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Electromembrane extraction of multi-class prohibited/restricted veterinary drugs from food samples – Exploring liquid membrane composition
Food Chemistry ( IF 8.5 ) Pub Date : 2024-12-26 , DOI: 10.1016/j.foodchem.2024.142680 Junling He, Yong Tang, Chiliang Lin, Shaoyun Peng, Stig Pedersen-Bjergaard, Frederik André Hansen, Chen Zhou
Food Chemistry ( IF 8.5 ) Pub Date : 2024-12-26 , DOI: 10.1016/j.foodchem.2024.142680 Junling He, Yong Tang, Chiliang Lin, Shaoyun Peng, Stig Pedersen-Bjergaard, Frederik André Hansen, Chen Zhou
Effective monitoring of veterinary drug residues in food is essential for legislation compliance and food safety, yet remains challenging due to low concentrations and complex matrices. This study introduced a miniaturized 96-well electromembrane extraction (EME) technique for pre-concentration and isolation 80 prohibited/restricted veterinary drugs from honey samples. Three liquid membranes were developed and characterized: V 1 (“V” for veterinary), a mixture of 2-undecanone and 0.5 % 2-nitro-p-cymene, was optimal for extraction of quinolones, tetracyclines, and β -agonists. V2, a mixture of 2-nitrophenyl octyl ether and a deep eutectic solution (formed upon mixing 6-methylcoumarin with thymol in a 1:1 w /w ratio) in a 1:1 v /v ratio, with the addition of 0.5 % di(2-ethylhexyl) phosphate (DEHP), was suitable for macrolides and sulfonamides extraction. V3, a deep eutectic solvent formed upon 1-decanoic acid and camphor in a 1:1 w /w ratio with 1 % DEHP, was suitable for aminoglycosides and β -lactams. Operational parameters were fine-tuned to achieve optimal extraction efficiencies, with recoveries ranging from 20.1–117.5 %, 20.3–91.9 %, and 20.1–118.8 % for V1, V2, and V3, respectively. High precision was observed for compounds with recoveries over 40 % (intra-day: 0.4–27.7 %; inter-day: 2.6–33.0 %), and matrix effects were generally within 80–120 %. This work established a theoretical framework for EME in food analysis, highlighting its potential as a powerful sample pretreatment method for the detection of veterinary drug residues. The results demonstrated the feasibility and advantages of using EME for ensuring food safety and regulatory compliance.
中文翻译:
从食品样品中电膜提取多类违禁/限制兽药 – 探索液膜成分
有效监测食品中的兽药残留对于法规遵从性和食品安全至关重要,但由于浓度低且基质复杂,仍然具有挑战性。本研究引入了一种小型化 96 孔电膜提取 (EME) 技术,用于从蜂蜜样品中预浓缩和分离 80 种违禁/限制兽药。开发并表征了三种液膜:V1(“V”代表兽医),2-十一酮和 0.5% 2-硝基对-伞草酮的混合物,是提取喹诺酮类、四环素类和β激动剂的最佳选择。V2 是 2-硝基苯基辛醚和深共熔溶液(将 6-甲基香豆素与百里香酚以 1:1 w/w 的比例混合形成)的混合物,以 1:1 v/v 的比例,加入 0.5% 磷酸二(2-乙基己基)磷酸酯 (DEHP),适用于大环内酯类和磺胺类药物的提取。V3 是一种由 1-癸酸和樟脑以 1:1 w/w 比例与 1% DEHP 形成的深共熔溶剂,适用于氨基糖苷类和 β-内酰胺类。对操作参数进行微调以实现最佳提取效率,V1、V2 和 V3 的回收率分别为 20.1–117.5 %、20.3–91.9 % 和 20.1–118.8 %。对于回收率超过 40 % 的化合物(日内:0.4–27.7 %;日间:2.6–33.0 %),观察到高精密度,基质效应通常在 80–120 % 之间。这项工作为食品分析中的 EME 建立了理论框架,突出了其作为检测兽药残留的强大样品预处理方法的潜力。结果证明了使用 EME 确保食品安全和法规合规性的可行性和优势。
更新日期:2024-12-26
中文翻译:
从食品样品中电膜提取多类违禁/限制兽药 – 探索液膜成分
有效监测食品中的兽药残留对于法规遵从性和食品安全至关重要,但由于浓度低且基质复杂,仍然具有挑战性。本研究引入了一种小型化 96 孔电膜提取 (EME) 技术,用于从蜂蜜样品中预浓缩和分离 80 种违禁/限制兽药。开发并表征了三种液膜:V1(“V”代表兽医),2-十一酮和 0.5% 2-硝基对-伞草酮的混合物,是提取喹诺酮类、四环素类和β激动剂的最佳选择。V2 是 2-硝基苯基辛醚和深共熔溶液(将 6-甲基香豆素与百里香酚以 1:1 w/w 的比例混合形成)的混合物,以 1:1 v/v 的比例,加入 0.5% 磷酸二(2-乙基己基)磷酸酯 (DEHP),适用于大环内酯类和磺胺类药物的提取。V3 是一种由 1-癸酸和樟脑以 1:1 w/w 比例与 1% DEHP 形成的深共熔溶剂,适用于氨基糖苷类和 β-内酰胺类。对操作参数进行微调以实现最佳提取效率,V1、V2 和 V3 的回收率分别为 20.1–117.5 %、20.3–91.9 % 和 20.1–118.8 %。对于回收率超过 40 % 的化合物(日内:0.4–27.7 %;日间:2.6–33.0 %),观察到高精密度,基质效应通常在 80–120 % 之间。这项工作为食品分析中的 EME 建立了理论框架,突出了其作为检测兽药残留的强大样品预处理方法的潜力。结果证明了使用 EME 确保食品安全和法规合规性的可行性和优势。