首页> 外文期刊>Journal of Agricultural and Food Chemistry >Determination of flubendazole and its metabolites in eggs and poultry muscle with liquid chromatography-tandem mass spectrometry.
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Determination of flubendazole and its metabolites in eggs and poultry muscle with liquid chromatography-tandem mass spectrometry.

机译:液相色谱-串联质谱法测定鸡蛋和禽肉中的氟苯达唑及其代谢产物。

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The optimization of a quantitative and sensitive LC-MS/MS method to determine flubendazole and its hydrolyzed and reduced metabolites in eggs and poultry muscle is described. The benzimidazole components were extracted from the two matrices with ethyl acetate after the sample mixtures had been made alkaline. The HPLC separation was performed on an RP C-18 column with gradient elution, using ammonium acetate and acetonitrile as mobile phase. The analytes were detected after atmospheric pressure electrospray ionization on a tandem quadrupole mass spectrometer in MS/MS mode. The components were measured by the MS/MS transition of the molecular ion to the most abundant daughter ion. The overall extraction recovery values for flubendazole, the hydrolyzed metabolite, and the reduced metabolite in eggs (fortification levels of 200, 400, and 800 microg kg(-1)) and muscle (fortification levels of 25, 50, and 100 microg kg(-1)) were, respectively, 77, 78, and 80% and 92, 95, and 90%. The trueness (fortification levels of 400 and 50 microg kg(-1), respectively, for eggs and muscle), expressed as a percentage of the added values for these analytes, was, respectively, 89, 100, and 86 and 110, 110, and 98%. The proposed MS detection method operating in the MS/MS mode is very selective and very sensitive. The limits of detection for flubendazole and its hydrolyzed and reduced metabolites in egg and muscle were, respectively, 0.19, 0.29, and 1.14 microg kg(-1) and 0.14, 0.75, and 0.31 microg kg(-1). The limits of quantification were, respectively, 1, 1, and 2 microg kg(-1) and 1, 1, and 1 microg kg(-1). The discussed method was applied to a pharmacokinetic study with turkeys. Residue concentrations in breast and thigh muscle of turkeys orally treated with flubendazole were quantified. Medicated feed containing 19.9 and 29.6 mg kg(-1) flubendazole was provided to the turkeys for seven consecutive days. For the trial with the recommended dose of 19.9 mg kg(-1), one day after the end of the treatment, the mean sum of the flubendazole plus hydrolyzed metabolite residue values in thigh and breast muscle declined to below the maximum residue limit (50 microg kg(-1)) and were, respectively, 36.6 and 54.1 microg kg(-1). The corresponding values with the higher dose of 29.6 mg kg(-1) were, respectively, 101.7 and 119.7 microg kg(-1).
机译:描述了定量和灵敏的LC-MS / MS方法的最佳方法,该方法可确定鸡蛋和家禽肌肉中的氟苯达唑及其水解和还原的代谢产物。将样品混合物制成碱性后,用乙酸乙酯从两种基质中萃取苯并咪唑组分。 HPLC分离在RP C-18柱上进行梯度洗脱,使用乙酸铵和乙腈作为流动相。在串联四极杆质谱仪上以MS / MS模式在大气压下电喷雾电离后检测分析物。通过分子离子到最丰富的子离子的MS / MS跃迁来测量组分。鸡蛋(强化水平分别为200、400和800微克kg(-1))和肌肉(强化水平分别为25、50和100微克kg(强化水平)下的氟苯达唑,水解代谢物和还原代谢物的总提取回收率值-1))分别为77%,78%和80%,以及92%,95%和90%。真实度(鸡蛋和肌肉的强化水平分别为400和50微克kg(-1)),以这些分析物的添加值的百分比表示,分别为89、100、86和110、110 ,和98%。所提出的以MS / MS模式运行的MS检测方法非常有选择性并且非常敏感。鸡蛋和肌肉中氟苯达唑及其水解和还原代谢产物的检出限分别为0.19、0.29和1.14 microg kg(-1)和0.14、0.75和0.31 microg kg(-1)。定量限分别为1、1和2微克kg(-1)和1、1和1微克kg(-1)。所讨论的方法应用于火鸡的药代动力学研究。定量分析了用氟苯达唑口服处理的火鸡的乳房和大腿肌肉中的残留浓度。连续7天向火鸡提供含19.9和29.6 mg kg(-1)氟苯达唑的药用饲料。对于建议剂量为19.9 mg kg(-1)的试验,在治疗结束后一天,大腿和胸肌中氟苯达唑加水解代谢物残留物的平均总和降至最大残留限量以下(50 microg kg(-1)),分别为36.6和54.1 microg kg(-1)。较高剂量29.6 mg kg(-1)的相应值分别为101.7和119.7 microg kg(-1)。

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