期刊文献+

高速逆流色谱法分离紫锥菊花色苷及其抗氧化性研究 被引量:14

Separation of Anthocyanins in Echinacea Purpurea Flower by High Speed Counter-current Chromatography and the Research on the Antioxidant Activity of the Anthocyanins
在线阅读 下载PDF
导出
摘要 建立了高速逆流色谱(HSCCC)分离制备紫锥菊花色苷类化合物的方法,并对所获得的2个花色苷单体进行了体外抗氧化性实验。以新鲜紫锥菊花瓣为原料,含0.1%HCl的60%乙醇为溶剂避光冷浸提取,经乙酸乙酯萃取和D101大孔吸附树脂(100 mL,2 cm×30 cm)纯化后,得2.1 g紫锥菊花色苷提取物干粉样品。以水-正丁醇-甲基叔丁基甲醚-乙腈-三氟乙酸(6∶3∶2∶1∶0.001)为HSCCC分离溶剂系统,上相为固定相,下相为流动相,流速2.0 mL/min,进样量160 mg,通过一次分离得到2种花色苷单体化合物,经HPLC检测其纯度分别达95.1%(9.8 mg)、98.2%(14.3 mg),MS及NMR技术鉴定其结构分别为矢车菊素-3-O-β-D葡萄糖苷(化合物1)和矢车菊素-3-O-(6″-O-丙二酰-β-D葡萄糖苷)(化合物2)。以Vc为对照组,对所获得的2种花色苷单体化合物进行了1,1-二苯基-2苦肼基(DPPH.)体外抗氧化性能评价,结果显示2种花色苷对DPPH.的半清除率(EC50)均小于10 mg/L,小于对照样Vc,表明2种花色苷均具有较强的自由基清除作用,且化合物1的清除能力强于化合物2。 An efficient method for the isolation and preparation of two anthocyanins,cyaniding 3-O-(β-D-giucopyranoside)(compound 1) and cyaniding 3-O-(6″-O-malonyl-β-D-glucopyranoside)(compound 2),from Echinacea purpurea flower by high speed counter-current chromatography(HSCCC) was established.The fresh flower was extracted with 60% ethanol(containing 0.1% HCl) at low temperature and dark conditions.2.1 g of crude sample for HSCCC was prepared after extracted with ethyl acetate and passed through an adsorbing column(2 cm× 30 cm,containing 100 mL D101 macroporous resin).Then water-n-butanol-methyl tert-butyl ether-acetonitrile-trifluoroacetic acid(6 ∶3 ∶2 ∶1 ∶0.001) was used as the two-phase solvent system,in which the upper phase was used as the stationary phase,while the lower phase was used as the mobile phase,the flow rate was set at 2.0 mL/min,and the revolution speed was 850 r/min.9.8 mg compound 1 with purity of 95.1% and 14.3 mg compound 2 with purity of 98.2% were obtained from 160 mg crude sample by one-step,as determined by high-performance liquid chromatography(HPLC).The chemical structures were identified by mass spectrometry(MS) and nuclear magnetic resonance imaging(NMR).Additionally,the antioxidant activities of the two compounds were also evaluated by the method of 1,1-diphenyl-2-picrylhydrazyl(DPPH·) radical scavenging assay with Vc as the control group.The results of antioxidative activity test showed that the two compounds have strong capacity of scavenging DPPH(EC5010 mg/L).Both of their EC50 were lower than that of Vc,and the scavenging ability of compound 1 was stronger than that of compound 2.
出处 《分析测试学报》 CAS CSCD 北大核心 2012年第1期45-50,共6页 Journal of Instrumental Analysis
基金 湖南省重大科技专项资助(NK07006)
关键词 高速逆流色谱 紫锥菊 花色苷 DPPH. 抗氧化性 high speed counter-current chromatography Echinacea purpurea anthocyanins DPPH· antioxidant activity
  • 相关文献

参考文献15

  • 1Bauer R,Wagner H.Econ.Med.Plant Res.,1991,5:253-321.
  • 2Singh N.A Comparison of both Water and Ethanol Extracts Prepared from Echinacea Purpurea and Echinacea Angustifoliaon the Response to Influenza A/PR/8/34 Infection in Mice.United States:Iowa State University,2011.
  • 3Sharma S,Anderson M,Schoop S,Hudson J.Phytomedicine,2010,17(8/9):563-568.
  • 4He J,Giusti M M.Annu.Rev.Food Sci.Technol.,2010,1:163-187.
  • 5Yun J W,Lee W S,Kim M J,Lu J N,Kang M H,Kim H G,Kim D C,Choi E J,Choi J Y.Food Chem.Toxicol.,2010,48(3):903-909.
  • 6Wallace T C.Adv.Nutrit.,2011,2:1-7.
  • 7Akkarachiyasit S,Yibchok-Anun S,Wacharasindhu S,Adisakwattana S.Molecules,2011,16(3):2075-2083.
  • 8Pauli G F,Pro S M,Friesen J B.J.Nat.Prod.,2008,71:1489-1508.
  • 9陆英,李佳银,罗晋,李觅路,刘仲华.高速逆流色谱制备分离紫甘薯花色苷[J].分析化学,2011,39(6):851-856. 被引量:29
  • 10Guo X,Wang D,Duan W,Du J,Wang X.Phytochem.Anal.,2010,21(3):268-272.

二级参考文献27

  • 1陈江弢,杨崇仁.当归属植物的研究进展[J].天然产物研究与开发,2004,16(4):359-365. 被引量:50
  • 2孔亮,于志远,邹汉法,孙乃昌,吴丽华,倪坚毅.高效液相色谱与质谱联用分析测定川芎中有效成分阿魏酸与藁本内酯[J].分析化学,2004,32(11):1501-1504. 被引量:22
  • 3苗爱东,梁乾德,刘勇,周喆,王升启.SPE-HPLC制备色谱法从当归挥发油中分离纯化Z-藁本内酯[J].中药材,2005,28(9):778-779. 被引量:10
  • 4宋萍萍,孙明毅,徐增莱,王年鹤.三种当归属植物的化学成分研究[J].中草药,2007,38(6):833-835. 被引量:38
  • 5LIU Z L,WANG J,SHEN P L,WANG C Y,SHEN Y J.Microwave-assisted extraction and high-speed counter-current chromatography purification of ferulic acid from Radix Angelicae sinensis[J].Sep Purif Technol,2006,52(1):18-21.
  • 6ITO Y.Golden rules and pitfalls in selecting optimum conditions for high-speed counter-current chromatography[J].J Chromatogr:A,2005,1065(2):145-168.
  • 7ITO Y.Principal,apparatus and methodology of high-speed countercurrent chromatography // ITO Y,CONWAY W D.High-speed countercurrent chromatography[M].New York:Wiley-Interscience Publication,1995.
  • 8YI L Z,LIANG Y Z,WU H,YUAN D L.The analysis of Radix Angelicae Sinensis(Danggui)[J].J Chromatogr:A,2009,1216(11):1991-2001.
  • 9GUNAWARDANA G,MCALPINE J.Preparative scale separation of natural products by countercurrent chromatography[M].New York:Marcel Deker Inc,1999.
  • 10ZHANG T Y.Separation and purification of natural products(medicinal herbs) by countercurrent chromatography //BERTHOD A.Countercurrent chromatography[M].Paris:Elsevier,2002.

共引文献33

同被引文献211

引证文献14

二级引证文献92

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