UCL Discovery
UCL home » Library Services » Electronic resources » UCL Discovery

Extrapolation of lung pharmacokinetics of Bedaquiline across species using Physiologically Based Pharmacokinetic modelling

Karakitsios, E; Della Pasqua, Oscar; Dokoumetzidis, A; (2025) Extrapolation of lung pharmacokinetics of Bedaquiline across species using Physiologically Based Pharmacokinetic modelling. British Journal of Clinical Pharmacology , 91 (11) pp. 3167-3178. 10.1002/bcp.70163. Green open access

[thumbnail of Walker_The impact of inter-infection time on antimicrobial resistance profiles in women with multiple urinary tract infections over time_VoR.pdf]
Preview
Text
Walker_The impact of inter-infection time on antimicrobial resistance profiles in women with multiple urinary tract infections over time_VoR.pdf

Download (631kB) | Preview

Abstract

AIMS: Bedaquiline (BDQ) is a first-in-class diarylquinoline (DARQ) and a potent anti-tuberculosis drug, vital in combating multi-drug resistant tuberculosis (TB). Understanding its lung pharmacokinetics (PK) across species is crucial for effective clinical translation. This study aimed to extrapolate BDQ’s lung PK from preclinical species to humans, focusing on healthy and TB-infected lung tissue. METHODS: Physiologically-based PK (PBPK) modelling was employed to simulate BDQ’s lung distribution in various pulmonary micro-compartments, including cellular lesions and caseous granulomas, using data from mice, rats and dogs. Complex interactions, such as lysosomal trapping within macrophages and anomalous diffusion within the caseum, utilising a catenary model and a time-dependent rate, were incorporated into the models to accurately represent BDQ’s unique PK profile. RESULTS: The study revealed intricate dynamics of BDQ’s lung distribution, with only free concentrations in lysosomes of macrophages surpassing the MIC of Mycobacterium tuberculosis in both mice and humans, indicating intracellular accumulation which may further explain the proven drug’s efficacy. Moreover, during the course of treatment in humans, adequate drug levels were achieved near the cellular rim but penetration into the inner caseous core was predicted to be limited. CONCLUSIONS: Understanding BDQ's lung PK is essential for optimising dosing strategies with new companion drugs. The findings underscore the need to characterise BDQ distribution within the caseum, as it shows extensive caseum binding. Moreover, the developed PBPK model can be applied to new promising DARQ analogues, facilitating their development as effective TB treatments.

Type: Article
Title: Extrapolation of lung pharmacokinetics of Bedaquiline across species using Physiologically Based Pharmacokinetic modelling
Open access status: An open access version is available from UCL Discovery
DOI: 10.1002/bcp.70163
Publisher version: https://doi.org/10.1002/bcp.70163
Language: English
Additional information: © The Author(s) 2025. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/).
Keywords: bedaquiline dose selection extrapolation physiologically-based pharmacokinetic modelling tissue pharmacokinetics tuberculosis
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > UCL School of Pharmacy
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > UCL School of Pharmacy > Pharmacology
URI: https://discovery.ucl.ac.uk/id/eprint/10209857
Downloads since deposit
4Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item