Development of F-18-labeled radiotracers for neuroreceptor imaging with positron emission tomography

作者：Brust Peter^*; van den Hoff Joerg; Steinbach Joerg

来源：Neuroscience Bulletin, 2014, 30(5): 777-811.

DOI：10.1007/s12264-014-1460-6

• Alzheimer's disease
• autoradiography
• blood-brain barrier
• brain tumor
• cholinergic system
• kinetic modeling
• metabolism
• molecular imaging
• neurodegeneration
• positron emission tomography
• precursor
• psychiatric disorder
• radiotracer
• sigma receptor

Positron emission tomography (PET) is an in vivo molecular imaging tool which is widely used in nuclear medicine for early diagnosis and treatment follow-up of many brain diseases. PET uses biomolecules as probes which are labeled with radionuclides of short half-lives, synthesized prior to the imaging studies. These probes are called radiotracers. Fluorine-18 is a radionuclide routinely used in the radiolabeling of neuroreceptor ligands for PET because of its favorable half-life of 109.8 min. The delivery of such radiotracers into the brain provides images of transport, metabolic, and neurotransmission processes on the molecular level. After a short introduction into the principles of PET, this review mainly focuses on the strategy of radiotracer development bridging from basic science to biomedical application. Successful radiotracer design as described here provides molecular probes which not only are useful for imaging of human brain diseases, but also allow molecular neuroreceptor imaging studies in various small-animal models of disease, including genetically-engineered animals. Furthermore, they provide a powerful tool for in vivo pharmacology during the process of pre-clinical drug development to identify new drug targets, to investigate pathophysiology, to discover potential drug candidates, and to evaluate the pharmacokinetics and pharmacodynamics of drugs in vivo.

• 出版日期2014-10