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Sci Rep. 2016 Dec 12;6:38773. doi: 10.1038/srep38773.

N-tert-butylmethanimine N-oxide is an efficient spin-trapping probe for EPR analysis of glutathione thiyl radical.

Author information

1
Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
2
Department of Environmental and Occupational Health, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Abstract

The electron spin resonance (EPR) spin-trapping technique allows detection of radical species with nanosecond half-lives. This technique is based on the high rates of addition of radicals to nitrones or nitroso compounds (spin traps; STs). The paramagnetic nitroxides (spin-adducts) formed as a result of reactions between STs and radical species are relatively stable compounds whose EPR spectra represent "structural fingerprints" of the parent radical species. Herein we report a novel protocol for the synthesis of N-tert-butylmethanimine N-oxide (EBN), which is the simplest nitrone containing an α-H and a tertiary α'-C atom. We present EPR spin-trapping proof that: (i) EBN is an efficient probe for the analysis of glutathione thiyl radical (GS); (ii) β-cyclodextrins increase the kinetic stability of the spin-adduct EBN/SG; and (iii) in aqueous solutions, EBN does not react with superoxide anion radical (O2-•) to form EBN/OOH to any significant extent. The data presented complement previous studies within the context of synthetic accessibility to EBN and efficient spin-trapping analysis of GS.

PMID:
27941944
PMCID:
PMC5150238
DOI:
10.1038/srep38773
[Indexed for MEDLINE]
Free PMC Article

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