A. Degenhardt et al., Preparative isolation of anthocyanins by high-speed countercurrent chromatography and application of the color activity concept to red wine, J AGR FOOD, 48(12), 2000, pp. 5812-5818
Red pigments were isolated from wine and grape-skin extracts using preparat
ive high-speed countercurrent chromatography (HSCCC) and identified by NMR
and MS techniques. Four solvent systems were developed in order to separate
anthocyanins with different polarities. Malvidin-3-glucoside was the major
component present in young red wines, and up to 500 mg of pure malvidin-3-
glucoside could be obtained from a single bottle of a red wine. Other isola
ted pigments were the malvidin- and peonidin-3,5-diglucosides, as well as a
cetyl-, coumaroyl-, and caffeoyl-derivatives of anthocyanins. Furthermore,
condensed red wine pigments formed from malvidin-3-glueoside (vitisin A and
acetylvitisin A) were isolated on a preparative scale. Isolated compounds
were used as standards for quantification of anthocyanius in a range of red
wines. The "color activity concept" was applied to red wine, and visual de
tection thresholds were determined far some of the isolated anthocyanins. M
ono-glucosides were found to exhibit lower visual detection thresholds than
diglucosides and acylated anthocyanins.