“…We have postulated that reactive oxygen species (ROS)-mediated degradation of the polymer matrix is responsible for accelerated in vivo degradation and drug release, however it is known that certain enzymes such as lipases, lysozymes and esterases exhibit biodegradative activity toward biodegradable polymers 48,31,49,50,30,32,29,51,52 . Here we employ our model to study the potential effects of enzymatic degradation under the assumption that degradative enzymes would have the same transportation kinetics and correlations 1 governing their diffusion into a microparticle as drug releasing from the microparticle.…”