A microfluidic chip integrated with a high-density PDMS-based microfiltration membrane for rapid isolation and detection of circulating tumor cells

被引:176
作者
Fan, Xiaoyun [1 ]
Jia, Chunping [1 ]
Yang, Jun [2 ]
Li, Gang [1 ,3 ]
Mao, Hongju [1 ]
Jin, Qinghui [1 ]
Zhao, Jianlong [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Microsyst & Informat Technol, State Key Lab Transducer Technol, Shanghai 200050, Peoples R China
[2] Nantong Univ, Dept Tumor Chemotherapy, Affiliated Hosp, Nantong 226001, Peoples R China
[3] Chongqing Univ, Sch Optoelect Engn, Chongqing 400044, Peoples R China
基金
中国国家自然科学基金;
关键词
Circulating tumor cells; Microfluidic chip; PDMS-based filter; Sacrificial film; BREAST-CANCER PATIENTS; PERIPHERAL-BLOOD; MICROCAVITY ARRAY; SIZE; DEVICE; ENUMERATION; CHALLENGES; CARCINOMA; CAPTURE; FLOW;
D O I
10.1016/j.bios.2015.04.080
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
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 CFCs 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. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:380 / 386
页数:7
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