Laboratory of Food Analysis, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460, 9000, Ghent, Belgium.
Department of Analytical Chemistry, University of Granada, Campus Fuentenueva s/n, 18071, Granada, Spain.
Anal Bioanal Chem. 2018 Sep;410(22):5567-5581. doi: 10.1007/s00216-018-1018-6. Epub 2018 Mar 24.
A fundamental step in addressing the global problem of mycotoxins is the development of highly sensitive, multi-class extraction and detection methods. This constitutes a field of research that has in recent years enjoyed a steady advance. Such methods, generally based on liquid chromatography coupled to mass spectrometry, are widely reported successfully detecting various mycotoxins in different food and feed samples. In this work, an innovative approach to multi-class mycotoxin control is proposed, offering specific advantages: a broader inclusion of more mycotoxin classes, robust and thorough extraction for all target compounds despite their varied chemical properties, and determination of all analytes from a single injection. The method involved the extraction and quantification of the main mycotoxins produced by Aspergillus, Fusarium, and Penicillium fungi, as well as their reported derivatives, together with 12 other compounds most commonly produced by Claviceps purpurea. The popularly reported QuEChERS technique has been reduced to a simple "salting-out liquid-liquid extraction" (SO-LLE) to obtain the most efficient extraction of the aforementioned mycotoxin classes in a very short time. This is in particular extremely important in ensuring correct determination of individual ergot alkaloids, for which short and robust sample preparation as well as short analytical sequences were key for minimizing the epimerization during analysis. The analyses of wheat and maize samples were performed using ultra-high performance liquid chromatography coupled with tandem mass spectrometry. Matrix-matched calibration curves were established and limits of quantification were below the maximum levels established by the EU regulation. The precision (repeatability and intermediate precision) was lower than 13% in all cases and recoveries ranged between 60 and 98% in maize and between 62 and 103% in wheat, fulfilling the current legislation. The method was applied to study the co-occurrence of these mycotoxins in wheat (n = 13) and maize (n = 15) samples from six European countries. A successful quantification of 23 different mycotoxins, from all major classes, in 85% of wheat and 93% of maize samples was achieved.
解决全球霉菌毒素问题的一个基本步骤是开发高灵敏度、多类别的提取和检测方法。近年来,这个领域的研究取得了稳步进展。这些方法通常基于液相色谱与质谱联用,广泛报道成功检测了不同食品和饲料样品中的各种霉菌毒素。在这项工作中,提出了一种多类霉菌毒素控制的创新方法,具有以下几个优势:更广泛地包含更多的霉菌毒素类别;对所有目标化合物进行稳健且彻底的提取,尽管它们的化学性质不同;以及从单个进样中同时测定所有分析物。该方法涉及提取和定量分析曲霉属、镰刀菌属和青霉属真菌产生的主要霉菌毒素及其报告的衍生物,以及紫堇单胞菌产生的其他 12 种最常见的化合物。流行的 QuEChERS 技术已被简化为简单的“盐析液液萃取”(SO-LLE),以在极短的时间内获得上述霉菌毒素类别的最有效提取。这对于正确测定个别麦角生物碱尤其重要,因为对于这些化合物,需要进行简短而稳健的样品制备和短的分析序列,以最小化分析过程中的差向异构化。使用超高效液相色谱与串联质谱法对小麦和玉米样品进行分析。建立了基质匹配校准曲线,定量限低于欧盟法规规定的最大限量。在所有情况下,精密度(重复性和中间精密度)均低于 13%,回收率在玉米中为 60%至 98%之间,在小麦中为 62%至 103%之间,符合现行法规。该方法应用于研究来自六个欧洲国家的小麦(n=13)和玉米(n=15)样品中这些霉菌毒素的共同存在情况。成功地定量了 23 种不同的霉菌毒素,来自所有主要类别,在 85%的小麦和 93%的玉米样品中都有定量结果。