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首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >G-Quadruplex-based DNAzyme for colorimetric detection of cocaine: Using magnetic nanoparticles as the separation and amplification element
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G-Quadruplex-based DNAzyme for colorimetric detection of cocaine: Using magnetic nanoparticles as the separation and amplification element

机译:基于G四联体的DNA酶用于可卡因的比色检测:使用磁性纳米颗粒作为分离和扩增元件

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摘要

The appearance of the aptamer provides good recognition elements for small molecules, especially for drugs. In this work, by combining the advantages of magnetic nanoparticles (MNPs) with colorimetric drug detection using hemin-G-quadruplex complex as the sensing element, we report a simple and sensitive DNAzyme-based colorimetric sensor for cocaine detection in a 3,3,5,5-tetramethylbenzidine sulfate (TMB)-H_2O_2 reaction system. The whole experimental processes are simplified. Cocaine aptamer fragments, SH-C2, are covalently labeled onto the amine-functionalized MNPs. When the target cocaine and another cocaine aptamer fragments (C1) grafted with G-riched strand AG4 (i.e. C1-AG4) are present simultaneously, the C2 layer on MNPs hybridizes partly with C1-AG4 to bind the cocaine. The C1-AG4 can be combinded with hemin to form DNAzyme which can effectively catalyze the H _2O_2-mediated oxidation of TMB, giving rise to a change in solution color. Importantly, using MNPs as the separation and amplification elements could effectively reduce the background signal and the interference from the real samples. A linear response from 0.1 μM to 20 μM is obtained for cocaine and a detection limit of 50 nM is achieved, which provides high sensitivity and selectivity to detect cocaine.
机译:适体的外观为小分子,尤其是药物提供了良好的识别元件。在这项工作中,通过将磁性纳米颗粒(MNP)的优势与使用hemin-G-quadplexplex复合体作为传感元件的比色药物检测相结合,我们报告了一种简单而灵敏的基于DNAzyme的比色传感器,可用于3,3, 5,5-四甲基联苯胺硫酸盐(TMB)-H_2O_2反应体系。整个实验过程得以简化。可卡因适体片段SH-C2被共价标记在胺官能化的MNP上。当目标可卡因和嫁接到富含G的链AG4(即C1-AG4)的另一个可卡因适体片段(C1)同时存在时,MNP上的C2层与C1-AG4部分杂交以结合可卡因。 C1-AG4可与血红素结合形成DNA酶,可有效催化H _2O_2介导的TMB氧化,从而引起溶液颜色的变化。重要的是,使用MNP作为分离和扩增元件可以有效降低背景信号和来自真实样品的干扰。可卡因的线性响应范围从0.1μM到20μM,检测限达到50 nM,这为检测可卡因提供了高灵敏度和选择性。

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