蒙药那如-3指纹图谱的HPLC-DAD技术研究
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  • 英文篇名:Study on fingerprint of Naru-3 by HPLC-DAD
  • 作者:曹人郦 ; 于永辉 ; 顾艳丽 ; 林娜 ; 王超 ; 李海鸥 ; 赛那 ; 刘勋 ; 王小凤 ; 杨彩静
  • 英文作者:CAO Ren-yi;YU Yong-hui;GU Yan-li;LIN Na;WANG Chao;LI Hai-ou;SAI Na;LIU Xun;WANG Xiao-feng;YANG Cai-jing;College of Pharmacy,Inner Mongolia Medical University;Institute of Chinese Materia Medica,China Academy of Chinese Medical Sciences;
  • 关键词:蒙药那如-3 ; HPLC指纹图谱 ; 制草乌 ; 荜茇 ; 诃子
  • 英文关键词:Mongolian medicine Naru-3;;HPLC fingerprinting;;Radix Aconitum kusnezoffii;;Piper longum L;;Myrobalan
  • 中文刊名:SZGY
  • 英文刊名:Lishizhen Medicine and Materia Medica Research
  • 机构:内蒙古医科大学药学院;中国中医科学院中药研究所;
  • 出版日期:2018-08-20
  • 出版单位:时珍国医国药
  • 年:2018
  • 期:v.29;No.276
  • 基金:国家自然科学基金面上项目(81673695);; 内蒙古自治区科技创新引导项目(1639002);; 内蒙古医科大学英才培育项目(YCPY2018055)
  • 语种:中文;
  • 页:SZGY201808027
  • 页数:5
  • CN:08
  • ISSN:42-1436/R
  • 分类号:91-95
摘要
目的建立蒙药那如-3的HPLC指纹图谱。方法采用高效液相-二极管阵列检测(HPLC-DAD),色谱柱ODS-C18(250×4. 6 mm,5μm),流动相甲醇-0. 1%磷酸梯度洗脱,柱温30℃,流速0. 8 ml·min-1,检测波长为280,235,343 nm。结果通过10批次蒙药那如-3的化学成分指纹图谱分析,建立了蒙药那如-3的对照指纹图谱,通过"中药色谱指纹图谱相似度评价系统(2004A版本)",计算出10批次蒙药那如-3指纹图谱相似度均在0. 9以上,并以单味药材与蒙药那如-3的HPLC图谱进行比较,归属了主要色谱峰。结论以胡椒碱为参照峰,280 nm波长下标识了25个共有峰,建立了蒙药那如-3指纹图谱。此方法准确性好,可靠快捷,重复性好,初步确定了主要色谱峰的处方来源,为以后更好地全面控制复方药材质量提供科学依据。
        Objective To establish HPLC fingerprinting of Mongolian medicine Na Ru-3. Methods HPLC-DAD,column ODS-C18( 250 × 4. 6 mm,5 m) and mobile phase methanol-0. 1% phosphoric acid were used for gradient elution. The column temperature was 30 ℃ and the flow rate was 0. 8 ml/min,detection wavelength was 280,235,343 nm. Results The control fingerprints of Mongolian medicine NaRu-3 were established by chemical composition fingerprinting analysis of 10 batches of Mongolian medicine NaRu-3. Ten fingerprints were obtained by " similarity evaluation system of chromatographic fingerprints of Chinese traditional medicine( 2004 A version) ". The similarities of the second Mongolian herbal medicine,NaRu-3 fingerprints,were all above 0. 9,and the main chromatographic peaks were attributed to the comparison of the HPLC profiles of the single herbs with those of Mongolian medicine. Conclusion Piperine was used as a reference peak,and 25 common peaks were identified at 280 nm wavelength. This method has good accuracy,reliability,quickness and good repeatability. The prescription source of the main chromatographic peaks was preliminarily determined to provide a scientific basis for better comprehensive control of the quality of compound medicinal materials in the future.
引文
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