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高效液相色谱柱前衍生化法快速测定三萜齐墩果酸和熊果酸的高灵敏度和选择性:响应面法优化三萜酸的提取和柱前衍生化。

Highly sensitive and selective pre-column derivatization high-performance liquid chromatography approach for rapid determination of triterpenes oleanolic and ursolic acids and application to Swertia species: optimization of triterpenic acids extraction and pre-column derivatization using response surface methodology.

机构信息

Northwest Plateau Institute of Biology, Chinese Academy of Sciences, Xining, 810001, PR China.

出版信息

Anal Chim Acta. 2011 Mar 4;688(2):208-18. doi: 10.1016/j.aca.2011.01.010. Epub 2011 Jan 18.

Abstract

Oleanolic acid (OA) and ursolic acid (UA) are the ubiquitous triterpenic acids in plant kingdom and have multiple biological effects. In the present study, a highly sensitive and selective method using a dual-sensitive probe 2-(5-benzoacridine)ethyl-p-toluenesulfonate (BAETS) as pre-column labeling reagent has been developed for rapid determination of the triterpenes OA and UA by HPLC with fluorescence detection (FLD) and online mass spectrometry identification. Response surface methodology as an efficient tool was employed to optimize the ultrasonic-assisted extraction of triterpenic acids from Swertia plants and the pre-column derivatization reaction, respectively, which ensured the highest triterpenic acids recoveries within the shortest extraction time and the sufficient labeling of the analyzed components. Fast separation of the isomers OA and UA could be achieved on a Hypersil BDS C8 column within 7 min. Both of OA and UA gave the good correlation coefficients of 0.9999. This developed method offered the satisfactory detection limits of 1.10 and 1.30 ng mL(-1) for UA and OA, respectively. When applied to Swertia species, it showed good reproducibility.

摘要

齐墩果酸(OA)和熊果酸(UA)是植物界中普遍存在的三萜酸,具有多种生物学效应。本研究采用双敏探针 2-(5-苯并吖啶基)乙基-对甲苯磺酸盐(BAETS)作为柱前衍生试剂,建立了一种快速测定三萜酸 OA 和 UA 的高效灵敏的 HPLC-FLD 在线质谱联用方法。响应面法作为一种有效的工具,分别用于优化超声辅助提取和柱前衍生反应,以确保在最短的提取时间内获得最高的三萜酸回收率和充分标记分析物。在 Hypersil BDS C8 柱上,异构体 OA 和 UA 可在 7 分钟内实现快速分离。OA 和 UA 的相关系数均为 0.9999。该方法对 UA 和 OA 的检测限分别为 1.10 和 1.30 ng·mL-1。应用于 Swertia 属植物时,具有良好的重现性。

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