Guo Yuna, Wang Yu, Liu Su, Yu Jinghua, Wang Hongzhi, Cui Min, Huang Jiadong
Key Laboratory of Chemical Sensing & Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, P.R. China.
Analyst. 2015 Jan 21;140(2):551-9. doi: 10.1039/c4an01463d.
A novel electrochemical immunosensor assay (EIA) for highly sensitive and specific detection of Escherichia coli O157:H7 has been developed. This immunosensor is constructed by the assembly of capture antibody on SG-PEDOT-AuNPs composites modified glass carbon electrode. In the presence of target E. coli O157:H7, horseradish peroxidase (HRP)-labeled antibody is captured on the electrode surface to form a sandwich-type system via the specific identification. As a result, E. coli O157:H7 detection is realized by outputting a redox current from electro-reduction of hydrogen peroxide reaction catalyzed by HRP. In our assay, the combination of the unique properties of sulfonated graphene (SG) and gold nanoparticles (AuNPs) can not only accelerate electron transfer on electrode interface, but also provide an excellent scaffold for the conjugation of capture antibody that significantly improves the target capture efficiency and enhances the sensitivity of the biosensor. The results reveal the calibration plot obtained for E. coli O157:H7 is approximately linear from 7.8 × 10-7.8 × 10(6) colony-forming unit (cfu) mL(-1) with the limit of detection of 3.4 × 10 cfu mL(-1). In addition, the biosensor has been successfully applied to the quantitative assay of E. coli O157:H7 in synthetic samples (spring water and milk). Hence, the developed electrochemical-based immunosensor might provide a useful and practical tool for E. coli O157:H7 determination and related food safety analysis and clinical diagnosis.
一种用于高灵敏度和特异性检测大肠杆菌O157:H7的新型电化学免疫传感器检测法(EIA)已被开发出来。这种免疫传感器是通过将捕获抗体组装在磺化石墨烯-聚(3,4-乙撑二氧噻吩)-金纳米颗粒(SG-PEDOT-AuNPs)复合材料修饰的玻碳电极上构建而成。在目标大肠杆菌O157:H7存在的情况下,辣根过氧化物酶(HRP)标记的抗体通过特异性识别被捕获在电极表面,形成夹心型体系。结果,通过输出由HRP催化的过氧化氢反应的电还原产生的氧化还原电流来实现大肠杆菌O157:H7的检测。在我们的检测方法中,磺化石墨烯(SG)和金纳米颗粒(AuNPs)的独特性质相结合,不仅可以加速电极界面上的电子转移,还能为捕获抗体的缀合提供一个优异的支架,显著提高目标捕获效率并增强生物传感器的灵敏度。结果表明,针对大肠杆菌O157:H7获得的校准曲线在7.8×10⁻⁷至7.8×10⁶菌落形成单位(cfu)mL⁻¹范围内近似呈线性,检测限为3.4×10 cfu mL⁻¹。此外,该生物传感器已成功应用于合成样品(泉水和牛奶)中大肠杆菌O157:H7的定量检测。因此,所开发的基于电化学的免疫传感器可能为大肠杆菌O157:H7的测定以及相关食品安全分析和临床诊断提供一种有用且实用的工具。