In the present study, the influence of polymeric concentration, its blend and drug loading
dose on the in vitro drug release pattern of alfuzosin hydrochloride from its transdermal patches has been
investigated. Ratio of EC and PVP and drug loading dose were selected as independent variables and their
influence on the percentage drug released at 24 h (Q24), drug release rate (KH) and time taken for 50%
drug release (t50%) were studied using statistical experimental designing. Ratio of EC and PVP was found
to be the main influential factor for all the dependent variables studied. Drug loading dose was also found
to influence the dependent variables but to a lesser extent. Physicochemical parameters of the prepared
patches were also evaluated. This study could be used as a screening method for further development of
transdermal delivery of alfuzosin hydrochloride and skin permeation studies.