Nerella Sridhar Goud, Singh Priti, Sanam Tulja, Digwal Chander Singh
Department of Neuroimaging and Interventional Radiology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research, Hyderabad, India.
Front Med (Lausanne). 2022 Feb 28;9:812270. doi: 10.3389/fmed.2022.812270. eCollection 2022.
Positron emission tomography with selective radioligands advances the drug discovery and development process by revealing information about target engagement, proof of mechanism, pharmacokinetic and pharmacodynamic profiles. Positron emission tomography (PET) is an essential and highly significant tool to study therapeutic drug development, dose regimen, and the drug plasma concentrations of new drug candidates. Selective radioligands bring up target-specific information in several disease states including cancer, cardiovascular, and neurological conditions by quantifying various rates of biological processes with PET, which are associated with its physiological changes in living subjects, thus it reveals disease progression and also advances the clinical investigation. This study explores the major roles, applications, and advances of PET molecular imaging in drug discovery and development process with a wide range of radiochemistry as well as clinical outcomes of positron-emitting carbon-11 and fluorine-18 radiotracers.
使用选择性放射性配体的正电子发射断层扫描通过揭示有关靶点结合、作用机制证明、药代动力学和药效学特征的信息,推动了药物发现和开发进程。正电子发射断层扫描(PET)是研究治疗性药物开发、给药方案以及新药候选物的药物血浆浓度的重要且极具意义的工具。选择性放射性配体通过用PET量化各种生物过程速率,在包括癌症、心血管和神经疾病等多种疾病状态下提供靶点特异性信息,这些生物过程速率与其在活体受试者中的生理变化相关,从而揭示疾病进展并推进临床研究。本研究探讨了PET分子成像在药物发现和开发过程中的主要作用、应用及进展,涉及广泛的放射化学以及正电子发射碳-11和氟-18放射性示踪剂的临床结果。