Development and Validation of a Method for the Determination of Quinolones in Muscle and Eggs by Liquid Chromatography-Tandem Mass Spectrometry

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作者
Loredana Annunziata
Pierina Visciano
Arianna Stramenga
Maria Novella Colagrande
Guido Campana
Giampiero Scortichini
Giacomo Migliorati
Dario Compagnone
机构
[1] Istituto Zooprofilattico Sperimentale dell’Abruzzo e del Molise “G. Caporale”,Faculty of BioScience and Technology for Food, Agriculture and Environment
[2] University of Teramo,undefined
[3] Istituto Zooprofilattico Sperimentale dell’Umbria e delle Marche,undefined
来源
Food Analytical Methods | 2016年 / 9卷
关键词
Quinolones; Muscle; Eggs; Liquid chromatography-tandem mass spectrometry; Method validation;
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摘要
In this study, the development and validation of a multiresidue method for the detection of 11 quinolones (marbofloxacin, norfloxacin, ciprofloxacin, danofloxacin, lomefloxacin, enrofloxacin, sarafloxacin, difloxacin, oxolinic acid, nalidixic acid, flumequine) in muscle and eggs were reported. The method involved an extraction with a methanol/metaphosphoric acid mixture and a clean up by Oasis hydrophilic-lipophilic balance (HLB) cartridge. The validation was performed according to the Commission Decision 2002/657/EC. Linearity, specificity, decision limit (CCα), detection capability (CCβ), recovery, precision (repeatability and within-laboratory reproducibility), and ruggedness were determined. Depending on the analytes, CCα and CCβ ranged from 113 to 234 μg/kg and from 126 to 282 μg/kg in muscle samples, whereas in eggs, these parameters were between 5.6 and 7.4 μg/kg and between 6.1 and 9.8 μg/kg, respectively. In both the examined matrices, the recovery values were always higher than 90 % and precision, calculated as relative standard deviation, was equal to or lower than 16 % for repeatability and 23 % for within-laboratory reproducibility. The described method can be considered adequate for the simultaneous determination and quantification of quinolones in the tested food matrices.
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页码:2308 / 2320
页数:12
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