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Standard addition method for the determination of pharmaceutical residues in drinking water by SPE-LC-MS/MS

机译:SPE-LC-MS / MS测定饮用水中药物残留的标准添加方法

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The study of the occurrence and fate of pharmaceutical compounds in drinking or waste water processes has become very popular in recent years. Liquid chromatography with tandem mass spectrometry is a powerful analytical tool often used to determine pharmaceutical residues at trace level in water. However, many steps may disrupt the analytical procedure and bias the results. A list of 27 environmentally relevant molecules, including various therapeutic classes and (cardiovascular, veterinary and human antibiotics, neuroleptics, non-steroidal anti-inflammatory drugs, hormones and other miscellaneous pharmaceutical compounds), was selected. In this work, a method was developed using ultra performance liquid chromatography coupled to tandem mass spectrometry (UPLC-MS/MS) and solid-phase extraction to determine the concentration of the 27 targeted pharmaceutical compounds at the nanogram per litre level. The matrix effect was evaluated from water sampled at different treatment stages. Conventional methods with external calibration and internal standard correction were compared with the standard addition method (SAM). An accurate determination of pharmaceutical compounds in drinking water was obtained by the SAM associated with UPLC-MS/MS. The developed method was used to evaluate the occurrence and fate of pharmaceutical compounds in some drinking water treatment plants in the west of France.
机译:近年来,在饮用水或废水处理过程中对药物化合物的产生和命运的研究已变得非常流行。液相色谱-串联质谱是一种功能强大的分析工具,通常用于测定水中痕量的药物残留。但是,许多步骤可能会干扰分析过程并使结果产生偏差。选择了27种与环境有关的分子,包括各种治疗类别和(心血管,兽用和人类抗生素,抗精神病药,非甾体抗炎药,激素和其他杂类药物)。在这项工作中,开发了一种使用超高效液相色谱与串联质谱(UPLC-MS / MS)和固相萃取相结合的方法,以确定以纳克/升为单位的27种目标药物化合物的浓度。从在不同处理阶段取样的水评估基质效应。将具有外部校准和内部标准校正的常规方法与标准添加方法(SAM)进行了比较。通过与UPLC-MS / MS关联的SAM,可以准确测定饮用水中的药物化合物。所开发的方法用于评估法国西部某些饮用水处理厂中药物化合物的发生和命运。

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