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Ultrasensitive Electrochemical Immunoassay of Staphylococcal Enterotoxin B in Food Using Enzyme-Nanosilica-Doped Carbon Nanotubes for Signal Amplification

机译:食品中葡萄球菌肠毒素B的超灵敏电化学免疫测定,使用酶-纳米二氧化硅掺杂的碳纳米管进行信号放大

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摘要

A new sandwich-type electrochemical immunoassay for ultrasensitive detection of staphylococcal enterotoxin B (SEB) in food was developed using horseradish peroxidase-nanosilica-doped multi-walled carbon nanotubes (HRPSiCNTs) for signal amplification. Rabbit polyclonal anti-SEB antibodies immobilized on the screen-printed carbon electrode (SPCE) and covalently bound to the HRPSiCNTs were used as capture antibodies and detection antibodies, respectively. In the presence of SEB analyte, the sandwich-type immunocomplex could be formed between the immobilized anti-SEB on the SPCE and anti-SEB-labeled HRPSiCNTs, and the carried HRP could catalyze the electrochemical reduction of H2O2 with the help of thionine. The high content of HRP in the HRPSiCNTs could greatly amplify the electrochemical signal. Under optimal conditions, the reduction current increased with the increase of SEB in the sample, and exhibited a dynamic range of 0.05-15 ng/mL with a low detection limit (LOD) of 10 pg/mL SEB (at 3σ). Intra- and interassay coefficients of variation were below 10%. In addition, the assay was evaluated with SEB spiked samples including watermelon juice, soymilk, apple juice, and pork food, receiving excellent correlation with results from commercially available enzyme-linked immunosorbent assay (ELISA).
机译:使用辣根过氧化物酶-纳米二氧化硅掺杂的多壁碳纳米管(HRPSiCNTs)进行信号放大,开发了一种用于食品中葡萄球菌肠毒素B(SEB)超灵敏检测的新型夹心型电化学免疫测定法。固定在丝网印刷的碳电极(SPCE)上并与HRPSiCNTs共价结合的兔多克隆抗SEB抗体分别用作捕获抗体和检测抗体。在存在SEB分析物的情况下,可以在SPCE上固定的抗SEB与抗SEB标记的HRPSiCNTs之间形成夹心型免疫复合物,并且携带的HRP可以在蛋氨酸的帮助下催化H2O2的电化学还原。 HRPSiCNTs中高含量的HRP可以大大放大电化学信号。在最佳条件下,还原电流随样品中SEB的增加而增加,并表现出0.05-15 ng / mL的动态范围,而SEB的低检测限(LOD)为10 pg / mL(在3σ)。批内和批间变异系数低于10%。此外,用SEB加标样品(包括西瓜汁,豆浆,苹果汁和猪肉食品)对测定进行了评估,与市售酶联免疫吸附测定(ELISA)的结果具有极好的相关性。

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