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Reduction of Antitumour Mitosenes in Non-Aqueous and Aqueous Environment. An Electron Spin Resonance and Cyclic Voltammetry Study
Authors:Marc Maliepaard   Nico J. De Mol  Lambert H. M. Janssen  Arnold r. Goeptar  Johan M. Te Koppele  Nico P. E. Vermeulen  Willem Verboom  David N. Reinhoudt
Affiliation: a Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Utrecht University, Utrecht, TB, The Netherlandsb Leiden/Amsterdam Center for Drug Research, Department of Pharmacochemistry, Division of Molecular Toxicology, Free University, Amsterdam, HV, The Netherlandsc Laboratory of Organic Chemistry, Faculty of Chemical Technology, University of Twente, Enschede, AE, The Netherlands
Abstract:Chemical reduction of mitosenes under aerobic conditions in DMSO showed characteristic ESR signals of the mitosene derived semiquinone free radicals. However, these signals diminished strongly upon addition of water to the reaction mixture, indicating a short lifetime of the mitosene semiquinone free radicals under aqueous conditions. In addition, enzymatic one-electron reduction of these mitosenes with either xanthine oxidase or purified NADPH cytochrome P450 reductase under anaerobic conditions showed no signals of the mitosene semiquinone free radicals. Subsequent cyclic voltammetry measurements demonstrated facilitation of the further one-electron reduction of the mitosene semiquinone free radicals in the presence of water in comparison with non-aqueous conditions. The present results strongly suggest that in the presence of water relatively stable hydroquinones are formed upon reduction of mitosenes. Consequently, the steady state concentrations of mitosene semiquinone free radicals will be lowered substantially in aqueous environment. Thus under physiological conditions, two-electron reduction and formation of the mitosene hydroquinone might be important in processes leading to DNA alkylation by these mitosenes.
Keywords:Mitosenes  Mitomycin C  Semiquinone free radical  reductive activation  hydroquinone
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