Mizuta Y, Masumizu T, Kohno M, Mori A, Packer L
Analytical Instruments Division, Jeol Ltd., Tokyo, Japan.
Biochem Mol Biol Int. 1997 Dec;43(5):1107-20. doi: 10.1080/15216549700204931.
A quantitative analysis of hydroxyl radical (.OH) generated in the Fe(2+)-hydrogen peroxide reaction system was explored by a spin-trapping method using 5,5-dimethyl-1-pyrroline-N-oxide (DMPO) combined with electron spin resonance spectroscopy. Based on the numerical analysis of Fenton-related reactions, the reduction of DMPO-OH adduct from 1:1 stoichiometry prominent at high concentrations of Fe2+ was consistent with a reaction model in which a molar amount of hydrogen peroxide was reduced by two molar amounts of Fe2+. Furthermore, time-dependent decrease in DMPO-OH quantity, apparent at much higher concentration of Fe2+, was proved due to the reaction not with Fe2+ but with Fe3+.
采用自旋捕获法,结合电子自旋共振光谱,利用5,5-二甲基-1-吡咯啉-N-氧化物(DMPO)对Fe(2+)-过氧化氢反应体系中产生的羟基自由基(·OH)进行了定量分析。基于对芬顿相关反应的数值分析,在高浓度Fe2+时显著的1:1化学计量比的DMPO-OH加合物的减少与一个反应模型一致,即一摩尔量的过氧化氢被两摩尔量的Fe2+还原。此外,在更高浓度的Fe2+下明显的DMPO-OH量随时间的减少被证明是由于其与Fe3+而非Fe2+的反应。