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      PET tracers based on (86)Y.

      1 , , ,
      Current radiopharmaceuticals

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          Abstract

          Positron emission tomography (PET) has become a powerful tool for probing biochemical processes in living subjects. PET imaging depends largely on the development of novel PET tracers labeled with positron-emitting radionuclides. Since the four traditional PET isotopes (18F, 11C, 13N, and 15O) are produced in a cyclotron and are short-lived, their use for long-term observation of biological processes in vivo is limited. In the last decades, extensive research in the development of other unconventional radionuclides (such as 64Cu, 68Ga, 89Zr, 86Y, and 124I) labeled tracers with half-lives complementary to the biological properties of their targeting agents has been conducted. Among these tracers, 86Y-based PET tracers have gained increasing attention since they are ideal surrogates for in vivo determination of biodistribution and dosimetry of therapeutic 90Y (pure β - emitter) pharmaceuticals. In this review article, we will brief introduce the physical characteristics, production, and radiochemistry of 86Y, and will summarize the current 86Y-based PET tracers used for molecular imaging and cancer detection in animal studies and in clinical trials.

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          Author and article information

          Journal
          Curr Radiopharm
          Current radiopharmaceuticals
          1874-4729
          1874-4710
          Apr 2011
          : 4
          : 2
          Affiliations
          [1 ] Medical Isotopes Research Center, Peking University, Beijing, China.
          Article
          CRP-4-2-122
          10.2174/1874471011104020122
          22191651
          09e3c342-5201-4eab-a899-0cc29bc23e18
          History

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