Escamilla-Gómez Vanessa, Campuzano Susana, Pedrero María, Pingarrón José M
Departamento Química Analítica, Facultad de CC. Químicas, Universidad Complutense de Madrid, E-28040 Madrid, Spain.
Biosens Bioelectron. 2009 Jul 15;24(11):3365-71. doi: 10.1016/j.bios.2009.04.047. Epub 2009 May 7.
Label-free electrochemical impedance immunosensors for the detection and quantification of Escherichia coli (E. coli) using self-assembled monolayers (SAMs)-modified gold screen-printed electrodes (AuSPEs) were developed. Two different immunosensor configurations were tested and compared. In the first one, the immunosensing design was based on the covalent immobilization of anti-E. coli at AuSPEs using the homobifunctional cross-linker 3,3'-dithiobis[sulfosuccinimidylpropionate] (DTSSP). The other one was based on the immobilization of the thiolated antibody onto the electrode surface. In both cases, the evaluation of the developed immunosensors performance was accomplished through the monitoring of the electron-transfer resistance detected by electrochemical impedance spectroscopy (EIS) in the presence of [Fe(CN)(6)(3-)]/[Fe(CN)(6)(4-)] as redox probe. The configuration using the thiolated antibodies gave rise to a better analytical performance, exhibiting a linear relationship between the increment in the electron-transfer resistance (DeltaR(et)) and the logarithmic value of the E. coli concentration in the 5-1.0 x 10(8) cfu mL(-1) range. The limit of detection achieved, with no need for preconcentration or pre-enrichment steps was 3.3 cfu mL(-1). The developed immunosensors showed a high selectivity against Staphylococcus aureus (S. aureus) and Salmonella choleraesuis (S. choleraesuis). The usefulness of the thiolated antibodies-based design for the rapid analysis (1h) of 10 cfu mL(-1)E. coli inoculated river and tap water samples was demonstrated.
开发了用于检测和定量大肠杆菌(E. coli)的无标记电化学阻抗免疫传感器,该传感器使用自组装单分子层(SAMs)修饰的金丝网印刷电极(AuSPEs)。测试并比较了两种不同的免疫传感器配置。在第一种配置中,免疫传感设计基于使用同双功能交联剂3,3'-二硫代双[磺基琥珀酰亚胺丙酸酯](DTSSP)将抗大肠杆菌共价固定在AuSPEs上。另一种配置基于将硫醇化抗体固定在电极表面。在这两种情况下,通过监测在存在[Fe(CN)₆³⁻]/[Fe(CN)₆⁴⁻]作为氧化还原探针时通过电化学阻抗谱(EIS)检测到的电子转移电阻,来评估所开发免疫传感器的性能。使用硫醇化抗体的配置产生了更好的分析性能,在5 - 1.0×10⁸ cfu mL⁻¹范围内,电子转移电阻的增量(ΔRet)与大肠杆菌浓度的对数值之间呈现线性关系。无需预浓缩或预富集步骤即可达到的检测限为3.3 cfu mL⁻¹。所开发的免疫传感器对金黄色葡萄球菌(S. aureus)和猪霍乱沙门氏菌(S. choleraesuis)显示出高选择性。证明了基于硫醇化抗体的设计对于快速分析(1小时)接种了10 cfu mL⁻¹大肠杆菌的河水和自来水样品的实用性。