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Biomedical subjects

J M Kauffmann

Publications and source records attributed to J M Kauffmann.

35 records · Page 2Linked to original sources

Redox behaviour of anti-tumor platinum (II) compounds (carboplatin) at solid electrodes.

The electroactivity of a cytostatic complex of platinum (II) possessing no halide ligand (carboplatin) has been studied in aqueous media using platinum and carbon paste electrodes. Cyclic voltammetry has been conducted in order to elucidate the redox behaviour of carboplatin as a function of chloride concentration. Reduction was not observed although oxidation was detected. The nature of the compounds formed during the electro-oxidation was directly related to free chloride ions. At the carbon paste electrode, the reduction of the oxidized species occurred in two steps with the formation of cis-platinum structures and a subsequent electrodeposition of platinum particles. The surface modification step at the carbon paste electrode has demonstrated electrocatalytic properties of the electrode towards platinum (II) complexes possessing halide ligands in their structures. Electrodeposition of platinum ions at a platinum electrode surface as well as a judicious choice of working parameters allows quantitative determinations in the concentration range 3 x 10(-4) - 1 x 10(-5) M.

Journal Article↗

[Not Available].

The analysis of pharmacologically active compounds using electrochemical techniques with modified electrodes is reviewed. Several physical and chemical methods for the immobilization of materials on to electrodes are available, and the resulting surfaces can be examined microscopically . Examples of these procedures and their analytical applications are given.

English Abstract↗

Electrochemical behaviour of tizanidine at solid electrodes.

The electrochemical behaviour of tizanidine [5-chloro(delta-2-imidazolinyl-2-amino)-4-benzothiadiazole-2,1,3], a centrally-active skeletal muscle relaxant has been investigated in aqueous media at the carbon paste electrode (CPE). Cyclic voltammetry at different pH values, controlled potential coulometry and comparative studies on three structurally related molecules have permitted identification of the oxidation site of tizanidine and suggest possible oxidation products in acidic media. The electrochemical reduction at the CPE occurred in one irreversible step and the reduction product (diamine derivative) was detected and characterized on the positive going scan in cyclic voltammetry. Quantitative measurements of tizanidine within the range 2 x 10(-5) M and 1 x 10(-4) M have been realized at the CPE using the differential pulse technique.

Carbon↗