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作 者:张慧[1] 杨孟妮 李洋[1] 刘娟[1] 李文婷 夏厚林[1] ZHANG Hui;YANG Meng-ni;LI Yang;LIU Juan;LI Wen-ting;XIA Hou-lin(School of Pharmacy, Chengdu University of Traditional Chinese Medicine," Key Laboratory of Standardization for Chinese Herbal Medicine, Ministry of Educatio;National Key Laboratory Breeding Base of Systematic Research, Development and Utilization of Chinese Medicine Resources, Chengdu 61113 7, Sichua)
机构地区:[1]成都中医药大学、中药材标准化教育部重点实验室、四川省中药资源系统研究与开发利用重点实验室-省部共建国家重点实验室培育基地
出 处:《中药与临床》2017年第4期10-13,共4页Pharmacy and Clinics of Chinese Materia Medica
摘 要:目的:建立藏茵陈4种有效成分的含量测定方法,并测定10批不同来源的含量。方法:采用HPLC(高效液相色谱法)法,同时测定藏茵陈中獐牙菜苦苷、龙胆苦苷、獐牙菜苷和芒果苷的含量,采用C18色谱柱(4.6 mm×250 mm,5μm),以甲醇-0.1%磷酸水溶液梯度洗脱,检测波长238 nm(獐牙菜苦苷)、274 nm(龙胆苦苷)、246 nm(獐牙菜苷)和258nm(芒果苷)。结果:建立了HPLC法同时测定藏茵陈中四种有效成分含量的方法,四种成分分离度良好,方法学考察符合要求。结论:本方法操作简便,结果准确,重复性好,可靠性好,可用于同时测定藏茵陈中四种有效成分的含量。Objective:To establish determination method of four effective components in Zangyinchen,and detect the content 5 of 10 batches samples from different sources.Method:High performance liquid chromatography(HPLC) method was used for the simultaneous determination of swertiamarin,gentiopicroside,swertiamarin and mangiferin in Zangyinchen on C18 column(4.6 mm × 250 mm,5 μm),with methanol-0.1% phosphoric acid water solution as mobile phase in gradient elution.The detection wavelength was set at 238 nm(swertiamarin),274 nm(gentiopicroside),243 nm(sweroside) and 258 nm(mangiferin).Result:The HPLC simultaneous determination of four effective components in Zangyinchen was established with good separation,and met the methodological requirements.Conclusion:The method is simple,accurate with ood repeatability and reliability,which can be used for the simultaneous determination of four effective components in Zangyinchen.
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