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作 者:王维聪[1] 王潮[1] 宋学英[1] 赵文华[1] 王桥[1]
机构地区:[1]首都医科大学化学生物学与药学院,北京100069
出 处:《中国中药杂志》2008年第6期656-659,共4页China Journal of Chinese Materia Medica
基 金:北京市属市管高等学校人才强教计划资助项目;首都医科大学科研基金(2006ZR09)
摘 要:目的:采用高效液相色谱测定44种中药中1,2,3,4,6-五-O-倍酰-D-葡萄糖(1,2,3,4,6-penta-O-galloyl-D-glucose,PGG)的含量。方法:以乙醇-水溶液(50∶50)为提取剂,在50~60 ℃的温度下超声1 h,从中药中提取PGG;采用Diamonsil C18(4. 6 mm×250 mm,5 μm)色谱柱,流动相为乙腈-2. 5 %醋酸水溶液(18∶82),紫外检测波长280 nm,流速1. 0 mL·min^-1。结果:PGG在1~150 μg·mL^-1呈良好的线性关系(r = 0. 999 4)。五倍子、牡丹皮、赤芍、白芍等17种中药中均含有PGG,且在五倍子、牡丹皮、赤芍、白芍中PGG含量较高。结论:本实验用简单快捷的方法考察了44种中药中PGG的含量,并准确测定了五倍子等17种含PGG中药中PGG的含量,为从中药中分离、纯化PGG以及中药的开发利用提供了实验基础。Objective: To determine 1, 2, 3, 4, 6-penta-O-galloyl-D-glucose (PGG) in forty four kinds of Chinese traditional medicines by HPLC. Method: The PGG was extracted with a solvent consisting of ethanol and water (50∶50) in ultrasonic bath at 50-60 ℃ for 1 hour. A Diamonsil C18 column (4. 6 mm×250 mm, 5 μm) was used for the separation and analysis of PGG with a mobile phase consisting of acetonitrile and 2. 5 % acetic acid solution (18∶82). The wavelength of detection was at 280 nm, and flow rate was set at 1. 0 mL·min^-1. Result: The calibration curve for PGG is linear over the range of 1-150 μg·mL^-1 (r=0. 999 4), and PGG was found in seventeen kinds of Chinese traditional medicines, such as gall tree peony bark, red peony root, white peony root,and so on. Conclusion: The contents of PGG were determined in forty four kinds of Chinese traditional medicines by a rapid and precision HPLC method.
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