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DNA的痕量分析:在使用金纳米颗粒的微芯片电泳中的预浓缩、分离及电化学检测

Trace analysis of DNA: preconcentration, separation, and electrochemical detection in microchip electrophoresis using Au nanoparticles.

作者信息

Shiddiky Muhammad J A, Shim Yoon-Bo

机构信息

Department of Chemistry, Pusan National University, Keumjeong-ku, Busan 609-735, South Korea.

出版信息

Anal Chem. 2007 May 15;79(10):3724-33. doi: 10.1021/ac0701177. Epub 2007 Apr 12.

Abstract

We have developed a simple and sensitive on-chip preconcentration, separation, and electrochemical detection (ED) method for trace analysis of DNA. The microchip comprised of three parallel channels: the first two are for the field-amplified sample stacking and subsequent field-amplified sampled injection steps, while the third one is for the microchip gel electrophoresis (MGE) with ED (MGE-ED). To improve preconcentration and separation performances of the method, the stacking and separation buffers containing the hydroxypropyl cellulose (HPC) matrix were modified with gold nanoparticles (AuNPs). The formation of AuNPs and HPC/AuNP-modified buffers were characterized by UV-visible spectroscopy and TEM experiments. The conducting polymer-modified electrode was also modified with AuNPs to enhance detection performances of the electrode. The conducting polymer/AuNP layers act as electrocatalysts for the direct detection of DNA based on their oxidation in a solution phase. The total sensitivity was improved by approximately 25 000-fold when compared with a conventional MGE-ED analysis. The calibration plots were linear (r2 = 0.9993) within the range of 0.003-1.0 pg/microL for a 20-bp DNA sample. The sensitivity was 0.20 nA/(fg/microL), with a detection limit of 5.7 amol in a 50-microL sample, based on S/N = 3. The applicability of the method for the analysis of 13 fragments present in a 100-bp DNA ladder was successfully demonstrated.

摘要

我们开发了一种用于DNA痕量分析的简单且灵敏的芯片上预浓缩、分离及电化学检测(ED)方法。该微芯片由三个平行通道组成:前两个用于场放大样品堆积及随后的场放大样品进样步骤,而第三个用于带有ED的微芯片凝胶电泳(MGE-ED)。为提高该方法的预浓缩和分离性能,用金纳米颗粒(AuNPs)对含有羟丙基纤维素(HPC)基质的堆积和分离缓冲液进行了改性。通过紫外可见光谱和透射电子显微镜实验对AuNPs的形成以及HPC/AuNP改性缓冲液进行了表征。导电聚合物修饰电极也用AuNPs进行了改性以增强电极的检测性能。导电聚合物/AuNP层基于其在溶液相中的氧化作用,作为直接检测DNA的电催化剂。与传统的MGE-ED分析相比,总灵敏度提高了约25000倍。对于20个碱基对的DNA样品,校准曲线在0.003 - 1.0 pg/μL范围内呈线性(r2 = 0.9993)。基于信噪比S/N = 3,在50 μL样品中的灵敏度为0.20 nA/(fg/μL),检测限为5.7 amol。成功证明了该方法对100个碱基对DNA阶梯中存在的13个片段进行分析的适用性。

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