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建立并验证了一种基于 QuEChERS 的液相色谱串联质谱法,用于测定香料中的多种真菌毒素。

Development and validation of a QuEChERS based liquid chromatography tandem mass spectrometry method for the determination of multiple mycotoxins in spices.

机构信息

nutriFOODchem unit, Department of Food Safety and Food Quality (partner in Food2Know), Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, B-9000 Ghent, Belgium.

出版信息

J Chromatogr A. 2013 Jul 5;1297:1-11. doi: 10.1016/j.chroma.2013.04.075. Epub 2013 Apr 30.

Abstract

A reliable and rapid method for the determination of multiple mycotoxins was developed using a QuEChERS (quick, easy, cheap, effective, rugged and safe) based extraction procedure in highly pigmented and complex spice matrices, namely red chilli (Capsicum annum ssp.), black and white pepper (Piper nigrum ssp.). High-performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS) was used for the quantification and confirmation of 17 chemically diversified mycotoxins. Different extraction procedures were studied and optimized in order to obtain better recoveries. Mycotoxins were extracted from the hydrated spices using acidified acetonitrile (1% formic acid), followed by partitioning with NaCl and anhydrous MgSO4; excluding the use of dispersive-solid phase extraction. Significant matrix effect was compensated using the matrix matched calibration curves. Electrospray ionization at positive mode was applied to simultaneously detect all the mycotoxins in a single run time of 20min. Multiple reaction monitoring mode, choosing at least two abundant fragment ions per analyte was applied. Coefficients of determination obtained were in the range of 0.9844-0.9997. Recoveries (ranging from 75% to 117%) were in accordance with the performance criteria required by the European Commission. Intra-day reproducibility ranged from 4% to 22% for most of the mycotoxins. The limit of quantification ranged from 2.3 to 146μgkg(-1). The validated method was finally applied to screen mycotoxins in ten of each spice matrix. Aflatoxins, ochratoxin, fumonisins, sterigmatocystin and citrinin were among the detected analytes. Positive findings were further confirmed using relative ion intensities. The potentiality of the method to be used for confirmatory purposes according to Commission Decision 2002/657/EC was assessed.

摘要

建立了一种基于 QuEChERS(快速、简便、廉价、有效、耐用和安全)的提取方法,用于从高度着色和复杂的香料基质(即红辣椒(Capsicum annum ssp.)、黑胡椒和白胡椒(Piper nigrum ssp.))中测定多种真菌毒素。采用高效液相色谱串联质谱法(HPLC-MS/MS)对 17 种化学多样性真菌毒素进行定量和确证。研究并优化了不同的提取程序,以获得更好的回收率。用酸化乙腈(1%甲酸)提取水合香料中的真菌毒素,然后用 NaCl 和无水 MgSO4 进行分配;不使用分散固相萃取。使用基质匹配校准曲线补偿了显著的基质效应。采用正电喷雾电离同时在 20min 的单个运行时间内检测所有真菌毒素。选择每个分析物至少两个丰富的碎片离子,应用多反应监测模式。得到的决定系数在 0.9844-0.9997 范围内。回收率(范围为 75%-117%)符合欧盟委员会要求的性能标准。大多数真菌毒素的日内重现性范围为 4%-22%。定量限范围为 2.3-146μgkg(-1)。最终将验证后的方法应用于十种每种香料基质的真菌毒素筛选。检测到的分析物包括黄曲霉毒素、赭曲霉毒素、伏马菌素、桔青霉素和桔霉素。使用相对离子强度进一步确认阳性结果。根据委员会决定 2002/657/EC 评估了该方法用于确证目的的潜力。

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