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Analysis of Multiple Endocrine Disruptors in Environmental Waters via Wide-Spectrum Solid-Phase Extraction and Dual-Polarity Ionization LC-Ion Trap-MS/MS

机译:广谱固相萃取和双极性电离LC-离子阱-MS / MS分析环境水中的多种内分泌干扰物

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An analytical method for the determination of 35 endocrine disrupting chemicals (EDCs) present in the aquatic environment was developed and validated. The procedure includes an off-line solid-phase extraction of 500-mL water samples using wide-spectrum polymer packing material combined with two LC-ESI-MS/MS runs, in negative and positive ionization modes. Limits of quantitation were established between 0.1 and 20.0 ng/L. Satisfactory recoveries were obtained ranging from 80.1 to 110.2%. Calibration, using deuterated internal standardization, was performed by linear regression analysis. Linearity (R~(2)>0.99) was demonstrated over individually specified ranges using seven calibration points for each analyte. Intrabatch and interbatch precision, as well as accuracy (n=5), were investigated at low, medium, and high concentrations. Precision for all compounds, expressed as the RSD, proved to be less than 17.8 and 20.0%, respectively, for intra- and interbatch. Accuracy, expressed as the mean recovery, was between 83.1 and 108.4% at all concentrations. Stability experiments showed no significant loss or deterioration for any of the analytes. Finally, the method was applied on real samples.
机译:开发并验证了一种用于确定水生环境中存在的35种内分泌干扰物(EDC)的分析方法。该程序包括使用广谱聚合物填充材料和两个LC-ESI-MS / MS运行以负电离和正电离模式对500 mL水样品进行离线固相萃取。定量限在0.1至20.0 ng / L之间。回收率令人满意,为80.1%至110.2%。通过线性回归分析,使用氘化内部标准化进行校准。使用每种分析物的七个校准点在单独指定的范围内证明了线性(R〜(2)> 0.99)。在低,中和高浓度下研究了批内和批间精度以及精度(n = 5)。批内和批间的所有化合物的精密度(分别表示为RSD)分别小于17.8%和20.0%。在所有浓度下,以平均回收率表示的准确度在83.1%至108.4%之间。稳定性实验表明,任何分析物均无明显损失或变质。最后,将该方法应用于真实样本。

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