Gang Li

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Organization: Chongqing University
Department: State Key Laboratory of Transducer Technology
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Co-reporter:Xiaoyun Fan, Chunping Jia, Jun Yang, Gang Li, Hongju Mao, Qinghui Jin, Jianlong Zhao
Biosensors and Bioelectronics 2015 Volume 71() pp:380-386
Publication Date(Web):15 September 2015
DOI:10.1016/j.bios.2015.04.080
•We developed a low-cost and efficient size-based CTC isolation microchip.•The chip used a precise and highly porous PDMS microfilter to isolate the larger CTCs from blood.•The PDMS microfilter was fabricated and transferred by combining a sacrificial film.•The chip showed a highly efficient isolation of CTCs from whole blood.Isolation of circulating tumor cells (CTCs) by size exclusion is a widely researched technique that offers the advantage of capturing tumor cells without reliance on cell surface expression markers. In this work, we report the development of a novel polydimethylsiloxane (PDMS) membrane filter-based microdevice for rapid and highly efficient isolation of CTCs from peripheral blood. A precise and highly porous PDMS microfilter was fabricated and integrated into the microfiltration chip by combining a sacrificial transferring film with a sandwich molding method. We achieved >90% recovery when isolating lung cancer cells from spiked blood samples, with a relatively high processing throughput of 10 mL/h. In contrast to existing CTC filtration systems, which rely on low-porosity track-etch filters or expensive lithography-based filters, our microfiltration chip does not require complex e-beam lithography or the reactive ion etching process, therefore it offers a low-cost alternative tool for highly efficient CTC enrichment and in situ analysis. Thus, this new microdevice has the potential for use in routine monitoring of cancer development and cancer therapy in a clinical setting.
Co-reporter:Yayun Fu, Hongbo Zhou, Chunping Jia, Fengxiang Jing, Qinghui Jin, Jianlong Zhao, Gang Li
Sensors and Actuators B: Chemical (June 2017) Volume 245() pp:414-422
Publication Date(Web):June 2017
DOI:10.1016/j.snb.2017.01.161
3-(3-HYDROXYPROPYL)-8-[(E)-2-(3-METHOXYPHENYL)ETHENYL]-7-METHYL-1-PROP-2-YNYLPURINE-2,6-DIONE
Caspase-3
Mitogen-activated protein kinase p38
Protein kinase Akt
Gelatinase B