SWCNTs modified nanoneedle biosensor for rapid detection of DNA

Darius Saadat-Moghaddam, Jong-Hoon Kim
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Abstract

The increasing availability of genetic information demands more simple and rapid methodology for nucleic acid testing. To this end, cumbersome procedural steps with long amplification time (>1 hour) for polymerase chain reaction (PCR) have been a major challenge for rapid identification of genetic information. This paper addresses the challenge of rapidly identifying genetic information. Unlike other amplification-based detection methods, a nanostructured needle modified with single-walled carbon nanotubes (SWCNTs) is capable of rapidly concentrating and detecting small amounts of DNA, due to a concentration and reaction step controlled by an electric field. The nanoneedle can detect DNA at the concentration of 100 attomolar (aM) in a given sample volume (e.g. 5 μL). Since the nanoneedle device does not require nucleic acid amplification, it is significantly faster and simpler than PCR approaches.
用于快速检测DNA的SWCNTs修饰纳米针生物传感器
随着遗传信息的日益丰富,对核酸检测方法的要求越来越高。为此,聚合酶链反应(PCR)繁琐的扩增时间长(>1小时)的程序步骤已成为快速鉴定遗传信息的主要挑战。本文解决了快速识别遗传信息的挑战。与其他基于扩增的检测方法不同,单壁碳纳米管(SWCNTs)修饰的纳米结构针能够快速浓缩并检测少量DNA,这是由于电场控制的浓度和反应步骤。在给定的样品体积(例如5 μL)中,纳米针可以检测浓度为100原子摩尔(aM)的DNA。由于纳米针装置不需要核酸扩增,它明显比PCR方法更快更简单。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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