Australian Centre for Pharmacometrics and Sansom Institute, School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, Australia.
Mayne Pharma International, Salisbury South, SA, Australia.
J Pharmacokinet Pharmacodyn. 2018 Apr;45(2):181-197. doi: 10.1007/s10928-017-9555-8. Epub 2017 Nov 17.
The aim of this study was to develop a population in vitro-in vivo pharmacokinetic model that simultaneously describe the absorption and accumulation kinetics of itraconazole (ICZ) and hydroxy-itraconazole (HICZ) in healthy subjects. The model integrated meta-models of gastrointestinal pH and gastrointestinal transit time and in vitro dissolution models of ICZ with the absorption and disposition kinetics of ICZ and HICZ. Mean concentration intravenous data, and single- and multi-dose oral data were used for model development. Model development was conducted in NONMEM in a stepwise manner. First, a model of intravenous data (systemic kinetics) was established and then extended to include the oral data. The latter was then extended to establish the in vitro-in vivo pharmacokinetic model. The systemic disposition of ICZ was best described by a 3-compartment model with oral absorption described by 4-transit compartments and HICZ distribution by a 1-compartment model. ICZ clearance was best described using a mixed inhibition model that allowed HICZ concentrations to inhibit the clearance of parent drug. HICZ clearance was described by Michaelis-Menten elimination kinetics. An in vitro-in vivo model was successfully established for both formulations. The presented model was able to describe ICZ and HICZ plasma concentrations over a wide range of oral and intravenous doses and allowed the exploration of complexities associated with the non-linear ICZ and HICZ kinetics. The model may provide insight into the variability in exposure of ICZ with respect to relating in vivo dissolution characteristics with in vivo disposition kinetics.
本研究旨在开发一种群体的体外-体内药代动力学模型,该模型能够同时描述健康受试者中伊曲康唑(ICZ)和羟基伊曲康唑(HICZ)的吸收和积累动力学。该模型整合了胃肠道 pH 值和胃肠道转运时间的元模型,以及 ICZ 的体外溶解模型,与 ICZ 和 HICZ 的吸收和处置动力学相结合。模型开发使用 NONMEM 分阶段进行。首先,建立静脉内数据(全身动力学)模型,然后扩展到包括口服数据。然后,进一步扩展以建立体外-体内药代动力学模型。ICZ 的全身处置最好通过 3 隔室模型来描述,口服吸收通过 4 个转运隔室来描述,HICZ 分布通过 1 个隔室模型来描述。ICZ 清除最好用混合抑制模型来描述,该模型允许 HICZ 浓度抑制母体药物的清除。HICZ 清除通过 Michaelis-Menten 消除动力学来描述。两种制剂均成功建立了体外-体内模型。所提出的模型能够描述广泛的口服和静脉内剂量的 ICZ 和 HICZ 血浆浓度,并允许探索与 ICZ 和 HICZ 动力学的非线性相关的复杂性。该模型可以深入了解与体内溶解特性与体内处置动力学相关的 ICZ 暴露的变异性。