Simultaneous determination of pharmaceuticals and metabolites in fish tissue by QuEChERS extraction and UHPLC Q/Orbitrap MS analysis

色谱法 探索者 化学 萃取(化学) 轨道轨道 质谱法 固相萃取 液相色谱-质谱法 样品制备 检出限 串联质谱法 分析物 高效液相色谱法 代谢物 基质(化学分析) 选择性反应监测
作者
Aggeliki G. Kalogeropoulou,Christina I. Kosma,Triantafyllos A. Albanis
出处
期刊:Analytical and Bioanalytical Chemistry [Springer Nature]
卷期号:413 (28): 7129-7140
标识
DOI:10.1007/s00216-021-03684-y
摘要

In recent years, the occurrence, fate, and adverse effects of pharmaceutically active compounds (PhACs) in aquatic organisms have become a noteworthy issue. In the present study, a rapid and sensitive multiresidue analytical method was developed for the determination of 18 parent PhACs and 5 metabolites in sea bream (Sparus aurata), by combining a modified QuEChERS (quick, easy, cheap, effective, rugged and safe) procedure with ultra-high performance liquid chromatography-Orbitrap-mass spectrometry (UHPLC-Orbitrap-MS). The method development involved optimization of extraction solvent, extraction salts, clean-up sorbents, and amount of sample evaluation, while identification on Orbitrap MS was based on accurate mass and further confirmation with MS/MS fragmentation. The developed method was validated, and linearity was higher than 0.99. Recoveries in all cases ranged between 62 and 107% (at 10, 50, and 100 ng g−1), while intra-day and inter-day precision, expressed as relative standard deviation, RSD, was lower than 4% and 7%, respectively. In addition, limits of quantification (LOQs) ranged between 0.5 and 19 ng g−1. The compounds presented a low matrix effect, between − 13 and 4%, while the expanded uncertainty U% estimated at the three spiking levels 10, 50, and 100 ng g−1 was found below 49% in all cases. Finally, the validated method was applied to sea bream samples from an aquaculture farm located in the Mediterranean Sea, with one positive finding for the antibiotic trimethoprim at a concentration of 26 ng g−1, presenting negligible human health risk.

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