NanoBioanalysis Group-Department of Physical and Analytical Chemistry, University of Oviedo, Julián Clavería 8, 33006, Oviedo, Spain.
IATA-CSIC, Avda Agustí Escardino 7, 46980, Paterna, Valencia, Spain.
Talanta. 2020 Mar 1;209:120465. doi: 10.1016/j.talanta.2019.120465. Epub 2019 Oct 11.
A direct competitive immunosensor for the electrochemical determination of Imidacloprid (IMD) pesticide on gold nanoparticle-modified screen-printed carbon electrodes (AuNP-SPCE) is here reported for the first time. Self-obtained specific monoclonal antibodies are immobilized on the AuNP-SPCE taking advantage of the AuNPs biofunctionalization abilities. In our biosensor design, free IMD in the sample competes with IMD conjugated with horseradish peroxidase (IMD-HRP) for the recognition by the antibodies. After that, 3,3',5,5'-Tetramethylbenzidine (TMB) is enzymatically oxidized by HRP, followed by the oxidized TMB reduction back at the surface of the SPCE. This process gives an associated catalytic current (analytical signal) that is inversely proportional to the IMD amount. The main parameters affecting the analytical signal have been optimized, reaching a good precision (repeatability with a RSD of 6%), accuracy (relative error of 6%), stability (up to one month), selectivity and an excellent limit of detection (LOD of 22 pmol L), below the maximum levels allowed by the legislation, with a wide response range (50-10000 pmol L). The detection through antibodies also allows to have an excellent selectivity against other pesticides potentially present in real samples. Low matrix effects were found when analysing IMD in tap water and watermelon samples. The electrochemical immunosensor was also validated with HPLC-MS/MS, the reference method used in official laboratories for IMD analysis, through statistical tests. Our findings make the electrochemical immunosensor as an outstanding method for the rapid and sensitive determination of IMD at the point-of-use.
一种基于金纳米粒子修饰的丝网印刷碳电极(AuNP-SPCE)的电化学测定吡虫啉(IMD)农药的直接竞争免疫传感器,在此首次报道。利用 AuNPs 的生物功能化能力,将自行获得的特异性单克隆抗体固定在 AuNP-SPCE 上。在我们的生物传感器设计中,样品中的游离 IMD 与辣根过氧化物酶偶联的 IMD(IMD-HRP)竞争与抗体的识别。之后,HRP 酶促氧化 3,3',5,5'-四甲基联苯胺(TMB),然后在 SPCE 表面还原氧化的 TMB。该过程给出与 IMD 量成反比的相关催化电流(分析信号)。已优化影响分析信号的主要参数,达到良好的精度(重复性 RSD 为 6%)、准确性(相对误差为 6%)、稳定性(长达一个月)、选择性和出色的检测限(LOD 为 22 pmol L),低于法规允许的最高水平,具有较宽的响应范围(50-10000 pmol L)。通过抗体进行检测还可以对实际样品中可能存在的其他农药具有出色的选择性。在分析自来水中和西瓜样品中的 IMD 时,发现基质效应较低。通过统计检验,通过与 HPLC-MS/MS 进行验证,HPLC-MS/MS 是官方实验室用于 IMD 分析的参考方法。我们的研究结果使电化学免疫传感器成为在现场快速灵敏测定 IMD 的杰出方法。