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首页> 外文期刊>Analytical and bioanalytical chemistry >Trace-level determination of pharmaceutical residues by LC-MS/MS in natural and treated waters. A pilot-survey study
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Trace-level determination of pharmaceutical residues by LC-MS/MS in natural and treated waters. A pilot-survey study

机译:通过LC-MS / MS在天然和处理后的水中进行痕量水平的药物残留测定。初步调查研究

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摘要

A pilot-survey study was performed by collecting samples (influent and effluent wastewaters, rivers and tap waters) from different locations in Europe (Spain, Belgium, Germany and Slovenia). A solid-phase extraction (SPE) followed by liquid chromatography-tandem mass spectrometry method was applied for the determination of pharmaceuticals (ibuprofen, naproxen, ketoprofen, diclofenac and clofibric acid). Method detection limits and method quantification limits were at the parts-per-trillion level (7.5-75 ng/L). The recovery rates of the SPE from deionized water and effluent wastewater samples spiked at 100- and 1,000-ng/L levels ranged from 87 to 95%. Identification criteria in compliance with the EU regulation for confirmatory methods of organic residues were applied. A detailed study of signal suppression evaluation for analysis of pharmaceutical residues in effluent wastewaters is presented.
机译:通过收集欧洲(西班牙,比利时,德国和斯洛文尼亚)不同地区的样本(废水和污水,河流和自来水)进行了试点研究。固相萃取(SPE),然后采用液相色谱-串联质谱法测定药物(布洛芬,萘普生,酮洛芬,双氯芬酸和氯纤维酸)。方法检测限和方法定量限为万亿分之一(7.5-75 ng / L)。从去离子水和废水样品中标出浓度分别为100和1,000 ng / L的固相萃取的回收率在87%至95%之间。应用符合欧盟规定的有机残留物确认方法的鉴定标准。提出了用于分析废水中药物残留的信号抑制评估的详细研究。

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