The aim of this study is to present a mathematical model of percutaneo
us absorption which considers the simultaneous penetration of drug by
transcellular and intercellular pathways, as well as movement of drug
between these two pathways. A two-layer mathematical model is formulat
ed and solutions to this model are obtained numerically for data sets
containing a range of physicochemical parameters relating to the percu
taneous pathways and model drugs. Detailed graphical output is present
ed of the drug concentration profiles with skin depth, the effect of l
ipophilicity on steady state fluxes and the total amount of drug deliv
ered, and the formation of drug depots within the skin. Many qualitati
ve similarities exist between the multiple pathway model presented and
previously proposed single and uncoupled pathway mathematical models.
However, the model presented reveals effects of changes to the physic
ochemical properties of the penetrant or the skin structure which are
not shown with a single or uncoupled pathway model.