Catalytic spectrofluorimetric determination of superoxide anion radical and superoxide dismutase activity using N,N-dimethylaniline as the substrate for horseradish peroxidase (HRP)

Spectrochim Acta A Mol Biomol Spectrosc. 2002 Oct;58(12):2557-62. doi: 10.1016/s1386-1425(02)00007-0.

Abstract

The coupled reaction of N,N-dimethylaniline (DMA) with 4-aminoantipyrine (4-AAP) using superoxide anion radical (O2-) as oxidizing agent under the catalysis of horseradish peroxidase (HRP) was studied. Based on the reaction, O2- produced by irradiating Vitamin B2, (VB2) was spectrophotometricly determined at 554 nm. The linear range of this method was 1.8 x 10(-6)-1.2 x 10(-4) mol l(-1) with a detection limit of 5.3 x 10(-7) mol l(-1). The effect of interferences on the determination of O2- was investigated. The proposed method was successfully applied to the determination of superoxide dismutase (SOD) activity in human blood and mouse blood.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age Factors
  • Ampyrone / metabolism
  • Aniline Compounds / metabolism
  • Animals
  • Catalysis
  • Horseradish Peroxidase / metabolism
  • Humans
  • Mice
  • Middle Aged
  • Riboflavin / radiation effects
  • Sensitivity and Specificity
  • Spectrometry, Fluorescence / methods*
  • Superoxide Dismutase / blood*
  • Superoxides / blood*
  • Superoxides / metabolism

Substances

  • Aniline Compounds
  • Ampyrone
  • Superoxides
  • N,N-dimethylaniline
  • Horseradish Peroxidase
  • Superoxide Dismutase
  • Riboflavin