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基于 AuPd NPs@UiO-66-NH/CoSe 和 RecJf 外切酶辅助信号放大的磺胺喹噁啉灵敏电化学适体传感器。

Sensitive electrochemical aptasensor for determination of sulfaquinoxaline based on AuPd NPs@UiO-66-NH/CoSe and RecJf exonuclease-assisted signal amplification.

机构信息

School of Food Science and Technology, Henan University of Technology, Zhengzhou, Henan, 450001, PR China.

School of Food Science and Technology, Henan University of Technology, Zhengzhou, Henan, 450001, PR China.

出版信息

Anal Chim Acta. 2021 Oct 16;1182:338948. doi: 10.1016/j.aca.2021.338948. Epub 2021 Aug 13.

DOI:10.1016/j.aca.2021.338948
PMID:34602189
Abstract

The authors designed a sensitive label-free electrochemical aptasensor for the detection of sulfaquinoxaline (SQX), including the AuPd NPs@UiO-66-NH/CoSe nanocomposites and RecJf exonuclease-assisted target recycle signal amplification strategy. AuPd NPs@UiO-66-NH/CoSe nanocomposite with excellent conductivity and numerous active sites was successfully synthesized to provide a favorable sensing platform and load more double-strand DNA (dsDNA) on the electrode surface. The negatively charged phosphate group of the oligonucleotide and [Fe (CN)] repel each other electrostatically, resulting in very low electrical signals. In the presence of SQX, its corresponding aptamer will be released from the double-stranded structure and then digested by RecJf exonuclease, which resulted in the SQX being released to initiate the next recycling to help amplify the DPV signal. Under the optimal conditions, the peak current has a linear relationship with the logarithmic of SQX concentration in the range of 1 pg/mL∼100 ng/mL and the obtained detection limit was 0.547 pg/mL. Furthermore, the contrasted aptasensor possess reliable specificity, reproducibility and stability toward SQX, and has been applied to detect SQX in pork samples with a satisfied recovery varied from 94.40% to 95.98%.

摘要

作者设计了一种用于检测磺胺喹噁啉(SQX)的灵敏无标记电化学适体传感器,包括 AuPd NPs@UiO-66-NH/CoSe 纳米复合材料和 RecJf 外切核酸酶辅助目标循环信号放大策略。成功合成了具有优异导电性和众多活性位点的 AuPd NPs@UiO-66-NH/CoSe 纳米复合材料,为传感器提供了有利的传感平台,并在电极表面负载了更多的双链 DNA(dsDNA)。寡核苷酸的带负电荷的磷酸基团和 [Fe(CN)] 之间存在静电排斥,导致电信号非常低。在 SQX 的存在下,其对应的适体将从双链结构中释放出来,然后被 RecJf 外切核酸酶消化,从而导致 SQX 被释放以启动下一次循环以帮助放大 DPV 信号。在最佳条件下,峰电流与 SQX 浓度的对数在 1 pg/mL∼100 ng/mL 的范围内呈线性关系,检测限为 0.547 pg/mL。此外,对比适体传感器对 SQX 具有可靠的特异性、重现性和稳定性,已应用于猪肉样品中 SQX 的检测,回收率在 94.40%至 95.98%之间。

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