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多维气相色谱-质谱法测定葡萄酒和葡萄汁中的3-烷基-2-甲氧基吡嗪。固相萃取法与顶空固相萃取法的比较。

Multidimensional gas chromatography-mass spectrometry determination of 3-alkyl-2-methoxypyrazines in wine and must. A comparison of solid-phase extraction and headspace solid-phase extraction methods.

作者信息

Culleré Laura, Escudero Ana, Campo Eva, Cacho Juan, Ferreira Vicente

机构信息

Department of Analytical Chemistry, Faculty of Sciences, University of Zaragoza, 50009 Zaragoza, Spain.

出版信息

J Chromatogr A. 2009 May 1;1216(18):4040-5. doi: 10.1016/j.chroma.2009.02.072. Epub 2009 Mar 3.

Abstract

Two different strategies for the quantitative determination of 3-alkyl-2-methoxypyrazines in wine and must have been developed and validated. Comparison between both the techniques has been presented and the most adequate has been applied to the determination of these compounds in different samples of wine, made from several varieties of grapes, and also in different samples of must made from Cabernet Sauvignon grapes. Both the methods consisted of a dynamic headspace coupled with a solid-phase extraction (HS-SPE) and solid-phase extraction (SPE) directly from the sample, coupled with multidimensional gas chromatography-mass spectrometry system (MDGC-MS). Both of them require resins LiChrolut EN, and analyte elution has been carried out with dichloromethane. The repeatability of both methodologies was evaluated at two concentration levels. The relative standard deviations (RSD%) were acceptable in every case, but smaller when working with HS-SPE. The recoveries obtained for the three analytes with the two methodologies were almost 100%, with the exception of IBMP, which had a recovery of only 70% with HS-SPE. The linearity was satisfactory with both methods for the range of occurrence of methoxypyrazines in wine and must. The limits of detection of the direct SPE technique were much lower than those of HS-SPE in every case. Direct SPE method detection limits ranged from 0.09 to 0.15 ng L(-1). The method based on direct SPE was chosen finally because it had better detection limits and was easier and quicker than the HS-SPE-based method. It has been applied to the determination of these components in 36 wine and 17 musts samples. The quantitative results suggest that the Spanish wines show meaningless amounts of these compounds. IBMP has been found just in between 1.9 and 15 ng L(-1).

摘要

已开发并验证了两种用于定量测定葡萄酒和葡萄汁中3-烷基-2-甲氧基吡嗪的不同策略。文中介绍了两种技术之间的比较,并将最合适的技术应用于测定不同品种葡萄制成的葡萄酒以及赤霞珠葡萄制成的葡萄汁的不同样品中的这些化合物。两种方法均包括动态顶空结合固相萃取(HS-SPE)以及直接从样品中进行固相萃取(SPE),并与多维气相色谱-质谱系统(MDGC-MS)联用。两者都需要LiChrolut EN树脂,且用二氯甲烷进行分析物洗脱。在两个浓度水平下评估了两种方法的重复性。在每种情况下,相对标准偏差(RSD%)都是可以接受的,但使用HS-SPE时相对较小。两种方法对三种分析物的回收率几乎均为100%,但异丁基甲氧基吡嗪(IBMP)除外,其在HS-SPE中的回收率仅为70%。对于葡萄酒和葡萄汁中甲氧基吡嗪的出现范围,两种方法的线性均令人满意。在每种情况下,直接SPE技术的检测限都远低于HS-SPE的检测限。直接SPE方法的检测限范围为0.09至0.15 ng L(-1)。最终选择了基于直接SPE的方法,因为它具有更好的检测限,并且比基于HS-SPE的方法更简便、快捷。它已应用于36个葡萄酒样品和17个葡萄汁样品中这些成分的测定。定量结果表明,西班牙葡萄酒中这些化合物的含量微不足道。仅在1.9至15 ng L(-1)之间检测到IBMP。

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