| Literature DB >> 26308650 |
Lu Wang1, Orit Jacobson2, Din Avdic1, Benjamin H Rotstein1, Ido D Weiss3, Lee Collier1, Xiaoyuan Chen4, Neil Vasdev5, Steven H Liang6.
Abstract
Azido (18) F-arenes are important and versatile building blocks for the radiolabeling of biomolecules via Huisgen cycloaddition ("click chemistry") for positron emission tomography (PET). However, routine access to such clickable agents is challenged by inefficient and/or poorly defined multistep radiochemical approaches. A high-yielding direct radiofluorination for azido (18) F-arenes was achieved through the development of an ortho-oxygen-stabilized iodonium derivative (OID). This OID strategy addresses an unmet need for a reliable azido (18) F-arene clickable agent for bioconjugation reactions. A ssDNA aptamer was radiolabeled with this agent and visualized in a xenograft mouse model of human colon cancer by PET, which demonstrates that this OID approach is a convenient and highly efficient way of labeling and tracking biomolecules.Entities:
Keywords: PET imaging; aptamers; bioconjugation; fluorine; radiopharmaceuticals
Mesh:
Substances:
Year: 2015 PMID: 26308650 PMCID: PMC4698351 DOI: 10.1002/anie.201505927
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336