1987
DOI: 10.1016/s0891-5849(87)80033-3
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Spin Trapping: ESR parameters of spin adducts 1474 1528V

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Cited by 1,672 publications
(1,049 citation statements)
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“…The predominant spin adduct formed ( fig.2B) consists of a triplet of doublets and can be computer-simulated using hyperfine coupling constants, ON = 1.58 mT, a& = 2.28 mT ( fig.ZC). These spectral parameters are consistent with those previously reported for DMPO-hydroxyethyl radical formed following the reaction of 'OH with ethanol [23]. Although at the concentration of ethanol used all 'OH formed should react with this reagent, the additional ESR lines observed in fig.2B show that a small fraction of DMPO-OH is also formed.…”
Section: Resultssupporting
confidence: 91%
See 1 more Smart Citation
“…The predominant spin adduct formed ( fig.2B) consists of a triplet of doublets and can be computer-simulated using hyperfine coupling constants, ON = 1.58 mT, a& = 2.28 mT ( fig.ZC). These spectral parameters are consistent with those previously reported for DMPO-hydroxyethyl radical formed following the reaction of 'OH with ethanol [23]. Although at the concentration of ethanol used all 'OH formed should react with this reagent, the additional ESR lines observed in fig.2B show that a small fraction of DMPO-OH is also formed.…”
Section: Resultssupporting
confidence: 91%
“…Reducing the instrument scan range from 2000 G to 100 G and the modulation amplitude from 10 G to 0.5 G, these additional 4 lines become well resolved into the 1:2:2:1 pattern shown in fig.lB. This ESR spectrum with hyperfine coupling constants, ON = a& = 1.49 mT, corresponds to the DMPO-OH spin adduct [23]. Since DMPO-OH may be formed by pathways other than the direct addition of 'OH to DMPO, an experiment was done reacting vanadyl sulfate (1 x 10m3 M) with Hz02 (1 x 10m3 M) in the presence of D,L-histidine (1 x 10-2 M) and the spin trap MNP (1 x 10e2 M) in order to verify the generation of 'OH.…”
Section: Resultsmentioning
confidence: 89%
“…2d). Even though these constants could be assigned to lipid radicals, spin trapping studies cannot readily distinguish between peroxyl (ROOÁ), alkoxyl (ROÁ) and alkyl (RÁ) adducts, owing to the similarity of the corresponding coupling constants (Buettner 1987).…”
Section: Lipid Radical Generation Of Isolated Liver ''Microsomes''mentioning
confidence: 99%
“…A major limitation of this technique is the inability to directly detect some highly reactive radical species with very short life (e.g. superoxide, hydroxyl radicals, sulfur centered radicals and alkoxyl radicals) [10]. Fortunately, this can be overcome through the use of spin traps, which are diamagnetic compounds (often nitrones or nitroso compounds) capable of yielding long-lived radical products upon reaction with free radicals [10].…”
Section: Introductionmentioning
confidence: 99%
“…superoxide, hydroxyl radicals, sulfur centered radicals and alkoxyl radicals) [10]. Fortunately, this can be overcome through the use of spin traps, which are diamagnetic compounds (often nitrones or nitroso compounds) capable of yielding long-lived radical products upon reaction with free radicals [10]. EPR spin trapping has been successfully used to elucidate many mechanistic questions [11][12][13].…”
Section: Introductionmentioning
confidence: 99%