Determination of Mycotoxins in Wheat Grain by LC-MS/MS using Modified QuEChERS Sample Preparation

IF 0.7 Q4 CHEMISTRY, ANALYTICAL
S. Senin, S. Midyk, V. Korniyenko, O. Konovalova, O. V. Berezovskyi, E. Ladohubets, I. Harkusha
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Abstract

The procedure of the mycotoxins determination in wheat grain was developed by LC-MS/MS using modified QuEChERS sample preparation. The method of simultaneous determination of six mycotoxins (aflatoxin B1, aflatoxin B2, aflatoxin G1, aflatoxin G2, T-2 toxin and zearalenone) in wheat grain was validated according to the following criteria: specificity, linearity, limits of detection (LOD), limits of quantification (LOQ), accuracy, and precision. The chromatographic and mass spectrometric conditions for separation and determination of the mycotoxins were optimized during the study. It was established that the most optimal mobile phase for the separation of six mycotoxins is 5 mМ ammonium formate solution in methanol : water : formic acid (5 : 94.9 : 0.1 by volume, eluent A and 95:4.9:0.1 by volume, eluent B). It was found that the correlation coefficients for six mycotoxins range from 0.9990 to 0.9998 (R2 > 0.995). Limits of detection (LOD) and limits of quantification (LOQ) of the mycotoxins are below the maximum permitted levels set by the European Union (EU). Percent recovery in the range from 88 to 103 % indicates the acceptability of the mycotoxin extraction procedure. The relative standard deviation (RSD, %) of the measurement results under conditions of repeatability ranged from 1.94 to 8.76 %. The obtained data suitability evaluation of method (validation) corresponds to criteria European Commission Regulation (EC) No. 401/2006. The validation results showed that LC-MS/MS method with using of modified QuEChERS sample preparation is effective and suitable for the simultaneous quantitation of mycotoxins in wheat grain.
改良QuEChERS样品制备的LC-MS/MS法测定小麦籽粒中的真菌毒素
采用改良的QuEChERS样品制备技术,建立了小麦中真菌毒素的LC-MS/MS检测方法。根据特异性、线性度、检出限(LOD)、定量限(LOQ)、准确度、精密度等标准,建立了同时测定小麦籽粒中黄曲霉毒素B1、黄曲霉毒素B2、黄曲霉毒素G1、黄曲霉毒素G2、T-2毒素和玉米赤霉烯酮6种真菌毒素的方法。优化了真菌毒素分离测定的色谱和质谱条件。结果表明,分离6种真菌毒素的最佳流动相为5 mМ甲酸铵溶液(5∶94.9∶0.1体积(洗脱液A)和95∶4.9∶0.1体积(洗脱液B)), 6种真菌毒素的相关系数为0.9990 ~ 0.9998 (R2 > 0.995)。真菌毒素的检出限(LOD)和定量限(LOQ)低于欧洲联盟(EU)规定的最大允许水平。回收率在88%至103%范围内表明霉菌毒素提取程序的可接受性。在重复性条件下,测定结果的相对标准偏差(RSD, %)范围为1.94 ~ 8.76%。获得的数据适用性评估方法(验证)符合欧盟委员会法规(EC) No 401/2006的标准。验证结果表明,采用改良的QuEChERS样品制备的LC-MS/MS方法是有效的,适用于小麦籽粒中真菌毒素的同时定量。
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来源期刊
CiteScore
1.00
自引率
14.30%
发文量
12
期刊介绍: The journal "Methods and objects of chemical analysis" is peer-review journal and publishes original articles of theoretical and experimental analysis on topical issues and bio-analytical chemistry, chemical and pharmaceutical analysis, as well as chemical metrology. Submitted works shall cover the results of completed studies and shall make scientific contributions to the relevant area of expertise. The journal publishes review articles, research articles and articles related to latest developments of analytical instrumentations.
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