Lee Ji Sun, Cho Soo Hee, Lim Chae Mi, Chang Moon Ik, Joo Hyun Jin, Bae Hojae, Park Hyun Jin
Imported Food Analysis Division, Seoul Regional Food and Drug Administration, 212 Mokdongjungang-ro, Yangcheon-Gu, Seoul, Republic of Korea.
Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University, 5-Ka, Anam-Dong, Sungbuk-Gu, Seoul, Republic of Korea.
PLoS One. 2017 Jan 13;12(1):e0169597. doi: 10.1371/journal.pone.0169597. eCollection 2017.
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.
本研究建立并验证了一种用于测定猪肉、鸡肉和马肉中甲苯咪唑及其水解和还原代谢物的液相色谱-串联质谱(LC-MS/MS)确证定量方法。将样品混合物碱化后,用乙酸乙酯提取驱虫化合物,然后使用反相C18柱进行液相色谱分离。流动相由含10 mM甲酸铵的水和甲醇组成,进行梯度洗脱。该确证方法根据欧盟要求进行了验证。评估的验证参数包括特异性、准确性、精密度(重复性和实验室内部再现性)、分析限(决策限和检测限)及适用性。结果表明,大多数参数符合欧盟要求。所有分析物的决策限(CCα)和检测能力(CCβ)范围为15.84至17.96 μgkg-1。所有分析物的检测限(LOD)和定量限(LOQ)分别为0.07 μgkg-1和0.2 μgkg-1。所建立的方法成功应用于主要城市市场采集的监测样品,证明其作为测定动物性食品中甲苯咪唑残留量监管工具具有巨大潜力。