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高效液相色谱法测定大鼠静脉注射山楂叶提取物后血浆中5种多酚类成分及其在药代动力学研究中的应用

HPLC determination of five polyphenols in rat plasma after intravenous administration of hawthorn leaves extract and its application to pharmacokinetic study.

作者信息

Wang Si-Yuan, Chai Ji-Yan, Zhang Wen-Jie, Liu Xun, DU Yang, Cheng Zhong-Zhe, Ying Xi-Xiang, Kang Ting-Guo

机构信息

Department of Pharmaceutical Analysis, School of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, China.

出版信息

Yakugaku Zasshi. 2010 Nov;130(11):1603-13. doi: 10.1248/yakushi.130.1603.

DOI:10.1248/yakushi.130.1603
PMID:21048422
Abstract

A simple and specific HPLC-UV method was developed to simultaneously determine five active compounds including vitexin-4"-O-glucoside (VG), vitexin-2"-O-rhamnoside (VR), vitexin (VIT), rutin (RUT) and hyperoside (HP) in rat plasma after intravenous administrating the hawthorn leaves extract (HLE). With baicalin as internal standard (I.S.), sample pretreatment involved a one-step extraction with methanol of 0.2 ml plasma. The HPLC assay was carried out using a Phenomsil C18 analytical column with UV detection at 332 nm. The mobile phase consisted of methanol-acetonitrile-tetrahydrofuran-1% glacial acetic acid (6:1.5:18.5:74, v/v/v/v). The calibration curves were liner over the range of 2.030-500.5, 0.1513-75.64, 0.2507-12.54, 0.5128-25.64 and 0.4032-20.16 µg/ml for VG, VR, VIT, RUT and HP, respectively. The relative standard deviations (RSD) of the intra- and inter-day precisions for the analysis of the five analytes were between 1.0 and 8.9% with accuracies (relative error) below 8.2% for the analysis of the five analytes. The average extraction recoveries of five analytes were more than 82.67 ± 4.74%. The HPLC method herein described was fully validated and successfully applied to the pharmacokinetic studies after intravenous administration of HLE solution to rats over three doses.

摘要

建立了一种简单且特异的高效液相色谱 - 紫外检测法(HPLC - UV),用于在静脉注射山楂叶提取物(HLE)后同时测定大鼠血浆中包括牡荆素 - 4'' - O - 葡萄糖苷(VG)、牡荆素 - 2'' - O - 鼠李糖苷(VR)、牡荆素(VIT)、芦丁(RUT)和金丝桃苷(HP)在内的五种活性化合物。以黄芩苷为内标(I.S.),样品预处理采用0.2 ml血浆一步甲醇萃取法。HPLC分析使用Phenomsil C18分析柱,在332 nm处进行紫外检测。流动相由甲醇 - 乙腈 - 四氢呋喃 - 1%冰醋酸(6:1.5:18.5:74,v/v/v/v)组成。校准曲线在2.030 - 500.5、0.1513 - 75.64、0.2507 - 12.54、0.5128 - 25.64和0.4032 - 20.16 μg/ml范围内分别对VG、VR、VIT、RUT和HP呈线性。五种分析物日内和日间精密度的相对标准偏差(RSD)在1.0%至8.9%之间,五种分析物分析的准确度(相对误差)低于8.2%。五种分析物的平均萃取回收率超过82.67 ± 4.74%。本文所述的HPLC方法经过充分验证,并成功应用于大鼠静脉注射三种剂量HLE溶液后的药代动力学研究。

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