Stripping voltammetry (SV), in common with all trace voltammetric anal
ytical techniques, suffers from poor signal-to-noise (S/N) ratios due
to external interference pick up and inherent generation of noise in t
he electrochemical system. In addition to other methods developed to s
mooth noisy data (such as time and frequency domain filtering), optimi
sation methods can also be used to reject the noise present in electro
chemical measurements. In this paper, an optimisation method, based on
a modified Simplex procedure, is presented. The method is based on mi
nimising the deviation (in terms of the mean square error) between the
recorded data and a theoretical model of the data. In this case, the
model was a response surface consisting of one or more peak-shaped fun
ctions of one of the following types: Gaussian (G), exponentially modi
fied Gaussian (EMG), Lorentzian (L), combined Gaussian-Lorentzian (GL)
and theoretical voltammetric peak (TVP). The method was successfully
applied to stripping signals obtained for the trace quantification of
riboflavin and for the simultaneous determination of zinc, cadmium lea
d and copper by SV.