藤黄药材的指纹图谱研究Fingerprint analysis of gamboge by HPLC
侯文洁;陈保来;萧伟;
HOU Wenjie1,3,CHEN Baolai2,3,XIAO Wei2,3*(1.Nanjing University of Chinese Medicine,Nanjing 210046,China; 2.Jangsu Kanion pharmaceutical Co.,Ltd.,Lianyungang 222001,China; 3.State Key Laboratory of Pharmaceutical New-tech for Chinese Medicine,Lianyungang 222001,China; 4.Enterprises Academician Workstations,Lianyungang 222001,China)
摘要(Abstract):
目的:建立藤黄药材的高效液相指纹图谱方法。方法:采用Luna C8(4.6 mm×250 mm,5μm)色谱柱,柱温25℃,以乙腈-0.1%冰乙酸水溶液为流动相梯度洗脱,检测波长362 nm,流速为1.0 mL·min-1。采用国家药典委员会出版的《中药色谱指纹图谱相似度评价》(2004年A版)软件,对11批不同批次的藤黄药材指纹图谱进行相似度计算。结果:各批藤黄药材中有13个共有峰,各峰分离度良好,各批次藤黄药材间共有峰的相对保留时间RSD均<1.0%,药材间相似度均>90%。结论:本方法具有良好的精密度、重复性、稳定性,各共有峰间分离度高,可用于藤黄药材的真伪鉴别和质量综合评价。
Objective: To establish the chromatographic fingerprint for the quality control of gamboge.Method: Analysis on a Luna C8(4.6 mm×250 mm,5 μm)column eluted with mobile phases containing acetonitrile and 0.1% glacial acetic acid in water in gradient mode.The flow rate was 1.0 mL·min-1 and the detection wavelength was at 362 nm.The temperature of column was 25 ℃.And data of 11 batches of gamboge samples from different sources were analysed by "similarity evaluation for chromatographic Fingerprint of Traditional Chinese Medicine" software.Result: Thirteen common peaks were selected in chromatograms,and all the common peeks were separated effectively.Conclusion: The precision,repeatability,and stability of this method were satisfying.The method developed can be used to identify and evaluate the quality of gamboge.
关键词(KeyWords):
藤黄;HPLC;指纹图谱
gamboge;HPLC;fingerprint
基金项目(Foundation): 国家“重大新药创制”科技重大专项(2008ZX09101-Z-024)
作者(Author):
侯文洁;陈保来;萧伟;
HOU Wenjie1,3,CHEN Baolai2,3,XIAO Wei2,3*(1.Nanjing University of Chinese Medicine,Nanjing 210046,China; 2.Jangsu Kanion pharmaceutical Co.,Ltd.,Lianyungang 222001,China; 3.State Key Laboratory of Pharmaceutical New-tech for Chinese Medicine,Lianyungang 222001,China; 4.Enterprises Academician Workstations,Lianyungang 222001,China)
Email:
DOI:
参考文献(References):
- [1]江苏新医学院.中药大辞典[M].上海:上海人民出版社,1977:2695.
- [2]贾明美,寿清耀,谭青,等.藤黄化学成分的研究[J].化学学报,2008,66(22):2513.
- [3]韩全斌,宋景政,乔春峰,等.藤黄中xanthone类化合物的定性定量分析[J].中国天然药物,2006,4:210.
- [4]张旭,柳文媛,冯锋,等.藤黄HPLC指纹图谱的研究[J].中国医药工业杂志,2003,34:605.
- [5]谢培山.中药色谱指纹图谱[M].北京:人民卫生出版社,2005:485.
- [6]屠鹏飞.中药指纹图谱指定的方法学探讨[C].现代化中药产业关键技术系列研讨会———国际色谱指纹评价中药质量研讨会.广州:广州药学会,2001.
- [7]国家药品监督管理局.中药注射剂指纹图谱研究的技术要求(暂行)[J].中成药,2000,22(10):671.
- 侯文洁
- 陈保来
- 萧伟
HOU Wenjie1- 3
- CHEN Baolai2
- 3
- XIAO Wei2
- 3*(1.Nanjing University of Chinese Medicine
- Nanjing 210046
- China
- 2.Jangsu Kanion pharmaceutical Co.
- Ltd.
- Lianyungang 222001
- China
- 3.State Key Laboratory of Pharmaceutical New-tech for Chinese Medicine
- Lianyungang 222001
- China
- 4.Enterprises Academician Workstations
- Lianyungang 222001
- China)
- 侯文洁
- 陈保来
- 萧伟
HOU Wenjie1- 3
- CHEN Baolai2
- 3
- XIAO Wei2
- 3*(1.Nanjing University of Chinese Medicine
- Nanjing 210046
- China
- 2.Jangsu Kanion pharmaceutical Co.
- Ltd.
- Lianyungang 222001
- China
- 3.State Key Laboratory of Pharmaceutical New-tech for Chinese Medicine
- Lianyungang 222001
- China
- 4.Enterprises Academician Workstations
- Lianyungang 222001
- China)