This book describes methods and procedures for conducting radiochemical reactions to prepare radiopharmaceuticals that are used in positron emission tomography (PET) imaging. Also highlighted in this volume are new methods for working with carbon-11 (C11) and fluorine-18 (F18), which are two of the most commonly used radionuclides in PET imaging. The reactions include solid-phase radiochemistry, transition-metal catalyzed radiochemistry, microfluidics, click chemistry, green radiochemistry and new strategies for radiopharmaceutical quality control. These detailed monographs provide readers the necessary information needed to reproduce these synthetic reactions and quality control methods in their own labs.
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Titolo: Radiochemical Syntheses : Further Radiopharmaceuticals for Positron Emission Tomography ( PET ) and New Strategies for Their Production
Autori: Scott - Kilbourn
Finitura: Copertina rigida
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