Technology - Positron Emission Tomography (PET) Imaging

Positron Emission Tomography Imaging

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Molecules accumulating at a specific target site may be labeled with a positron emitting radionuclide. The emitted positron traverses a short distance until it collides with an electron, annihilating into two gamma rays of 511 KeV. The coincident detection of the two gamma rays that are emitted ˜180 degrees apart from each other can be recorded and used to reconstruct an image showing the location and amount of positron radionuclides in the body of a living subject. PET imaging relies upon clearance of PET probe from non-target site and accumulation of probe at target sites over time.

Positron Emission Tomography Imaging

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PET reporter genes and PET reporter probes enable imaging non-invasively all living mammals regardless of size

  • Transgene expression (Gene therapy monitoring)
  • Endogenous gene expression
  • Cell kinetics (Cell therapy, regenerative medicine and cancer therapy)
  • Protein-protein interactions
  • Signal transduction
  • Pharmacodynamics, or molecular effects of external factors such as administered therapeutic agents

PET Reporter Genes & PET Reporter Probes

  • Enzyme based: PET reporter probe accumulates in cells expressing its PET reporter gene due to entrapment caused by enzyme encoded by PET reporter gene
  • Receptor based: PET reporter probe accumulates on the membrane or inside cells by binding to a protein receptor encoded by the PET reporter gene
  • Transporter based: PET reporter probe accumulates in cells through a transporter protein encoded by the PET reporter gene

Advantages of PET

  • Relatively high sensitivity (highest sensitivity for imaging large animals and humans)
  • Trace dose of imaging probe, unlikely to have pharmacological or toxic effects
  • Quantitative molecular imaging modality makes it suitable for kinetic modeling applications and tracking pharmacokinetics of therapeutic agents
  • PET/CT allows accurate determination of anatomical location of probe activity
  • Very low tissue attenuation (which can be corrected) hence no depth limitation
  • Higher spatial resolution than optical imaging
  • Ability to image metabolism, apoptosis, proliferation, cellular transporters, cell receptors, oxygen availability, gene expression and cell kinetics, non-invasively in living subjects at multiple time points