Tissue residues and urinary excretion of zilpaterol in sheep treated for 10 days with dietary zilpaterol

被引:24
作者
Shelver, WL [1 ]
Smith, DJ [1 ]
机构
[1] USDA ARS, Biosci Res Lab, Fargo, ND 58105 USA
关键词
analysis; ELISA; HPLC; LC-MS/MS; zilpaterol; residue;
D O I
10.1021/jf060552m
中图分类号
S [农业科学];
学科分类号
09 [农学];
摘要
Zilpaterol is beta-adrenergic growth promoter approved in Mexico and South Africa for use in cattle. Understanding the rates of zilpaterol depletion from tissues and urine is of interest for the development of strategies to detect the off-label use of zilpaterol. Eight sheep were fed 0.15 mg/kg/day dietary zilpaterol hydrochloride (Zilmax) for 10 consecutive days; two sheep each were slaughtered 0, 2, 5, and 9 days after discontinuation of exposure to the zilpaterol-containing diet. Tissue zilpaterol levels rapidly decreased during the withdrawal period. On the basis of LC-MS/MS-ES (external standard) measurements, liver zilpaterol residues in sheep were 29.3, 1.5, 0.13, and 0.10 ng/g after 0, 2, 5, and 9 day withdrawal periods, respectively; kidney residues were 29.6, 1.10, and 0.09 ng/g and below the detection limit; and muscle residues were 13.3, 0.86, 0.12, and 0.08 ng/g at the same respective withdrawal periods. Between- animal variation in urinary zilpaterol concentrations during the feeding period was considerable, although zilpaterol concentrations converged somewhat as steady state was reached. During the first 3 days of the withdrawal period, zilpaterol elimination followed a first-order excretion pattern, having an average elimination half- life of 15.3 +/- 1.8 h. Urinary zilpaterol concentrations during the withdrawal period were determined using ELISA, HPLC-fluorescence, LC-MS/MS-ES (external standard), and LC-MSMS-IS (internal standard). Comparison of these methods showed a high correlation with each other. With the exception of LC-MS/MS-IS, the regression coefficients of the linear equations with a zero intercept were between 0.90 and 1.25, indicating the near equivalence of the methods. Because of its simplicity, ELISA is a convenient assay for determining zilpaterol levels in urine giving similar results to HPLC-fluorescence and LC-MS/MS-ES without requiring the extensive cleanup of the latter methods.
引用
收藏
页码:4155 / 4161
页数:7
相关论文
共 22 条
[1]
[Anonymous], REV SANIDAD MILITAR
[2]
[Anonymous], 1996, OFF J EUR COMMUNIT L, pL125
[3]
[Anonymous], PUBLIC HLTH EPIDEMIO
[4]
Food poisoning by clenbuterol in Portugal [J].
Barbosa, J ;
Cruz, C ;
Martins, J ;
Silva, JM ;
Neves, C ;
Alves, C ;
Ramos, F ;
Da Silveira, MIN .
FOOD ADDITIVES AND CONTAMINANTS PART A-CHEMISTRY ANALYSIS CONTROL EXPOSURE & RISK ASSESSMENT, 2005, 22 (06) :563-566
[5]
BENVILLE PE, 1970, J AGR FOOD CHEM, V18, P948, DOI 10.1021/jf60171a010
[6]
Determination of clenbuterol, ractopamine and zilpaterol in liver and urine by liquid chromatography tandem mass spectrometry [J].
Blanca, J ;
Muñoz, P ;
Morgado, M ;
Méndez, N ;
Aranda, A ;
Reuvers, T ;
Hooghuis, H .
ANALYTICA CHIMICA ACTA, 2005, 529 (1-2) :199-205
[7]
Bocca B, 2003, J AOAC INT, V86, P8
[8]
Extraction, clean-up and gas chromatography-mass spectrometry characterization of zilpaterol as feed additive in fattening cattle [J].
Bocca, B ;
Di Mattia, M ;
Cartoni, C ;
Fiori, M ;
Felli, M ;
Neri, B ;
Brambilla, G .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2003, 783 (01) :141-149
[9]
Clinical and pharmacological profile in a clenbuterol epidemic poisoning of contaminated beef meat in Italy [J].
Brambilla, G ;
Cenci, T ;
Franconi, F ;
Galarini, R ;
Macrì, A ;
Rondoni, F ;
Strozzi, M ;
Loizzo, A .
TOXICOLOGY LETTERS, 2000, 114 (1-3) :47-53
[10]
Performance enhancing drugs (doping agents) and sudden death - a case report and review of the literature [J].
Hausmann, R ;
Hammer, S ;
Betz, P .
INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 1998, 111 (05) :261-264