Factors that influence the deoxyribose oxidation assay for Fenton reaction products

Free Radic Biol Med. 1991;11(4):353-60. doi: 10.1016/0891-5849(91)90151-r.

Abstract

The mechanism of oxidation of deoxyribose to thiobarbituric acid-reactive products by Fenton systems consisting of H2O2 and either Fe2+ or Fe2+ (EDTA) has been studied. With Fe2+ (EDTA), dependences of product yield on reactant concentrations are consistent with a reaction involving OH.. With Fe2+ in 5-50 mM phosphate buffer, yields of oxidation products were much higher and increased with increasing deoxyribose concentration up to 30 mM. The product yield varied with H2O2 and Fe2+ concentrations in a way to suggest competition between deoxyribose and both reactants. Deoxyribose oxidation by Fe2+ and H2O2 was enhanced 1.5-fold by adding superoxide dismutase, even though superoxide generated by xanthine oxidase increased deoxyribose oxidation. These results are not as expected for a reaction involving free OH. or site localized OH. product on the deoxyribose. They can be accommodated by a mechanism of deoxyribose oxidation involving an iron(IV) species formed from H2O2 and Fe2+, but the overall conclusion is that the system is too complex for definitive identification of the Fenton oxidant.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Deoxyribose*
  • Edetic Acid
  • Free Radicals
  • Hydrogen Peroxide*
  • Hydroxides
  • Hydroxyl Radical
  • Indicators and Reagents
  • Iron*
  • Kinetics
  • Oxidation-Reduction
  • Thiobarbiturates

Substances

  • Fenton's reagent
  • Free Radicals
  • Hydroxides
  • Indicators and Reagents
  • Thiobarbiturates
  • Hydroxyl Radical
  • Deoxyribose
  • Edetic Acid
  • Hydrogen Peroxide
  • Iron
  • thiobarbituric acid