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Current Radiopharmaceuticals

Volume 4 Issue 2
ISSN: 1874-4710
eISSN: 1874-4729

 

   All Titles

  Recent Advances in Copper Radiopharmaceuticals
  pp.109-121 (13) Authors: Guiyang Hao, Ajay N. Singh, Orhan K. Oz, Xiankai Sun
doi: 10.2174/1874471011104020109
 
 
      Abstract

Copper has five radioisotopes (60Cu, 61Cu, 62Cu, 64Cu, and 67Cu) that can be used in copper radiopharmaceuticals. These radioisotopes decay by mixed emissions of β+, β-, and γ with a wide range of half-lives from 9.74 min (62Cu) to 2.58 d (67Cu), which enable the design and synthesis of a variety of radiopharmaceuticals for different biomedical applications in diagnostic and therapeutic nuclear medicine. However, due to the availability and production cost, the research efforts in copper radiopharmaceuticals are mainly focused on the use of 64Cu (t1/2 = 12.7 h; 17.4% β+, 43% EC, 39% β-), a radioisotope with low positron energy (E β+max = 0.656 MeV) that is ideal for positron emission tomography (PET) imaging quantification and β- emissions along with Auger electron for radiotherapy. Driven by the ever-increasing availability of preclinical and clinical PET scanners, a considerable interest has been seen in the development of novel copper radiopharmaceuticals in the past decade for a variety of diseases as represented by PET imaging of cancer. To avoid unnecessary literature redundancy, this review focuses on the unrepresented research aspects of copper chemistry (e.g. electrochemistry) and their uses in the evaluation of novel nuclear imaging probe design and recent advances in the field towards the practical use of copper radiopharmaceuticals.

 
  Keywords: Copper radioisotope, bifunctional chelator, multivalent effect, non-standard PET nuclide, imaging probe, immuno-PET, radioimmunoconjugate, PET, molecular imaging, Chemistry of Copper
  Affiliation: Department of Radiology and Advanced Imaging Research Center, University of Texas Southwestern Medical Center at Dallas, 2201 Inwood Road, Texas 75390-8542, USA.
 
  Key: New Content Free Content Open Access Plus Subscribed Content

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