Polymers grafted to substrates have traditionally been considered stable because of the covalent bonds that hold the polymers attached to the substrate. However, several recent reports have indicated that grafted polymers may detach from substrates under specific conditions. In this work, we report on a systematic study of polymer degrafting involving polycationic brushes with different degrees of quaternization (DQ mol %), which have been incubated in three different buffer solutions (pH 4, 7.4, and 9) with the same ionic strength of 0.05 M. We have varied the molecular weight (MW) and grafting density (sigma) of the polymer brushes using a combinatorial setup to examine the effect of MW, sigma, and DQ on polymer degrafting. Furthermore, we explored the effect of the bonding environment at the base of the initiator (mono- vs. tri-functional) of the grafted polymer layer at the substrate on the overall stability of polymer brushes on the substrate. The two major findings in this paper are (1) degrafting of polycationic grafts from flat silica substrate increases with increasing DQ of the polymer and (2) polymer degrafting likely occurs both in the initiator ester group and the silane head-group at the silicon substrate.