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Single-step multiresidue determination of ten multiclass veterinary drugs in pork, milk, and eggs using liquid chromatography with tandem mass spectrometry
被引:21
|作者:
Park, Jin-A
[1
]
Zhang, Dan
[1
]
Kim, Dong-Soon
[1
]
Kim, Seong-Kwan
[1
]
Cho, Kyeong-Su
[1
]
Jeong, Dana
[1
]
Shim, Jae-Han
[2
]
Kim, Jin-Suk
[1
]
Abd El-Aty, A. M.
[1
,3
]
Shin, Ho-Chul
[1
]
机构:
[1] Konkuk Univ, Dept Vet Pharmacol & Toxicol, Coll Vet Med, Seoul 143701, South Korea
[2] Chonnam Natl Univ, Biotechnol Res Inst, Coll Agr & Life Sci, Gwangju, South Korea
[3] Cairo Univ, Dept Pharmacol, Fac Vet Med, Giza 12211, Egypt
关键词:
Animal food products;
Liquid-phase extraction;
Multiresidue analysis;
Tandem mass spectrometry;
Veterinary drugs;
CHICKEN MUSCLE;
RESIDUES;
VALIDATION;
EXTRACTION;
BOVINE;
LC;
PORCINE;
QUICK;
CHEAP;
D O I:
10.1002/jssc.201500501
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
A multiclass, multiresidue determination method is reported for the detection of ten veterinary drugs, including scopolamine, metoclopramide, acriflavine, berberine, tripelennamine, diphenhydramine, acrinol, triamcinolone, loperamide, and roxithromycin in pork, milk, and eggs. The method involves a simple extraction using 0.1% formic acid in acetonitrile, followed by defatting with n-hexane, centrifugation, and filtration prior to liquid chromatography with tandem mass spectrometric analysis. As ion suppression and enhancement effects are reported, matrix-matched calibrations are used for quantification, with determination coefficients >= 0.9765. For the majority of the tested analytes, the intra-and interday accuracy (expressed as recovery %) range from 70.6 to 94.6% and from 70.1 to 93.3%, respectively, and the precision (expressed as relative standard deviation) ranges from 0.5 to 19.8% and from 2.8 to 18.4% in allmatrices. The limits of quantification range between 0.5 and 10 ng/g. The validated tandem mass spectrometry method is successfully applied to market samples; the target analytes are not detected in any of the tested samples. In terms of accuracy, no extract cleanup is deemed necessary. The developed method is feasible for the simultaneous detection of the tested analytes in pork, milk, and eggs.
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页码:2772 / 2780
页数:9
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