Brunner Martin, Müller Markus
Department of Clinical Pharmacology, Division of Clinical Pharmacokinetics, University of Vienna Medical School, Allgemeines Krankenhaus, Währinger Gürtel 18-20, 1090 Vienna, Austria.
Eur J Clin Pharmacol. 2002 Jul;58(4):227-34. doi: 10.1007/s00228-002-0475-0. Epub 2002 May 23.
Microdialysis (MD) is a catheter-based sampling method that provides the opportunity to directly study tumor drug exposure and metabolism in a minimally invasive way. Tumor drug exposure, which is directly linked to clinical outcome, may be substantially reduced due to diffusion barriers in solid tumors. Therefore plasma drug profiles are frequently inappropriate for predicting outcome in oncology. This contribution focuses on the application of MD in preclinical and clinical oncological research and presents an overview of the current literature. It is concluded that MD, in combination with pharmacokinetic/pharmacodynamic modeling, has the potential to contribute to the design of optimal treatment schedules and to select appropriate drug candidates, doses, and dosing intervals for established and new anticancer drugs.
微透析(MD)是一种基于导管的采样方法,它提供了以微创方式直接研究肿瘤药物暴露和代谢的机会。与临床结果直接相关的肿瘤药物暴露,可能会因实体瘤中的扩散障碍而大幅降低。因此,血浆药物谱通常不适用于预测肿瘤学中的结果。本文着重探讨MD在临床前和临床肿瘤学研究中的应用,并对当前文献进行综述。得出的结论是,MD与药代动力学/药效学建模相结合,有潜力为优化治疗方案的设计做出贡献,并为已有的和新的抗癌药物选择合适的候选药物、剂量和给药间隔。