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

✍ Scribed by Soon Sung Lim; Min Young Lee; Hong Ryul Ahn; Soon Jung Choi; Jae-Yong Lee; Sang Hoon Jung

• Publisher: John Wiley and Sons
• Year: 2011
• Tongue: English
• Weight: 228 KB
• Volume: 34
• Category: Article
• ISSN: 1615-9306
• DOI: 10.1002/jssc.201100484

✦ Synopsis

Abstract

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 ^1^H‐ and ^13^C‐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‐β‐D‐glucopyranoside, 80.04 mg of 3‐deoxohirsutenonol 5‐O‐β‐D‐glucopyranoside, and 91.0 mg of hirsutenone were obtained with purity of 94.7, 90.5, and 98.6%, respectively.