An impressive variety of new methodologies for the preparation of 18 F-labelled tracers and
ligands has appeared over the last decade. Most strategies of the newly developed …

Incorporation of [18F] fluorine into PET radiotracer structure has traditionally been
accomplished via nucleophilic pathways. The [18F] fluoride is generated in an aqueous …

New radiolabeled probes for positron-emission tomography (PET) are providing an ever-
increasing ability to answer diverse research and clinical questions and to facilitate the …

Positron emission tomography (PET) has proven to be an invaluable tool in the staging and
management of disease in oncology; however,[18F] fluorodeoxyglucose ([18F] FDG) …

Recent droplet-based radiochemistry platforms have enabled reactions in< 10 µL volumes,
providing many advantages including minimal reagent consumption, fast synthesis times …

Microfluidic techniques are increasingly being used to synthesize positron-emitting
radiopharmaceuticals. Several reports demonstrate higher incorporation yields, with shorter …

Electrochemical fluorination of methyl (phenylthio) acetate was achieved using
tetrabutylammonium fluoride (TBAF). Electrochemical fluorination was performed under …

This review addresses progress in the radionuclide diagnosis of oncological diseases using
radiopharmaceutical preparations (RPP) based on labeled glucose derivatives. Most …

The pathogenesis of many socially significant diseases such as neurodegenerative
dementias and neuroendocrine tumours involves imbalance of neurotransmitters. Among …

Одним из основных условий, определяющих успешное применение технологий
ядерной медицины, является получение и введение пациенту …