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基于生理学的药物纳米颗粒药代动力学(PBPK)建模

Physiologically Based Pharmacokinetic (PBPK) Modeling of Pharmaceutical Nanoparticles.

作者信息

Li Min, Zou Peng, Tyner Katherine, Lee Sau

机构信息

Office of Pharmaceutical Quality, US Food and Drug Administration, Silver Spring, Maryland, USA.

Office of Clinical Pharmacology, US Food and Drug Administration, Silver Spring, Maryland, USA.

出版信息

AAPS J. 2017 Jan;19(1):26-42. doi: 10.1208/s12248-016-0010-3. Epub 2016 Nov 10.

Abstract

With the great interests in the discovery and development of drug products containing nanoparticles, there is a great demand of quantitative tools for assessing quality, safety, and efficacy of these products. Physiologically based pharmacokinetic (PBPK) modeling and simulation approaches provide excellent tools for describing and predicting in vivo absorption, distribution, metabolism, and excretion (ADME) of nanoparticles administered through various routes. PBPK modeling of nanoparticles is an emerging field, and more than 20 PBPK models of nanoparticles used in pharmaceutical products have been published in the past decade. This review provides an overview of the ADME characteristics of nanoparticles and how these ADME processes are described in PBPK models. Recent advances in PBPK modeling of pharmaceutical nanoparticles are summarized. The major challenges in model development and validation and possible solutions are also discussed.

摘要

随着对含纳米颗粒药物产品的发现和开发产生了浓厚兴趣,对评估这些产品的质量、安全性和有效性的定量工具也有巨大需求。基于生理的药代动力学(PBPK)建模和模拟方法为描述和预测通过各种途径给药的纳米颗粒在体内的吸收、分布、代谢和排泄(ADME)提供了出色的工具。纳米颗粒的PBPK建模是一个新兴领域,在过去十年中已发表了20多个用于药品的纳米颗粒PBPK模型。本综述概述了纳米颗粒的ADME特性以及这些ADME过程在PBPK模型中是如何描述的。总结了药物纳米颗粒PBPK建模的最新进展。还讨论了模型开发和验证中的主要挑战以及可能的解决方案。

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