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利用真空辅助顶空固相微萃取的多功能性和基于离子液体的 GC 固定相的选择性,通过挥发性和半挥发性馏分来区分乳香属树脂。

Exploiting the versatility of vacuum-assisted headspace solid-phase microextraction in combination with the selectivity of ionic liquid-based GC stationary phases to discriminate Boswellia spp. resins through their volatile and semivolatile fractions.

机构信息

Dipartimento di Scienza e Tecnologia del Farmaco, Università di Torino, Turin, Italy.

出版信息

J Sep Sci. 2020 May;43(9-10):1879-1889. doi: 10.1002/jssc.202000084. Epub 2020 Mar 12.

DOI:10.1002/jssc.202000084
PMID:32072762
Abstract

The frankincense resins, secreted from Boswellia species, are an uncommon example of a natural raw material where every class of terpenoids is present in similar proportions. Diterpenoids (serratol, incensole, and incensole acetate) are used to discriminate samples from different species and origins. Headspace solid-phase microextraction has been used for frankincense analysis, although it requires long sampling time for medium- to low-volatility markers; headspace solid-phase microextraction under vacuum can overcome this limit. Gas chromatography is used for analysis but the separation of incensole and serratol needs polar stationary phases. In this study, we develop a method to discriminate frankincenses based on vacuum-assisted headspace solid-phase microextraction combined with fast gas chromatography-mass spectrometry with ionic liquid-based stationary phases. The optimized conditions for solid samples were: air evacuation below 0°C, 15 min of incubation time, and 15 min of extraction time. Losses of volatiles due to vial air-evacuation in the presence of the sample were minimized by sample amount above 100 mg and low sample temperature. Fast gas chromatography provides the baseline separation of all markers in 20 min. By applying vacuum sampling and fast gas chromatography, the total analysis was reduced to 50 min compared to 120 min (60 min sampling plus 60 min analysis) as previously reported. The method was successfully applied to commercial frankincense samples.

摘要

乳香树脂是从乳香属植物分泌出来的一种不常见的天然原料,萜类化合物的每一类都以相似的比例存在。二萜类化合物(蛇麻脂醇、乳香醇和乳香醇乙酸酯)被用于区分不同物种和来源的样本。顶空固相微萃取已被用于乳香分析,但对于中低挥发性标志物,它需要较长的采样时间;在真空中进行顶空固相微萃取可以克服这个限制。气相色谱法用于分析,但乳香醇和蛇麻脂醇的分离需要使用极性固定相。在这项研究中,我们开发了一种基于真空辅助顶空固相微萃取结合基于离子液体的固定相的快速气相色谱-质谱法来区分乳香的方法。对固体样品的优化条件为:低于 0°C 的空气排空、15 分钟的孵育时间和 15 分钟的提取时间。通过使用超过 100 毫克的样品量和低样品温度,可以最大限度地减少由于样品存在而导致的挥发性物质在小瓶空气排空过程中的损失。快速气相色谱在 20 分钟内提供了所有标志物的基线分离。通过应用真空采样和快速气相色谱,与之前报道的 120 分钟(60 分钟采样加 60 分钟分析)相比,总分析时间减少到 50 分钟。该方法成功应用于商业乳香样品。

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