Abstract

A confirmatory and quantitative method of liquid chromatography-tandem mass spectrometry (LC-MS/MS) for the determination of mebendazole and its hydrolyzed and reduced metabolites in pork, chicken, and horse muscles was developed and validated in this study. Anthelmintic compounds were extracted with ethyl acetate after sample mixture was made alkaline followed by liquid chromatographic separation using a reversed phase C18 column. Gradient elution was performed with a mobile phase consisting of water containing 10 mM ammonium formate and methanol. This confirmatory method was validated according to EU requirements. Evaluated validation parameters included specificity, accuracy, precision (repeatability and within-laboratory reproducibility), analytical limits (decision limit and detection limit), and applicability. Most parameters were proved to be conforming to the EU requirements. The decision limit (CCα) and detection capability (CCβ) for all analytes ranged from 15.84 to 17.96 μgkg-1. The limit of detection (LOD) and the limit of quantification (LOQ) for all analytes were 0.07 μgkg-1 and 0.2 μgkg-1, respectively. The developed method was successfully applied to monitoring samples collected from the markets in major cities and proven great potential to be used as a regulatory tool to determine mebendazole residues in animal based foods.

Highlights

  • Mebendazole (MEB), a benzimidazole anthelmintic, is widely used in veterinary medicine [1, 2]

  • This method showed low recovery rate for the detection of mebendazole residues, especially in the case of hydrolyzed metabolite (HMEB) in pork (Fig 2). This could be due to high protein and fat contents in this type of matrix that can often interfere with the analytical procedure [15]

  • Sample preparation procedure described in this study was based on the liquid-liquid extraction (LLE) method reported by De Ruyck et al [17]

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Summary

Introduction

Mebendazole (MEB), a benzimidazole anthelmintic, is widely used in veterinary medicine [1, 2]. This compound is an orally active broad-spectrum anthelmintic that is effective against numerous species of nematodes and cestodes in the gastrointestinal track of animals [3]. The standard analytical method for MEB residues using dimethylsulphoxide (DMSO) extraction followed by purification with solid phase extraction (SPE) depicted in Korean Food Standards Codex resulted in low HMEB recovery rate from edible tissues of pork [6]. To effectively control MEB residues in animal products, a confirmatory and quantitative method capable of detecting the complete range of marker residues is urgently needed

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