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正电子发射断层成像在药物发现中的应用。

Positron emission tomographic imaging in drug discovery.

机构信息

Lee Kong Chian School of Medicine, Nanyang Technological University, 59 Nanyang Drive, Singapore 636921, Singapore.

Lee Kong Chian School of Medicine, Nanyang Technological University, 59 Nanyang Drive, Singapore 636921, Singapore; Cognitive Neuroimaging Centre, 59 Nanyang Drive, Nanyang Technological University, Singapore 636921, Singapore.

出版信息

Drug Discov Today. 2022 Jan;27(1):280-291. doi: 10.1016/j.drudis.2021.07.025. Epub 2021 Jul 28.

Abstract

Positron emission tomography (PET) is an extensively used nuclear functional imaging technique, especially for central nervous system (CNS) and oncological disorders. Currently, drug development is a lengthy and costly pursuit. Imaging with PET radiotracers could be an effective way to hasten drug discovery and advancement, because it facilitates the monitoring of key facets, such as receptor occupancy quantification, drug biodistribution, pharmacokinetic (PK) analyses, validation of target engagement, treatment monitoring, and measurement of neurotransmitter concentrations. These parameters demand careful analyses for the robust appraisal of newly formulated drugs during preclinical and clinical trials. In this review, we discuss the usage of PET imaging in radiopharmaceutical development; drug development approaches with PET imaging; and PET developments in oncological and cardiac drug discovery.

摘要

正电子发射断层扫描(PET)是一种广泛应用于核医学的功能成像技术,尤其适用于中枢神经系统(CNS)和肿瘤疾病的诊断。目前,药物研发是一项漫长而昂贵的工作。使用 PET 放射性示踪剂进行成像可能是加速药物发现和进展的有效方法,因为它有助于监测关键方面,如受体占有率定量、药物生物分布、药代动力学(PK)分析、靶标结合验证、治疗监测以及神经递质浓度的测量。这些参数需要进行仔细分析,以在临床前和临床试验中对新配方药物进行稳健评估。在本文中,我们将讨论 PET 成像在放射性药物开发中的应用、使用 PET 成像的药物开发方法以及在肿瘤和心脏药物发现中的 PET 发展。

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