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作 者:胡君萍[1] 迪丽拜尔.马木提 李渊[1] 柳惠斌[2] 杨建华[3]
机构地区:[1]新疆医科大学药学院,乌鲁木齐830011 [2]新疆医科大学附属肿瘤医院,乌鲁木齐830011 [3]新疆医科大学第一附属医院,乌鲁木齐830011
出 处:《中国实验方剂学杂志》2014年第17期65-68,共4页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家自然科学基金项目(30960526)
摘 要:目的:建立同时测定维药毛菊苣和菊苣中5种化学成分含量的UPLC分析方法。方法:采用UPLC,Hypersil BDS C18柱(4.6 mm×250 mm,5μm),乙腈-0.4%磷酸溶液为流动相梯度洗脱,流速1.0 mL·min^-1,柱温30℃,检测波长254 nm,进样量10μL。结果:秦皮甲素、秦皮乙素、山莴苣素、菊苣酸、山莴苣苦素分别在0.025~0.225,0.01~0.05,0.2~1.0,0.1~0.5,0.24~1.20μg线性关系良好,相关系数分别为0.999 3,0.999 9,0.999 8,0.999 9,0.999 9,平均加样回收率分别为99.37%,98.66%,99.63%,100.05%,99.97%。结论:《中国药典》收载两种菊苣的各成分含量差异很大,毛菊苣以山莴苣苦素、山莴苣素和秦皮乙素含量较高,菊苣以菊苣酸含量高,药材的质量控制和评价值得进一步研究。Objective: This study was conduct to establish an UPLC method for the simultaneous determination of five components aesculin,esculetin,lactucin,cichoric acid and lactucopicrin in Uyghur drug Cichorium glandulosum and C. intybus. Method: Hypersil BDS C18(4.6 mm ×250 mm,5 μm) was used as the stationary phase. The mobile phase was composed of acetonitrile and 0. 4% phosphoric acid aqueous with a gradient elution. The flow rate was 1. 0 mL·min^-1. Column temperature was 30 ℃. The detection wavelength was 254 nm.Result: All calibration curves showed good linear regression(r 〉0. 999 3) within test ranges. The validation data indicated excellent precision and good recovery. Conclusion: The method was successfully applied to quantify five components in C. glandulosum and C. intybus,which could be used as comprehensive quality evaluation of Cichorium.
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