Food Safety Assurance Center, Kirin Group Office Co., Ltd., 1-13-5 Fukuura Kanazawa-ku, Yokohama, 236-0004, Japan.
Rapid Commun Mass Spectrom. 2011 Dec 15;25(23):3481-90. doi: 10.1002/rcm.5250.
A method coupling liquid chromatography with tandem mass spectrometry (LC/MS/MS) was developed for the simultaneous quantitative determination of trichothecenes, nivalenol, deoxynivalenol, deoxynivalenol-3-glucoside, fusarenon-X, 3-acetyldeoxynivalenol, 15-acetyldeoxynivalenol, isotrichodermin, calonectrin, 3-deacetylcalonectrin, 15-deacetylcalonectrin, 3,15-diacetylnivalenol, 4,15-diacetylnivalenol, 3,15-diacetyldeoxynivalenol, and 3,4,15-triacetylnivalenol. The analytical parameters of trichothecenes and their derivatives were optimized to enable their highly sensitive detection. Evaluation of clean-up procedures using Multisep #226 and #227 indicated that Multisep #227 was more suitable for their simultaneous detection in wheat. In performance validation studies using the LC/MS/MS method with Multisep #227 cleanup, good recoveries ranging from 84% to 115% with relative standard deviations from 0.4% to 7.2% were measured. The limits of detection and quantification ranged from 0.03 to 1.4 ng·g(-1) and from 0.1 to 4.7 ng·g(-1) , respectively. The effect of matrices using matrix-matched calibration was estimated to range from 80% to 117% after Multisep #227 cleanup. Multisep #227 clean-up procedure with matrix-free standard calibration achieved accurate quantification without having a considerable effect on matrix compounds. Using the developed method, several trichothecene derivatives and precursors were detected in fungally inoculated wheat samples. The developed LC/MS/MS method is a practical technique that can be used for the quantification of trichothecenes in wheat. This study is the first report of an analytical method used for the simultaneous quantification of major trichothecenes, their derivatives and precursors.
建立了一种同时定量测定单端孢霉烯族毒素、雪腐镰刀菌烯醇、脱氧雪腐镰刀菌烯醇、脱氧雪腐镰刀菌烯醇-3-葡萄糖苷、呋甾烯酮、3-乙酰脱氧雪腐镰刀菌烯醇、15-乙酰脱氧雪腐镰刀菌烯醇、交链孢酚、卡尔农毒素、3-去乙酰卡尔农毒素、15-去乙酰卡尔农毒素、3,15-二乙酰基雪腐镰刀菌烯醇、4,15-二乙酰基雪腐镰刀菌烯醇、3,15-二乙酰基脱氧雪腐镰刀菌烯醇和 3,4,15-三乙酰基雪腐镰刀菌烯醇的液相色谱-串联质谱(LC/MS/MS)方法。优化了单端孢霉烯族毒素及其衍生物的分析参数,以实现其高灵敏度检测。使用 Multisep #226 和 #227 对净化程序进行评估表明,Multisep #227 更适合同时检测小麦中的单端孢霉烯族毒素。在使用 Multisep #227 净化的 LC/MS/MS 方法进行性能验证研究中,测量到的回收率范围为 84%至 115%,相对标准偏差范围为 0.4%至 7.2%。检测限和定量限范围分别为 0.03 至 1.4 ng·g(-1)和 0.1 至 4.7 ng·g(-1)。使用 Multisep #227 净化后,基质效应估计范围为 80%至 117%。使用无基质标准校准的 Multisep #227 净化程序可实现准确的定量,而对基质化合物没有显著影响。使用所开发的方法,在真菌接种的小麦样品中检测到几种单端孢霉烯族毒素衍生物和前体。所开发的 LC/MS/MS 方法是一种实用技术,可用于小麦中单端孢霉烯族毒素的定量。本研究首次报道了一种用于同时定量测定主要单端孢霉烯族毒素、其衍生物和前体的分析方法。