“…Below, we develop a mathematical model for drug release from the inserts that takes both resistances into account and explains all the observed trends in the drug release profiles. Since the drug loading is above the solubility limit, the hydrated conjunctival inserts contain drug in three forms [32]: (i) free drug dissolved in the fluid that hydrates the gel, (ii) drug adsorbed on the polymer surface, and (iii) drug present as aggregates/particles. On exposing the inserts to PBS, the un-aggregated drug diffuses out of the insert to reduce the free concentration of the drug below the solubility limit, which leads to dissolution of the drug particles.…”