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Electrochemical Cloth-Based DNA Sensors (ECDSs): A New Class of Electrochemical Gene Sensors

机译:基于电化学布的DNA传感器(ECDS):一类新的电化学基因传感器

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摘要

Electrochemical (EC) sensors have been widely developed for DNA detection, but they are seldom used in a simple, economic, and efficient manner. In this work, for the first time, EC cloth-based DNA sensors (ECDSs) are developed as a new class of EC DNA sensors, without the need for cumbersome chip fabrication and high-cost peripheral facilities. Carbon ink- and solid wax-based screen printing were used to produce ultracheap sensing devices (the cost of one sensor is estimated to be $0.045). Also, a CdTe QDs/MWCNTs nanocomposite (CdTe-MWCNTs) was applied to modify the sensing interface to obtain a stronger EC signal. Specifically, the newly developed double linear hybridization chain reaction (DL-HCR) greatly amplified the EC signal, relative to the conventional linear HCR. Under optimized conditions, target DNA (TD) samples (75-bp DNA fragments prepared via PCR amplification) were determined in a range from 20 fM to 5 nM, with a detection limit of 8.74 fM and relative standard deviations of 2.04% and 4.75% for intra- and inter-assays at 50 pM TD, respectively. Additionally, the ECDSs had an acceptable storage stability and high selectivity. Importantly, the ECDSs, coupled with simple enzyme digestion, could detect genomic DNA from Listeria monocytogenes (L. monocytogenes), and a detection limit of 0.039 ng/mu L was obtained. When coupled with enzyme digestion and PCR amplification, the ECDSs could determine L. monocytogenes in milk samples, with detection limits of approximately 1.64 X 10(4) and 11 CFU/mL. These results demonstrate that the method offers a broad prospect for cost-effective, reliable, and highly sensitive gene-sensing applications.
机译:电化学(EC)传感器已广泛开发用于DNA检测,但它们很少以简单,经济和有效的方式使用。在这项工作中,首次开发EC布料的DNA传感器(ECDS)作为新的EC DNA传感器,无需繁琐的芯片制造和高成本的周边设施。使用碳油墨和固体蜡基丝网印刷来生产超速EAP传感装置(一个传感器的成本估计为0.045美元)。此外,施加CDTE QDS / MWCNT纳米复合材料(CDTE-MWCNT)以改变感测界面以获得更强的EC信号。具体地,新开发的双线性杂交链反应(DL-HCR)相对于常规线性HCR大大扩增EC信号。在优化条件下,靶DNA(Td)样品(通过PCR扩增制备的75bp DNA片段)在20 fm至5nm的范围内测定,检测限为8.74 fm,相对标准偏差为2.04%和4.75%对于50pm Td的分析和分析分别。另外,ECDS具有可接受的存储稳定性和高选择性。重要的是,与简单的酶消化相结合的ECDS可以检测来自李斯特菌单核细胞增生(L.单核细胞元)的基因组DNA,并获得0.039ng / mu L的检测限。当与酶消化和PCR扩增结合时,ECDS可以在牛奶样品中确定L.单核细胞生成,检测限约1.64×10(4)和11CFU / mL。这些结果表明,该方法为具有成本效益,可靠和高度敏感的基因传感应用提供了广泛的前景。

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  • 来源
    《Analytical chemistry》 |2020年第11期|共9页
  • 作者单位

    South China Normal Univ MOE Key Lab Laser Life Sci Guangzhou 510631 Peoples R China;

    South China Normal Univ MOE Key Lab Laser Life Sci Guangzhou 510631 Peoples R China;

    South China Normal Univ MOE Key Lab Laser Life Sci Guangzhou 510631 Peoples R China;

    South China Normal Univ MOE Key Lab Laser Life Sci Guangzhou 510631 Peoples R China;

    South China Univ Technol Guangzhou Peoples Hosp 1 Sch Med Dept Lab Med Guangzhou 510180 Peoples R China;

    South China Normal Univ MOE Key Lab Laser Life Sci Guangzhou 510631 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
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