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Electrochemical DNA biosensor based on gold nanorods for detecting hepatitis B virus

机译:基于金纳米棒的电化学DNA生物传感器检测乙肝病毒

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摘要

The purpose of this work was to fabricate an electrochemical DNA biosensor for detecting hepatitis B virus. Gold nanorods (GNRs), which are known for their conductivity, were used to increase surface area and consequently increase the immobilization of single-stranded DNA (ss-DNA) on the modified gold electrode. The GNRs were characterized via transmission electron microscopy. The morphology of the gold electrode before and after modification with GNRs was characterized by scanning electron microscopy. Atomic-force microscopy was used to evaluate the morphology of the GNR electrode surface before and after interaction with ss-DNA. Cyclic voltammetry was used to monitor DNA immobilization and hybridization, using [Co(phen)(3)](3+) as an electrochemical indicator. The target DNA sequences were quantified at a linear range from 1.0 x 10(-12) to 10.0 x 10(-6) mol L-1, with a detection limit of 2.0 x 10(-12) mol L-1 by 3 sigma. The biosensor had good specificity for distinguishing complementary DNA in the presence of non-complementary and mismatched DNA sequences.
机译:这项工作的目的是制造用于检测乙型肝炎病毒的电化学DNA生物传感器。金纳米棒(GNRs)以其导电性而闻名,可用于增加表面积,从而提高单链DNA(ss-DNA)在修饰金电极上的固定性。通过透射电子显微镜表征GNR。通过扫描电子显微镜表征了用GNR修饰之前和之后的金电极的形态。原子力显微镜用于评估GNR电极表面与ss-DNA相互作用之前和之后的形态。使用[Co(phen)(3)](3+)作为电化学指示剂,使用循环伏安法监测DNA固定化和杂交。靶DNA序列的定量范围为1.0 x 10(-12)到10.0 x 10(-6)mol L-1,检测限为2.0 x 10(-12)mol L-1(3 sigma) 。该生物传感器具有很好的特异性,可以在存在非互补和错配的DNA序列时区分互补的DNA。

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