Preparative Separation of Phenolic Compounds from Halimodendron halodendron by High-Speed Counter-Current Chromatography 英文参考文献.docVIP
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Preparative Separation of Phenolic Compounds from Halimodendron halodendron by High-Speed Counter-Current Chromatography 英文参考文献
Molecules 2010, 15, 5998-6007; doi:10.3390/moleculeOPEN ACCESS
molecules
ISSN 1420-3049
/journal/molecules
Article
Preparative Separation of Phenolic Compounds from
Halimodendron halodendron by High-Speed
Counter-Current Chromatography
Jihua Wang 1, Haifeng Gao 1, Jianglin Zhao 1, Qi Wang 1, Ligang Zhou 1,*, Jianguo Han 2,
Zhu Yu 2 and Fuyu Yang 2
1
College of Agronomy and Biotechnology, China Agricultural University, Beijing 100193, China
2
College of Animal Science and Technology, China Agricultural University, Beijing 100193, China
* Author to whom correspondence should be addressed; E-Mail: lgzhou@;
Tel.: +86 10
Received: 30 July 2010; in revised form: 16 August 2010 / Accepted: 27 August 2010 /
Published: 31 August 2010
Abstract: Three phenolic compounds, p-hydroxybenzoic acid (1), isorhamnetin-3-O-β-D-
rutinoside (2), and 3,3-di-O-methylquercetin (5), along with a phenolic mixture were
successfully separated from the ethyl acetate crude extract of Halimodendron halodendron
by high-speed counter-current chromatography (HSCCC) with chloroform-methanol-
water-acetic acid (4:3:2:0.05, v/v) as the two-phase solvent system. The phenolic mixture
from HSCCC was further separated by preparative HPLC and purified by Sephadex LH-20
to afford quercetin (3) and 3-O-methylquercetin (4). Seven hundred mg of ethyl acetate
crude extract was separated by HSCCC to obtain six fractions which were then analyzed
by high performance liquid chromatography (HPLC). The HSCCC separation obtained
total of 80 mg of the mixture of quercetin (3) and 3-O-methylquercetin (4) (26.43% and
71.89%, respectively) in fraction 2, 14 mg of 3,3-di-O-methylquercetin (5) at 95.14% of
purity in fraction 3, 15 mg of p-hydroxybenzoic acid (1) at 92.83% of purity in fraction 5,
12 mg of isorhamnetin-3-O-β-D-rutinoside (2) at 97.99% of purity in fraction 6. This is the
first time these phenolic compounds have been o
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