Within a wide study designed to the development of a transdermal deliv
ery system of clonazepam, in the present work the in vitro permeation
behaviour of the drug from a series of alcoholic-gel or emulsion-gel f
ormulations containing various enhancing agents was investigated. Phys
icochemical properties of each gel and drug kinetic permeation paramet
ers were determined. The flux of the drug was found to be principally
influenced by both the drug solubility in the vehicle and the formulat
ion viscosity. The results indicated the great importance of a proper
choice of the vehicle for optimization of drug delivery. The formulati
ons containing isopropanol gave the best results, yielding a flux of c
lonazepam up to four times greater than in the absence of enhancer.