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Automated Radiochemical Synthesis of [18F]3F4AP: A Novel PET Tracer for Imaging Demyelinating Diseases
Published on: May 29, 2017
Synthesis of ligand-functionalized water-soluble [18F]YF3 nanoparticles for PET imaging
Liqin Xiong1, Bin Shen, Deepak Behera
1Stanford Molecular Imaging Program (MIPS), Department of Radiology, Stanford University, Stanford, CA 94305-5484, USA. xiongliqin@sjtu.edu.cn
Abstract:
We report a simple, efficient synthesis of novel (18)F-labeled imaging agents based on YF3 nanoparticles. Targeting ligands and antitumor drug molecules can be introduced onto the YF3 nanoparticles in a one-pot synthesis. The (18)F-labeling reaction proceeds in aqueous solutions at room temperature with excellent radiolabeling yields (>80%) in a very short time (5-10 min). (18)F-labeled YF3 nanoparticles displayed high stability in mouse and human serum, and their application for mapping lymph nodes in live rats after local injection has also been demonstrated.

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