The determination of thiomalate in physiological fluids by high-performance liquid chromatography and electrochemical
Journal of Pharmaceutical and Biomedical Analysis
|January 1, 1983
Abstract:
Methods are described for the determination of free thiomalate in the plasma and urine of patients receiving the anti-rheumatic drug sodium aurothiomalate. Thiomalate is separated by reversed-phase chromatography and detected using a gold electrochemical cell. Plasma analyses require maximal sensitivity while urine estimations require selectivity rather than sensitivity: different phosphate buffer-methanol eluents and electrode potentials are used. On-column sensitivity for thiomalate is 40 fmol injected.
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