期刊文献+

采用顶空气相色谱-质谱技术对不同产地莪术进行快速鉴别 被引量:1

Headspace GC-MS for fast identification of Rhizoma curcuma of different origins
原文传递
导出
摘要 目的运用顶空气相色谱-质谱(HS-GC/MS)结合化学计量学方法对不同产地莪术进行鉴别,以便莪术的质量控制研究。方法采用HP-5石英毛细管色谱柱(30 m×0.32 mm,0.25μm),进样口温度250℃,柱初始温度为50℃,保持3 min,以20℃/min升至150℃,最后以2℃/min升至200℃,保持10 min,分流比10∶1。载气为氦气,流速:1.0 mL/min。顶空瓶区域温度:90℃;样品瓶加热平衡时间:30 min;进样量:1.5 mL。结合主成分分析和聚类分析方法对数据进行分析。结果在15个批次的样品的图谱中选取18个共有色谱峰进行鉴定,采用主成分分析法能够有效地区分四川、广西和云南等不同产地的莪术药材,并明确了对药材造成差异的主要成分为β-榄香烯、莰烯、β-蒎烯、p-menth-1-en-8-ol、桉叶素、8,9-去氢-9-甲酰基-环异长叶烯。结论应用HS-GC/MS技术与化学计量学方法相结合,建立了鉴别区分不同产地来源的莪术药材的方法,并找到了莪术中对分类起主要作用的特征性成分。 Objective To distinguish Rhizoma curcuma of different origins using headspace-gas chromatography/mass spectrometry (HS-GC/MS) combined with principal components analysis (PCA) and hierarchical cluster analysis (HCA), so as to help the quality control of Rhizoma curcuma. Methods HP-5 capillary column (30 mX 0.32 mm, 0.25μm) was used under the following condition: inlet temperature: 250℃, initial column temperature: 50℃maintained for 3 min, then increasing to 150℃ at 20℃/rain and to 200℃ at 2℃/min, maintained for 10 min, with the split ratio being 10 : 1. The carrier gas was helium, with flow rate being 1.0 mL/min, hadspace vials regional temperature being 90℃, vials heating equilibration time being 30 rain, and injection volume being 1.5 mL. The effect of extract separation conditions, temperature of the vial and equilibrium time on the extraction volatile components of Rhizoma curcuma were observed. Results PCA could distinguish 18 common peaks of 15 batches of Rhizoma curcurna from Sichuan, Guangxi and Yunnan, and it was confirmed thatβ-elemene, camphene, β-pinene, p-menth-l-en-8-ol, eucalyptol, and cycloisolongifolene, 8, 9-dehydro 9-formyl were the main components to cause differences in Rhizoma curcuma of different origins. Conclusion We have established a method combining HS-GC/MS with PCA and HCA to distinguish Rhizoma curcuma of different origins, and we have also identified the major characteristic components of Rhizoma curcuma of different origins.
出处 《第二军医大学学报》 CAS CSCD 北大核心 2013年第2期190-194,共5页 Academic Journal of Second Military Medical University
基金 国家自然科学基金(81273472)~~
关键词 莪术 顶空气相色谱-质谱法 主成分分析 聚类分析 Rhizoma curcuma headspace-gas chromatography mass spectrometry principal component analysis hierarchical cluster analysis
  • 相关文献

参考文献13

  • 1国家药典委员会.中华人民共和国药典 一部[S]北京:中国医药科技出版社,2010257.
  • 2Deng C H,Ji J,Li N,Yu Y J Duan G L Zhang X M. Fast determination of curcumol,curdione and germacrone in three species of Curcuma rhizomes by microwave-assisted extraction followed by headspace solidphase microextraction and gas chromatography-mass spectrometry[J].Journal of Chromatography A,2006.115-120.
  • 3Cao J,Qi M L,Fang L H,Zhou S,Fu R N,Zhang P P. Solid-phase microextraction-gas chromatographicmass spectrometric analysis of volatile compounds from Curcuma wenyujin Y.H.Chen et C.Ling[J].Journal of Pharmaceutical and Biomedical Analysis,2006.552-558.
  • 4郑良,朱华勇,沈慧,周先礼,赵静.GC-MS分析山东野花椒果皮中挥发油的化学成分[J].华西药学杂志,2009,24(4):386-388. 被引量:8
  • 5王建,赵应学.广西莪术种内变异类型中不同颜色挥发油化学成分分析[J].中草药,2009,40(11):1726-1727. 被引量:9
  • 6林朝展,柴玲,祝晨蔯,赵钟祥,张翠仙.枇杷叶紫珠叶挥发油化学成分的研究[J].时珍国医国药,2010,21(9):2275-2277. 被引量:11
  • 7Yang F Q,Li S P,Chen Y,Lao S C Wang Y T Dong T T X. Identification and quantitation of eleven sesquiterpenes in three species of Curcuma rhizomes by pressurized liquid extraction and gas chromatographymass spectrometry[J].Journal of Pharmaceutical and Biomedical Analysis,2005.552-558.
  • 8Yang F Q,Li S P,Zhao J,Lao S C Wang Y T. Optimization of GC-MS conditions based on resolution and stability of analytes for simultaneous determination of nine sesquiterpenoids in three species of Curcuma rhizomes[J].Journal of Pharmaceutical and Biomedical Analysis,2007.73-82.
  • 9Yang F Q,Wang Y T,Li S P. Simultaneous determination of 11 characteristic components in three species of Curcuma rhizomes using pressurized liquid extraction and high-performance liquid chromatography[J].Journal of Chromatography A,2006.226-231.
  • 10张园,张琦,王贤亲.固相萃取-气相色谱串联质谱法测定温莪术中19种有机氯和有机磷农药残留[J].药物分析杂志,2012,32(1):95-99. 被引量:12

二级参考文献39

共引文献56

同被引文献12

引证文献1

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部