首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Development and validation of a liquid chromatography/atmospheric pressure photoionization-tandem mass spectrometric method for the analysis of mycotoxins subjected to commission regulation (EC) No. 1881/2006 In cereals
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Development and validation of a liquid chromatography/atmospheric pressure photoionization-tandem mass spectrometric method for the analysis of mycotoxins subjected to commission regulation (EC) No. 1881/2006 In cereals

机译:谷物中受霉菌毒素分析的液相色谱/大气压光电离串联质谱分析方法的开发和验证(EC)1881/2006

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摘要

A sensitive and reliable liquid chromatography/photoionization (APPI) tandem mass spectrometry method has been developed for determining nine selected mycotoxins in wheat and maize samples. The analytes were chosen on the basis of the mycotoxins under EU Commission Regulation (EC) No. 1881/2006, i.e., deoxynivalenol (DON), zearalenone (ZON), aflatoxins (AFs), and ochratoxin A (OTA), and considering the possibility of a near future regulation for T-2 and HT-2 toxins. Mycotoxins were extracted from samples by means of an one-step solvent extraction without any cleanup. The developed multi-mycotoxin method permits simultaneous, simple, and rapid determination of several co-existing toxins separated in a single chromatographic run, in which AFs, T-2 and HT-2 toxin are acquired in positive, while OTA, DON and ZON in negative mode. Although a moderate signal suppression was noticeable, matrix effect did not give significant differences at p=0.05. Then, calibration in standard solution were used for quantitation. Based on the EU Commission Decision 2002/657/EC, the method was in-house validated in terms of ruggedness, specificity, linearity, trueness, within-laboratory reproducibility, decision limit (CC α) and detection capability (CC β). For all the analytes, the regression coefficient r ranged between 0.8752 (DON in wheat) and 0.9465 (ZON in maize), biases related to mean concentrations were from -13% to +12% of the nominal spiking level, and the overall within-laboratory reproducibility ranged 3-16%; finally, CC α values did not differ more than 20% and CC β not more than 42% from their respective maximum limit. Method quantification limits ranged from 1/20 (AFG1) to 1/4 (AFG2 and OTA) the maximum limit established by European Union in the Commission Regulation (EC) No. 1881/2006 and its subsequent amendments.
机译:已经开发了一种灵敏可靠的液相色谱/光电离(APPI)串联质谱方法,用于测定小麦和玉米样品中的九种选定的霉菌毒素。根据欧盟委员会法规(EC)1881/2006的霉菌毒素选择分析物,即脱氧雪腐烯醇(DON),玉米赤霉烯酮(ZON),黄曲霉毒素(AFs)和曲霉毒素A(OTA),并考虑T-2和HT-2毒素在不久的将来可能会受到管制。通过一步溶剂萃取从样品中提取真菌毒素,而无需进行任何纯化。发达的多真菌毒素方法可同时,简单,快速地测定单次色谱分离的几种共存毒素,其中AF,T-2和HT-2毒素为阳性,而OTA,DON和ZON为阳性在否定模式下。尽管中等程度的信号抑制是明显的,但在p = 0.05时,基质效应并未产生显着差异。然后,将标准溶液中的标定用于定量。根据欧盟委员会第2002/657 / EC号决定,该方法在坚固性,特异性,线性,真实性,实验室内可重复性,决策极限(CCα)和检测能力(CCβ)方面进行了内部验证。对于所有分析物,回归系数r介于0.8752(小麦中的DON)和0.9465(玉米中的ZON)之间,与平均浓度相关的偏差为标称加标水平的-13%至+ 12%,总体在-实验室重现性为3-16%;最后,CCα值与其各自的最大限值之差不超过20%,CCβ值之差不超过42%。方法的定量限为欧盟在委员会法规(EC)第1881/2006号及其后续修正案中确定的最大限度的1/20(AFG1)至1/4(AFG2和OTA)。

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