Effect of triacylglycerol structure on the antioxidant activity of γ-oryzanol

Food Chem. 2022 Feb 15:370:130974. doi: 10.1016/j.foodchem.2021.130974. Epub 2021 Aug 29.

Abstract

In this study, the triacylglycerol structure of vegetable oils was removed and the effects of this removal were observed on the antioxidant efficiency of γ-oryzanol. A sigmoidal-model was used for calculating kinetic parameters relevant to the initiation and propagation phases during the peroxidation of soybean, corn, sesame, and olive oils as well as their fatty acid methyl esters. Removing the triacylglycerol structure caused an increase in the antioxidant activity of γ-oryzanol (26.49%) by affecting both inhibitory mechanisms, i.e. hydrogen-donating (7.80%) and electron-transfer (14.72%). Unexpectedly, the antioxidant performance of γ-oryzanol continued even when the induction period had ended. During the propagation phase, the highest antioxidant activity was observed in the fatty acid methyl esters of soybean oil (3.86) based on hydroperoxides decomposition. An evaluation of how the endergonic activated complexes formed could indicate that the removal of the triacylglycerol structure increased the effective collisions between the γ-oryzanol molecules and free radicals.

Keywords: Antioxidant activity; Mass transfer; Oxidation kinetic; Sigmoidal model.

MeSH terms

  • Antioxidants*
  • Phenylpropionates*
  • Plant Oils
  • Triglycerides

Substances

  • Antioxidants
  • Phenylpropionates
  • Plant Oils
  • Triglycerides
  • gamma-oryzanol