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适配体/量子点电化学同时检测多种小分子。

Aptamer/quantum dot-based simultaneous electrochemical detection of multiple small molecules.

机构信息

Key Laboratory on Luminescence and Real-Time Analysis, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.

出版信息

Anal Chim Acta. 2011 Mar 4;688(2):99-103. doi: 10.1016/j.aca.2010.12.017. Epub 2010 Dec 16.

Abstract

A novel strategy for "signal on" and sensitive one-spot simultaneous detection of multiple small molecular analytes based on electrochemically encoded barcode quantum dot (QD) tags is described. The target analytes, adenosine triphosphate (ATP) and cocaine, respectively, are sandwiched between the corresponding set of surface-immobilized primary binding aptamers and the secondary binding aptamer/QD bioconjugates. The captured QDs yield distinct electrochemical signatures after acid dissolution, whose position and size reflect the identity and level, respectively, of the corresponding target analytes. Due to the inherent amplification feature of the QD labels and the "signal on" detection scheme, as well as the sensitive monitoring of the metal ions released upon acid dissolution of the QD labels, low detection limits of 30 nM and 50 nM were obtained for ATP and cocaine, respectively, in our assays. Our multi-analyte sensing system also shows high specificity to target analytes and promising applicability to complex sample matrix, which makes the proposed assay protocol an attractive route for screening of small molecules in clinical diagnosis.

摘要

一种基于电化学编码条码量子点(QD)标签的新型“信号开启”和敏感的单点同时检测多种小分子分析物的策略被描述。目标分析物,三磷酸腺苷(ATP)和可卡因,分别夹在相应的一组表面固定的初级结合适体和二级结合适体/QD 生物缀合物之间。捕获的 QD 在酸溶解后产生独特的电化学特征,其位置和大小分别反映相应目标分析物的身份和水平。由于 QD 标签的固有放大特性和“信号开启”检测方案,以及对 QD 标签酸溶解释放的金属离子的敏感监测,在我们的测定中,ATP 和可卡因的检测限分别低至 30 nM 和 50 nM。我们的多分析物传感系统对目标分析物也表现出高特异性和复杂样品基质的应用前景,这使得所提出的测定方案成为临床诊断中小分子筛选的有吸引力的途径。

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