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pubmed-article:14769880pubmed:abstractTextWe studied the mechanism of formation of oxygen radicals during ferrous ion-induced decomposition of linoleic acid hydroperoxide using the spin trapping and chemiluminescence methods. The formation of the superoxide anion (O2*-) was verified in the present study. The hydroxyl radical is also generated through Fenton type decomposition of hydrogen peroxide produced on disproportionation of O2*-. A carbon-centered radical was detected using 5-(diethoxyphosphoryl)-5-methyl-1-pyrroline N-oxide (DEPMPO) as a spin trap. Alkoxyl radical formation is essential for the conversion of linoleic acid hydroperoxide into the peroxyl radical by ferrous ion. It is likely that the alkoxyl radical [R1CH(O*)R2] is converted into the hydroxylcarbon radical [R1C*(OH)R2] in water, and that this carbon radical reacts with oxygen to give the alpha-hydroxyperoxyl radical [R1R2C(OH)OO*], which decomposes into the carbocation [R1C+(OH)R2] and O2*-.lld:pubmed
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pubmed-article:14769880pubmed:dateRevised2011-11-17lld:pubmed
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pubmed-article:14769880pubmed:articleTitleFormation of superoxide anion during ferrous ion-induced decomposition of linoleic acid hydroperoxide under aerobic conditions.lld:pubmed
pubmed-article:14769880pubmed:affiliationDepartment of Photon and Free Radical Research, Japan Immunoresearch Laboratories, 351-1 Nishiyokote-cho, Takasaki 370-0021. kambayashi@pub.m.kanazawa-u.ac.jplld:pubmed
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