| dc.contributor.author |
de Beer D. |
|
| dc.contributor.author |
Jerz G. |
|
| dc.contributor.author |
Joubert E. |
|
| dc.contributor.author |
Wray V. |
|
| dc.contributor.author |
Winterhalter P. |
|
| dc.date.accessioned |
2011-05-15T15:59:34Z |
|
| dc.date.available |
2011-05-15T15:59:34Z |
|
| dc.date.issued |
2009 |
|
| dc.identifier.citation |
Journal of Chromatography A |
|
| dc.identifier.citation |
1216 |
|
| dc.identifier.citation |
19 |
|
| dc.identifier.issn |
219673 |
|
| dc.identifier.other |
10.1016/j.chroma.2009.02.056 |
|
| dc.identifier.uri |
http://hdl.handle.net/10019.1/11252 |
|
| dc.description.abstract |
Isomangiferin was isolated from Cyclopia subternata using a multi-step process including extraction, liquid-liquid partitioning, high-speed counter-current chromatography (HSCCC) and semi-preparative reversed-phase high-performance liquid chromatography (HPLC). Enrichment of phenolic compounds in a methanol extract of C. subternata leaves was conducted using liquid-liquid partitioning with ethyl acetate-methanol-water (1:1:2, v/v). The enriched fraction was further fractionated using HSCCC with a ternary solvent system consisting of tert-butyl methyl ether-n-butanol-acetonitrile-water (3:1:1:5, v/v). Isomangiferin was isolated by semi-preparative reversed-phase HPLC from a fraction containing mostly mangiferin and isomangiferin. The chemical structure of isomangiferin was confirmed by LC-high-resolution electrospray ionization MS, as well as one- and two-dimensional NMR spectroscopy. © 2009 Elsevier B.V. All rights reserved. |
|
| dc.subject |
Counter-current chromatography |
|
| dc.subject |
Cyclopia subternata |
|
| dc.subject |
Fabaceae |
|
| dc.subject |
Isomangiferin |
|
| dc.subject |
Mangiferin |
|
| dc.subject |
NMR spectroscopy |
|
| dc.subject |
Xanthones |
|
| dc.subject |
Acetonitrile |
|
| dc.subject |
Body fluids |
|
| dc.subject |
Bubbles (in fluids) |
|
| dc.subject |
Chromatographic analysis |
|
| dc.subject |
Chromatography |
|
| dc.subject |
Electrospray ionization |
|
| dc.subject |
Esters |
|
| dc.subject |
Ethers |
|
| dc.subject |
High performance liquid chromatography |
|
| dc.subject |
High pressure liquid chromatography |
|
| dc.subject |
Liquids |
|
| dc.subject |
Methanol |
|
| dc.subject |
Nuclear magnetic resonance |
|
| dc.subject |
Nuclear magnetic resonance spectroscopy |
|
| dc.subject |
Organic solvents |
|
| dc.subject |
Phenols |
|
| dc.subject |
Solvent extraction |
|
| dc.subject |
acetic acid ethyl ester |
|
| dc.subject |
coumaric acid |
|
| dc.subject |
eriocitrin |
|
| dc.subject |
hesperidin |
|
| dc.subject |
isomangiferin |
|
| dc.subject |
luteolin |
|
| dc.subject |
mangiferin |
|
| dc.subject |
methanol |
|
| dc.subject |
phenol derivative |
|
| dc.subject |
scolymoside |
|
| dc.subject |
unclassified drug |
|
| dc.subject |
water |
|
| dc.subject |
article |
|
| dc.subject |
carbon nuclear magnetic resonance |
|
| dc.subject |
counter current chromatography |
|
| dc.subject |
Cyclopia subternata |
|
| dc.subject |
drug isolation |
|
| dc.subject |
drug structure |
|
| dc.subject |
electrospray mass spectrometry |
|
| dc.subject |
extraction |
|
| dc.subject |
heteronuclear multiple bond correlation |
|
| dc.subject |
high performance liquid chromatography |
|
| dc.subject |
medicinal plant |
|
| dc.subject |
nonhuman |
|
| dc.subject |
plant leaf |
|
| dc.subject |
priority journal |
|
| dc.subject |
proton nuclear magnetic resonance |
|
| dc.subject |
Chromatography, High Pressure Liquid |
|
| dc.subject |
Countercurrent Distribution |
|
| dc.subject |
Cyclopia Plant |
|
| dc.subject |
Methanol |
|
| dc.subject |
Nuclear Magnetic Resonance, Biomolecular |
|
| dc.subject |
Plant Extracts |
|
| dc.subject |
Xanthones |
|
| dc.subject |
Cyclopia subternata |
|
| dc.subject |
Fabaceae |
|
| dc.title |
Isolation of isomangiferin from honeybush (Cyclopia subternata) using high-speed counter-current chromatography and high-performance liquid chromatography |
|
| dc.type |
Article |
|
| dc.description.version |
Article |
|