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机构地区:[1]山东阿如拉药物研究开发有限公司,山东济南250101
出 处:《中国医学创新》2013年第20期129-132,共4页Medical Innovation of China
摘 要:目的:研究并提高藏药前列宁胶囊的质量标准。方法:采用薄层色谱法鉴别红花、诃子、菥蓂子、藏茜草;采用高效液相色谱法同时测定没食子酸和羟基红花黄色素A。结果:薄层色谱显色清晰,阴性对照无干扰。没食子酸在33.76~337.6μg/ml浓度范围内线性关系良好,r=0.9996,平均加样回收率为98.35%,RSD为1.36%。羟基红花黄色素A在2.68~26.80μg/ml浓度范围内线性关系良好,r=0.9998,平均加样回收率为99.03%,RSD为0.72%。结论:该方法简便、可行、可靠,可用于控制前列宁胶囊的质量。Objective:To study and upgrade the quality standard of Tibetan Medicine Qianliening Capsule.Method:TLC method was used to identify Flos Carthami,Terminalia Chebula,Semen Thlaspi and Radix et Rhizoma Rubiae;Hplc was used for the determination of Gallic acid and Hydroxy Safflor yellow A.Result:Flos Carthami,Terminalia Chebula,Semen Thlaspi and Radix et Rhizoma Rubiae could be identified by TLC without the interference of negative control.Gallic acid and Hydroxy Safflor yellow A could be determined at the same time.Gallic acid was linear in the concentration range of 33.76-337.6μg/mL, r =0.9996.The average recovery rate was 98.35%,RSD=1.36%;Hydroxy Safflor yellow A had a good linear in the concentration range of 2.68-26.80 μg/ml, r =0.9998.The average recovery rate was 99.03%,RSD=0.72%.Conclusion:The method is simple, feasible,reliable,and can be effectively used for the quality control of Qianliening Capsule.
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