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使用多壁碳纳米管修饰的丝网印刷碳电极快速检测单链DNA和RNA

Rapid detection of ssDNA and RNA using multi-walled carbon nanotubes modified screen-printed carbon electrode.

作者信息

Ye Yongkang, Ju Huangxian

机构信息

Department of Chemistry, Institute of Analytical Science, Key Laboratory of Analytical Chemistry for Life Science, Nanjing University, Nanjing 210093, PR China.

出版信息

Biosens Bioelectron. 2005 Nov 15;21(5):735-41. doi: 10.1016/j.bios.2005.01.004.

Abstract

A method for rapid sensitive detection of DNA or RNA was designed using a composite screen-printed carbon electrode modified with multi-walled carbon nanotubes (MWNTs). MWNTs showed catalytic characteristics for the direct electrochemical oxidation of guanine or adenine residues of signal strand DNA (ssDNA) and adenine residues of RNA, leading to indicator-free detection of ssDNA and RNA concentrations. With an accumulation time of 5 min, the proposed method could be used for detection of calf thymus ssDNA ranging from 17.0 to 345 microg ml(-1) with a detection limit of 2.0 microg ml(-1) at 3 sigma and yeast tRNA ranging from 8.2 microg ml(-1) to 4.1 mg ml(-1). AC impedance was employed to characterize the surface of modified electrodes. The advantages of convenient fabrication, low-cost detection, short analysis time and combination with nanotechnology for increasing the sensitivity made the subject worthy of special emphasis in the research programs and sources of new commercial products.

摘要

设计了一种使用多壁碳纳米管(MWNTs)修饰的复合丝网印刷碳电极快速灵敏检测DNA或RNA的方法。多壁碳纳米管对信号链DNA(ssDNA)的鸟嘌呤或腺嘌呤残基以及RNA的腺嘌呤残基的直接电化学氧化具有催化特性,从而实现了对ssDNA和RNA浓度的无指示剂检测。在5分钟的积累时间下,该方法可用于检测浓度范围为17.0至345微克/毫升的小牛胸腺ssDNA,在3σ时检测限为2.0微克/毫升,以及浓度范围为8.2微克/毫升至4.1毫克/毫升的酵母tRNA。采用交流阻抗对修饰电极表面进行表征。该方法具有制备方便、检测成本低、分析时间短以及与纳米技术结合以提高灵敏度等优点,使其在研究项目和新型商业产品来源中值得特别关注。

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