E. Lissi et al., ON THE USE OF THE QUENCHING OF LUMINOL LUMINESCENCE TO EVALUATE SOD ACTIVITY, Free radical biology & medicine, 16(6), 1994, pp. 833-837
Addition of horseradish peroxidase to a luminol solution (pH = 9.4) pr
oduces a burst of light followed by a steady luminescence that lasts f
or 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 empl
oyed to evaluate SOD activity in SOD-containing samples. However, the
light intensity can also be quenched by additives, such as Trolox, tha
t 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.