Preparative isolation and purification of atractylon and atractylenolide III from the Chinese medicinal plant Atractylodes macrocephala by high-speed counter-current chromatography

被引:55
作者
Zhao, Chunxia [1 ]
He, Chaohong [1 ]
机构
[1] Zhejiang Univ, Dept Chem Engn, Hangzhou 310027, Peoples R China
关键词
atractylon; atractylenolide III; Atractylodes macrocephala; high-speed counter-current chromatography (HSCCC);
D O I
10.1002/jssc.200500464
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学]; 081704 [应用化学];
摘要
The medicinal plant Atractylodes macrocephala (Baizhu in Chinese) has been widely used in traditional Chinese medicine for energy and stomach complaints, treatment of dyspepsia and anorexia, anti-inflammation, anticancer and for increasing assimilation. A high-speed counter-current chromatography (HSCCC) method was developed for the preparative separation and purification of two main bioactive components, namely, atractylon and atractylenolide III from A. macrocephala by using light petroleum (60-90 degrees C)-ethyl acetate-ethanol-water (4:1:4:1 v/v) as the two-phase solvent system in dual-mode elution. Compared with the separation using the normal-mode elution, the dual-mode HSCCC can be achieved with shorter elution time. Atractylenolide III (32.1 mg) at 99.0% purity and 319.6 mg atractylon at 97.8% purity could be obtained from 1000 mg crude sample in a single run. The recoveries of atractylenolide III and atractylon were 95.4 and 92.6%, respectively.
引用
收藏
页码:1630 / 1636
页数:7
相关论文
共 27 条
[1]
Dual-mode high-speed counter-current chromatography:: retention, resolution and examples [J].
Agnely, M ;
Thiébaut, D .
JOURNAL OF CHROMATOGRAPHY A, 1997, 790 (1-2) :17-30
[2]
Isolation of carotenoids from plant materials and dietary supplements by high-speed counter-current chromatography [J].
Aman, R ;
Carle, R ;
Conrad, J ;
Beifuss, U ;
Schieber, A .
JOURNAL OF CHROMATOGRAPHY A, 2005, 1074 (1-2) :99-105
[3]
Modeling the performance of pilot-scale countercurrent chromatography: Scale-up predictions and experimental verification of erythromycin separation [J].
Booth, AJ ;
Sutherland, IA ;
Lye, GJ .
BIOTECHNOLOGY AND BIOENGINEERING, 2003, 81 (06) :640-649
[4]
CHEN J-M, 1991, Acta Botanica Sinica, V33, P164
[5]
*CHIN PHARM COMM, 1999, PHARM PEOPL REP CHIN, P84
[6]
Relationship between the flow-rate of the mobile phase and retention of the stationary phase in counter-current chromatography [J].
Du, QZ ;
Wu, CJ ;
Qian, GJ ;
Wu, PD ;
Ito, Y .
JOURNAL OF CHROMATOGRAPHY A, 1999, 835 (1-2) :231-235
[7]
ENDO K, 1979, CHEM PHARM BULL, V12, P755
[8]
Single-step preparative separation of barbinervic acid and its epimer (rotungenic acid), along with two other pentacyclic triterpene acids from the leaves of Diospyros kaki using HSCCC [J].
Fan, JP ;
He, CH .
JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES, 2006, 29 (06) :815-827
[9]
EXTENDED OCTANOL-WATER PARTITION-COEFFICIENT DETERMINATION BY DUAL-MODE CENTRIFUGAL PARTITION CHROMATOGRAPHY [J].
GLUCK, SJ ;
MARTIN, EJ .
JOURNAL OF LIQUID CHROMATOGRAPHY, 1990, 13 (18) :3559-3570
[10]
HIKINO H, 1964, CHEM PHARM BULL, V12, P755