高效液相色谱法检测加味芍药甘草颗粒中芍药苷、甘草酸的含量  

Determination of Peoniflorin and Glycyrrhizic Acid in Modified Shaoyao Gancao Granules by High Performance Liquid Chromatography

作　　者：陆彦[1] 彭拓华[1] 

机构地区：[1]广东省药物研究所,广东广州510440

出　　处：《广州中医药大学学报》2009年第1期66-69,共4页Journal of Guangzhou University of Traditional Chinese Medicine

摘　　要：【目的】建立加味芍药甘草颗粒中芍药苷及甘草酸的含量测定方法。【方法】采用反相高效液相色谱法,色谱条件：乙腈（A）-10 g/L冰醋酸水溶液（B）（调pH3.5）,流速1.0 mL/min;检测波长250 nm,柱温为室温,进样量20μL。梯度洗脱程序：体积分数18%A、0～5 min,体积分数19%～29%A、6～10 min,体积分数30%～45%A、11～25 min（A＋B=100%）。【结果】芍药苷及甘草酸分别在1.916～122.6、2.625～168μg/mL范围内成良好线性关系,平均回收率芍药苷为101.12%,甘草酸为99.68%。【结论】本测定方法简便可行、重复性好,可用于加味芍药甘草颗粒中有效成分芍药苷和甘草酸的含量测定。Objective To establish a method for the determination of peoniflorin and glycyrrhizic acid in modified Shaoyao Gancao Granules.Methods Reversed-phase high performance liquid chromatography（HPLC） was used.The chromatographic condition was as follows： Diamonsil C18 column（4.6mm ×250mm,5μm）,column temperature being room temperature,mobile phase consisting of acetonitrile（A）-10g/L acetic acid（B） with adjusting pH value being 3.5,flowing rate at 1.0mL/min,detective wavelength at 250nm,and the injection volume being 20μL.The gradient elution procedure was as follows： elution with 18% A for 0～5 min,elution with 19%～29% A for 6～10 min,elution with 30%～45% A for 11～25min,and A＋B=100%.Results Peoniflorin at the concentration of 1.916～122.6μg/L and glycyrrhizic acid at the concentration of 2.625～168μg/L showed a good linearity.The mean recovery was 101.12% for peoniflorin and 99.68% for glycyrrhizic acid.Conclusion This method is simple and reproducible,and can be used for the determination of peoniflorin and glycyrrhizic acid in modified Shaoyao Gancao Granules.

关 键 词：加味芍药甘草颗粒/化学 芍药苷/分析 甘草酸/分析 色谱法 高压液相 

分 类 号：R284.1[医药卫生—中药学]