Zhao Minmin, Ding Weijing, Wang Shuang, Wang Chunying, Du Yingfeng, Xu Huijun, Wang Qiao, Jin Shumin
Department of Pharmaceutical Analysis, School of Pharmacy, Hebei Medical University, Shijiazhuang 050017, PR China; Jincheng General Hospital, General Hospital (Medical Group) of Shanxi Jincheng Anthracite Mining Group, Jincheng 048006, PR China.
Department of Pharmaceutical Analysis, School of Pharmacy, Hebei Medical University, Shijiazhuang 050017, PR China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2016 Jul 1;1025:25-32. doi: 10.1016/j.jchromb.2016.04.042. Epub 2016 Apr 30.
A high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method was developed for the simultaneous determination of nine coumarins including aesculin, aesculetin, fraxin, fraxetin, scopoletin, isoscopoletin, 6-hydroxy-7,8-dimethoxy coumarin, 8-hydroxy-6,7-dimethoxy coumarin and umbelliferone in rat plasma using nodakenin as the internal standard (IS). The plasma samples were pretreated by a one-step direct protein precipitation with methanol. The chromatographic separation was carried out on a C18 column with a gradient mobile phase consisting of methanol and water (containing 0.05% acetic acid). All analytes and IS were quantitated through electrospray ionization in negative ion multiple reaction monitoring (MRM) mode. This method was fully validated in terms of the sensitivity, specificity, accuracy, precision (intra- and inter-day), matrix effect, recovery as well as the stability of the analyte under various conditions, and the results satisfied the requirements of biological sample measurement. The validated method was successfully applied to pharmacokinetic study of the nine coumarins in rat plasma after oral administration of Fraxini Cortex aqueous extract, among which the pharmacokinetics of four coumarins including fraxetin, isoscopoletin, 6-hydroxy-7,8-dimethoxy coumarin and 8-hydroxy-6,7-dimethoxy coumarin were studied for the first time.
建立了一种高效液相色谱-串联质谱(HPLC-MS/MS)法,以紫花前胡苷为内标,同时测定大鼠血浆中秦皮甲素、秦皮乙素、秦皮苷、秦皮素、东莨菪内酯、异东莨菪内酯、6-羟基-7,8-二甲氧基香豆素、8-羟基-6,7-二甲氧基香豆素和伞形花内酯9种香豆素类成分。血浆样品采用甲醇一步直接沉淀蛋白法进行预处理。色谱分离在C18柱上进行,流动相为甲醇和水(含0.05%乙酸)的梯度洗脱。所有分析物和内标均通过电喷雾电离在负离子多反应监测(MRM)模式下进行定量。该方法在灵敏度、特异性、准确性、精密度(日内和日间)、基质效应、回收率以及分析物在各种条件下的稳定性等方面均得到充分验证,结果满足生物样品测定要求。该验证方法成功应用于大鼠口服秦皮水煎液后血浆中9种香豆素类成分的药代动力学研究,其中对秦皮素、异东莨菪内酯、6-羟基-7,8-二甲氧基香豆素和8-羟基-6,7-二甲氧基香豆素4种香豆素类成分的药代动力学进行了首次研究。