Podunavac Ivana, Kukkar Manil, Léguillier Vincent, Rizzotto Francesco, Pavlovic Zoran, Janjušević Ljiljana, Costache Vlad, Radonic Vasa, Vidic Jasmina
University of Novi Sad, BioSense Institute, 21000 Novi Sad, Serbia.
Université Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, UMR 1319, 78350 Jouy-en-Josas, France.
Talanta. 2023 Jul 1;259:124557. doi: 10.1016/j.talanta.2023.124557. Epub 2023 Apr 17.
Gold electrodes are one of most prevalent substrates in electrochemical biosensors because they can be easily and highly efficiently functionalized with thiolated biomolecules. However, conventional methods to fabricate gold electrodes are costly, time-consuming and require onerous equipment. Here, an affordable method for rapid fabrication of an electrochemical immunosensor for Escherichia coli detection is presented. The gold electrode was generated using 24-karat gold leaves and lowcost polyvinyl chloride adhesive sheets covered with an insulating PTFE layer. The goldleaf electrode (GLE) was patterned using laser ablation and characterized by cyclic voltammetry, electrochemical impedance spectroscopy, scanning electronic microscopy, contact angle and 3D profiling. The GLEs were modified by a self-assembled mercaptopropionic monolayer, followed by surface activation to allow binding of the specific anti-E. coli antibody via carbodiimide linking. The biosensor showed a detection limit of 2 CFU/mL and a linear dynamic range of 10-10 CFU/mL for E. coli cells. No false positive signals were obtained from control bacteria. The obtained results demonstrated suitability of GLE for use in biosensors with high reliability and reproducibility. It is foreseeable that our work will inspire design of point-of-need biosensors broadly applicable in low-resource settings.
金电极是电化学生物传感器中最普遍的基底之一,因为它们可以很容易且高效地用硫醇化生物分子进行功能化修饰。然而,传统的金电极制造方法成本高、耗时且需要昂贵的设备。在此,我们提出一种经济实惠的方法,用于快速制造用于检测大肠杆菌的电化学免疫传感器。金电极是使用24K金叶和覆盖有绝缘聚四氟乙烯层的低成本聚氯乙烯胶粘片制成的。金叶电极(GLE)通过激光烧蚀进行图案化,并通过循环伏安法、电化学阻抗谱、扫描电子显微镜、接触角和三维轮廓分析进行表征。GLE先用自组装的巯基丙酸单层进行修饰,然后进行表面活化,以便通过碳二亚胺连接使特异性抗大肠杆菌抗体结合。该生物传感器对大肠杆菌细胞的检测限为2 CFU/mL,线性动态范围为10-10 CFU/mL。对照细菌未获得假阳性信号。所得结果表明GLE适用于具有高可靠性和可重复性的生物传感器。可以预见,我们的工作将激发适用于低资源环境的即时检测生物传感器的设计。