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健康成年人全血、外周血单个核细胞和中性粒细胞中阿奇霉素的群体药代动力学。

Population pharmacokinetics of azithromycin in whole blood, peripheral blood mononuclear cells, and polymorphonuclear cells in healthy adults.

机构信息

Division of Pharmacotherapy and Experimental Therapeutics, University of North Carolina Eshelman School of Pharmacy, Chapel Hill, North Carolina, USA.

1] Division of Pharmacotherapy and Experimental Therapeutics, University of North Carolina Eshelman School of Pharmacy, Chapel Hill, North Carolina, USA [2] Clinical Pharmacology Modeling and Simulation, GlaxoSmithKline, Research Triangle Park, North Carolina, USA.

出版信息

CPT Pharmacometrics Syst Pharmacol. 2014 Mar 5;3(3):e103. doi: 10.1038/psp.2013.80.

Abstract

Azithromycin's extensive distribution to proinflammatory cells, including peripheral blood mononuclear cells (PBMCs) and polymorphonuclear cells (PMNs), may be important to its antimicrobial and anti-inflammatory properties. The need to simultaneously predict azithromycin concentrations in whole blood ("blood"), PBMCs, and PMNs motivated this investigation. A single-dose study in 20 healthy adults was conducted, and nonlinear mixed effects modeling was used to simultaneously describe azithromycin concentrations in blood, PBMCs, and PMNs (simultaneous PK model). Data were well described by a four-compartment mamillary model. Apparent central clearance and volume of distribution estimates were 67.3 l/hour and 336 l (interindividual variability of 114 and 122%, respectively). Bootstrapping and visual predictive checks showed adequate model performance. Azithromycin concentrations in blood, PBMCs, and PMNs from external studies of healthy adults and cystic fibrosis patients were within the 5th and 95th percentiles of model simulations. This novel empirical model can be used to predict azithromycin concentrations in blood, PBMCs, and PMNs with different dosing regimens.

摘要

阿奇霉素广泛分布于促炎细胞,包括外周血单核细胞(PBMC)和多形核细胞(PMN),这可能对其抗菌和抗炎特性很重要。需要同时预测全血(“血液”)、PBMC 和 PMN 中的阿奇霉素浓度,这促使了这项研究。在 20 名健康成年人中进行了一项单剂量研究,并使用非线性混合效应模型同时描述血液、PBMC 和 PMN 中的阿奇霉素浓度(同时 PK 模型)。数据通过四个隔室乳突模型得到了很好的描述。表观中心清除率和分布容积估计值分别为 67.3 l/h 和 336 l(个体间变异性分别为 114%和 122%)。自举和可视化预测检查表明模型性能良好。来自健康成年人和囊性纤维化患者的外部研究中血液、PBMC 和 PMN 中的阿奇霉素浓度在模型模拟的第 5 和第 95 百分位数范围内。这种新的经验模型可用于预测不同给药方案下血液、PBMC 和 PMN 中的阿奇霉素浓度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82d2/4039392/5d2c0fb6ff44/psp201380f1.jpg

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