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基于生理的药代动力学模型在预测药物转运体作用中的应用:科学与监管视角

The Application of Physiologically Based Pharmacokinetic Modeling to Predict the Role of Drug Transporters: Scientific and Regulatory Perspectives.

作者信息

Pan Yuzhuo, Hsu Vicky, Grimstein Manuela, Zhang Lei, Arya Vikram, Sinha Vikram, Grillo Joseph A, Zhao Ping

机构信息

Office of Clinical Pharmacology, Office of Translational Sciences, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, MD, USA.

Current affiliation: Office of Generic Drugs, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, MD, USA.

出版信息

J Clin Pharmacol. 2016 Jul;56 Suppl 7:S122-31. doi: 10.1002/jcph.740.

Abstract

Transporters play an important role in drug absorption, disposition, and drug action. The evaluation of drug transporters requires a comprehensive understanding of transporter biology and pharmacology. Physiologically based pharmacokinetic (PBPK) models may offer an integrative platform to quantitatively evaluate the role of drug transporters and its interplay with other drug disposition processes such as passive drug diffusion and elimination by metabolizing enzymes. To date, PBPK modeling and simulations integrating drug transporters lag behind that for drug-metabolizing enzymes. In addition, predictive performance of PBPK has not been well established for predicting the role of drug transporters in the pharmacokinetics of a drug. To enhance overall predictive performance of transporter-based PBPK models, it is necessary to have a detailed understanding of transporter biology for proper representation in the models and to have a quantitative understanding of the contribution of transporters in the absorption and metabolism of a drug. This article summarizes PBPK-based submissions evaluating the role of drug transporters to the Office of Clinical Pharmacology of the US Food and Drug Administration.

摘要

转运体在药物吸收、处置及药物作用过程中发挥着重要作用。对药物转运体的评估需要全面了解转运体生物学和药理学知识。基于生理学的药代动力学(PBPK)模型可为定量评估药物转运体的作用及其与其他药物处置过程(如被动药物扩散和代谢酶消除)之间的相互作用提供一个综合平台。迄今为止,整合药物转运体的PBPK建模与模拟落后于针对药物代谢酶的相关研究。此外,PBPK在预测药物转运体在药物药代动力学中的作用方面,其预测性能尚未得到充分确立。为提高基于转运体的PBPK模型的整体预测性能,有必要详细了解转运体生物学以便在模型中进行恰当表述,同时还需定量了解转运体在药物吸收和代谢中的贡献。本文总结了向美国食品药品监督管理局临床药理学办公室提交的基于PBPK评估药物转运体作用的相关材料。

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