Microfluidic techniques for high throughput single cell analysis

被引:115
|
作者
Reece, Amy [1 ]
Xia, Bingzhao [1 ]
Jiang, Zhongliang [1 ]
Noren, Benjamin [1 ]
McBride, Ralph [1 ]
Oakey, John [1 ]
机构
[1] Univ Wyoming, Dept Chem Engn, 1000 East Univ Ave, Laramie, WY 82070 USA
基金
美国国家科学基金会;
关键词
CIRCULATING TUMOR-CELLS; LABEL-FREE; INERTIAL MICROFLUIDICS; DROPLET MICROFLUIDICS; NANOLITER DROPLETS; INDIVIDUAL CELLS; CHIP; SEPARATION; PLATFORM; FILTRATION;
D O I
10.1016/j.copbio.2016.02.015
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The microfabrication of microfluidic control systems and the development of increasingly sensitive molecular amplification tools have enabled the miniaturization of single cells analytical platforms. Only recently has the throughput of these platforms increased to a level at which populations can be screened at the single cell level. Techniques based upon both active and passive manipulation are now capable of discriminating between single cell phenotypes for sorting, diagnostic or prognostic applications in a variety of clinical scenarios. The introduction of multiphase microfluidics enables the segmentation of single cells into biochemically discrete picoliter environments. The combination of these techniques are enabling a class of single cell analytical platforms within great potential for data driven biomedicine, genomics and transcriptomics.
引用
收藏
页码:90 / 96
页数:7
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