On the use of the quenching of luminol luminescence to evaluate SOD activity

Free Radic Biol Med. 1994 Jun;16(6):833-7. doi: 10.1016/0891-5849(94)90200-3.

Abstract

Addition of horseradish peroxidase to a luminol solution (pH = 9.4) produces a burst of light followed by a steady luminescence that lasts for several minutes. This steady-state luminescence is readily quenched by SOD, with a Q1/2 concentration (the additive concentration needed to decrease by one-half the emitted luminescence intensity) of c.a. 4 ng/ml (14 mU/ml). The luminescence intensity decrease can then be employed to evaluate SOD activity in SOD-containing samples. However, the light intensity can also be quenched by additives, such as Trolox, that are able to trap luminol-derived intermediates. It is proposed that double quenching experiments must be performed in order to be able to relate the observed effect of an additive to its SOD-like activity.

MeSH terms

  • Antioxidants
  • Chromans
  • Horseradish Peroxidase
  • Indicators and Reagents
  • Kinetics
  • Light
  • Luminescent Measurements
  • Luminol*
  • Potentiometry / methods
  • Superoxide Dismutase / analysis
  • Superoxide Dismutase / metabolism*
  • Time Factors

Substances

  • Antioxidants
  • Chromans
  • Indicators and Reagents
  • Luminol
  • Horseradish Peroxidase
  • Superoxide Dismutase
  • 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid