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牛黄清宫丸质量标准的研究 被引量:2

Studies on Quality Standard of Niuhuang Qinggong Pills
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摘要 目的:建立牛黄清宫丸质量标准。方法:采用TLC法对处方中大黄、栀子、金银花进行了定性鉴别,并用HPLC法对处方中黄芩进行了含量测定,采用Diamonsil C18色谱柱,以甲醇-水-磷酸(46:54:0.2)为流动相,流速为1.0mL·min^-1,检测波长为280nm。结果:薄层色谱斑点清晰,易于识别,专属性强;黄芩苷线性范围为0.1175~1.175μg(r=1.0000),平均加样回收率为99.5%,RSD为1.6%。结论:本方法操作简便,快速、准确、灵敏度高,重复性好,提高后的质量标准更有效的控制该制剂的质量。 Objective: To determine the quality standard of Niuhuang Qinggong Pills. Methods: Radix Et Rhizoma Rhei, Fructus Gardeniae, Flos Lonicerae Japonicae in Niuhuang Qinggong Pills were identified by TLC. The content of Baicalin was determined by HPLC. Using ODS column, Methanol-Water- Phosphoric acid (46: 54: 0. 2) as the mobile phase at flow rate of 1.0 mL ·min^-1, wavelength of the detection was 280 nm. Results:The qualitative identification with TLC were specific. The liner range of Baicalin was 0. 117 5 - 1. 175μg(r = 1. 000 0); the recovery was 99. 5% (RSD = 1.6% ). Conclusion: This method is simple,rapid,accurate,highly sensitive and well reproducible. This method can be used for the quality control of Niuhuang Qinggong Pills.
出处 《中国药品标准》 CAS 2011年第2期131-135,共5页 Drug Standards of China
关键词 牛黄清宫丸 薄层色谱 黄芩苷 高效液相色谱 Niuhuang Qinggong Pills Quality control TLC Baicalin HPLC
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参考文献2

  • 1《卫生部药品标准》.中药成方制剂[s].第六册.
  • 2国家药典委员会.《中国药典》一部[S].北京:化学工业出版社,2005:152.

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