Hydrogels are a network of polymer chains with properties that absorb, store and transport solutions. A hydrogel membrane has a permeability that allows influx and excretion. Therefore, it is the ideal material for medicated membranes. This study investigates the crosslinking of poly(vinyl alcohol) (PVA) hydrogel membranes using different agents and explores the usability of the candidate membranes as drug delivery systems. The model protein, bovine albumin serum (BSA), was used to test the stability and controlled drug release rate characteristics of the candidate hydrogel membranes. This investigation also evaluated the stability different crosslinkers for hydrogel membranes. Glutaraldehyde (GA) and an alternative crosslinking method of ultraviolet irradiation with the sensitizer, sodium benzoate (SB), were used to crosslink PVA containing BSA. In GA crosslinked membranes, BSA release diffusion experiments showed 48%, 45%, and 63% recovery of protein at pH 6.5, 7.4 and 8.0, respectively; this confirmed that this system is suited for physiological conditions and controlled release. Although SB has been used for membrane fabrication, our Fourier Transform Infrared Spectroscopy (FTIR) and Thermogravimetric Analysis (TGA) results indicate that UV(SB)-crosslinked films are not suited for drug delivery, despite the release of BSA
