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Positron Emission Tomography (PET) is an imaging modality
that allows visualization of physiological, biochemical and pharmacological
functions in living animals and humans using radiopharmaceuticals labeled with
positron emitting nuclides. Direct quantitative information on the
pharmacokinetics of drugs, their therapeutic and toxic effects can be obtained.
Commonly used positron emitting radionuclides are oxygen-15, nitrogen-13, carbon-11
and fluorine-18 with half-lives of 2, 10, 20 and 110 minutes, respectively.
Other longer-lived positron emitting isotopes such as bromine-76, and copper-64
are also sometimes employed. Until recently, PET studies were limited to humans
and large animals such as dogs, monkeys and pigs due to the spatial resolution
of the existing PET scanners. Now, new commercial PET scanners fully dedicated
to small laboratory animals such as mice and rats are available. A specific
advantage of using small animal PET scanners is the possibility to study animal
models of disease, perform fast, dynamic studies and also longitudinal studies
to follow disease progression in the same animal. The main goal of this group
is the development of specific PET radioligands for diagnostic application in
neurology, oncology and cardiology.
Keywords:
Molecular Imaging, PET radiopharmaceuticals, Drug Development, GMP-validation
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