Simplification of Methods for PET Radiopharmaceutical Syntheses

[摘要] In an attempt to develop simplified methods for radiochemical synthesis of radiopharmaceuticals useful in Positron Emission Tomography (PET), current commercially available automated synthesis apparati were evaluated for use with solid phase synthesis, thin-film techniques, microwave-accelerated chemistry, and click chemistry approaches. Using combinations of these techniques, it was shown that these automated synthesis systems can be simply and effectively used to support the synthesis of a wide variety of carbon-11 and fluorine-18 labeled compounds, representing all of the major types of compounds synthesized and using all of the common radiochemical precursors available. These techniques are available for use to deliver clinically useful amounts of PET radiopharmaceuticals with chemical and radiochemical purities and high specific activities, suitable for human administration.

[发布日期] 2011-12-27 [发布机构] University of Michigan, Ann Arbor, MI

[关键词] 60 Applied Life Sciences Positron, Radiopharmaceutical, Synthesis;Positron, Radiopharmaceutical, Synthesis