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作 者:陈飞[1] 段秀俊[1] 金龙[1] 薛慧清[1] 史静超[1] 周然[1]
机构地区:[1]山西中医学院,山西太原030024
出 处:《山西中医学院学报》2016年第2期35-38,共4页Journal of Shanxi College of Traditional Chinese Medicine
基 金:国家科技重大专项重大新药创制项目(2010ZX09102-210);山西省科技产业化环境建设项目(2012061014-3)
摘 要:目的:建立风湿宁胶囊的鉴别方法及含量测定方法。方法:鉴别采用薄层色谱法,含量测定采用高效液相色谱法。结果:独活、青风藤、血竭与肉桂的薄层鉴别图谱中,斑点清晰,阴性无干扰;血竭及青风藤的HPLC测定方法,血竭素线性范围0.116μg^0.581μg,Y=3×10~6X-13 854(r=0.999 6),平均回收率为100.86%,RSD为2.14%(n=6);青藤碱线性范围0.2μg^1.6μg,Y=18.13X-0.005 5(r=0.999 1),平均回收率为100.96%,RSD为2.34%(n=6)。结论:鉴别及含量测定方法专属性强,重复性好,准确度高,可用于风湿宁胶囊的质量控制。Objective:To establish the methods for identification and content determination of Fengshining capsules.Methods:TLC was used for identification,HPLC was used for determination. Results:Spots of Radix Angelicae,Caulis Sinomenii seu Diploclisiae,Resina Draconis and Casssia Barktree were clear,and the blank test didn′ t show interference.Linear range of dracorhodin was 0.116 μg ~0.581 μg,the regression equation was Y =3 ×10~6X-13 854(r =0.999 6),the average recovery rate was 100.86%,and RSD was 2.14%(n =6);the linear range of sinomenine was 0.2 μg ~1.6 μg,the regression equation was Y=18.13X-0.005 5(r=0.999 1),the average recovery rate was 100.96%,and RSD was 2.34%(n=6).Conclusion:The methods for identification and content determination have good specificity,repeatability and accuracy and could be used to control the quality of Fengshining capsules.
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