Quantitative determination of dexamethasone in bovine plasma and tissues by liquid chromatography-atmospheric pressure chemical ionization-tandem mass spectrometry to monitor residue depletion kinetics

被引:24
作者
Cherlet, M [1 ]
De Baere, S [1 ]
Croubels, S [1 ]
De Backer, P [1 ]
机构
[1] Univ Ghent, Fac Vet Med, Dept Pharmacol Pharm & Toxicol, B-9820 Merelbeke, Belgium
关键词
dexamethasone; LC-APCI-MS/MS; quantification; validation; intravenous administration; residue depletion kinetics;
D O I
10.1016/j.aca.2004.07.014
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Dexamethasone, (DXM) is a synthetic glucocorticoid that is authorized for therapeutic use in veterinary medicine. The European Community (EC) fixed a maximum residue limit (MRL) at 2 ng g(-1) for liver, 0.75 ng g(-1) for muscle and kidney tissues and 0.3 ng ml(-1) for milk, while its use as a growth-promotor is completely banned. We developed earlier a LC-APCI-MS/MS method capable of quantifying such low MRL levels in milk. Minor modifications-concerning only the extraction procedure-were sufficient to allow the quantification of these levels as well in tissue samples. Validation results according to EC requirements concerning linearity, accuracy and precision were satisfactory. Limits of quantification of 0.375 ng g(-1) were obtained for muscle and kidney tissues and of 1 ng g(-1) for liver tissue, i.e. half the MRLs. Limits of detection were 0.09, 0.13 and 0.33 ng g(-1) for muscle, kidney and liver tissues, respectively. Decision limits (CCalpha) were 1.2 ng g(-1) for muscle and kidney tissues and 2.2 ng g(-1) for liver tissue, while detection capabilities (CCbeta) were 1.8, 1.9 and 2.5 ng g(-1) for muscle, kidney and liver tissues, respectively. A simple deproteinization step with concentrated trichloroacetic acid followed by an extraction with ethyl acetate was sufficient to quantify DXM in plasma samples with a limit of quantification of 1 ng ml(-1). After intravenous injection of DXM to cattle, a distribution within 30 min was observed followed by a phase of slow elimination characterized by a half-life of 9.2 h. In muscle tissue, low levels of DXM were found and a quick elimination was observed, with the DXM level falling below the MRL within 4 days after administration. Higher DXM levels were found in liver tissue compared to kidney tissue up to 4 days after administration. Nevertheless, in liver tissue DXM was below the MRL after 8 days of withdrawal time, while it was still as high as 2.5 ng g(-1) in kidney tissue. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:361 / 369
页数:9
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