Development and Optimization of Extraction Methodologies for the Determination of Antibiotics in Honey by UHPLC-ToF-MS.

Helena Rodrigues, Marta Leite, Beatriz Oliveira, Andreia Freitas
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Abstract

Background: The administration of antibiotics to food-producing animals, including bees, is a common practice employed to prevent or treat bacterial diseases. Such practices may result in the presence of veterinary residues in honey, potentially compromising the safety and health of consumers. In the European Union, maximum residue limits (MRLs) have not been established for pharmacological substances in honey. In this context, the development of accurate and robust analytical methodologies is of paramount importance for the appropriate risk assessment.

Objective: This study aimed to develop and optimize a multi-class method for the determination of veterinary drug residues from seven classes (β-lactams, lincosamides, macrolides, quinolones, sulfonamides, tetracyclines and diaminopyrimidines) using ultra-high performance liquid chromatography coupled to time-of-flight mass spectrometry (UHPLC-ToF-MS).

Methods: A preliminary assessment was conducted to evaluate the feasibility of solid-liquid extraction, given the complex matrix of compounds present in honey, by analysing different solvent solutions in acetonitrile, methanol, water, and/or McIlvaine buffer. The subsequent phase of the study involved the optimisation of a purification/clean-up method. This was achieved by comparing the efficacy of several solid-phase extraction (SPE) and QuEChERS protocols.

Results: The results indicated that the most efficacious extraction were acetonitrile-based solutions, specifically acetic acid 1% and formic acid 0.1% in ACN-H2O (80:20, v/v). Finally, the method with the most optimal analytical performance in terms of recovery and matrix effect entailed an initial extraction step with formic acid 0.1% in ACN-H2O (80:20, v/v), followed by a modified QuEChERS protocol.

Conclusion: Acidified organic solvents in combination with QuEChERS method revealed to be the most effective for the determination of antibiotics in honey, ensuring optimum extraction with minimum matrix interference.

Highlights: The developed analytical protocol with further detection by high resolution mass spectrometry will be important to assess health risks and to add value to the consumption of honey and honey-based products.

UHPLC-ToF-MS测定蜂蜜中抗生素提取方法的建立与优化。
背景:对包括蜜蜂在内的食用动物使用抗生素是预防或治疗细菌性疾病的一种常见做法。这种做法可能导致蜂蜜中存在兽药残留,可能危及消费者的安全和健康。在欧盟,蜂蜜中药理学物质的最大残留限量(MRLs)尚未建立。在这方面,发展准确和可靠的分析方法对于适当的风险评估至关重要。目的:建立并优化超高效液相色谱-飞行时间质谱联用(UHPLC-ToF-MS)测定7类兽药残留(β-内酰胺类、lincoamide类、大环内酯类、喹诺酮类、磺胺类、四环素类和二氨基嘧啶类)的多类方法。方法:考虑到蜂蜜中化合物的复杂基质,通过分析乙腈、甲醇、水和/或McIlvaine缓冲液的不同溶剂溶液,对固液萃取的可行性进行了初步评估。研究的后续阶段涉及净化/清理方法的优化。这是通过比较几种固相萃取(SPE)和QuEChERS协议的效果来实现的。结果:以乙腈为溶剂,乙酸1%和甲酸0.1%为ACN-H2O (80:20, v/v),提取效果最佳。最后,在回收率和基质效应方面具有最佳分析性能的方法是:用0.1%的甲酸在ACN-H2O (80:20, v/v)中进行初始提取步骤,然后采用改进的QuEChERS方案。结论:酸化有机溶剂联用QuEChERS法测定蜂蜜中抗生素含量最有效,提取效果最佳,基质干扰最小。重点:通过高分辨率质谱法进一步检测开发的分析方案对于评估健康风险和增加蜂蜜和蜂蜜基产品的消费价值非常重要。
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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