2016-06-032016-06-032015Gordillo Arrobas, B., Rodríguez Pulido, F.J., González Miret, M.L., Quijada Morín, N., Rivas Gonzalo, J.C., García Estévez, I.,...,Escribano Bailón, M.T. (2015). Application of differential colorimetry to evaluate anthocyanin-flavonol-flavanol ternary copigmentation interactions in model solutions. Journal of Agricultural and Food Chemistry, 63 (35), 7645-7653.0021-8561http://hdl.handle.net/11441/41856The combined effect of anthocyanin−flavanol−flavonol ternary interactions on the colorimetric and chemical stability of malvidin-3-glucoside has been studied. Model solutions with fixed malvidin-3-glucoside/(+)-catechin ratio (MC) and variable quercetin-3-β-D-glucoside concentration (MC+Q) and solutions with fixed malvidin-3-glucoside/quercetin-3-β-Dglucoside ratio (MQ) and variable (+)-catechin concentration (MQ+C) were tested at levels closer to those existing in wines. Color variations during storage were evaluated by differential colorimetry. Changes in the anthocyanin concentration were monitored by HPLC-DAD. CIELAB color-difference formulas were demonstrated to be of practical interest to assess the stronger and more stable interaction of quercetin-3-β-D-glucoside with MC binary mixture than (+)-catechin with MQ mixture. The results imply that MC+Q ternary solutions kept their intensity and bluish tonalities for a longer time in comparison to MQ+C solutions. The stability of malvidin-3-glucoside improves when the concentration of quercetin-3-β-D-glucoside increases in MC+Q mixtures, whereas the addition of (+)-catechin in MQ+C mixtures resulted in an opposite effectapplication/pdfengAttribution-NonCommercial-NoDerivatives 4.0 Internacionalhttp://creativecommons.org/licenses/by-nc-nd/4.0/ternary copigmentationmalvidin-3-glucoside(+)-catechinquercetin-3-β-D-glucosidedifferential colorimetryApplication of differential colorimetry to evaluate anthocyanin-flavonol-flavanol ternary copigmentation interactions in model solutionsinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccesshttp://dx.doi.org/10.1021/acs.jafc.5b00181https://idus.us.es/xmlui/handle/11441/41856