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Enzyme-linked immunosorbent assay and immunochromatographic strip for rapid detection of atrazine in water samples
Authors:Yu Na  Wei Sheng  Meng Yuan  Lingling Li  Bing Liu  Yan Zhang  Shuo Wang
Institution:1. Institute of Analytical Science, Shaanxi Provincial Key Laboratory of Electroanalytical Chemistry, Northwest University, Xi’an, Shaanxi, 710069, People’s Republic of China
Abstract:We have developed a heterologous direct competitive enzyme-linked immunosorbent assay (ELISA) and a colloidal gold-based immunochromatographic (ICG) strip for the determination of the herbicide atrazine in water samples. The ELISA had a half-maximum inhibition concentration (IC50) of 0.12 ng mL?1 and a limit of detection (LOD, calculated as the IC15 value) of 0.01 ng mL?1. The average of recoveries for all spiked water samples was 96.5%. There was a good correlation between the data determined by this ELISA and those obtained by high performance liquid chromatography (HPLC) (r 2 ?=?0.996). The visual LOD of the ICG strip assay was 2 ng mL?1. The assay process only took 10 min, and no sample pretreatment was required. Its high specificity, sensitivity and fast detection made the strip well suited for on-site screening of atrazine in water samples. Both the ELISA and the ICG strip assay are useful for rapid analysis of a large number of water samples at low cost.
Figure
A heterologous direct competitive enzyme-linked immunosorbent assay (ELISA) and a colloidal gold-based immunochromatographic (ICG) strip assay are proposed for the determination of the herbicide atrazine in water samples.
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