Linking biomimetic binding measurements to pharmacokinetic models of volume of distribution and hepatic clearance
Year: 2026
Type: article
Abstract: Background and purpose: The steady-state volume of distribution reflects the extent to which drugs partition between plasma and tissues and is closely related to the tissue-to-plasma partition coefficient. In pharmacokinetics, different modelling frameworks have led to ongoing debate regarding the role of plasma protein binding and the importance of unbound drug exposure in determining both distribution and clearance. This review aims to clarify the relationship between distribution and elimination models and to assess how experimental binding measurements can support their mechanistic interpretation. Experimental approach: ), clearance and half-life were analysed alongside biomimetic chromatographic measurements of drug binding to human serum albumin and phospholipid membranes using immobilized artificial membrane (IAM) chromatography. Literature data for marketed drugs were evaluated to examine how these experimental descriptors relate to distribution and clearance behaviour. Key results: , while plasma protein binding influences both distribution and clearance through its effect on the fraction of drug unbound in plasma. The apparent paradox of plasma protein binding arises because changes in unbound fraction affect both processes simultaneously. Conclusion: This work demonstrates that biomimetic binding measurements provide a mechanistically meaningful bridge between physicochemical properties and pharmacokinetic behaviour. By integrating experimental binding data with pharmacokinetic models, the study advances understanding of how distribution and clearance are linked, supporting more informed decision-making in early drug discovery while highlighting that clearance remains influenced by additional factors beyond non-specific binding.
Source: ADMET & DMPK
DOI: 10.5599/admet.3311
Author: Klara Livia Valko
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: diamond
OpenAlex ID: W7159970545