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A competitive immunoassay based on gold nanoparticles for the detection of chromium in water sampies

机译:一种基于金纳米颗粒的竞争性免疫测定法,用于检测水样中的铬

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摘要

A competitive enzyme-linked immunosorbent assay (ELISA) based on colloidal gold nanoparticles modified with a monoclonal antibody and horseradish peroxidase (HRP) was developed and validated for the quantitative determination of chromium in water samples. The monoclonal antibody against Cr(III)-EDTA secreted by the hybridoma cell line 5G12C5 was prepared through cell fusion. The ELISA conditions were optimized using the chessboard method and the sensitivity and specificity of this assay were determined. The results show that this competitive immunoassay has a half maximum inhibition concentration (IC50) of 3.85 ng mL~(-1) and a limit of detection (LOD) of 0.1 ng mL~(-1). Specificity assays revealed that the cross-reactivities (CRs) of this assay with 10 other common metal ions were all below 1%. The accuracy of this immunoassay was confirmed by using certified reference materials (GSBZ50027-94, GSB07-1187-2000). Furthermore, the assay was used to detect the concentrations of Cr(vi) and total chromium in local surface water samples after the pretreatment procedure. The data show that the results of this method correlated well with those obtained from atomic absorption spectroscopy (AAS) (R~2 = 0.9728), and that this method is capable of detecting the amount of total chromium and Cr(vi).
机译:基于单克隆抗体和辣根过氧化物酶(HRP)修饰的胶体金纳米颗粒的竞争性酶联免疫吸附测定(ELISA)得以开发,并已用于定量测定水中的铬。通过细胞融合制备由杂交瘤细胞系5G12C5分泌的针对Cr(III)-EDTA的单克隆抗体。使用棋盘法优化了ELISA条件,并确定了该测定的灵敏度和特异性。结果表明,该竞争性免疫测定的最大半数抑制浓度(IC50)为3.85 ng mL〜(-1),检测极限(LOD)为0.1 ng mL〜(-1)。特异性测定表明,该测定与其他10种常见金属离子的交叉反应性(CR)均低于1%。该免疫测定的准确性通过使用认证的参考材料(GSBZ50027-94,GSB07-1187-2000)进行了确认。此外,该方法还用于检测预处理程序后局部地表水样品中Cr(vi)和总铬的浓度。数据表明,该方法的结果与通过原子吸收光谱法(AAS)获得的结果具有很好的相关性(R〜2 = 0.9728),并且该方法能够检测总铬和Cr(vi)的量。

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