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炎症:转化研究中药代动力学/药效动力学变异性的来源规划。

Inflammation: planning for a source of pharmacokinetic/pharmacodynamic variability in translational studies.

机构信息

Department of Clinical Pharmacology/Modeling and Simulation, GlaxoSmithKline, Research Triangle Park, North Carolina, USA.

出版信息

Clin Pharmacol Ther. 2010 Apr;87(4):488-91. doi: 10.1038/clpt.2009.258. Epub 2010 Feb 10.

Abstract

The impact of inflammation on variability in the pharmacokinetics (PK) and pharmacodynamics (PD) of drugs should be considered in the design, analysis, and interpretation of clinical pharmacology studies. Data suggest that the metabolism and transport of drugs, as well as the expression of receptors, may change in the presence of inflammation. The clinical implications of these changes are not straightforward; they may vary depending on whether the inflammation is active or controlled and may change with time and successful treatment of the inflammation.

摘要

在设计、分析和解释临床药理学研究时,应考虑炎症对药物药代动力学(PK)和药效动力学(PD)变异性的影响。有数据表明,在炎症存在的情况下,药物的代谢和转运以及受体的表达可能会发生变化。这些变化的临床意义并不简单;它们可能因炎症是活跃的还是得到控制的而有所不同,并且可能随时间和炎症的成功治疗而变化。

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