首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Amperometric immunoassay for the detection of Salmonella pullorum using a screen - printed carbon electrode modified with gold nanoparticle-coated reduced graphene oxide and immunomagnetic beads
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Amperometric immunoassay for the detection of Salmonella pullorum using a screen - printed carbon electrode modified with gold nanoparticle-coated reduced graphene oxide and immunomagnetic beads

机译:使用丝网印刷碳电极修饰金纳米粒子涂层的氧化石墨烯和免疫磁珠修饰的安培沙门氏菌的安培免疫分析

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The article describes a sandwich electrochemical immunoassay for detecting the food pathogen Salmonella pullorum (S. pullorum). The assay is based on the use of immunomagnetic beads (IMB) and reduced graphene oxide coated with gold nanoparticles (rGO/AuNPs) acting as an electrochemical label. The IMB were prepared via conjugation of antibody against S. pullorum (Ab(1)) to silica coated magnetic beads (SiO2/Fe3O4) and were used to capture S. pullorum from the sample. The rGO/AuNP were prepared by co-reduction of chloroauric acid and graphene oxide and then linked to secondary antibody (Ab(2)). This conjugate served as a label in a sandwich immunoassay to produce signals. The electrochemical immunoassay was carried out by immobilizing the rGO/AuNP/Ab(2)/S/IMB complex on a four channel screen-printed carbon electrode (4-SPCE). The assay involves the following steps: (a) Exposure of the modified 4-SPCE to the sample; (b) Electro-oxidation of the modified 4-SPCE in 0.2 M HCl; and (c) Differential pulse voltammetry (DPV). It is found that the use of the rGO/AuNP leads to strong signal amplification. The DPV signal (at an optimal working potential of +1.25 V vs. Ag/AgCl for 120 s) is linearly related to the logarithm of the concentration of S. pullorum in the range from 10(2) to 10(6) CFUa <...mLaEuro3/4(1). The detection limit is as low as 89 CFUa <...mLaEuro3/4(1). This nanoparticle-based immunoassay excels by its low cost and ease of operation, thereby providing a promising tool in clinical analysis.
机译:该文章介绍了一种夹心电化学免疫测定法,用于检测食物病原体沙门氏菌(S. Pullorum)。该测定基于使用免疫磁珠(IMB)和涂有金纳米颗粒(rGO / AuNPs)的还原氧化石墨烯作为电化学标记。通过将抗白痢链球菌(Ab(1))的抗体与二氧化硅包被的磁珠(SiO2 / Fe3O4)偶联来制备IMB,并将其用于从样品中捕获白痢链球菌。通过共还原氯金酸和氧化石墨烯制备rGO / AuNP,然后与二抗(Ab(2))连接。该缀合物在三明治免疫测定中用作标记以产生信号。通过将rGO / AuNP / Ab(2)/ S / IMB复合物固定在四通道丝网印刷碳电极(4-SPCE)上进行电化学免疫分析。该测定包括以下步骤:(a)将修饰的4-SPCE暴露于样品中; (b)在0.2 M HCl中将修饰的4-SPCE电氧化; (c)差分脉冲伏安法(DPV)。发现rGO / AuNP的使用导致强烈的信号放大。 DPV信号(在+1.25 V相对于Ag / AgCl的最佳工作电位下持续120 s)与白痢链球菌浓度在10(2)至10(6)CFUa <的对数线性相关... mLaEuro3 / 4(1)。检测限低至89 CFUa <... mLaEuro3 / 4(1)。这种基于纳米颗粒的免疫测定法以其低成本和易于操作而著称,从而为临床分析提供了有希望的工具。

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