Journal
INORGANICA CHIMICA ACTA
Volume 363, Issue 6, Pages 1316-1319Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.ica.2010.01.038
Keywords
Copper-64; PET; Radiopharmaceuticals; Bis(thiosemicarbazones)
Categories
Funding
- Medical Research Council [G0001237, G9439390, G0600986] Funding Source: researchfish
- National Institute for Health Research [NF-SI-0508-10327] Funding Source: researchfish
- MRC [G9439390, G0001237, G0600986] Funding Source: UKRI
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To facilitate the development of PET radiopharmaceuticals labelled with the positron-emitting radioisotope copper-64 (t(1/2) = 12.7 h) we have developed a fully automated method for its regular productions. Using the Ni-64(p,n) Cu-64 nuclear reaction applied on a 16.5 MeV PETtrace cyclotron the radioisotope is generated in good yields (up to 2 GBq at end-of-synthesis) within 4 h irradiations on nickel-64 (99.6% enrichment) plated onto a gold disk. Based on ion exchange chromatography an automated method has been devised for efficient extraction of the copper-64 in good radionuclide and chemical purity, with ICP-OES analysis determining the concentration of the copper to be 0.14-1.5 ppm. The specific radioactivities of the copper-64 at end-of-synthesis were calculated to be 9.62-77 GB/mu mol. The copper-64 radioisotope obtained from this method was then applied to the radiosynthesis of the hypoxia markers, Cu-64-ATSM and Cu-64-ATSE, which were obtained in good radiochemical yields of >95%. (C) 2010 Elsevier B.V. All rights reserved.
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