Multiclass detection and quantitation of antibiotics and veterinary drugs in shrimps by fast liquid chromatography time-of-flight mass spectrometry

被引:89
作者
Villar-Pulido, Marina [1 ]
Gilbert-Lopez, Bienvenida [1 ]
Garcia-Reyes, Juan F. [1 ]
Ramos Martos, Natividad [1 ]
Molina-Diaz, Antonio [1 ]
机构
[1] Univ Jaen, Dept Phys & Analyt Chem, Analyt Chem Res Grp FQM 323, Jaen 23071, Spain
关键词
Multiresidue; Antibiotics; Shrimps; Seafood; Liquid chromatography; Mass spectrometry; MALACHITE GREEN; SAMPLE PREPARATION; RESIDUE ANALYSIS; BOVINE MUSCLE; TROUT MUSCLE; MILK; QUANTIFICATION; CONFIRMATION; VALIDATION; MATRICES;
D O I
10.1016/j.talanta.2011.06.036
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A fast liquid chromatography time-of-flight mass spectrometry (LC-TOFMS) method has been developed for simultaneous quantitative multiclass determination of residues of selected antibiotics and other veterinary drugs (benzalkonium chloride, ethoxyquin, leucomalachite green (LMG), malachite green (MG), mebendazole, sulfadiazine, sulfadimethoxine, sulfamethazine, sulfamethizole, sulfanilamide, sulfapyridine, sulfathiazole and trimethoprim) in shrimps. Different sample treatment methodologies were tested for the extraction of the targeted species based on either liquid partitioning with different solvents, solid-phase extraction or and matrix solid-phase dispersion. The final selected extraction method consisted of solid-liquid extraction protocol using acetonitrile as solvent followed by a clean-up step with primary secondary amine (QuEChERS). Recovery rates for the extraction of the selected multiclass chemicals were in the range 58-133%. Subsequent identification, confirmation and quantitation were carried out by LC-TOFMS analysis using a reverse-phase C-18 column with 1.8 mu m particle size. The confirmation of the target species was based on accurate mass measurements of the protonated molecules ([M+H](+)) and their fragment ions, obtaining routine accuracy errors lower than 2 ppm in most cases. The optimized LC-TOFMS method displayed excellent sensitivity for the studied analytes, with limits of detection (LODs) in the range 0.06-7 mu g kg(-1). Finally, the proposed method was successfully applied to the analysis of 12 shrimp samples collected from different supermarkets, showing the potential applicability of the method for ultratrace detection of these chemicals in such complex matrix. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1419 / 1427
页数:9
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