Development of an LC-MS/MS method for analysis of levamisole in poultry and livestock products.

IF 1.7
Ya-Chun Chou, Pei-Jie Zheng, Chih-Neng Huang, Shu-Han Chang, Ya-Min Kao, Mei-Chih Lin, Lih-Ching Chiueh, Su-Hsiang Tseng
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Abstract

Background: Levamisole is an imidazothiazole anthelmintic agent widely used in poultry and livestock. In Taiwan, the Ministry of Health and Welfare has established MRLs ranging from 0.01 to 1 μg/g for eggs, milk, and various livestock and poultry tissues.

Objective: To support regulatory monitoring, a chiral LC-MS/MS method with simple sample preparation was developed for determining levamisole residues in chicken muscle, porcine muscle, liver, kidney, fat, poultry eggs, and milk from food-producing animals.

Method: Separation of levamisole and its enantiomer dexamisole was achieved using an Astec Cyclobond I 2000 DMP column with 100 mM ammonium acetate and acetonitrile as the mobile phase. The sample was extracted with acetonitrile/methanol (95:5, v/v) containing 1% formic acid, followed by clean-up with acetonitrile-saturated n-hexane.

Results: The method demonstrated good linearity (r > 0.995, 0.5-25 ng/mL) for three quantitative methods in all tested matrices. The method achieved a LOQ of 0.005 μg/g in all matrices. While the pre-spiked tissue calibration curve provided higher recoveries (96.3%-110.1%) by compensating for both matrix effects and analyte losses during extraction, it was more labor-intensive. In contrast, the matrix-matched calibration curve and ISTD-normalized solvent calibration curve offered slightly lower recoveries (84.8%-100.4%) but showed greater practicality for routine monitoring. All calibration strategies met the accuracy and precision criteria specified in European Commission Decision 2002/657/EC and the TFDA validation guidelines. Furthermore, levamisole residues were not detected in any of the 10 commercial livestock and poultry products analyzed, confirming the applicability of the method for food surveillance.

Conclusions: A simple and rapid LC-MS/MS method was developed for the determination of levamisole in poultry and livestock matrices, demonstrating satisfactory sensitivity, accuracy, and selectivity. The method is suitable for routine monitoring and large-scale surveillance of levamisole residues in food products.

Highlights: Development and validation of an LC-MS/MS method involving simple solvent extraction for chiral determination of levamisole in livestock and poultry products with satisfactory sensitivity, accuracy, and selectivity.

禽畜产品中左旋咪唑的LC-MS/MS分析方法的建立。
背景:左旋咪唑是一种广泛应用于畜禽的咪唑类驱虫剂。在台湾,卫生福利部已经确定了鸡蛋、牛奶和各种畜禽组织的最大残留限量为0.01至1 μg/g。目的:建立一种简单制样的手性LC-MS/MS方法,用于测定鸡肌肉、猪肌肉、肝脏、肾脏、脂肪、禽蛋和奶制品中的左旋咪唑残留量,为监管监测提供支持。方法:采用Astec Cyclobond I 2000 DMP色谱柱,以100 mM醋酸铵和乙腈为流动相,对左旋咪唑及其对映体地塞米索进行分离。样品用含有1%甲酸的乙腈/甲醇(95:5,v/v)提取,然后用乙腈饱和正己烷清理。结果:该方法对3种定量方法均具有良好的线性关系(r为0 0.995,0.5 ~ 25 ng/mL)。该方法的定量限为0.005 μg/g。虽然加标前组织校准曲线通过补偿基质效应和萃取过程中分析物的损失提供了更高的回收率(96.3%-110.1%),但其劳动强度较大。相比之下,基质匹配校准曲线和istd归一化溶剂校准曲线的回收率略低(84.8% ~ 100.4%),但在常规监测中表现出更大的实用性。所有校准策略均符合欧盟委员会决议2002/657/EC和TFDA验证指南中规定的准确度和精密度标准。此外,在分析的10种商品畜禽产品中均未检测到左旋咪唑残留,证实了该方法在食品监测中的适用性。结论:建立了一种简便、快速的LC-MS/MS测定家禽和家畜基质中左旋咪唑的方法,具有良好的灵敏度、准确性和选择性。该方法适用于食品中左旋咪唑残留的常规监测和大规模监测。重点:建立了一种简单溶剂萃取的LC-MS/MS方法,用于畜禽产品中左旋咪唑的手性测定,具有良好的灵敏度、准确性和选择性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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