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一种用于数字环介导等温DNA扩增检测的LED驱动的金纳米颗粒-聚二甲基硅氧烷微流控芯片及集成装置。

An LED-Driven AuNPs-PDMS Microfluidic Chip and Integrated Device for the Detection of Digital Loop-Mediated Isothermal DNA Amplification.

作者信息

Zhang Zengming, Zhao Shuhao, Hu Fei, Yang Guangpu, Li Juan, Tian Hui, Peng Niancai

机构信息

State Key Laboratory for Manufacturing Systems Engineering, Xi'an Jiaotong University, Xi'an, 710054, Shaanxi, China.

出版信息

Micromachines (Basel). 2020 Feb 8;11(2):177. doi: 10.3390/mi11020177.

Abstract

The sensitive quantification of low-abundance nucleic acids holds importance for a range of clinical applications and biological studies. In this study, we describe a facile microfluidic chip for absolute DNA quantifications based on the digital loop-mediated isothermal amplification (digital LAMP) method. This microfluidic chip integrates a cross-flow channel for droplet generation with a micro-cavity for droplet tiling. DNA templates in the LAMP reagent were divided into ~20,000 water-in-oil droplets at the cross-flow channel. The droplets were then tiled in the micro-cavity for isothermal amplification and fluorescent detection. Different from the existing polydimethylsiloxane (PDMS) microfluidic chips, this study incorporates gold nanoparticles (AuNPs) into PDMS substrate through silica coating and dodecanol modification. The digital LAMP chip prepared by AuNPs-PDMS combines the benefits of the microstructure manufacturing performance of PDMS with the light-to-heat conversion advantages of AuNPs. Upon illumination with a near infrared (NIR) LED, the droplets were stably and efficiently heated by the AuNPs in PDMS. We further introduce an integrated device with a NIR heating unit and a fluorescent detection unit. The system could detect HBV (hepatitis B virus)-DNA at a concentration of 1 × 10 to 1 × 10 copies/μL. The LED-driven digital LAMP chip and the integrated device; therefore, demonstrate high accuracy and excellent performance for the absolute quantification of low-abundance nucleic acids, showing the advantages of integration, miniaturization, cost, and power consumption.

摘要

低丰度核酸的灵敏定量对于一系列临床应用和生物学研究都具有重要意义。在本研究中,我们描述了一种基于数字环介导等温扩增(数字LAMP)方法用于绝对DNA定量的简易微流控芯片。该微流控芯片将用于液滴生成的错流通道与用于液滴平铺的微腔集成在一起。LAMP试剂中的DNA模板在错流通道处被分成约20,000个油包水液滴。然后将这些液滴平铺在微腔中进行等温扩增和荧光检测。与现有的聚二甲基硅氧烷(PDMS)微流控芯片不同,本研究通过二氧化硅涂层和十二烷醇修饰将金纳米颗粒(AuNPs)掺入PDMS基板中。由AuNPs-PDMS制备的数字LAMP芯片结合了PDMS的微结构制造性能优势和AuNPs的光热转换优势。在用近红外(NIR)LED照射时,PDMS中的AuNPs能稳定且高效地加热液滴。我们还引入了一种带有近红外加热单元和荧光检测单元的集成装置。该系统能够检测浓度为1×10至1×10拷贝/μL的乙肝病毒(HBV)-DNA。因此,LED驱动的数字LAMP芯片和集成装置在低丰度核酸的绝对定量方面展现出高精度和卓越性能,体现了集成化、小型化、成本及功耗方面的优势。

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