AbbreviationsA+,A-F L+,L-QSAR sd sgn High and low amphiphilicity Fisher criterion High and low lipophilicity Quantitative structure-activity relationships Standard deviation sgn = -1 for acids and sgn = 1 for bases
Symbols
A , B, C, D, E, it Adjustable parametersDispositionfunction with the time of exposure ( t ) and physico-chemical properties (pp) of both the drugs and biological systems as variables Actual drug concentration Concentration of free non-ionized molecules in aqueous compartments Equipotent concentration eliciting the fraction X of the maximum effect Drug concentration in the entry compartment Diffusion coefficient in the diffusion layer with the effective thickness h Z , , , , , = 0 for cis-derivatives and Ztrans = 1 for trans-derivatives