Abstract
AbstractVoltammetric sensing of analytes in biological fluids is frequently accompanied by non-linear effects due to the analyte/matrix interactions. A theoretical approach is developed to describe such effects when standard addition methods are applied. Several asymptotic models are described considering equilibrium-like and kinetic-like interaction models and possible co-diffusion effects. Experimental data for non-linear features which appear in voltammetric sensing of serotonin and noradrenalin in urine are in satisfactory agreement with theoretical predictions.
Publisher
Springer Science and Business Media LLC
Subject
Electrical and Electronic Engineering,Electrochemistry,Condensed Matter Physics,General Materials Science,Energy Engineering and Power Technology,Materials Chemistry