药效学
医学
水痘带状疱疹病毒
药代动力学
阿昔洛韦
单纯疱疹病毒
药理学
人口
病毒载量
病毒
病毒学
疱疹病毒科
病毒性疾病
环境卫生
作者
Geeske F. Grit,Anne‐Grete Märtson,Marjolein Knoester,Marlous Toren-Wielema,Daan J. Touw
出处
期刊:Pharmaceutics
[MDPI AG]
日期:2022-10-27
卷期号:14 (11): 2311-2311
被引量:2
标识
DOI:10.3390/pharmaceutics14112311
摘要
Background: Acyclovir and valacyclovir are used for the treatment and prophylaxis of infections with herpes simplex virus (HSV) and varicella zoster virus (VZV). The aim of this study is to provide insight into the pharmacodynamics (PD) of (val)acyclovir. Methods: Patients were retrospectively selected, based on therapeutic drug monitoring for acyclovir, to create a population pharmacokinetic (PK) model in Pmetrics. This PK model was used to develop a PK/PD model to study the effect of acyclovir levels on VZV viral load in plasma in immunocompromised patients. Results: Immunocompromised patients with known VZV viral loads in plasma were included for PK/PD modelling (N = 4, with 23 measure points); they were part of the population of 43 patients used for PK model building. The PK/PD model described the data well (r2 = 0.83). This is a hopeful first step in clarifying the pharmacodynamics of acyclovir; however, the data in this study are limited. Conclusions: Our preliminary PK/PD model can be used in further research to determine the effect of acyclovir levels on VZV viral load.
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