[HTML][HTML] Application of a physiologically based pharmacokinetic model to characterize time-dependent metabolism of voriconazole in children and support dose …

Y Zhang, S Zhao, C Wang, P Zhou… - Frontiers in Pharmacology, 2021 - frontiersin.org
Background: Voriconazole is a potent antifungal drug with complex pharmacokinetics
caused by time-dependent inhibition and polymorphisms of metabolizing enzymes. It also …

A physiologically based pharmacokinetic model for voriconazole disposition predicts intestinal first-pass metabolism in children

NR Zane, DR Thakker - Clinical pharmacokinetics, 2014 - Springer
Abstract Background and Objectives The effect of ontogeny in drug-metabolizing enzymes
on pediatric pharmacokinetics is poorly predicted. Voriconazole, a potent antifungal, is …

Pediatric clinical pharmacology of voriconazole: role of pharmacokinetic/pharmacodynamic modeling in pharmacotherapy

RS Kadam, JN Van Den Anker - Clinical pharmacokinetics, 2016 - Springer
Voriconazole is a potent antifungal agent used for the treatment of invasive fungal infections
caused by Aspergillus and Candida species in adult and pediatric patients. Voriconazole …

Population pharmacokinetic analysis of voriconazole plasma concentration data from pediatric studies

MO Karlsson, I Lutsar, PA Milligan - Antimicrobial agents and …, 2009 - Am Soc Microbiol
Voriconazole is a potent triazole with broad-spectrum antifungal activity against clinically
significant and emerging pathogens. The present population pharmacokinetic analysis …

A physiologically based pharmacokinetic model of voriconazole integrating time-dependent inhibition of CYP3A4, genetic polymorphisms of CYP2C19 and …

X Li, S Frechen, D Moj, T Lehr, M Taubert, C Hsin… - Clinical …, 2020 - Springer
Background Voriconazole, a first-line antifungal drug, exhibits nonlinear pharmacokinetics
(PK), together with large interindividual variability but a narrow therapeutic range, and …

Impact of CYP2C19 phenotype and drug-drug interactions on voriconazole concentration in pediatric patients

X Tian, C Zhang, Z Qin, D Wang, J Yang… - Antimicrobial Agents …, 2021 - Am Soc Microbiol
ABSTRACT Voriconazole (VRC), a first-line agent for the treatment of invasive fungal
infections, is mainly metabolized by human cytochrome P450 (CYP) 2C19. In this study, a …

[HTML][HTML] Pharmacogenetic analysis of voriconazole treatment in children

R Tilen, P Paioni, AN Goetschi, R Goers, I Seibert… - Pharmaceutics, 2022 - mdpi.com
Voriconazole is among the first-line antifungal drugs to treat invasive fungal infections in
children and known for its pronounced inter-and intraindividual pharmacokinetic variability …

[HTML][HTML] Population pharmacokinetics of voriconazole and the role of CYP2C19 genotype on treatment optimization in pediatric patients

L Hu, S Huang, Q Huang, J Huang, Z Feng, G He - Plos one, 2023 - journals.plos.org
The aim of this study was to evaluate factors that impact on voriconazole (VRC) population
pharmacokinetic (PPK) parameters and explore the optimal dosing regimen for different …

[HTML][HTML] Voriconazole: a review of population pharmacokinetic analyses

C Shi, Y Xiao, Y Mao, J Wu, N Lin - Clinical pharmacokinetics, 2019 - Springer
Numerous population pharmacokinetic studies on voriconazole have been conducted in
recent years. This review aimed to comprehensively summarize the population …

A physiologically based pharmacokinetic model of voriconazole in human CNS—Integrating time-dependent inhibition of CYP3A4, genetic polymorphisms of …

L Dong, X Zhuang, T Yang, K Yan, Y Cai - International Journal of …, 2024 - Elsevier
Objectives Voriconazole is a classical antifungal drug that is often used to treat CNS fungal
infections due to its permeability through the BBB. However, its clinical use remains …