“…1,3,4 Quantitative aspects of diffusion through this layer have attracted considerable experimental and theoretical study in connection with topical and transdermal drug delivery 2,5-7 as well as risk assessment of chemical exposure. [8][9][10] At steady state, such passage is characterized by a permeability coefficient P SC/w , measurable in vitro, representing the constant of proportionality between permeant flux J (mol/cm 2 Ás) through an SC sample and the driving difference in permeant concentrations between two aqueous solutions separated by the sample. (The subscript ''w'' represents shorthand designating the aqueous solution environment at a prescribed pH.)…”