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

机译:基于适体/量子点的同时电化学检测多个小分子

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摘要

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.
机译:描述了一种基于电化学编码条形码量子点(QD)标签的“信号开启”和灵敏的单点同时检测多种小分子分析物的新颖策略。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一级结合适体和二级结合适体/ QD生物缀合物之间。酸溶解后,捕获的QD产生明显的电化学特征,其位置和大小分别反映了相应目标分析物的身份和水平。由于QD标签固有的扩增功能和“信号开启”检测方案,以及对酸溶解QD标签​​后释放的金属离子的灵敏监测,因此获得了30 nM和50 nM的低检测限在我们的检测方法中分别为ATP和可卡因。我们的多分析物传感系统还显示出对目标分析物的高度特异性,并有望应用于复杂的样品基质,这使得拟议的分析方案成为在临床诊断中筛选小分子的诱人途径。

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