Microsystems for the Capture of Low-Abundance Cells

被引:110
作者
Dharmasiri, Udara [1 ,3 ]
Witek, Malgorzata A. [1 ,3 ]
Adams, Andre A. [1 ,4 ]
Soper, Steven A. [1 ,2 ,3 ]
机构
[1] Louisiana State Univ, Dept Chem, Baton Rouge, LA 70803 USA
[2] Louisiana State Univ, Dept Engn Mech, Baton Rouge, LA 70803 USA
[3] Louisiana State Univ, Ctr Biomodular Multiscale Syst, Baton Rouge, LA 70803 USA
[4] USN, Ctr Biomol Sci & Engn, Res Lab, Washington, DC 20375 USA
来源
ANNUAL REVIEW OF ANALYTICAL CHEMISTRY, VOL 3 | 2010年 / 3卷
关键词
cell capture and enumeration; circulating tumor cells; size-based selection; immunoaffinity capture; fluorescence-activated sorters; dielectrophoretic separation; CIRCULATING TUMOR-CELLS; BLOOD MONONUCLEAR-CELLS; BREAST-CANCER CELLS; PERIPHERAL-BLOOD; CAPILLARY-ELECTROPHORESIS; MONOCLONAL-ANTIBODIES; MICROFLUIDIC SYSTEM; PROGENITOR CELLS; PROGNOSTIC VALUE; FLOW-CYTOMETRY;
D O I
10.1146/annurev.anchem.111808.073610
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Efficient selection and enumeration of low-abundance biological cells are highly important in a variety of applications. For example, the clinical utility of circulating tumor cells (CTCs) in peripheral blood is recognized as a viable biomarker for the management of various cancers, in which the clinically relevant number of CTCs per 7.5 ml of blood is two to five. Although there are several methods for isolating rare cells from a variety of heterogeneous samples, such as immunomagnetic-assisted cell sorting and fluorescence-activated cell sorting, they are fraught with challenges. Microsystem-based technologies are providing new opportunities for selecting and isolating rare cells from complex, heterogeneous samples. Such approaches involve reductions in target-cell loss, process automation, and minimization of contamination issues. In this review, we introduce different application areas requiring rare cell analysis, conventional techniques for their selection, and finally microsystem approaches for low-abundance-cell isolation and enumeration.
引用
收藏
页码:409 / 431
页数:23
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