Radiopharmaceuticals: From Molecular Imaging to Targeted Radionuclide Therapy

Authors

  • P. August Schubiger
  • Jürgen Grünberg
  • Simon Mensah Ametamey
  • Michael Honer
  • Elisa Garcia-Garayoa
  • Peter Bläuenstein
  • Robert Waibel
  • Ilse Novak-Hofer
  • Roger Schibli

DOI:

https://doi.org/10.2533/000942904777677489

Keywords:

Molecular imaging, Pet-tracer, Radioimmunotherapy, Radionuclide therapy, Radiopharmaceuticals

Abstract

The research and development of smart radiodrugs is the goal of the Center of Radiopharmaceutical Science of ETH, PSI, and USZ. Positron Emission Tomography (PET) allows the non-invasive visualization of biochemical processes within the body. Radiolabeled PET-tracers allow the study of neurophysiological diseases like Alzheimer, Parkinson's disease or the imaging of metastatic tumors. PET-techniques are nowadays an important part of routine nuclear medicine diagnosis. Tumor-cell targeting biomolecules (e.g. antibodies or peptides) coupled to therapeutic radionuclides can sterilize the malignant cells while sparing healthy tissue. This so-called targeted radionuclide therapy has made tremendous progress in the recent years and the first approved radiotherapeutics are available for clinical use.

Downloads

Published

2004-10-01

How to Cite

[1]
P. A. Schubiger, J. Grünberg, S. M. Ametamey, M. Honer, E. Garcia-Garayoa, P. Bläuenstein, R. Waibel, I. Novak-Hofer, R. Schibli, Chimia 2004, 58, 731, DOI: 10.2533/000942904777677489.