High-speed counter-current chromatography assisted preparative isolation of phenolic compounds from the flowers of Chrysanthemum morifolium cv. Fubaiju

被引:5
|
作者
Dong, Xiaowei [1 ]
Huang, Hongping [1 ]
Wang, Rong [1 ]
Luo, Shiyu [1 ]
Mi, Yahui [1 ]
Pan, Yuqing [1 ]
Shen, Wei [1 ]
Cui, Jiamin [1 ]
Hu, Xiaolong [1 ]
Cheng, Xuexiang [2 ,3 ]
Shi, Xinhong [1 ]
Wang, Hao [1 ]
机构
[1] China Pharmaceut Univ, Sch Tradit Chinese Pharm, State Key Lab Nat Med, Nanjing 210009, Peoples R China
[2] Hubei Fenghuang Baiyunshan Pharmaceut Co Ltd, Macheng, Peoples R China
[3] Hubei Univ Chinese Med, Sch Pharm, Wuhan, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
antioxidant; Chrysanthemum morifolium cv; Fubaiju; high-speed counter-current chromatography; phenolic compounds; retinal protection; FLAVONOIDS; SEPARATION; IDENTIFICATION; PURIFICATION; ISOMERS; ACIDS;
D O I
10.1002/jssc.202300172
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Chrysanthemum morifolium cv. Fubaiju is rich in phenolic compounds with various benefits such as anti-inflammatory, antioxidant, and cardiovascular protection. In this study, 12 phenolic compounds, including five flavonoid glycosides and seven quinic acid derivatives, were successfully separated from the flowers of Chrysanthemum morifolium cv. Fubaiju by high-speed counter-current chromatography and preparative high-performance liquid chromatography. Ethyl acetate-n-butanol-acetonitrile-water-acetic acid (5:0.5:2.5:5:0.25, v/v/v/v/v) was selected as solvent system to separate six fractions from the flowers of Chrysanthemum morifolium cv. Fubaiju, and 20% aqueous acetonitrile (containing 0.1% formic acid) was chosen to be the elution solvent in preparative high-performance liquid chromatography for purifying the fractions above. Luteolin-7-O-& beta;-D-glucoside (1), luteolin-7-O-& beta;-D-glucuronide (2), apigenin-7-O-& beta;-D-glucoside (3), luteolin-7-O-& beta;-D-rutinoside (4), diosmetin-7-O-& beta;-D-glucoside (5), chlorogenic acid (6), 1,5-dicaffeoylquinic acid (7), 1,4-dicaffeoylquinic acid (8), 3,4-dicaffeoylquinic acid (9), 3,4-dicaffeoyl-epi-quinic acid (10), 3,5-dicaffeoylquinic acid (11), and 4,5-dicaffeoylquinic acid (12) were isolated with purities all above 95%, respectively. In addition, all isolates were evaluated for their protective effects on H2O2-induced oxidative damage in adult retinal pigment epithelial cells.
引用
收藏
页数:10
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