Development of a Dynamic Physiologically Based Mechanistic Kidney Model to Predict Renal Clearance. (11th August 2018)

• Record Type: Journal Article
• Authors: Huang, Weize; Isoherranen, Nina
• Is Part Of: CPT: pharmacometrics & systems pharmacology. Volume 7:Number 9(2018)
• Page Start: 593
• Page End: 602
• Publication Date: 2018-08-11
• Subjects: Pharmacokinetics -- Periodicals; Pharmacology -- Periodicals; Pharmacokinetics; Periodicals; 615.05
• DOI: 10.1002/psp4.12321
• Languages: English
• ISSNs: 2163-8306

Abstract

Abstract : Renal clearance is usually predicted via empirical approaches including quantitative structure activity relationship and allometric scaling. Recently, mechanistic prediction approaches using in silico kidney models have been proposed. However, empirical scaling factors are typically used to adjust for either passive diffusion or active secretion, to acceptably predict renal clearances. The goal of this study was to establish a renal clearance simulation tool that allows prediction of renal clearance (filtration and pH‐dependent passive reabsorption) from in vitro permeability data. A 35‐compartment physiologically based mechanistic kidney model was developed based on human physiology. The model was verified using 46 test compounds, including neutrals, acids, bases, and zwitterions. The feasibility of incorporating active secretion and pH‐dependent bidirectional passive diffusion into the model was demonstrated using para‐aminohippuric acid (PAH), cimetidine, memantine, and salicylic acid. The developed model enables simulation of renal clearance from in vitro permeability data, with predicted renal clearance within twofold of observed for 87% of the test drugs.