Chitosan as an antioxidant alternative to sulphites in oenology: EPR investigation of inhibitory mechanisms

Food Chem. 2019 Jul 1:285:67-76. doi: 10.1016/j.foodchem.2019.01.155. Epub 2019 Jan 31.

Abstract

The efficacy against oxidative degradation in model and sulphite-free white wines of two commercial, insoluble chitosans (one being approved for winemaking) were investigated by electron paramagnetic resonance (EPR). Both compounds at various doses significantly inhibited the formation of α-(4-pyridyl-1-oxide)-N-t-butylnitrone (4-POBN)-1-hydroxyethyl adducts under normal wine storage conditions. Pre-incubation with 2 g/L chitosan followed by filtration had a better effect than adding 50 mg/L sulphur dioxide to the experimental Chardonnay wine on the release of 4-POBN adducts after 6 days of incubation with 100 μM iron(II). In a relevant photooxidative system acetaldehyde formation was significantly reduced after 6 days of incubation. Parallel EPR tests were performed to assess the importance of metal chelation (iron and copper) versus direct scavenging of hydroxyl radicals on the effect of chitosan. The present data support the potentiality of using biocompatible chitosan as a healthier complement and/or alternative to sulphur dioxide against white wine oxidative spoilage.

Keywords: Antioxidant; Chitosan; EPR spin trapping; Hydroxyl radical scavenging activity; Metal chelation; Photooxidation; Sulphur dioxide-free wines.

MeSH terms

  • Antioxidants / chemistry*
  • Chelating Agents / chemistry
  • Chitosan / chemistry*
  • Electron Spin Resonance Spectroscopy
  • Ferrous Compounds / chemistry
  • Hydroxyl Radical / chemistry
  • Pyridines / chemistry
  • Spin Labels
  • Sulfites / chemistry*
  • Wine / analysis

Substances

  • Antioxidants
  • Chelating Agents
  • Ferrous Compounds
  • Pyridines
  • Spin Labels
  • Sulfites
  • alpha-(4-pyridyl-1-oxide)-N-tert-butylnitrone
  • Hydroxyl Radical
  • Chitosan