首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Development and in-house validation of a robust and sensitive solid-phase extraction liquid chromatography/tandem mass spectrometry method for the quantitative determination of aflatoxins B1, B2, G 1, G2, ochratoxin A, deoxynivalenol, zearalenone, T-2 and HT-2 toxins in cereal-based foods
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Development and in-house validation of a robust and sensitive solid-phase extraction liquid chromatography/tandem mass spectrometry method for the quantitative determination of aflatoxins B1, B2, G 1, G2, ochratoxin A, deoxynivalenol, zearalenone, T-2 and HT-2 toxins in cereal-based foods

机译:建立可靠的固相萃取液相色谱/串联质谱方法,用于定量测定黄曲霉毒素B1,B2,G 1,G2,曲霉毒素A,脱氧雪腐酚,玉米赤霉烯酮,T-2和HT-谷物食品中的2种毒素

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A sensitive and robust liquid chromatography/tandem mass spectrometry (LC/MS/MS) method was developed for the simultaneous determination of aflatoxins (B1, B2, G1, G2), ochratoxin A, deoxynivalenol, zearalenone, T-2 and HT-2 toxins in cereal-based foods. Samples were extracted with a mixture of acetonitrile/water (84:16, v/v) and cleaned up through a polymeric solid-phase extraction column. Detection and quantification of the nine mycotoxins were performed by reversed-phase liquid chromatography coupled with electrospray ionization triple quadrupole mass spectrometry (LC/ESI-MS/MS), using fully 13C-isotope-labelled mycotoxins as internal standards. The method was validated in-house for five different cereal processed products, namely barley, oat and durum wheat flours, rye- and wheat-based crisp bread. Recoveries and repeatability of the whole analytical procedure were evaluated at contamination levels encompassing the EU maximum permitted levels for each tested mycotoxin. Recoveries ranged from 89 to 108% for deoxynivalenol, from 73 to 114% for aflatoxins, from 85 to 114% for T-2 and HT-2 toxins, from 64 to 97% for zearalenone, from 74 to 102% for ochratoxin A. Relative standard deviations were less than 16% for all tested mycotoxins and matrices. Limits of detection (signal-to-noise ratio 3:1) ranged from 0.1 to 59.2 μg/kg. The trueness of the results obtained by the proposed method was demonstrated by analysis of reference materials for aflatoxins, deoxynivalenol, zearalenone. The use of inexpensive clean-up cartridges and the increasing availability of less expensive LC/MS/MS instrumentation strengthen the potential of the proposed method for its effective application for reliable routine analysis to assess compliance of tested cereal products with current regulation.
机译:建立了灵敏且稳定的液相色谱/串联质谱(LC / MS / MS)方法,用于同时测定黄曲霉毒素(B1,B2,G1,G2),ra曲霉毒素A,脱氧雪腐酚,玉米赤霉烯酮,T-2和HT-2谷类食品中的毒素。用乙腈/水(84:16,v / v)的混合物萃取样品,并通过聚合物固相萃取柱进行净化。使用完全13 C同位素标记的霉菌毒素作为内标,通过反相液相色谱结合电喷雾电离三重四极杆质谱(LC / ESI-MS / MS)对9种霉菌毒素进行检测和定量。该方法已在内部针对五种不同的谷物加工产品进行了验证,即大麦,燕麦和硬质小麦粉,黑麦和小麦基脆面包。评估了整个分析过程的回收率和可重复性,其污染水平包括每种被测真菌毒素的欧盟最大允许水平。脱氧雪腐烯醇的回收率从89%到108%,黄曲霉毒素的回收率从73%到114%,T-2和HT-2毒素的回收率从85%到114%,玉米赤霉烯酮的回收率从64%到97%,曲毒素A的回收率从74%到102%。所有测试的霉菌毒素和基质的相对标准偏差均小于16%。检测限(信噪比3:1)在0.1至59.2μg/ kg之间。通过对黄曲霉毒素,脱氧雪腐烯酚,玉米赤霉烯酮的参考物质进行分析,证明了所提出方法获得的结果的真实性。使用廉价的净化柱以及价格越来越便宜的LC / MS / MS仪器的可用性不断提高,增强了该方法在有效进行可靠的常规分析以评估受测谷物产品是否符合现行法规方面的潜力。

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