核酸
循环肿瘤细胞
溶解
化学
数字聚合酶链反应
微流控
分子生物学
癌症研究
聚合酶链反应
癌症
纳米技术
基因
生物化学
生物
材料科学
遗传学
转移
作者
Yanmin Wang,Wanlei Gao,Man Wu,Xiaofen Zhang,Wei Liu,Yang Zhou,Chunping Jia,Hui Cong,Xiang Chen,Jianlong Zhao
出处
期刊:Talanta
[Elsevier BV]
日期:2021-01-07
卷期号:225: 122057-122057
被引量:18
标识
DOI:10.1016/j.talanta.2020.122057
摘要
Microfluidics has become a reliable platform for circulating tumor cells (CTCs) detection because of its high integration, small size, low consumption of reagents and rapid response. Here, we developed a multifunctional microfluidic device consists of three parts, including CTCs capture area, single-layer membrane valves area, and microcavity nucleic acid detection and analysis region based on digital polymerase chain reaction (dPCR), allowing CTCs capture, lysis, and genetic characterization to be performed on a single chip. The CTCs capture chip is coupled to the nucleic acid detection chip via a control valve. CTCs were firstly trapped in the CTC capture area, and then lysed using proteinase K to release nucleic acids. Subsequently CTCs lysate was transferred into nucleic acid detection area consisting of 12800 micro-cavity chambers for nucleic acids detection. To evaluate the performance of this chip, this study detected EGFR-L858R mutation in lung cancer cell lines H1975 and A549 cells, as well as leukocytes from normal donors. The results showed that positive signals were only observed in H1975 cells, and the detected value had a high linear relationship with the expected value (R2 = 0.9897). In conclusion, this multi-functional microfluidic chip that integrates CTCs capture, lysis and nucleic acid detection can successfully detect gene mutations in CTCs, providing reference for tumor-targeted drugs and precise diagnosis and treatment.
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