Takashi Michida

アルカリ処理した塩化メチレン中の電気化学的 P-450 モデル系によるジフェニルスルフィドの酸化

Dichloromethane containing metalloporphyrins [meso-tetraphenylporphyrinatomanganese(III) chloride (1) or meso-tetraphenylporphyrinatoiron(III) chloride (2)] and Bu4NClO4 was treated with an aqueous solution of NaOH (5%), and subjected to controlled potential electrolysis at -1.0 V (vs. S.C.E. (saturated calomel electrode)) in a divided cell after addition of diphenyl sulfide (3). Diphenyl sulfoxide (4) and diphenyl sulfone (5) were found in an electrolyzed solution as the reaction products. Results obtained from cyclic voltammetry and visible spectrometry suggested that the treatment of dichloromethane containing metalloporphyrins with the aqueous solution of NaOH did not change the fifth ligand of metalloporphyrins from Cl to OH. On the electrode, dissolved dioxygen was reduced to hydrogen peroxide. Compounds 1 and 2 catalyze the oxidation of 3 by hydrogen peroxide without imidazole. Compound 2 showed higher selectivity than compound 1.

Electrochemical immunoassay combined with column liquid chromatography: determination of phenytoin in human serum

A new electrochemical immunoassay combined with column liquid chromatography has been developed for the determination of phenytoin in human serum. Phenytoin was labelled with the electrochemically active nitroxide, and the separation of the free labelled antigen from other electrochemically active compounds in serum was accomplished by the use of gel chromatography. Serum samples were mixed with the antibody and the labelled antigen, incubated for 90 min, and then a 100-microliter aliquot of the mixture was directly injected to the column, which was equipped with an electrochemical detector. With 10 microliter of serum, the smallest detectable concentration of phenytoin was 2 micrograms/ml.