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Appl Radiat Isot ; 140: 294-299, 2018 Oct.
Article in English | MEDLINE | ID: mdl-30098587

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 ±â€¯5.3 GBq/µmol (0.86 ±â€¯0.14 mCi/nmol) (n = 3) at the end of synthesis. Radiochemical purity was greater than 98%, and total synthesis time was ~90 min.


Subject(s)
Fluorine Radioisotopes/chemistry , Glucagon-Like Peptide 1/analogs & derivatives , Maleimides/chemistry , Maleimides/chemical synthesis , Radiopharmaceuticals/chemistry , Radiopharmaceuticals/chemical synthesis , Animals , Chromatography, High Pressure Liquid , Glucagon-Like Peptide 1/chemical synthesis , Glucagon-Like Peptide 1/chemistry , Glucagon-Like Peptide 1/standards , Maleimides/standards , Peptides/chemistry , Proteins/chemistry , Quality Control , Radiochemistry/instrumentation , Radiochemistry/methods , Radiopharmaceuticals/standards , Sulfhydryl Reagents/chemical synthesis , Sulfhydryl Reagents/chemistry
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