Department of Imaging Physics Research, The University of Texas, M.D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030, USA ; Department of Biomedical Engineering, The University of Texas at Austin, 1 University Station, C0800, Austin, Texas 78712, USA.
Department of Systems Biology, The University of Texas, M.D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030, USA.
Biomicrofluidics. 2013 Jan 16;7(1):11807. doi: 10.1063/1.4774304. eCollection 2013.
Circulating tumor cells (CTCs) are prognostic markers for the recurrence of cancer and may carry molecular information relevant to cancer diagnosis. Dielectrophoresis (DEP) has been proposed as a molecular marker-independent approach for isolating CTCs from blood and has been shown to be broadly applicable to different types of cancers. However, existing batch-mode microfluidic DEP methods have been unable to process 10 ml clinical blood specimens rapidly enough. To achieve the required processing rates of 10(6) nucleated cells/min, we describe a continuous flow microfluidic processing chamber into which the peripheral blood mononuclear cell fraction of a clinical specimen is slowly injected, deionized by diffusion, and then subjected to a balance of DEP, sedimentation and hydrodynamic lift forces. These forces cause tumor cells to be transported close to the floor of the chamber, while blood cells are carried about three cell diameters above them. The tumor cells are isolated by skimming them from the bottom of the chamber while the blood cells flow to waste. The principles, design, and modeling of the continuous-flow system are presented. To illustrate operation of the technology, we demonstrate the isolation of circulating colon tumor cells from clinical specimens and verify the tumor origin of these cells by molecular analysis.
循环肿瘤细胞(CTCs)是癌症复发的预后标志物,可能携带与癌症诊断相关的分子信息。介电泳(DEP)已被提议作为一种独立于分子标志物的方法,从血液中分离 CTCs,并且已经被证明广泛适用于不同类型的癌症。然而,现有的批量微流控 DEP 方法无法快速处理 10ml 的临床血液标本。为了达到所需的 10(6)个核细胞/分钟的处理速率,我们描述了一种连续流动微流控处理室,将临床标本的外周血单核细胞部分缓慢注入其中,通过扩散去离子化,然后施加介电泳、沉淀和流体动力升力的平衡。这些力导致肿瘤细胞被运送到靠近腔室底部的位置,而血细胞则被带到它们上方约三个细胞直径的位置。通过从腔室底部撇取肿瘤细胞来实现肿瘤细胞的分离,而血细胞则流向废物。本文介绍了连续流动系统的原理、设计和建模。为了说明该技术的操作,我们展示了从临床标本中分离循环结肠肿瘤细胞,并通过分子分析验证了这些细胞的肿瘤来源。