REQUIMTE/LAQV, Instituto Superior de Engenharia do Porto, Instituto Politécnico do Porto, 4200-072 Porto, Portugal; REQUIMTE/LAQV, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto, 4169-007 Porto, Portugal.
REQUIMTE/LAQV, Departamento de Engenharia Química, Faculdade de Engenharia, Universidade do Porto, 4200-465 Porto, Portugal.
Talanta. 2019 Mar 1;194:134-142. doi: 10.1016/j.talanta.2018.10.024. Epub 2018 Oct 12.
Polymeric ion selective electrodes are highly sensitive to changes in zero current ion flow and this offers a route to signal amplification in label-free potentiometric immunosensors. In this work, a label-free potentiometric immunosensor toward Salmonella typhimurium (ST) assembled in a home-made pipette-tip electrode is described. The signal-output amplification was implemented on a gold nanoparticle polymer inclusion membrane (AuNPs-PIM) which was used as sensing platform and for antibody immobilization. Additionally, a marker ion was used to detect the antibody-antigen binding event at the electrode surface. The immunosensor construction was performed in several steps: i) gold salt ions extraction in PVC membrane; ii) AuNPs formation using NaEDTA as reduction agent; iii) antibody anti-Salmonella conjugation on AuNPs-PIM in pipette-tip electrodes. The potential shift observed in potentiometric measurements was derived simply from the blocking effect in the ionic flux caused by antigen-antibody conjugation, without no extra steps, mimetizing the ion-channel sensors. A detection limit of 6 cells mL was attained. As proof-of-concept, recovery studies were performed in spiked commercial apple juice samples with success. Due to the simplicity of use, the appealing cost of equipment and sensor production and being able to provide a quick analytical response (less than 1 h for a complete assay, including sample preparation for analysis), this scheme represents a good prototype device for the detection of foodborne pathogens like ST or other immune-responsive bacteria.
聚合离子选择性电极对零电流离子流动的变化非常敏感,这为无标记电位免疫传感器中的信号放大提供了一种途径。在这项工作中,描述了一种在自制的微量滴定电极中组装的针对鼠伤寒沙门氏菌(ST)的无标记电位免疫传感器。信号输出放大是在金纳米粒子聚合物包容膜(AuNPs-PIM)上实现的,该膜用作传感平台和抗体固定化。此外,还使用标记离子来检测电极表面的抗体-抗原结合事件。免疫传感器的构建分以下几个步骤进行:i)在 PVC 膜中提取金盐离子;ii)使用 NaEDTA 作为还原剂形成 AuNPs;iii)在微量滴定电极上将抗沙门氏菌抗体共轭到 AuNPs-PIM 上。在电位测量中观察到的电位偏移仅仅是由于抗原-抗体结合引起的离子通量的阻断效应,而无需额外的步骤,模拟了离子通道传感器。检测限达到 6 个细胞 mL。作为概念验证,在添加了商业苹果汁样品中进行了回收研究,取得了成功。由于使用简单、设备和传感器生产成本低廉、能够快速提供分析响应(对于完整的分析,包括样品制备,少于 1 小时),该方案代表了用于检测食源性病原体(如 ST 或其他免疫反应性细菌)的良好原型设备。