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Automation of a Positron-emission Tomography (PET) Radiotracer Synthesis Protocol for Clinical Production
1SOFIE, 2Department of Molecular & Medical Pharmacology,David Geffen School of Medicine, University of California, Los Angeles (UCLA), 3Ahmanson Translational Imaging Division,University of California, Los Angeles (UCLA), 4Crump Institute for Molecular Imaging,University of California, Los Angeles (UCLA)
Bölümler
- 00:04Başlık
- 00:53Synthesis Protocol Automation
- 02:13Setup for Automated Synthesis
- 05:25Automated Synthesis, Purification and Formulation, and Post-Run System Shutdown
- 09:10Results: Representative Quality Control Test Data Summary for Three Validation Batches
- 09:33Conclusion
Positron-emission tomography (PET) imaging sites that are involved in multiple early clinical research trials need robust and versatile radiotracer manufacturing capabilities. Using the radiotracer [18F]Clofarabine as an example, we illustrate how to automate the synthesis of a radiotracer using a flexible, cassette-based radiosynthesizer and validate the synthesis for clinical use.
