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生物治疗药物和药物靶点的组织生物分析以支持药代动力学/药效学。

Tissue bioanalysis of biotherapeutics and drug targets to support PK/PD.

作者信息

Neubert Hendrik, Fountain Scott, King Lindsay, Clark Tracey, Weng Yan, O'Hara Denise M, Li Wenlin, Leung Sheldon, Ray Chad, Palandra Joe, Ocaña Mireia Fernández, Chen Jianqing, Ji Chengjie, Wang Mengmeng, Long Kimberly, Gorovits Boris, Fluhler Eric

机构信息

Pharmacokinetics Dynamics & Metabolism, Pfizer Inc., 1 Burtt Road, Andover, MA 01810, USA.

出版信息

Bioanalysis. 2012 Nov;4(21):2589-604. doi: 10.4155/bio.12.234.

Abstract

Contemporary drug discovery leverages quantitative modeling and simulation with increasing emphasis, both to gain deeper knowledge of drug targets and mechanisms as well as improve predictions between preclinical models and clinical applications, such as first-in-human dose projections. Proliferation of novel biotherapeutic modalities increases the need for applied PK/PD modeling as a quantitative tool to advance new therapies. Of particular relevance is the understanding of exposure, target binding and associated pharmacology at the target site of interest. Bioanalytical methods are key to informing PK/PD models and require assessment of both PK and PD end points. Where targets are sequestered in tissues (noncirculating), the ability to quantitatively measure drug or biomarker in tissue compartments becomes particularly important. This perspective provides an overview of contemporary applications of quantitative bioanalysis in tissue compartments as applied to PK and PD assessments associated with novel biotherapeutics. Case studies and key references are provided.

摘要

当代药物研发越来越重视利用定量建模和模拟,以更深入地了解药物靶点和作用机制,并改善临床前模型与临床应用之间的预测,例如首次人体给药剂量预测。新型生物治疗方式的不断涌现,增加了应用药代动力学/药效学(PK/PD)建模作为推进新疗法的定量工具的需求。特别重要的是要了解在感兴趣的靶点部位的暴露情况、靶点结合及相关药理学。生物分析方法是为PK/PD模型提供信息的关键,需要对PK和PD终点进行评估。当靶点存在于组织中(非循环状态)时,定量测量组织隔室中的药物或生物标志物的能力就变得尤为重要。本文概述了定量生物分析在组织隔室中的当代应用,这些应用适用于与新型生物治疗相关的PK和PD评估。文中提供了案例研究和关键参考文献。

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