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升清胶囊定性定量方法研究
引用本文:宋锦锋,李娟. 升清胶囊定性定量方法研究[J]. 中南药学, 2012, 10(3): 192-195
作者姓名:宋锦锋  李娟
作者单位:1. 湖南省岳阳市食品药品检验所,湖南岳阳,414000
2. 长沙医学院,长沙,410219
摘    要:目的 研究升清胶囊定性定量方法.方法 对大黄进行了显微鉴别采用TLC法对升清胶囊中虎杖及陈皮进行定性鉴别;采用HPLC法对方中大黄及虎杖的主要成分大黄素进行了定量分析.色谱柱为C18柱(250 mm×4.6mm,5 μm),流动相为甲醇-0.1%磷酸溶液(85∶15),流速1.0 mL·min-1,检测波长为254 nm,柱温为室温.结果 定性鉴别明显清晰,阴性样品无干扰;大黄素对照品在0.048 5~0.388 0邸进样量与峰面积呈良好线性关系,平均加样回收率为99.2%,RSD=0.80% (n=6).结论 方法简便可行,结果准确可靠,重现性好,可作为本产品的质量控制方法.

关 键 词:升清胶囊  质量标准  薄层色谱  高效液相色谱  大黄素

Qualitative and quantitive method for Shengqing Jiaonang
SONG Jin-feng , LI Juan. Qualitative and quantitive method for Shengqing Jiaonang[J]. Central South Pharmacy, 2012, 10(3): 192-195
Authors:SONG Jin-feng    LI Juan
Affiliation:1.Yueyang Institute for Food and Drug Control,Yueyang Hunan 414000;2.Changsha Medical College,Changsha 410219)
Abstract:Objective To establish the qualitative and quantitive methods for Shengqing Jiaonang.Method Rheum palmatum L.was identified by microscopic identification.Polygonum cuspidatum Sieb.et Zucc.and citrus reticulata Blanco were identified by TLC.The content of emodin was determined by HPLC.The separation was performed on C18 column with methanol-0.1% phosphoric acid solution(85∶15)as the mobile phase.The flow rate was 1.0 mL·min-1.The wavelength was 254 nm.The column temperature was room temperature.Results The TLC spots were fairly clear,and the negative sample showed no interference.The emodin was linear over 0.048 5-0.388 0 μg,the average recovery was 99.2%,and the RSD was 0.80%(n=6).Conclusion The method is simple,reliable,accurate,and can be used as the quality control method for Shengqing Jiaonang.
Keywords:Shengqing Jiaonang  quality standard  TLC  HPLC  emodin
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