Quantitative determination of dihydrostreptomycin in bovine tissues and milk by liquid chromatography-electrospray ionization-tandem mass spectrometry

被引:38
|
作者
Cherlet, Marc [1 ]
De Baere, Siegrid [1 ]
De Backer, Patrick [1 ]
机构
[1] Univ Ghent, Fac Vet Med, Dept Pharmacol Toxicol Biochem & Oran Physiol, B-9820 Merelbeke, Belgium
来源
JOURNAL OF MASS SPECTROMETRY | 2007年 / 42卷 / 05期
关键词
dihydrostreptomycin tissue and milk residues; weak cation exchange solid-phase clean-up; liquid chromatography/electrospray ionization mass spectrometry; validation;
D O I
10.1002/jms.1194
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Dihydrostreptomycin (DHS) is an aminoglycoside antibiotic used in veterinary medicine in combination with benzylpenicillin for the treatment of bacterial infections in cattle, pigs and sheep. A method to determine its residues in edible tissues of cattle, as well as in milk, was developed and validated. Extraction of DHS from the tissues was performed using a liquid extraction with a 10 mm phosphate buffer containing 2% (w/v) trichloroacetic acid, while milk samples were treated with a 50% (w/v) trichloroacetic acid solution, followed by a solid-phase clean-up procedure on a carboxypropyl (CBA) weak cation exchange column. Ion-pair chromatography, using a mixture of 20 mm pentafluoropropionic acid in water and acetonitrile as the mobile phase, was used to retain DHS and the internal standard streptomycin (STR) on a Nucleosil (5 mu m) reversed-phase C18 column. The components were detected and quantified by electrospray ionization (ESI) tandem mass spectrometry. The method could be validated according to EC (European Community) requirements with respect to linearity, trueness and precision, the latter evaluated at the maximum residue limit (MRL) - 1000 ng g(-1) for kidney, 500 ng g(-1) for muscle, liver and fat, and 200 ng g(-1) for milk -, at one-half of the MRL and at one and a half times the MRL. A limit of quantification of 10 ng g(-1) and 1 ng ml(-1) was obtained for all tissues and for milk, respectively, which is far below one-half of the MRL as requested, while the limit of detection was in the low ppb range, varying between 1.9 and 4.2 ng g(-1) for the different tissues tested, and being 0.6 ng ml(-1) for milk. The method was used for the monitoring of DHS residues in incurred tissue and milk samples coming from cattle medicated with DHS in combination with benzylpenicillin by intramuscular injection, in order to evaluate withdrawal times. Copyright (c) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:647 / 656
页数:10
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