Symons T, Tocher J H, Tocher D A, Edwards D I
Chemotherapy Research Unit, Polytechnic of East London.
Free Radic Res Commun. 1991;14(1):33-40. doi: 10.3109/10715769109088939.
The electrochemical behaviour of three nitrofuran compounds, nitrofurazone, nitrofurantoin and furazolidone, has been studied in three solvent types; aprotic, aqueous and mixed, and at four working electrodes. Particular attention has focused on the 1-electron RNO2/RNO2.- couple as measured by the cyclic voltammetric mode. Using Hg in aqueous buffer, reduction of the NO2 group proceeds directly to the hydroxylamine with no intermediate stages being identified. Addition of an aprotic solvent gave a 2-stage reduction, initially forming the RNO2.- species. At all solid electrodes, however, the RNO2/RNO2.- couple was identified under simple aqueous conditions. The switch to a mixed aqueous/aprotic solvent medium produced only minor changes in the response compared with the situation on Hg. This presents the opportunity of using nitrofuran complexes as model systems for the redox behaviour of nitro aromatic compounds in general at solid electrode surfaces where the latters' more negative reduction potentials makes direct study difficult. The conditions have been defined whereby we can examine pH effects and RNO2.- biological target interactions in simple aqueous media to allow the further refinement of the electrolytic model system for studying bio-reducible drug action.
已在三种溶剂类型(非质子溶剂、水性溶剂和混合溶剂)以及四种工作电极上研究了三种硝基呋喃化合物(呋喃西林、呋喃妥因和呋喃唑酮)的电化学行为。特别关注通过循环伏安法测量的单电子RNO₂/RNO₂⁻ 电对。在水性缓冲液中使用汞时,NO₂基团的还原直接进行到羟胺,未发现中间阶段。添加非质子溶剂会产生两阶段还原,最初形成RNO₂⁻ 物种。然而,在所有固体电极上,在简单的水性条件下都能识别出RNO₂/RNO₂⁻ 电对。与在汞电极上的情况相比,切换到水性/非质子混合溶剂介质只会使响应产生微小变化。这为将硝基呋喃配合物用作一般硝基芳香化合物在固体电极表面氧化还原行为的模型系统提供了机会,因为后者更负的还原电位使得直接研究变得困难。已经确定了相关条件,据此我们可以在简单的水性介质中研究pH效应和RNO₂⁻ 与生物靶点的相互作用,以便进一步完善用于研究生物可还原药物作用的电解模型系统。