Three methods of manipulating the kinetics of hydrolysis of polymer co
njugates were evaluated. It was demonstrated that either first-order z
ero-order or S-shaped kinetic profiles could be achieved by systematic
changes in the chemical composition of several series of model side-c
hain substituted polyacrylates. The changes in kinetics were shown to
arise from an increase in the rate constant during solvolysis, resulti
ng from predictable changes in either the water content, secondary str
ucture, or LCST of the polymer conjugate.