RT Journal Article SR Electronic T1 Intracellular and intra-organ concentrations of small molecule drugs: theory, practice, and promise JF Drug Metabolism and Disposition JO Drug Metab Dispos FD American Society for Pharmacology and Experimental Therapeutics SP dmd.118.085951 DO 10.1124/dmd.118.085951 A1 Dennis Allen Smith A1 Malcolm Rowland YR 2019 UL http://dmd.aspetjournals.org/content/early/2019/03/25/dmd.118.085951.abstract AB The distribution of a drug within the body should be considered as involving movement of unbound drug between the various aqueous spaces of the body. At true steady state, even for a compound of restricted lipoidal permeability, unbound concentrations in all aqueous compartments (blood, extracellular, intracellular) are considered identical, unless a compartment has a clearance /transport process. In contrast, total drug concentrations may differ greatly reflecting binding or partitioning into constituents of each compartment. For most highly lipid permeable drugs, this uniform unbound concentration is expected to apply. However, many compounds have restricted lipoidal permeability and are subjected to transport / clearance processes causing a gradient between intracellular and extracellular unbound concentrations even at steady state. Additional concerns arise where the drug target resides in a site of limited vascularity. Many misleading assumptions about drug concentrations and access to drug targets are based on total drug. Correction if made is usually by measuring tissue binding, but this is limited by the lack of homogenicity of the organ or compartment. Rather than looking for technology to measure the unbound concentration it may be better to focus on designing high lipoidal permeable molecules with a high chance of achieving a uniform unbound drug concentration. It is hoped this manuscript will stimulate greater understanding of the path from circulation to cell interior and thereby, in part, avoid or minimise the need to provide the experimentally very determining, and sometimes still questionable, answer to this problem.