利用超高效液相色谱-串联质谱法测定乙氧基喹,并对鸡蛋、蛋制品和家禽中的乙氧基喹残留物进行新加坡调查。

IF 2.3 3区 农林科学 Q2 CHEMISTRY, APPLIED
Xiau Yi Tan, Zan Xin Chin, Sew Lay Chua, Ken Kah Meng Lee, Yuansheng Wu, Joanne Sheot Harn Chan
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引用次数: 0

摘要

本研究开发了一种先进的超高效液相色谱-串联质谱(UPLC-MS/MS)方法,用于定量检测乙氧基醌(EQ)。该方法采用了独特的抗氧化剂添加萃取步骤,旨在防止乙氧基喹分解并保持分析精度。该方法可有效测定鸡蛋、加工蛋制品、家禽肌肉、三文鱼和液态奶中的乙氧基喹残留量。该方法在鸡蛋、牛奶、鲑鱼和鸡肉中的定量限(LOQ)分别为 1.5 微克/千克、1.9 微克/千克、2.1 微克/千克和 1.2 微克/千克。EQ 的回收率为 79.2% 至 107.6%,相对标准偏差 (RSD) 低于 8.4%。新加坡对不同种类的鸡蛋和家禽肌肉中的 EQ 含量进行了监测研究,共检测了 140 个样本。所有样本的 EQ 残余量均低于美国食物及药物管理局(FDA)规定的最高残余限量(每公斤 500 微克)。部分来自中国的腌制和腌制鸡蛋样本检出较高浓度的 EQ。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determination of ethoxyquin by ultra-high performance liquid chromatography with tandem mass spectrometry and a Singapore survey of ethoxyquin residues in eggs, egg products and poultry.

In this study, an advanced ultra-high performance liquid chromatography with tandem mass spectrometry (UPLC-MS/MS) method was developed for quantifying ethoxyquin (EQ). The approach employed a distinctive antioxidant added extraction step designed to prevent ethoxyquin decomposition and maintain analytical precision. This method effectively determines residue levels of EQ in eggs, processed egg products, poultry muscle, salmon, and liquid milk. The method was shown to have a limit of quantitation (LOQ) for eggs, milk, salmon, and chicken muscle of 1.5 µg/kg, 1.9 µg/kg, 2.1 µg/kg, and 1.2 µg/kg, respectively. The recoveries of EQ ranged from 79.2% to 107.6%, with a relative standard deviation (RSD) below 8.4%. A surveillance study for the presence of EQ in different types of eggs and poultry muscle available in Singapore was conducted and a total of 140 samples were tested. EQ residues in all samples were found to be below the U.S. Food and Drug Administration (FDA) MRLs of 500 µg/kg. Some samples of salted and preserved eggs from China were detected with higher concentration of EQ.

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来源期刊
CiteScore
7.40
自引率
6.90%
发文量
136
审稿时长
3 months
期刊介绍: Food Additives & Contaminants: Part A publishes original research papers and critical reviews covering analytical methodology, occurrence, persistence, safety evaluation, detoxification and regulatory control of natural and man-made additives and contaminants in the food and animal feed chain. Papers are published in the areas of food additives including flavourings, pesticide and veterinary drug residues, environmental contaminants, plant toxins, mycotoxins, marine biotoxins, trace elements, migration from food packaging, food process contaminants, adulteration, authenticity and allergenicity of foods. Papers are published on animal feed where residues and contaminants can give rise to food safety concerns. Contributions cover chemistry, biochemistry and bioavailability of these substances, factors affecting levels during production, processing, packaging and storage; the development of novel foods and processes; exposure and risk assessment.
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