Reversed-Phase Ion-Pair Chromatography of Anthocyanins in Red Wines

A reversed-phase ion-pair chromatographic method has been developed for the separation of anthocyanins from red wines. Separation of anthocyanin monoglucosides can be achieved with a gradient mode elution using tetrabutylammonium hydrogen sulfate as a counter-ion, phosphoric acid, and methanol—aceto...

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Published inJournal of chromatographic science Vol. 35; no. 4; pp. 161 - 164
Main Authors Peña, Araceli, Garcia, Veronica, de la Luz Romero, Ma, Capella, Santiago
Format Journal Article
LanguageEnglish
Published Niles, IL Oxford University Press 01.04.1997
Preston Publications
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Summary:A reversed-phase ion-pair chromatographic method has been developed for the separation of anthocyanins from red wines. Separation of anthocyanin monoglucosides can be achieved with a gradient mode elution using tetrabutylammonium hydrogen sulfate as a counter-ion, phosphoric acid, and methanol—acetonitrile—water in the mobile phase (pH = 2). This technique allows a relatively fast separation and identification of different anthocyanins in one run without prior treatment of the wine or derivatization of the compounds; it also avoids both the use of low pH (below 2) and, consequently, the degradation of the column. The order of elution of anthocyanin monoglucosides does not change in this mode of chromatography; they elute in the order of their polarity, as is typical in reversed-phase chromatography (delphinidin, cyanidin, petunidin, peonidin, and malvidin monoglucoside). Therefore, this characteristic profile is useful for the identification of anthocyanins of Vitis vinifera in red wines.
Bibliography:istex:614FE2C7B03D6A00693AA16AB38190866B65C4FF
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ISSN:0021-9665
1945-239X
DOI:10.1093/chromsci/35.4.161