“…The drug partitioning was assessed from the retention volume, which was expressed as a capacity factor, K s , normalized with respect to the amount of immobilized phospholipids, and can be used for semi‐quantitative analysis of solute–membrane interaction 3, 4. For normalization of the results obtained on gel beds with different amounts of phospholipids, and for elimination of the dead volume of the system, a logarithm of the normalized retention values, K s , for a drug was calculated by using Eqn 1: where V r is the retention volume of the drug, V o is the retention volume of a small and hydrophilic reference ion (whereby the dead volume of the system is eliminated) and A is the amount of immobilized phospholipids 7. Using chemometric tools to predict drug and chemical tissue distribution, membrane permeability or biphasic system partition is of major importance in physicochemical, environmental, and life sciences 8.…”