Irakli Maria N, Skendi Adriana, Papageorgiou Maria D
HellenicAgricultural Organization - Demeter, Plant Breeding and Genetic Resources Institute, PO Box 60458 57001, Thermi, Thessaloniki, Greece.
Department of Food Technology, Alexander Technological Educational Institute of Thessaloniki (ATEITh), PO Box 141, GR 57400, Thessaloniki, Greece.
J Chromatogr Sci. 2017 Aug 1;55(7):690-696. doi: 10.1093/chromsci/bmx022.
Aflatoxins, deoxynivalenol, ochratoxin A and zearalenone are the most important mycotoxins that everyone on its own, in groups or simultaneously contaminate cereals. The external layers of cereal grains (bran) apart from health promoting ingredients are also the most contaminated part with reference to mycotoxin's presence. Therefore, consumption of a high fiber wheat-based diet represent an increased risk to consumer's health. The objective of this study was to develop a simple and reliable high performance liquid chromatography method for the simultaneous determination of these mycotoxins in wheat bran (WB). A double extraction was applied with phosphate buffered saline/methanol and for the clean-up a multi-immunoaffinity column was utilized. The detection was carried out with diode-array and fluorescence detectors linked with a post-column photochemical reactor. After optimization of the chromatographic conditions, all mycotoxins were eluted within ~26 min. Limits of detection for each mycotoxin (0.12-12.58 µg/kg) were below the maximum levels provisioned by European Union regulations. Good linearity was observed for the analytes (r2 ≥ 0.9980). The recovery of analyzed mycotoxins ranged from 70.2 to 105.8%, with a relative standard deviation <12%. The method was successfully applied to quantify mycotoxins in 34 WB samples obtained after pearling of grains that were collected from different regions of Greece.
黄曲霉毒素、脱氧雪腐镰刀菌烯醇、赭曲霉毒素A和玉米赤霉烯酮是最重要的霉菌毒素,它们各自、成组或同时污染谷物。谷物颗粒的外层(麸皮)除了含有促进健康的成分外,也是霉菌毒素污染最严重的部分。因此,食用以高纤维小麦为基础的饮食会增加消费者健康风险。本研究的目的是开发一种简单可靠的高效液相色谱法,用于同时测定麦麸(WB)中的这些霉菌毒素。采用磷酸盐缓冲盐水/甲醇进行两次萃取,并使用多免疫亲和柱进行净化。使用与柱后光化学反应器相连的二极管阵列和荧光检测器进行检测。优化色谱条件后,所有霉菌毒素在约26分钟内洗脱。每种霉菌毒素的检测限(0.12 - 12.58 µg/kg)低于欧盟法规规定的最大限量。分析物具有良好的线性关系(r2≥0.9980)。分析的霉菌毒素回收率在70.2%至105.8%之间,相对标准偏差<12%。该方法成功应用于对从希腊不同地区收集的谷物脱壳后获得的34个WB样品中的霉菌毒素进行定量分析。