首页> 外文期刊>American Journal of Analytical Chemistry >Utilization of Dispersive Liquid-Liquid Microextraction Coupled with HPLC-UV as a Sensitive and Efficient Method for the Extraction and Determination of Oleanolic Acid and Ursolic Acid in Chinese Medicinal Herbs
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Utilization of Dispersive Liquid-Liquid Microextraction Coupled with HPLC-UV as a Sensitive and Efficient Method for the Extraction and Determination of Oleanolic Acid and Ursolic Acid in Chinese Medicinal Herbs

机译:分散液-液微萃取-高效液相色谱-紫外光法联用灵敏高效提取中草药中齐墩果酸和熊果酸

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Isomeric triterpenic acids of oleanolic acid (OA) and ursolic acid (UA) both have very low ultraviolet absorption and always exist in the same plant, so the separation and simultaneous determination of them have been a difficult task. In this study, a sensitive method combining dispersive liquid-liquid microextraction (DLLME) with HPLC-UV was developed for the extraction and determination of OA and UA in traditional Chinese medicinal herbs (CMHs). Variables influencing DLLME such as type and volume of extraction solvent, volume of dispersive solvent, ionic strength, aqueous phase pH, extraction time, centrifugation speed and time, and sample volume were investigated and optimized. Under the optimum conditions, both OA and UA attained favorable extraction efficiencies with enrichment factors 1378 and 933, respectively. The linear dynamic ranges of 0.07 - 30.4 μg?mL–1 for OA and 0.08 - 33.6 μg?mL–1 for UA were obtained with square correlation coefficients of 0.9963. The detection limits of OA and UA were both 0.02 μg?mL–1. The method recoveries ranged between 88.2% - 116.2% for OA and 85.7% - 108.2% for UA with the RSDs (n = 5) lower than 8.6%. The proposed method was successfully applied to concentrate and simultaneously determine these two triterpenic acids in Hedyotis diffusa and Eriobotrya japonica samples.
机译:齐墩果酸(OA)和熊果酸(UA)的异三萜酸都具有非常低的紫外线吸收,并且总是存在于同一植物中,因此分离和同时测定它们是一项艰巨的任务。在这项研究中,开发了一种结合液-液微萃取(DLLME)和HPLC-UV的灵敏方法,用于中草药(CMHs)中OA和UA的提取和测定。研究并优化了影响DLLME的变量,例如萃取溶剂的类型和体积,分散溶剂的体积,离子强度,水相pH,萃取时间,离心速度和时间以及样品量。在最佳条件下,OA和UA均获得了良好的提取效率,富集系数分别为1378和933。 OA的线性动态范围为0.07-30.4μg?mL–1,UA的线性动态范围为0.08-33.6μg?mL–1,平方相关系数为0.9963。 OA和UA的检出限均为0.02μg?mL–1。该方法的回收率在OA的88.2%至116.2%之间,在UA的85.7%至108.2%之间,且RSD(n = 5)低于8.6%。所提出的方法已成功地应用于浓缩和同时测定白花蛇舌草和日本堇草样品中的这两种三萜酸。

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