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. 2002 Nov 22;299(1):155-9.
doi: 10.1016/s0006-291x(02)02594-9.

One-electron oxidation of "photo-Fenton" reagents and inhibition of lipid peroxidation

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One-electron oxidation of "photo-Fenton" reagents and inhibition of lipid peroxidation

Darren Tobin et al. Biochem Biophys Res Commun. .

Abstract

The "photo-Fenton" reagent, 2-mercaptopyridine N-oxide (MPO), which releases a hydroxyl radical on ultraviolet irradiation, has been found to act as an antioxidant. In the peroxidation of linoleate initiated by a water-soluble azo-initiator, MPO has about one-third the activity of the water-soluble vitamin E analogue Trolox C. In contrast, the oxygen-containing analogue, 2-hydroxypyridine N-oxide (HPO), does not have measurable antioxidant activity in this system. Both reagents react with hydroxyl radical with second order rate constants very close to the diffusion-controlled limit. With the less oxidising dithiocyanate radical anion, MPO reacts approximately 50 times more rapidly than HPO at pH>7. The more reducing properties of MPO result in its activity as an antioxidant and make it less suitable than HPO as a source of hydroxyl radicals for investigation of oxidative stress in biological systems.

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