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通过在具有亲水膜涂层的聚二甲基硅氧烷的自驱动微流控芯片上进行等温扩增来对 DNA 进行数字量化。

Digital quantification of DNA via isothermal amplification on a self-driven microfluidic chip featuring hydrophilic film-coated polydimethylsiloxane.

机构信息

Department of Power Mechanical Engineering, National Tsing Hua University, Hsinchu, Taiwan, ROC.

Coretronic Corporation, Miaoli, Taiwan, ROC.

出版信息

Biosens Bioelectron. 2018 Jan 15;99:547-554. doi: 10.1016/j.bios.2017.08.026. Epub 2017 Aug 12.

DOI:10.1016/j.bios.2017.08.026
PMID:28823979
Abstract

Loop-mediated isothermal amplification (LAMP) is a DNA amplification approach characterized by high sensitivity and specificity. In "digital LAMP", small quantities of both template DNA and reagents are encapsulated within a droplet or microwell, allowing for analysis of precious nucleic acid samples in shorter amounts of time relative to traditional DNA amplification protocols (e.g., PCR) with an improved limit of detection. In this study, an integrated, self-driven microfluidic chip was designed to carry out digital LAMP. The entire quantification process could be automatically performed on this chip via capillary forces enabled through microwells comprised of polydimethylsiloxane (PDMS) surfaces coated with a hydrophilic film; no external pumps were required. Moreover, digitized droplets could be separated from each other by normally-closed microvalves. The contact angle of the hydrophilic film-coated PDMS surface was only 14.3°. This is the first time that a rapid (30min) and simple method has been used to create hydrophilic PDMS surfaces that allow for digital LAMP to be performed in a self-driven microfluidic device. As a proof of concept, amplification of a gene specific to a vancomycin-resistant Enterococcus strain was performed on the developed microfluidic chip within 30min, and the limit of detection was only 11 copies with a volume of 30μL. This device may therefore become a promising tool for clinical diagnosis and point-of-care applications.

摘要

环介导等温扩增 (LAMP) 是一种 DNA 扩增方法,其特点是具有高灵敏度和特异性。在“数字 LAMP”中,少量的模板 DNA 和试剂都被封装在液滴或微井中,与传统的 DNA 扩增方法(如 PCR)相比,可以在更短的时间内分析更少量的珍贵核酸样本,并且检测限得到改善。在这项研究中,设计了一种集成的、自驱动的微流控芯片来进行数字 LAMP。通过微井中的毛细作用力,可以在该芯片上自动执行整个定量过程,这些微井由涂有亲水膜的聚二甲基硅氧烷 (PDMS) 表面组成,不需要外部泵。此外,通过常闭微阀可以将数字化的液滴彼此分离。涂有亲水膜的 PDMS 表面的接触角仅为 14.3°。这是首次使用快速(30min)且简单的方法来创建亲水 PDMS 表面,从而可以在自驱动微流控设备中进行数字 LAMP。作为概念验证,在开发的微流控芯片上,在 30min 内对耐万古霉素肠球菌菌株特异性基因进行了扩增,检测限仅为 11 拷贝,体积为 30μL。因此,该设备可能成为临床诊断和即时护理应用的有前途的工具。

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