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Analysis of Microcystins in Drinking Water by ELISA and LC/MS/MS

机译:ELISA和LC / MS / MS分析饮用水中的微囊藻毒素

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Enzyme-linked immunosorbent assay (ELISA) and liquid chromatography/tandem mass spectrometry (LC/MS/MS) were compared for analyzing microcystins in water. ELISA results of microcystin-LR spiked into raw water samples were close to the spike concentrations, but method variability was ±25%. However, ELISA-derived microcystin- LA concentrations were two to three times higher than the spike concentrations obtained using the kit-provided microcystin-LR standards, indicating the need for variant-appropriate ELISA standards. LC/MS/MS results agreed with spike concentrations for all variants in reagent water, but matrix suppression was observed in some raw waters. In bench-scale studies, ozonated microcystins generated low-level positive responses by ELISA and a protein phosphatase inhibition assay, even though microcystins were not detected by LC/MS/MS. These findings indicate that ELISA results—particularly in treated water—should be interpreted with caution because of the possibility of false-positives, relatively high variability, and differential detection of some variants.
机译:比较了酶联免疫吸附测定(ELISA)和液相色谱/串联质谱(LC / MS / MS)来分析水中的微囊藻毒素。加标在原水样品中的微囊藻毒素-LR的ELISA结果与加标浓度接近,但方法变异性为±25%。但是,源自ELISA的微囊藻毒素LA浓度是使用试剂盒提供的微囊藻毒素LR标准品获得的加标浓度的2至3倍,这表明需要适用于变体的ELISA标准。 LC / MS / MS结果与试剂水中所有变体的加标浓度一致,但在某些原水中观察到基质抑制。在实验室规模的研究中,即使LC / MS / MS未检测到微囊藻毒素,臭氧化的微囊藻毒素也可通过ELISA和蛋白磷酸酶抑制试验产生低水平的阳性反应。这些发现表明,ELISA结果(特别是在处理过的水中)应谨慎解释,因为可能会出现假阳性,相对较高的变异性以及某些变异的差异检测。

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