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基于适配体的安培法测定氨苄西林,使用单链 DNA 结合蛋白和 DNA 功能化金纳米粒子。

Aptamer based voltammetric determination of ampicillin using a single-stranded DNA binding protein and DNA functionalized gold nanoparticles.

机构信息

College of Resources and Environment, Key Laboratory of Agricultural Environment in Universities of Shandong, Shandong Agricultural University, Taian, 271018, People's Republic of China.

College of Chemistry and Material Science, Shandong Agricultural University, 271018, Taian, Shandong, People's Republic of China.

出版信息

Mikrochim Acta. 2017 Dec 20;185(1):68. doi: 10.1007/s00604-017-2566-8.

Abstract

An aptamer based method is described for the electrochemical determination of ampicillin. It is based on the use of DNA aptamer, DNA functionalized gold nanoparticles (DNA-AuNPs), and single-stranded DNA binding protein (ssDNA-BP). When the aptamer hybridizes with the target DNA on the AuNPs, the ssDNA-BP is captured on the electrode surface via its specific interaction with ss-DNA. This results in a decreased electrochemical signal of the redox probe Fe(CN) which is measured best at a voltage of 0.188 mV (vs. reference electrode). In the presence of ampicillin, the formation of aptamer-ampicillin conjugate blocks the further immobilization of DNA-AuNPs and ssDNA-BP, and this leads to an increased response. The method has a linear reposne that convers the 1 pM to 5 nM ampicillin concentration range, with a 0.38 pM detection limit (at an S/N ratio of 3). The assay is selective, stable and reproducible. It was applied to the determination of ampicillin in spiked milk samples where it gave recoveries ranging from 95.5 to 105.5%. Graphical abstract Schematic of a simple and sensitive electrochemical apta-biosensor for ampicillin detection. It is based on the use of gold nanoparticles (AuNPs), DNA aptamer, DNA functionalized AuNPs (DNA-AuNPs), and single-strand DNA binding protein (SSBP).

摘要

一种基于适体的电化学测定方法被描述用于氨苄西林的检测。该方法基于使用 DNA 适体、DNA 功能化金纳米粒子(DNA-AuNPs)和单链 DNA 结合蛋白(ssDNA-BP)。当适体与 AuNPs 上的靶 DNA 杂交时,ssDNA-BP 通过其与 ss-DNA 的特异性相互作用被捕获在电极表面。这导致氧化还原探针 Fe(CN)的电化学信号降低,其最佳测量电压为 0.188 mV(相对于参比电极)。在氨苄西林存在下,适体-氨苄西林缀合物的形成阻止了 DNA-AuNPs 和 ssDNA-BP 的进一步固定,这导致响应增加。该方法具有线性响应,可将 1 pM 至 5 nM 的氨苄西林浓度范围转换,检测限为 0.38 pM(信噪比为 3)。该测定具有选择性、稳定性和重现性。它被应用于加标牛奶样品中氨苄西林的测定,回收率范围为 95.5%至 105.5%。

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