Cathodic stripping voltammetry of NADH in presence of Cu2+
Original paper
Abstract
The adsorption and accumulation of NADH and the Cu2+-NADH system at the mercury electrode surface was examined using differential pulse cathodic stripping voltammetry (DPCSV). The method was developed for analytical trace determination of NADH. Experimental and operational parameters for the quantitative determination of NADH were optimized and the detection limit was found to be 9.960 × 10–8 mol/L. The effect of some interferences (e.g. purine compounds, amino acids and some metal ions) was considered.
Keywords
Mercury Detection Limit NADH Electrode Surface Purine
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© Springer-Verlag Berlin Heidelberg 1998