zhifeng
dc.date.accessioned2019-02-28T11:04:44Z
dc.date.available2019-02-28T11:04:44Z
dc.date.copyright9/21/2018 12:00:00 AM
dc.date.issued2018
dc.identifier.issn1932-6181
dc.identifier.othermed_012_04_041004.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4252440
dc.description.abstractDetection and capture of circulating tumor cells (CTCs) with microfluidic chips hold significance in cancer prognosis, diagnosis, and anti-cancer treatment. The counting of CTCs provides potential tools to evaluate cancer stages as well as treatment progress. However, facing the challenge of rareness in blood, the precise enumeration of CTCs is challenging. In the present research, we designed an inertial-deformability hybrid microfluidic chip using a long spiral channel with trapezoid-circular pillars and a capture zone. To clinically validate the device, the microfluidic chip has been tested for the whole blood and lysed blood with a small number of CTCs (colorectal and nonsmall-cell lung cancer) spiked in. The capture efficiency reaches over 90% for three types of cancer cell lines at the flow rate of 1.5 mL/h. Following numerical modeling was conducted to explain the working principle and working condition (Reynolds number below 10 and Dean number around 1). This design extended the effective capture length, improved the capture efficiency, and made the CTC enumeration much easier. We believe that this hybrid chip is promising clinically in the CTCs enumeration, evaluation of cancer therapy, and pharmacological responses.
dc.publisherThe American Society of Mechanical Engineers (ASME)
dc.titleAn Inertia-Deformability Hybrid Circulating Tumor Cell Chip: Design, Clinical Test, and Numerical Analysis
dc.typeJournal Paper
dc.journal.volume12
dc.journal.issue4
dc.journal.titleJournal of Medical Devices
dc.identifier.doi10.1115/1.4040986
dc.journal.fristpage41004
dc.journal.lastpage041004-6
dc.treeJournal of Medical Devices:;2018:;volume( 012 ):;issue: 004
dc.contenttypeFulltext


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