Development of an SPME-GC-MS/MS procedure for the monitoring of 2-phenoxyethanol in anaesthetised fish

被引:9
作者
Klimankova, Eva [1 ]
Riddellova, Katerina [1 ]
Hajslova, Jana [1 ]
Poustka, Jan [1 ]
Kolarova, Jitka [2 ]
Kocourek, Vladimir [1 ]
机构
[1] Inst Chem Technol, Fac Food & Biochem Technol, Dept Food Chem & Anal, CR-16628 Prague 6, Czech Republic
[2] Univ S Bohemia Ceske Budejovice, Res Inst Fish Culture & Hydrobiol Vodnany, Vodnany 38925, Czech Republic
关键词
solid phase microextraction; 2-phenoxyethanol; fish samples; matrix modification; gas chromatography (GC); ion trap mass spectrometry (ITMS);
D O I
10.1016/j.talanta.2008.01.035
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
2-Phenoxyethanol (ethylene glycol monophenyl ether, C8H10O2) is a promising anaesthetic agent used in fisheries and aquaculture. The aim of this study was to develop a fast and easy method to determine 2-phenoxyethanol residue levels in fish tissue and blood plasma, and, subsequently, to use the method to monitor the dynamics of 2-phenoxyethanol residues in fish treated with anaesthetic. We developed a new procedure that employs solid phase microextraction (SPME) of the target analyte from the sample headspace followed by gas chromatography-mass spectrometry (GC-MS). Both sample handling, aimed at maximum transfer of 2-phenoxyethanol into the headspace, and SPME-GC-MS conditions were carefully optimised. Using a divinylbenzene/Carboxen/polydimethylsiloxane (PDMS/CAR/DVB) fiber for 60 min sampling at 30 degrees C and an ion trap detector operated in MS/MS mode, we obtained detection (LOD) and quantification (LOQ) limits of 0.03 and 0.1 mg kg(-1) of sample, respectively. The method was linear in a range of 0.1-250 mg kg(-1) and, depending on the sample matrix and spiking level, a repeatability (expressed as relative standard deviation, R.S.D.) of between 3% and 11% was obtained. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1082 / 1088
页数:7
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