| Literature DB >> 31280104 |
Zonghua Luo1, Jiwei Gu1, Robert C Dennett1, Gregory G Gaehle1, Joel S Perlmutter2, Delphine L Chen1, Tammie L S Benzinger1, Zhude Tu3.
Abstract
Automated synthesis of a radiopharmaceutical 3-((2-fluoro-4-(5-(2'-methyl-2-(trifluoromethyl)-[1,1'-biphenyl]-4-yl)-1,2,4-oxadiazol-3-yl)benzyl) (methyl-11C)amino)propanoic acid ([11C]CS1P1) for PET imaging sphingosine-1 phosphate receptor 1 (S1P1) was accomplished by a two-step-one-pot procedure in a Siemens CTI methylation automated module using TR-19 cyclotron. The synthesis of [11C]CS1P1 was successfully validated under current Good Manufacturing Practices (cGMP) conditions, resulting in a consistent average radiochemical yield of ∼15%, molar activity of ∼3129 GBq/μmol (decay corrected to end of bombardment, EOB), and radiochemical purity > 95%. The radiopharmaceutical product meets all quality control criteria for human use for an Investigational New Drug (IND) application to permit human studies.Entities:
Keywords: Automation; Positron emission tomography; Radiopharmaceutical; Sphingosine-1 phosphate receptor 1; [(11)C]CS1P1
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Year: 2019 PMID: 31280104 PMCID: PMC6708718 DOI: 10.1016/j.apradiso.2019.06.029
Source DB: PubMed Journal: Appl Radiat Isot ISSN: 0969-8043 Impact factor: 1.513