循环肿瘤细胞捕获微流体装置中蛋白质固定的优化

M. Gaskill, C. Launiere, D. Eddington
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引用次数: 1

摘要

利用微流控装置分离血液中转移性循环肿瘤细胞(CTCs)是一种很有前途的癌症检测方法。在本研究中,利用微流控通道内内皮-白细胞粘附分子-1 (E-selectin)和抗上皮细胞粘附分子(Anti-EpCAM)的蛋白模式来提高捕获效率。为了创建这种蛋白质图案,必须首先优化蛋白质固定方法,以允许最大限度地捕获ctc,并且由于增加涂层厚度而使细胞通过设备的流速增加最小。利用光引发聚丙烯酸(PAA)接枝聚合和硅烷化反应将蛋白质固定在交替区域。利用干涉仪测量和荧光标记,最小化PAA高度,优化蛋白固定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optimization of Protein Immobilization in Microfludic Devices for Circulating Tumor Cell Capture
The isolation of metastatic circulating tumor cells (CTCs) within the blood using microfluidic devices is a promising method for the detection of cancer. In this study, protein patterning of endothelial-leukocyte adhesion molecule-1 (E-selectin) and anti-epitheal-cell-adhesion-molecule (Anti-EpCAM) within microfluidic channels is utilized to improve the capture efficiency. To create this protein patterning the protein immobilization method must first be optimized to allow for maximum capture of CTCs and minimal increase in the flow rate of cells through the device due to added coating thickness. Proteins are immobilized in alternating regions using photo-initiated graft polymerization of polyacrylic acid (PAA) and a silanization reaction. Using interferometer measurements and fluorescent tagging, PAA height was minimized and protein immobilization was optimized.
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