PET radiotracer

PET radiotracer is a type of radioligand that is used for the diagnostic purposes via positron emission tomography imaging technique.[1][2]

PET radiotracer
A carbon-11 labelled radiopharmaceutical
SynonymsPET-ligand
Purposeused for diagnosis in combination with PET

Mechanism
A fully automated radiosynthesis interface of PET-radiotracers

PET is a functional imaging technique that produces a three-dimensional image of functional processes in the body. The system detects pairs of gamma rays emitted indirectly by a positron-emitting radionuclide (tracer), which is introduced into the body on a biologically active molecule.[3]

Pharmacology

In in vivo systems it is often used to quantify the binding of a test molecule to the binding site of radioligand. The higher the affinity of the molecule the more radioligand is displaced from the binding site and the increasing radioactive decay can be measured by scintillography. This assay is commonly used to calculate binding constant of molecules to receptors. Due to the probable injuries of PET-radiotracers, they could not be administrated in the normal doses of the medications. Therefore, the binding affinity (PKD) of the PET-tracers must be high. In addition, since via the PET imaging technique is desired to investigate a function accurately, the selectivity of bindings to the specific targets is very important.[1]

See also

References
  1. Wadsak Wolfgang, Mitterhauser Markus (2010). "Basics and principles of radiopharmaceuticals for PET/CT". European Journal of Radiology. 73 (3): 461–469. doi:10.1016/j.ejrad.2009.12.022. PMID 20181453.
  2. Bailey, D.L; D.W. Townsend; P.E. Valk; M.N. Maisey (2005). Positron Emission Tomography: Basic Sciences. Secaucus, NJ: Springer-Verlag. ISBN 1-85233-798-2.
  3. Carlson, Neil (January 22, 2012). Physiology of Behavior. Methods and Strategies of Research. 11th edition. Pearson. p. 151. ISBN 978-0205239399.
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