We compare two of the most successful models for the description and analysis
of drug release data. The fractal kinetics approach leading to release profiles
described by a Weibull function and the fractional kinetics approach leading to
release profiles described by a Mittag-Leffler function. We used Monte Carlo
simulations to generate artificial release data from euclidean and fractal
substrates. We have also used real release data from the literature and found
that both models are capable in describing release data up to roughly 85%
of the release. For larger times both models systematically overestimate the
number of particles remaining in the release device