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作 者:崔晓红[1] 奇海涛[2] 生宁[2] 张兰桐[2] 田亚平[2] 郑旭光[2]
机构地区:[1]河北医科大学第二医院药剂科,石家庄050017 [2]河北医科大学药学院药物分析教研室,石家庄050017
出 处:《药物分析杂志》2014年第3期432-436,共5页Chinese Journal of Pharmaceutical Analysis
摘 要:目的:采用HPLC法同时测定益肝康颗粒(丹参、黄芪、赤芍、当归等)中活性成分没食子酸、丹参素、芍药苷、丹酚酸B和丹参酮Ⅱ。的含量。方法:采用c。。反相色谱柱,以甲醇-乙睛-0.1%磷酸水溶液为流动相梯度洗脱,检测波长为芍药苷230nm,没食子酸、丹参素、丹酚酸B、丹参酮IIA 270nm。结果:没食子酸、丹参素、芍药苷、丹酚酸B和丹参酮ⅡA进样量分别在30.1~376.8、452.7—5659.2、201.6~2520、1657.0~20712.0、54.336~679.2μg·mL^-1范围内呈良好的线性关系,平均回收率分别为102.5%、104.7%、99.4%、105.0%、102.9%。结论:该方法简捷,快速,可靠,可用于控制该制剂的质量。Objective: To develop a method for determining the contents of gallic acid,tanshinol, paeoniflorin, salvianolic acid B and tanshinone II A in Yi gan kang granules. Methods: The analytical column was an ODS col- umn. The mobile phase consisted of acetonitrile - 0. 1% phosphoric acid aqueous solution using gradient elution. The detection wavelength of paeoniflorin was 230 nm, and the wavelength for gallic acid, tanshinol, salvianolic acid B and tanshinone II A detection was set at 270 nm. Results : The calibration curves of gallic acid, tanshinol, pae- oniflorin, salvianolic acid B and tanshinone II A showed good linearity in the ranges of 30. 1 - 376.8,452.7 - 5659.2,201.6 - 2520,1657.0 - 20712.0 and 54. 336 - 679.2 μg · mL-1 , and the average recoveries were 102. 5% , 104.7% ,99.4% , 105.0% and 102.9% , respectively. Conclusions : The method is simple, rapid, reli- able and can be used for drug quality control. This method replenishes the insufficient quality control of Yi gan kang granules.
关 键 词:益肝康颗粒 没食子酸 丹参素 芍药苷 丹酚酸B 丹参酮ⅡA 含量测定 质量控制 HPLC—DAD
分 类 号:R917[医药卫生—药物分析学]
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