Carbon-11 Radiopharmaceuticals - Radiopharmacy Aspects

  • C. Halldin
  • S-O. Nilsson
Part of the Developments in Nuclear Medicine book series (DNUM, volume 22)

Abstract

Examples of the routine production of some 11C-labelled PET radiopharmaceuticals which have been set up for patient application are discussed. This includes recommendations and general guidelines for safety and procedures for the a) preparation of the radionuclide and the primary precursors b) synthesis of some secondary precursors c) synthesis, purification, analysis and membrane filtration of some selected 11C-receptor ligands and d) metabolite studies. Furthermore, radiopharmacy aspects as quality assurance and quality control are discussed. The general quality criterias described are the following: a) radionuclidic purity b) chemical purity c) radiochemical purity d) specific radioactivity e) pharmaceutical quality and f) stability and shelf-life.

Keywords

Positron Emission Tomography High Performance Liquid Chromatography Radiochemical Purity Methyl Iodide Ethyl Iodide 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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© Springer Science+Business Media Dordrecht 1992

Authors and Affiliations

  • C. Halldin
  • S-O. Nilsson

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