Literature DB >> 3029206

A demonstration that O2- is a crucial intermediate in the high quantum yield luminescence of luminol.

E K Miller, I Fridovich.   

Abstract

The chemiluminescence of luminol, due to its reaction with alkaline H2O2, is inhibited by superoxide dismutase or by hydroxyl radical scavengers. Hematin markedly enhances this H2O2-induced luminescence of luminol and lessens, but does not eliminate, the sensitivity towards these inhibitors. Reaction mechanisms are proposed to account for these results. Since luminol luminescence depends upon a reaction between the luminol radical and O2-, and since the luminol radical can reduce dioxygen to O2-, superoxide dismutase-inhibitable luminol luminescence cannot be reliably used as a detector of O2- production.

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Year:  1986        PMID: 3029206     DOI: 10.1016/s0748-5514(86)80058-7

Source DB:  PubMed          Journal:  J Free Radic Biol Med        ISSN: 0748-5514


  3 in total

1.  A coelenterazine-based luminescence assay to quantify high-molecular-weight superoxide anion scavenger activities.

Authors:  Livia Saleh; Christoph Plieth
Journal:  Nat Protoc       Date:  2010-09-16       Impact factor: 13.491

2.  Peroxynitrite-induced luminol chemiluminescence.

Authors:  R Radi; T P Cosgrove; J S Beckman; B A Freeman
Journal:  Biochem J       Date:  1993-02-15       Impact factor: 3.857

3.  Peroxide-Induced Liberation of Iron from Heme Switches Catalysis during Luminol Reaction and Causes Loss of Light and Heterodyning of Luminescence Kinetics.

Authors:  Christoph Plieth
Journal:  ACS Omega       Date:  2019-02-14
  3 in total

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