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开发低分子量的 PET 和 SPECT 成像剂。

Developing Low Molecular Weight PET and SPECT Imaging Agents.

机构信息

Monash Institute of Pharmaceutical Sciences, Monash University, 381 Royal Parade Parkville, Victoria 3052, Australia.

ETH Zürich, Department of Chemistry and Applied Biosciences Center for Radiopharmaceutical Sciences, Vladimir-Prelog Weg 1-5/10, 8093, Zürich, Switzerland.

出版信息

ChemMedChem. 2024 Aug 1;19(15):e202400094. doi: 10.1002/cmdc.202400094. Epub 2024 May 22.

Abstract

Imaging agents for positron emission tomography (PET) and single-photon emission computerized tomography (SPECT) have shown their utility in many situations, answering clinical questions related to drug development and medical considerations. The discovery and development of imaging agents follow a well-understood process, with variations related to available starting points and to the envisaged imaging application. This article describes the general development path leading from the expression of an imaging need and project initiation to a clinically usable imaging agent. The definition of the project rationale, the design and optimization of early leads, and the assessment of the imaging potential of an imaging agent candidate are followed by preclinical and clinical development activities that differ from those required for therapeutic agents. These include radiolabeling with a positron emitter and first-in-human clinical studies, to rapidly evaluate the ability of a new imaging agent to address the questions it was designed to answer.

摘要

正电子发射断层扫描(PET)和单光子发射计算机断层扫描(SPECT)的成像剂在许多情况下都显示出了它们的效用,能够回答与药物开发和医学考虑相关的临床问题。成像剂的发现和开发遵循一个众所周知的过程,其变化与可用的起点和预期的成像应用有关。本文描述了从表达成像需求和项目启动到临床可用成像剂的一般开发路径。该路径包括项目基本原理的定义、早期先导化合物的设计和优化,以及候选成像剂的成像潜力评估,然后是临床前和临床开发活动,这与治疗剂所需的开发活动不同。这些活动包括用正电子发射体进行放射性标记,以及进行首例人体临床研究,以快速评估新的成像剂解决其设计所要回答的问题的能力。

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