液相色谱-串联质谱法测定牛、猪、鸡和土耳其组织中的替米考星,单实验室验证。

John Matt Rodewald, Thomas J Burnett, Sharon L Brunelle, Clive Ward, Mark R Coleman
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引用次数: 0

摘要

背景:建立了一种LC-MS/MS方法,用于测定和确认牛、猪、鸡和土耳其组织(肝、肾、肌肉和皮肤/脂肪)以及牛奶中替米考星的含量。目的:对该方法进行单实验室验证,以确定方法性能参数。方法:考虑到所研究的各种组织和牛奶中的法典、欧盟最大残留限量和美国耐受性,动物组织和牛奶在4个浓度下进行强化,范围从最低最大残留限量(MRL)或耐受性的0.5倍到最高最大残留限量或耐量的2倍。对介入组织进行分析,以验证该方法的准确性。结果:使用加权(1/x)回归,数据显示了矩阵匹配校准曲线的线性。在强化组织中,回收率在83.3%-107.1%之间。重复性精密度(RSDr)在0.465%-13.4%之间,中间精密度(RSMi)在2.24%-14.7%之间。在发生的组织中验证了该方法的重复性,范围从3.41%到16.0%。该方法的检测和定量极限如下所示,因基质而异。在所有基质中检查了一种确认性过渡离子,并符合美国和欧盟的质谱确认标准。当方法参数发生微小变化,并估计分析物在强化组织、提取物、标准溶液和基质匹配标准中的稳定性时,该方法被证明是稳健的。结论:数据符合AOAC兽医残留方法利益相关者小组对单实验室验证研究的要求,以及美国食品药品监督管理局兽医工业指导中心208号(VICH GL49)的要求。亮点:基于法典和欧盟最大残留限量以及美国的耐受性,LC-MS/MS方法被证明适用于测定和确认牛、猪、鸡和土耳其组织以及牛奶中替米考星的残留量。
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Determination of Tilmicosin in Bovine, Swine, Chicken, and Turkey Tissues by Liquid Chromatography With Tandem Mass Spectrometry, Single-Laboratory Validation.

Background: An LC-MS/MS method was developed for determination and confirmation of tilmicosin in bovine, swine, chicken, and turkey tissues (liver, kidney, muscle, and skin/fat) and bovine milk.

Objective: The method was subjected to single-laboratory validation to establish method performance parameters.

Method: Animal tissues and bovine milk were fortified at four concentrations ranging from 0.5 times the lowest maximum residue limit (MRL) or tolerance to 2 times the highest MRL or tolerance considering the Codex and EU MRLs and the US tolerances in the various tissues and milk studied. Incurred tissues were analyzed to verify the precision of the method.

Results: The data demonstrated linearity of matrix-matched calibration curves using a weighted (1/×) regression. Recoveries varied from 83.3 to 107.1%. Repeatability precision (RSDr) ranged from 0.465 to 13.4% and intermediate precision (RSDi) ranged from 2.24 to 14.7% in fortified tissue. Repeatability of the method was verified in incurred tissues, ranging from 3.41 to 16.0%. The limits of detection and quantitation of the method are presented and vary by matrix. One confirmatory transition ion was examined across all matrixes and met US and EU criteria for mass spectrometry confirmation. The method was shown to be robust when small changes in method parameters were made, and stability of the analyte in fortified tissues, extracts, standard solutions, and matrix-matched standards was estimated.

Conclusions: The data satisfy the requirements of the AOAC Stakeholder Panel for Veterinary Drug Residue Methods for single-laboratory validation studies and the U.S. Food and Drug Administration Center for Veterinary Medicine Guidance for Industry #208 (VICH GL49).

Highlights: The LC-MS/MS method was demonstrated to be suitable for determination and confirmation of tilmicosin residues in bovine, swine, chicken, and turkey tissues and bovine milk based on Codex and EU MRLs and US tolerances.

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