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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >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
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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

机译:超高效液相色谱-四极杆-线性离子阱串联质谱法快速,全面地对地表水和处理后水中的人类和兽药及其代谢产物进行多残留分析

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摘要

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).
机译:本工作描述了一种分析方法的开发,该方法基于自动离线固相萃取(SPE),然后将超高效液相色谱与四极杆线性离子阱串联质谱联用(UPLC-QqLIT)进行测定。地表水和处理后的水中(进水和出水废水,河流,水库,海水和饮用水)中的81种药用残留物,涵盖各种治疗组及其主要代谢产物。为了明确识别和确认,每个化合物监测两个选定的反应监测(SRM)过渡。通过校正基质效应必不可少的内标方法进行定量。此外,为了获得用于确认阳性结果的额外工具,进行了信息依赖获取(IDA)实验,其中SRM作为调查扫描,而增强的产物离子(EPI)扫描作为依赖扫描。通过谱库搜索进行化合物鉴定,将在一种固定碰撞能量下获得的EPI光谱与谱库中存在的那些相匹配。该方法的主要优点是通过减少某些基质的提取量,减少大量药物的快速分离,其高灵敏度(低ng / L范围内的检测极限)实现了自动化并加快了样品制备的速度。选择性(由于使用了串联质谱),可靠性,因为大量同位素标记的化合物被用作定量的内标,最后是自来水,水库和海水的分析,因为有关这些基质中药物的存在信息仍然稀疏。作为验证程序的一部分,开发的方法用于分析加泰罗尼亚(西班牙东北)不同地点的废水和地表水中的药物残留。

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