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使用激光烧蚀塑料层压板制造的并行微流道固定装置,用于电化学和化学发光生物检测 DNA。

A parallel microfluidic channel fixture fabricated using laser ablated plastic laminates for electrochemical and chemiluminescent biodetection of DNA.

机构信息

Biosensors and Nanomaterials, Sandia National Laboratories, P.O. Box 5800, MS-0892, Albuquerque, New Mexico 87185, USA.

出版信息

Biomicrofluidics. 2011 Dec;5(4):44115-4411514. doi: 10.1063/1.3664694. Epub 2011 Dec 15.

Abstract

Herein is described the fabrication and use of a plastic multilayer 3-channel microfluidic fixture. Multilayer devices were produced by laser machining of plastic polymethylmethacrylate and polyethyleneterapthalate laminates by ablation. The fixture consisted of an array of nine individually addressable gold or gold/ITO working electrodes, and a resistive platinum heating element. Laser machining of both the fluidic pathways in the plastic laminates, and the stencil masks used for thermal evaporation to form electrode regions on the plastic laminates, enabled rapid and inexpensive implementation of design changes. Electrochemiluminescence reactions in the fixture were achieved and monitored through ITO electrodes. Electroaddressable aryl diazonium chemistry was employed to selectively pattern gold electrodes for electrochemical multianalyte DNA detection from double stranded DNA (dsDNA) samples. Electrochemical detection of dsDNA was achieved by melting of dsDNA molecules in solution with the integrated heater, allowing detection of DNA sequences specific to breast and colorectal cancers with a non-specific binding control. Following detection, the array surface could be renewed via high temperature (95 °C) stripping using the integrated heating element. This versatile and simple method for prototyping devices shows potential for further development of highly integrated, multi-functional bioanalytical devices.

摘要

本文描述了一种塑料多层 3 通道微流控夹具的制作和使用。多层器件是通过激光烧蚀对聚甲基丙烯酸甲酯和聚对苯二甲酸乙二醇酯层压板进行激光加工制造的。该夹具由 9 个可单独寻址的金或金/ITO 工作电极阵列和一个电阻式铂加热元件组成。对塑料层压板中的流体通道以及用于热蒸发以在塑料层压板上形成电极区域的模板掩模进行激光加工,使得设计变更的快速和低成本实现成为可能。通过 ITO 电极实现并监测夹具中的电化学发光反应。电寻址芳基重氮化学被用于选择性地对金电极进行图案化,以从双链 DNA(dsDNA)样品中进行电化学多分析物 DNA 检测。通过集成加热器使溶液中的 dsDNA 分子熔化来实现 dsDNA 的电化学检测,从而可以检测到具有非特异性结合对照的乳腺癌和结直肠癌的特异性 DNA 序列。检测后,通过集成加热元件在高温(95°C)下进行剥离,可对阵列表面进行更新。这种用于原型设备的通用且简单的方法显示出进一步开发高度集成、多功能生物分析设备的潜力。

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