[Analysis of volatile aroma components in tobacco by gas chromatography-mass spectrometry coupled with headspace solid phase microextraction].

Xiao-Long Yao, Ya-Yun Ma, Yuan Li, Gao-Jian Shi, Qian-Wei Zhou, Yu-Hai Zhang, Ning-Jie Luo, Lin Zhang, Bin Li, Nan Deng, Ling-Jie Meng
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Abstract

Volatile flavor compounds play vital roles when evaluating the flavor and quality of tobacco products. Pretreatment is always required owing to the wide range of flavor compounds and the complexity of the tobacco matrix. Solvent extraction (SE), steam distillation (SD), simultaneous distillation extraction (SDE), supercritical fluid extraction (SFE), and solid phase microextraction (SPME) are methods commonly used to extract and purify volatile flavor compounds. Among these methods, SPME coupled with headspace (HS) sampling has gained considerable attention in a variety of research fields because it combines sampling, extraction, concentration, and sample injection into a single procedure to deliver advantages that include convenient and simple sample preparation, small sample volumes, high sensitivities, and convenient operation.In this study, HS-SPME coupled with gas chromatography-mass spectrometry (GC-MS) was used to analyze the volatile aroma components in tobacco leaves. First, extraction efficiency was optimized by carefully evaluating multiple parameters, including types of solid phase microextraction fibers, extraction temperature, adsorption time, and desorption time. The number of chromatographic peaks, total chromatographic peak area, number of identified compounds, and internal-standard peak areas were used as indices. The optimized protocol involves incubating tobacco powder (1.0 g) under 80 ℃, extraction with an 80 μm divinylbenzene/carboxen/polydimethylsiloxane (DVB/CWR/PDMS) SPME needle for 30 min, followed by desorption from the fiber for a sufficient time (8 min). These conditions led to a 1.6% RSD for the internal-standard peak area across five replicate experiments; hence, the developed method is highly repeatable. The volatile aroma components in tobacco leaves obtained from five different production areas were analyzed using the optimized parameters. A total of 107 volatile aroma compounds were identified, among which ketones, aromatics, and heterocyclic compounds accounted for more than 70% of the total volatile aroma components (excluding neophytadiene). Tobacco leaves obtained from the Shangluo region contained the highest amount of total volatile aroma compounds, followed by leaves from Ankang, Hanzhong, Baoji, and Yan'an regions. Orthogonal partial least squares-discriminant analysis (OPLS-DA) was used to determine the main differential components from the various production regions, which identified 14 differential compounds (primarily ketones and alcohols). This study provides a theoretical basis and reference for further exploring key volatile flavor compounds in leaves sourced from different production areas, as well as for identifying flavor-indicator substances and improving the quality of tobacco leaves.

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[顶空固相微萃取-气相色谱-质谱法分析烟草中挥发性香气成分]。
挥发性香料在评价烟草制品的风味和质量方面起着至关重要的作用。由于香精化合物的种类繁多和烟叶基质的复杂性,预处理一直是需要的。溶剂萃取(SE)、蒸汽蒸馏(SD)、同时蒸馏萃取(SDE)、超临界流体萃取(SFE)和固相微萃取(SPME)是提取和纯化挥发性风味化合物的常用方法。在这些方法中,SPME与顶空(HS)采样相结合的方法因其将采样、提取、浓缩、进样等工序结合在一起,具有制样方便、简单、样品体积小、灵敏度高、操作方便等优点而受到了广泛的关注。采用HS-SPME联用气相色谱-质谱联用技术对烟叶中挥发性香气成分进行了分析。首先,通过对固相微萃取纤维类型、萃取温度、吸附时间、解吸时间等参数的综合评价,优化萃取效率。以色谱峰数、色谱总峰面积、鉴定化合物数和内标峰面积为指标。优化后的方案为:烟草粉末(1.0 g)在80℃下培养,用80 μm二乙烯苯/碳/聚二甲基硅氧烷(DVB/CWR/PDMS) SPME针提取30 min,然后从纤维中脱附足够的时间(8 min)。这些条件导致5次重复实验的内标峰面积的RSD为1.6%,因此,所开发的方法具有高度可重复性。利用优化后的参数对5个不同产地烟叶的挥发性香气成分进行了分析。共鉴定出107种挥发性香气化合物,其中酮类、芳烃类和杂环类化合物占总挥发性香气成分的70%以上(不含新苔二烯)。商洛地区烟叶总挥发性香气化合物含量最高,安康、汉中、宝鸡和延安地区次之。采用正交偏最小二乘判别分析(OPLS-DA)确定了不同产地的主要差异成分,鉴定出14种差异化合物(主要是酮类和醇类)。本研究为进一步探索不同产地烟叶中关键挥发性风味物质,鉴定风味指示物质,提高烟叶品质提供理论依据和参考依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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