Antioxidant activity and calcium binding of isomeric hydroxybenzoates

The association constant for calcium binding to hydroxybenzoates in aqueous 0.16 M NaCl at 25 °C was found electrochemically to have the value Kass = 280 mol L−1 with ΔHo = −51 kJ mol−1, ΔSo = −122 J mol−1 K−1 for the 2-isomer (salicylate), Kass = 7 mol L−1 with ΔHo = −39 kJ mol−1, ΔSo = −116 J mol−...

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Main Authors: Zichen Zhao, Martina Vavrusova, Leif Horsfelt Skibsted
Format: Article
Language:English
Published: Elsevier 2018-04-01
Series:Journal of Food and Drug Analysis
Online Access:http://www.sciencedirect.com/science/article/pii/S1021949817301370
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spelling doaj-6201682bd27e45ef8257320d3efa03972020-11-24T23:21:59ZengElsevierJournal of Food and Drug Analysis1021-94982018-04-01262591598Antioxidant activity and calcium binding of isomeric hydroxybenzoatesZichen Zhao0Martina Vavrusova1Leif Horsfelt Skibsted2Department of Food Science, University of Copenhagen, Rolighedsvej 30, DK-1958 Frederiksberg C, DenmarkDepartment of Food Science, University of Copenhagen, Rolighedsvej 30, DK-1958 Frederiksberg C, DenmarkCorresponding author.; Department of Food Science, University of Copenhagen, Rolighedsvej 30, DK-1958 Frederiksberg C, DenmarkThe association constant for calcium binding to hydroxybenzoates in aqueous 0.16 M NaCl at 25 °C was found electrochemically to have the value Kass = 280 mol L−1 with ΔHo = −51 kJ mol−1, ΔSo = −122 J mol−1 K−1 for the 2-isomer (salicylate), Kass = 7 mol L−1 with ΔHo = −39 kJ mol−1, ΔSo = −116 J mol−1 K−1 for the 3-isomer, and Kass = 8 mol L−1 with ΔHo = −51 kJ mol−1, ΔSo = −155 J mol−1 K−1 for the 4-isomer. The 3- and 4-isomers were found more efficient as antioxidants than the 2-isomer in decreasing oxygen consumption rate in a peroxidating methyl linoleate emulsion and less sensitive to presence of calcium. All isomers were found prooxidative for iron-catalyzed initiation of oxidation due to enhanced radical formation as shown by electron spin resonance spectroscopy. Calcium salicylate was found to have low solubility with a solubility product Ksp = 4.49·10−6 based on activity with ΔHo = 67 kJ mol−1, ΔSo = 123 J mol−1 K−1 for dissolution in water, when corrected for the strong complex formation. Calcium in food and beverages may thus lower antioxidant activity of plant phenols through complexation or by precipitation. Keywords: Antioxidant activity, Calcium binding, 2-Hydroxybenzoate, 3-Hydroxybenzoate, 4-Hydroxybenzoatehttp://www.sciencedirect.com/science/article/pii/S1021949817301370
collection DOAJ
language English
format Article
sources DOAJ
author Zichen Zhao
Martina Vavrusova
Leif Horsfelt Skibsted
spellingShingle Zichen Zhao
Martina Vavrusova
Leif Horsfelt Skibsted
Antioxidant activity and calcium binding of isomeric hydroxybenzoates
Journal of Food and Drug Analysis
author_facet Zichen Zhao
Martina Vavrusova
Leif Horsfelt Skibsted
author_sort Zichen Zhao
title Antioxidant activity and calcium binding of isomeric hydroxybenzoates
title_short Antioxidant activity and calcium binding of isomeric hydroxybenzoates
title_full Antioxidant activity and calcium binding of isomeric hydroxybenzoates
title_fullStr Antioxidant activity and calcium binding of isomeric hydroxybenzoates
title_full_unstemmed Antioxidant activity and calcium binding of isomeric hydroxybenzoates
title_sort antioxidant activity and calcium binding of isomeric hydroxybenzoates
publisher Elsevier
series Journal of Food and Drug Analysis
issn 1021-9498
publishDate 2018-04-01
description The association constant for calcium binding to hydroxybenzoates in aqueous 0.16 M NaCl at 25 °C was found electrochemically to have the value Kass = 280 mol L−1 with ΔHo = −51 kJ mol−1, ΔSo = −122 J mol−1 K−1 for the 2-isomer (salicylate), Kass = 7 mol L−1 with ΔHo = −39 kJ mol−1, ΔSo = −116 J mol−1 K−1 for the 3-isomer, and Kass = 8 mol L−1 with ΔHo = −51 kJ mol−1, ΔSo = −155 J mol−1 K−1 for the 4-isomer. The 3- and 4-isomers were found more efficient as antioxidants than the 2-isomer in decreasing oxygen consumption rate in a peroxidating methyl linoleate emulsion and less sensitive to presence of calcium. All isomers were found prooxidative for iron-catalyzed initiation of oxidation due to enhanced radical formation as shown by electron spin resonance spectroscopy. Calcium salicylate was found to have low solubility with a solubility product Ksp = 4.49·10−6 based on activity with ΔHo = 67 kJ mol−1, ΔSo = 123 J mol−1 K−1 for dissolution in water, when corrected for the strong complex formation. Calcium in food and beverages may thus lower antioxidant activity of plant phenols through complexation or by precipitation. Keywords: Antioxidant activity, Calcium binding, 2-Hydroxybenzoate, 3-Hydroxybenzoate, 4-Hydroxybenzoate
url http://www.sciencedirect.com/science/article/pii/S1021949817301370
work_keys_str_mv AT zichenzhao antioxidantactivityandcalciumbindingofisomerichydroxybenzoates
AT martinavavrusova antioxidantactivityandcalciumbindingofisomerichydroxybenzoates
AT leifhorsfeltskibsted antioxidantactivityandcalciumbindingofisomerichydroxybenzoates
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