Antfolk Maria, Magnusson Cecilia, Augustsson Per, Lilja Hans, Laurell Thomas
Department of Biomedical Engineering, Lund University , Ole Römers väg 3, 22363 Lund, Sweden.
Department of Translational Medicine, Lund University , Jan Waldenströms gata 35, 205 02 Malmö, Sweden.
Anal Chem. 2015 Sep 15;87(18):9322-8. doi: 10.1021/acs.analchem.5b02023. Epub 2015 Sep 3.
Enrichment of rare cells from peripheral blood has emerged as a means to enable noninvasive diagnostics and development of personalized drugs, commonly associated with a prerequisite to concentrate the enriched rare cell population prior to molecular analysis or culture. However, common concentration by centrifugation has important limitations when processing low cell numbers. Here, we report on an integrated acoustophoresis-based rare cell enrichment system combined with integrated concentration. Polystyrene 7 μm microparticles could be separated from 5 μm particles with a recovery of 99.3 ± 0.3% at a contamination of 0.1 ± 0.03%, with an overall 25.7 ± 1.7-fold concentration of the recovered 7 μm particles. At a flow rate of 100 μL/min, breast cancer cells (MCF7) spiked into red blood cell-lysed human blood were separated with an efficiency of 91.8 ± 1.0% with a contamination of 0.6 ± 0.1% from white blood cells with a 23.8 ± 1.3-fold concentration of cancer cells. The recovery of prostate cancer cells (DU145) spiked into whole blood was 84.1 ± 2.1% with 0.2 ± 0.04% contamination of white blood cells with a 9.6 ± 0.4-fold concentration of cancer cells. This simultaneous on-chip separation and concentration shows feasibility of future acoustofluidic systems for rapid label-free enrichment and molecular characterization of circulating tumor cells using peripheral venous blood in clinical practice.
从外周血中富集稀有细胞已成为实现无创诊断和开发个性化药物的一种手段,这通常需要在进行分子分析或培养之前对富集的稀有细胞群体进行浓缩。然而,在处理低细胞数量时,通过离心进行的常规浓缩存在重要局限性。在此,我们报告了一种基于集成声泳的稀有细胞富集系统,并结合了集成浓缩功能。聚苯乙烯7μm微粒能够与5μm微粒分离,在污染率为0.1±0.03%的情况下回收率为99.3±0.3%,回收的7μm微粒总体浓缩了25.7±1.7倍。在流速为100μL/min时,添加到经红细胞裂解的人血中的乳腺癌细胞(MCF7)的分离效率为91.8±1.0%,来自白细胞的污染率为0.6±0.1%,癌细胞浓缩了23.8±1.3倍。添加到全血中的前列腺癌细胞(DU145)的回收率为84.1±2.1%,白细胞污染率为0.2±0.04%,癌细胞浓缩了9.6±0.4倍。这种同时进行的芯片上分离和浓缩显示了未来声流控系统用于在临床实践中使用外周静脉血对循环肿瘤细胞进行快速无标记富集和分子表征的可行性。