Label-Free, Microfluidic Separation of Human Breast Carcinoma and Epithelial Cells by Adhesion Difference

K. Kwon, Sang Ho Lee, Byungkyu Kim, Min Cheol Park, P. Kim, K. Suh
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引用次数: 3

Abstract

A simple, label-free microfluidic separation of cancer cells by exploiting difference in cell adhesion. To maximize the adhesion difference, three types of polymeric nanostructures (50 nm pillars, 50 nm perpendicular and parallel lines with respect to the direction of flow) were fabricated using UV- assisted capillary moulding onto glass substrate of PDMS microfluidic channel. The adhesion force of human breast epithelial cells (MCF10A) and human breast carcinoma (MCF7) was measured independently by injecting each cell line into the microfluidic device followed by culture for a period of time (e.g., one, two, and three hours). Then, the cells bound to the floor of a microfluidic channel were detached by increasing the flow rate of medium in a stepwise fashion. The adhesion force of MCF10A was always higher than that of MCF cells regardless of culture time and surface nanotopography at all flow rates, resulting in a label-free separation of cancer cells. For the cell types used in our study, the optimum separation was found for 2 hours culture on 50 nm parallel line pattern followed by flow-induced detachment at a flow rate of 300 mul/min
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人乳腺癌细胞与上皮细胞黏附差异的无标记微流体分离
一个简单的,无标记的微流体分离癌细胞利用细胞粘附的差异。为了最大限度地提高粘着差异,采用紫外辅助毛细管模塑技术在PDMS微流控通道玻璃基板上制备了三种类型的聚合物纳米结构(50 nm柱状、50 nm垂直和50 nm平行的流动方向)。人乳腺上皮细胞(MCF10A)和人乳腺癌细胞(MCF7)的粘附力分别通过将每个细胞系注射到微流控装置中,然后培养一段时间(如1、2、3小时)来独立测量。然后,通过逐步增加介质的流速,将结合在微流控通道底端的细胞分离出来。在所有流速下,无论培养时间和表面纳米形貌如何,MCF10A的黏附力始终高于MCF细胞,导致癌细胞无标记分离。对于我们所使用的细胞类型,最佳分离方法是在50 nm平行线上培养2小时,然后在300 μ l/min的流速下进行流动诱导分离
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