首页 | 本学科首页   官方微博 | 高级检索  
     


Efficient methods for isolating five phytochemicals from Gentiana macrophylla using high‐performance countercurrent chromatography
Authors:Taewoong Rho  Mila Jung  Min Won Lee  Young‐Won Chin  Kee Dong Yoon
Affiliation:1. College of Pharmacy and Integrated Research Institute of Pharmaceutical Sciences, The Catholic University of Korea, Bucheon, Republic of Korea;2. Laboratory of Pharmacognosy and Natural Product Derived Medicine, College of Pharmacy, Chung‐Ang University, Seoul, Republic of Korea;3. College of Pharmacy, Dongguk University‐Seoul, Goyang, Republic of Korea
Abstract:Efficient high‐performance countercurrent chromatography methods were developed to isolate five typical compounds from the extracts of Gentiana macrophylla. n‐Butanol‐soluble extract of G. macrophylla contained three hydrophilic iridoids, loganic acid ( 1 ), swertiamarin ( 2 ) and gentiopicroside ( 3 ), and a chromene derivative, macrophylloside D ( 4 ) which were successfully isolated by flow rate gradient (1.5 mL/min in 0–60 min, 5.0 mL/min in 60–120 min), and consecutive flow rate gradient HPCCC using n‐butanol/0.1% aqueous trifluoroacetic acid (1:1, v/v, normal phase mode) system. The yields of 1 – 4 were 22, 16, 122, and 6 mg, respectively, with purities over 97% in a flow rate gradient high‐performance countercurrent chromatography, and consecutive flow rate gradient high‐performance countercurrent chromatography gave 1 , 2 , 3 (54, 41, 348 mg, respectively, purities over 97%) and 4 (13 mg, purity at 95%) from 750 mg of sample. The main compound in methylene chloride soluble extract, 2‐methoxyanofinic acid, was successfully separated by n‐hexane/ethyl acetate/methanol/water (4:6:4:6, v/v/v/v, flow‐rate: 4 mL/min, reversed phase mode) condition. The structures of five isolates were elucidated by 1H, 13C NMR and ESI‐Q‐TOF‐MS spectroscopic data which were compared with previously reported values.
Keywords:Chromens  Gentiana macrophylla  High‐performance countercurrent chromatography  Iridoids
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号