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Simultaneous analysis of Alternaria toxins and citrinin in tomato: an optimised method using liquid chromatography-tandem mass spectrometry

机译:同时分析番茄中的链霉菌毒素和柠檬素:液相色谱-串联质谱法的优化方法

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摘要

Alternaria toxins and citrinin are mycotoxins produced by fungi growing on different raw materials and agricultural commodities. Maximum levels of these toxins in foods are currently under consideration by the European Commission as a risk management measure. In this study, a new quantitative method is described for the determination of five Alternaria toxins and citrinin in tomato and tomato juice samples based on LC-MS/MS detection. Samples were extracted with pure methanol, followed by a derivatisation step with 2,4-dinitrophenylhydrazine to improve the determination of tenuazonic acid and to decrease the wide polarity difference between the compounds of interest. Samples were purified on hydrophilic-modified styrene polymer solid-phase extraction cartridges. High-performance liquid chromatographic columns packed with different core–shell materials were tested for the separation of toxins and a C-18 phase was in the final method applied to achieve sufficient separation of all relevant analytes. A key element of this approach was to prove successful transferability of the method to three different triple quadrupole mass spectrometers. A full single laboratory method validation was performed on two LC-MS/MS systems and performance characteristics met the predefined requirements. Moreover, the method was used in an international proficiency test and the satisfactory z-scores obtained (−0.1 to 0.8 in tomato juice samples) demonstrated the reliability of the approach described. The method will be validated in an inter-laboratory collaborative study and if the criteria for method precision are met, the method will be proposed as a new Work Item to the European Committee for Standardisation.
机译:交链孢霉毒素和西林毒素是真菌生长在不同原料和农产品上产生的霉菌毒素。欧盟委员会目前正在考虑将食品中这些毒素的最高含量作为一种风险管理措施。在这项研究中,描述了一种新的定量方法,用于基于LC-MS / MS检测的方法来测定番茄和番茄汁样品中的五种链霉菌毒素和西林毒素。样品用纯甲醇萃取,然后用2,4-二硝基苯肼进行衍生化步骤,以改善Tenuazonic酸的测定并减少目标化合物之间的宽极性差异。样品在亲水改性的苯乙烯聚合物固相萃取柱上纯化。测试了填充有不同核-壳材料的高性能液相色谱柱中毒素的分离,最后一种方法中使用C-18相以实现所有相关分析物的充分分离。该方法的关键要素是证明该方法可成功转移至三种不同的三重四极杆质谱仪。在两个LC-MS / MS系统上进行了完整的单一实验室方法验证,并且性能特征符合预定义的要求。此外,该方法已在国际水平测试中使用,所获得的令人满意的Z值(番茄汁样品中的-0.1至0.8)证明了上述方法的可靠性。该方法将在实验室间的协作研究中得到验证,如果满足方法精度的标准,则该方法将作为欧洲标准化委员会的新工作项目提出。

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