| Literature DB >> 30098587 |
Keunpoong Lim1, Jim Ropchan2, Dale O Kiesewetter3, Xiaoyuan Chen3, Yiyun Huang2.
Abstract
In the process of developing [18F]FBEM coupled target peptide, we have instituted a robust automated synthesis of [18F]FBEM, a sulfhydryl (-SH) site specific agent for radiolabeling of peptides and proteins. The radiosynthesis generated 1.67-3.89 GBq (45.1-105.1 mCi, 7.5-18.8% non-decay corrected yield) of [18F]FBEM from 22.2 GBq (600 mCi) of starting [18F]fluoride with molar activity of 31.8 ± 5.3 GBq/µmol (0.86 ± 0.14 mCi/nmol) (n = 3) at the end of synthesis. Radiochemical purity was greater than 98%, and total synthesis time was ~90 min.Entities:
Keywords: Automation; PET; Radiotracer synthesis; Thiol(-SH)-specific; [(18)F]FBEM
Mesh:
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Year: 2018 PMID: 30098587 PMCID: PMC6119497 DOI: 10.1016/j.apradiso.2018.07.033
Source DB: PubMed Journal: Appl Radiat Isot ISSN: 0969-8043 Impact factor: 1.513