作者: Viktoria V. Sursyakova , Galina V. Burmakina , Anatoly I. Rubaylo
关键词: Chromatography 、 Analyte 、 Capillary electrophoresis 、 Electrolyte 、 Analytical chemistry 、 Electrophoresis 、 Stability constants of complexes 、 Capillary action 、 Ligand (biochemistry) 、 Chemistry 、 Kinetics
摘要: The influence of analyte concentration when compared with the a charged ligand in background electrolyte (BGE) on measured values electrophoretic mobilities and stability constants (association, binding or formation constants) is studied using capillary electrophoresis (CE) dynamic mathematical simulator CE. study performed labile complexes (with fast kinetics) iron (III) 5-sulfosalicylate ions (ISC) as an example. It shown that because zone not equal to BGE, considerable changes migration times are observed, resulting systematic errors constant values. Of crucial significance slope dependence mobility decrease equilibrium concentration. Without prior information this accurately evaluate for similar systems, total must be at least >50-100 higher than analyte. Experimental ISC peak fronting difference between direction experimental pH simulation allow assuming presence wall interaction.