ESR spin trapping studies into the nature of the oxidizing species formed in the Fenton reaction: pitfalls associated with the use of 5,5-dimethyl-1-pyrroline-N-oxide in the detection of the hydroxyl radical.

ESR spin trapping studies into the nature of the oxidizing species formed in the Fenton reaction: pitfalls associated with the use of 5,5-dimethyl-1-pyrroline-N-oxide in the detection of the hydroxyl radical.
复制标题

ESR 自旋捕获研究芬顿反应中形成的氧化物质的性质:与使用 5,5-二甲基-1-吡咯啉-N-氧化物检测羟基自由基相关的陷阱。

DOI:
--
复制
发表时间:
1993
期刊:
Free Radical Research Communications
影响因子:
--
通讯作者:
M. Burkitt
M. Burkitt
中科院分区:
--
文献类型:
--
作者:
M. Burkitt

文献摘要

参考文献

被引文献

相似文献

一些研究者已经质疑了广泛持有的观点,即羟基自由基是亚铁离子和过氧化氢反应中形成的主要氧化剂。在最近的研究中,使用ESR自旋捕获技术。Yamazaki和Piette发现,在Fe 2+和H2 O2之间的反应中,氧化剂形成的化学计量常常显示出与预期值1:1的显著偏差(I. Yamazaki和L. H. 03 The Dog(1990)113,7588-7593)。为了解释这些观察结果,有人提出,形成了额外的氧化物质,如铁离子(FeO 2+),特别是当铁以高浓度存在并与EDTA螯合时。在本文中,它表明,二次反应,涉及铁的氧化还原循环和铁的自旋陷阱5,5-二甲基-1-吡咯啉-N-氧化物(DMPO)的羟基自由基加合物的氧化,山崎和Piette所采用的反应条件下操作。因此,氧化剂形成的化学计量可以合理化,而不需要设想除了羟基自由基之外的氧化物质的形成。它也表明,铁(III)配合物的PAN-PAC可以直接与DMPO反应,形成DMPO羟基自由基加合物(DMPO/OH)在不存在过氧化氢。因此,为了避免形成(DMPO/OH)作为伪影,建议在使用DMPO的实验中,不应将C13 PAC用作去除含有外源铁的试剂。
Several investigators have challenged the widely held view that the hydroxyl radical is the primary oxidant formed in the reaction between the ferrous ion and hydrogen peroxide. In recent studies, using the ESR spin trapping technique. Yamazaki and Piette found that the stoichiometry of oxidant formation in the reaction between Fe2+ and H2O2 often shows a marked deviation from the expected value of 1:1 (I. Yamazaki and L. H. Piette (1990) J. Am. Chem. Soc. 113, 7588-7593). In order to account for these observations, it was suggested that additional oxidizing species are formed, such as the ferryl ion (FeO2+), particularly when iron is present at high concentration and chelated to EDTA. In this paper it is shown that secondary reactions, involving the redox cycling of iron and the oxidation of the hydroxyl radical adduct of the spin trap 5,5-dimethyl-1-pyrroline-N-oxide (DMPO) by iron, operate under the reaction conditions employed by Yamazaki and Piette. Consequently, the stoichiometry of oxidant formation can be rationalized without the need to envisage the formation of oxidizing species other than the hydroxyl radical. It is also demonstrated that the iron(III) complex of DETAPAC can react directly with DMPO to form the DMPO hydroxyl radical adduct (DMPO/OH) in the absence of hydrogen peroxide. Therefore, to avoid the formation of (DMPO/OH) as an artefact, it is suggested that DETAPAC should not be used as a reagent to inactivate containing adventitious iron in experiments using DMPO.
.OH 和 .O2 的 DMPO 自旋加合物的细胞诱导衰变。
DOI: 10.1016/0891-5849(89)90115-9
发表时间: 1989
影响因子: 7.4
作者:
Samuni,A;Samuni,A;Swartz,HM
通讯作者: Swartz,HM
DOI: 10.1016/s0021-9258(19)62677-3
发表时间: 1986-05
期刊: The Journal of biological chemistry
影响因子: --
作者:
J. D. Rush;Willem H. Koppenolg
通讯作者: J. D. Rush;Willem H. Koppenolg
DOI: 10.1016/s0021-9258(18)77389-4
发表时间: 1990-08
期刊: The Journal of biological chemistry
影响因子: --
作者:
I. Yamazaki;L. Piette
通讯作者: I. Yamazaki;L. Piette
DOI: 10.1016/0162-0134(87)80027-2
发表时间: 1987-03-01
影响因子: 3.9
作者:
RUSH, JD;KOPPENOL, WH
通讯作者: KOPPENOL, WH