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用于即时护理应用的基于毛细管驱动的样品加载和反应器密封的实时 PCR 芯片。

Real-time PCR array chip with capillary-driven sample loading and reactor sealing for point-of-care applications.

机构信息

BioMEMS Laboratory, School of Mechanical and Aerospace Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798, Singapore.

出版信息

Biomed Microdevices. 2009 Oct;11(5):1007-20. doi: 10.1007/s10544-009-9318-4. Epub 2009 May 7.

Abstract

A major challenge for the lab-on-a-chip (LOC) community is to develop point-of-care diagnostic chips that do not use instruments. Such instruments include pumping or liquid handling devices for distribution of patient's nucleic-acid test sample among an array of reactors and microvalves or mechanical parts to seal these reactors. In this paper, we report the development of a primer pair pre-loaded PCR array chip, in which the loading of the PCR mixture into an array of reactors and subsequent sealing of the reactors were realized by a novel capillary-based microfluidics with a manual two-step pipetting operations. The chip is capable of performing simultaneous (parallel) analyses of multiple gene targets and its performance was tested by amplifying twelve different gene targets against cDNA template from human hepatocellular carcinoma using SYBR Green I fluorescent dye. The versatility and reproducibility of the PCR-array chip are demonstrated by real-time PCR amplification of the BNI-1 fragment of SARS cDNA cloned in a plasmid vector. The reactor-to-reactor diffusion of the pre-loaded primer pairs in the chip is investigated to eliminate the possibility of primer cross-contamination. Key technical issues such as PCR mixture loss in gas-permeable PDMS chip layer and bubble generation due to different PDMS-glass bonding methods are investigated.

摘要

对于芯片实验室(LOC)社区来说,一个主要的挑战是开发不需要仪器的即时诊断芯片。这些仪器包括用于将患者的核酸测试样本分配到一系列反应器中的泵送或液体处理设备,以及用于密封这些反应器的微阀或机械部件。在本文中,我们报告了一种预加载引物对的 PCR 阵列芯片的开发,其中通过新型基于毛细管的微流控技术以及手动两步移液操作实现了将 PCR 混合物加载到一系列反应器中并随后密封这些反应器。该芯片能够同时(平行)分析多个基因靶标,其性能通过使用 SYBR Green I 荧光染料对来自人肝癌的 cDNA 模板进行十二种不同基因靶标的扩增来测试。通过实时 PCR 扩增克隆在质粒载体中的 SARS cDNA 的 BNI-1 片段,展示了 PCR 阵列芯片的多功能性和可重复性。研究了芯片中预加载的引物对的在反应器之间的扩散,以消除引物交叉污染的可能性。研究了诸如在透气 PDMS 芯片层中 PCR 混合物的损失以及由于不同的 PDMS-玻璃键合方法而产生气泡等关键技术问题。

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