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采用超高效液相色谱-四极杆线性离子阱串联质谱法快速全面地分析地表水中广泛的人用和兽用药物及其部分代谢物。

Fast and comprehensive multi-residue analysis of a broad range of human and veterinary pharmaceuticals and some of their metabolites in surface and treated waters by ultra-high-performance liquid chromatography coupled to quadrupole-linear ion trap tandem mass spectrometry.

机构信息

Catalan Institute for Water Research (ICRA), C/Emili Grahit 101, 17003 Girona, Spain.

出版信息

J Chromatogr A. 2012 Jul 27;1248:104-21. doi: 10.1016/j.chroma.2012.05.084. Epub 2012 May 29.

Abstract

The present work describes the development of an analytical method, based on automated off-line solid phase extraction (SPE) followed by ultra-high-performance liquid chromatography coupled to quadrupole linear ion trap tandem mass spectrometry (UPLC-QqLIT) for the determination of 81 pharmaceutical residues, covering various therapeutic groups, and some of their main metabolites, in surface and treated waters (influent and effluent wastewaters, river, reservoir, sea and drinking water). For unequivocal identification and confirmation, two selected reaction monitoring (SRM) transitions per compound are monitored. Quantification is performed by the internal standard approach, indispensable to correct matrix effects. Moreover, to obtain an extra tool for confirmation of positive findings, an information dependent acquisition (IDA) experiment was performed, with SRM as survey scan and an enhanced product ion (EPI) scan as dependent scan. Compound identification was carried out by library search, matching the EPI spectra achieved at one fixed collision energy with those present in a library. The main advantages of the method are automation and speed-up of sample preparation by the reduction of extraction volumes for some matrices, the fast separation of a big number of pharmaceuticals, its high sensitivity (limits of detection in the low ng/L range), selectivity, due to the use of tandem mass spectrometry, reliability since a significant number of isotopically labeled compounds are used as internal standards for quantification and finally, the analysis of tap, reservoir and sea waters, since information about occurrence of pharmaceuticals in these matrices is still sparse. As part of the validation procedure, the method developed was applied to the analysis of pharmaceutical residues in waste and surface waters from different sites in Catalonia (North East of Spain).

摘要

本工作描述了一种分析方法的开发,该方法基于自动化离线固相萃取(SPE),随后进行超高效液相色谱-四极杆线性离子阱串联质谱(UPLC-QqLIT)分析,用于测定 81 种药物残留,涵盖了各种治疗组和它们的一些主要代谢物,在地表水和处理水中(进水和废水、河流、水库、海洋和饮用水)。为了进行明确的鉴定和确证,每个化合物监测两个选择反应监测(SRM)转换。采用内标法进行定量,这对于校正基质效应是必不可少的。此外,为了获得阳性发现的确证的额外工具,进行了信息依赖采集(IDA)实验,其中 SRM 作为调查扫描,增强的产物离子(EPI)扫描作为依赖扫描。化合物的鉴定通过库搜索进行,将在一个固定碰撞能量下获得的 EPI 谱与库中存在的谱进行匹配。该方法的主要优点是通过减少某些基质的提取体积,实现了自动化和样品制备的加速,快速分离大量药物,由于采用串联质谱,具有高灵敏度(检测限在低 ng/L 范围内)、选择性,由于使用了大量同位素标记化合物作为内标进行定量,最后,还可以分析自来水、水库和海水,因为关于这些基质中药物存在的信息仍然很少。作为验证程序的一部分,该方法应用于分析来自西班牙东北部加泰罗尼亚不同地点的废水和地表水的药物残留。

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