Kinetic modeling in pre-clinical positron emission tomography

Z Med Phys. 2014 Dec;24(4):274-85. doi: 10.1016/j.zemedi.2014.02.003. Epub 2014 Mar 12.

Abstract

Pre-clinical positron emission tomography (PET) has evolved in the last few years from pure visualization of radiotracer uptake and distribution towards quantification of the physiological parameters. For reliable and reproducible quantification the kinetic modeling methods used to obtain relevant parameters of radiotracer tissue interaction are important. Here we present different kinetic modeling techniques with a focus on compartmental models including plasma input models and reference tissue input models. The experimental challenges off deriving the plasma input function in rodents and the effect of anesthesia are discussed. Finally, in vivo application of kinetic modeling in various areas of pre-clinical research is presented and compared to human data.

Keywords: Kompartiment-Modelle; Plasma-Input-Modelle; Positron emission tomography (PET); Positronen-Emissions-Tomographie (PET); Quantifizierung; Referenzregion-Modelle; compartmental models; kinetic modeling; kinetische Modellierung; plasma input models; quantification; reference tissue input models.

Publication types

  • Review

MeSH terms

  • Animals
  • Computer Simulation
  • Humans
  • Image Interpretation, Computer-Assisted / methods*
  • Kinetics
  • Metabolic Clearance Rate
  • Models, Biological*
  • Organ Specificity
  • Positron-Emission Tomography / methods*
  • Radiopharmaceuticals / blood*
  • Radiopharmaceuticals / pharmacokinetics*
  • Species Specificity
  • Tissue Distribution

Substances

  • Radiopharmaceuticals