Preparative isolation and purification of antioxidative diarylheptanoid derivatives from Alnus japonica by high-speed counter-current chromatography

被引:17
作者
Lim, Soon Sung [4 ]
Lee, Min Young [2 ]
Ahn, Hong Ryul [1 ]
Choi, Soon Jung [1 ]
Lee, Jae-Yong [2 ,3 ]
Jung, Sang Hoon [1 ]
机构
[1] Korea Inst Sci & Technol KIST Gangneung Inst, Funct Food Ctr, Taejon 210340, Gangneung, South Korea
[2] Hallym Univ, Ctr Efficacy Assessment & Dev Funct Foods & Drugs, Chunchon, South Korea
[3] Hallym Univ, Dept Biochem, Coll Med, Chunchon, South Korea
[4] Hallym Univ, Dept Food Sci & Nutr, Chunchon, South Korea
关键词
Alnus japonica; Diarylheptanoids; High-speed counter-current chromatography; Online HPLC-2; 2'-azino-bis(3-ethylbenzthiazoline-6-sulphonic acid) plus bioassay; ABTS RADICAL-CATION; ONLINE; BARK; HIRSUTA; IDENTIFICATION; ISOFLAVONOIDS; EXPRESSION; LICORICE; CELLS; ESTER;
D O I
10.1002/jssc.201100484
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This study employed the online HPLC-2,2'-azino-bis(3-ethylbenzthiazoline-6-sulphonic acid) (ABTS)+ bioassay to rapidly determine the antioxidant compounds occurring in the crude extract of Alnus japonica. The negative peaks of the ABTS+ radical scavenging detection system, which indicated the presence of antioxidant activity, were monitored by measuring the decrease in absorbance at 734 nm. The ABTS+-based antioxidant activity profile showed that three negative peaks exhibited antioxidant activity. High-speed counter-current chromatography (HSCCC) was used for preparative scale separation of the three active peaks from the extract. The purity of the isolated compounds was analyzed by HPLC and their structures were identified by 1H- and 13C-nuclear magnetic resonance spectrometry (NMR), heteronuclear multiple bond correlation (HMBC), and heteronuclear single quantum correlation (HSQC). Two solvent systems composed of n-hexane/ethylacetate/methanol/water (4:6:4:6, v/v) and of ethyl acetate/methanol/water (1:0.1:1, v/v) were performed in high-speed counter-current chromatography. Consequently, a total of 527 mg of hirsutanonol 5-O-beta-D-glucopyranoside, 80.04 mg of 3-deoxohirsutenonol 5-O-beta-D-glucopyranoside, and 91.0 mg of hirsutenone were obtained with purity of 94.7, 90.5, and 98.6%, respectively.
引用
收藏
页码:3344 / 3352
页数:9
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