Department of Analytical Chemistry, Faculty of Chemical Technology, University of Pardubice, Pardubice, Czech Republic.
J Sep Sci. 2013 Feb;36(4):764-72. doi: 10.1002/jssc.201200714. Epub 2013 Jan 28.
A method employing the direct immersion solid-phase microextraction followed by GC-MS analysis is presented for the determination of essential oils components in herbal tea infusions, i.e. their direct content in the liquid phase. The extraction performances were compared using five different microextraction fibres. Significant parameters affecting sorption process such as sample amount, sorption and desorption time and temperature, stirring speed, pH adjustment and effect of ionic strength were optimised and discussed. By optimising the key parameters, a detection limits (LOD = S/N × 3) for ten target marker compounds were obtained in the range from 5.3 to 48.2 ng/mL with recoveries ranged between 93.03 and 100.50%. Intra-day and inter-day repeatability at three concentration levels were found to be 1.1-15.3 and 7.2-15.5% RSD, respectively. Finally, the optimised procedure enabling a rapid and simple analysis of essential oils was applied for the direct determination of these compounds in ten herbal tea infusions.
一种采用直接浸没法固相微萃取结合 GC-MS 分析的方法被提出,用于测定草药茶浸提液中的精油成分,即它们在液相中的直接含量。使用五种不同的微萃取纤维比较了萃取性能。对影响吸附过程的重要参数(如样品量、吸附和解吸时间和温度、搅拌速度、pH 值调节和离子强度的影响)进行了优化和讨论。通过优化关键参数,在 5.3 至 48.2 ng/mL 的范围内,十种目标标记化合物的检测限(LOD = S/N × 3)为 5.3 至 48.2 ng/mL,回收率在 93.03%至 100.50%之间。在三个浓度水平下,日内和日间重复性的 RSD 分别为 1.1-15.3%和 7.2-15.5%。最后,优化后的程序能够快速、简单地分析精油,用于直接测定十种草药茶浸提液中的这些化合物。