| Literature DB >> 29191024 |
Emilie M F Billaud1, Sarah Belderbos2, Frederik Cleeren1, Wim Maes3, Marlies Van de Wouwer3, Michel Koole4, Alfons Verbruggen1, Uwe Himmelreich2, Nick Geukens3, Guy Bormans1.
Abstract
In cancer research, pretargeted positron emission tomography (PET) imaging has emerged as an effective two-step approach that combines the excellent target affinity and selectivity of antibodies with the advantages of using short-lived radionuclides such as fluorine-18. One possible approach is based on the bioorthogonal inverse-electron-demand Diels-Alder (IEDDA) reaction between tetrazines and trans-cyclooctene (TCO) derivatives. Here, we report the first successful use of an 18F-labeled small TCO compound, [18F]1 recently developed in our laboratory, to perform pretargeted immuno-PET imaging. The study was performed in an ovarian carcinoma mouse model, using a trastuzumab-tetrazine conjugate.Entities:
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Year: 2017 PMID: 29191024 DOI: 10.1021/acs.bioconjchem.7b00635
Source DB: PubMed Journal: Bioconjug Chem ISSN: 1043-1802 Impact factor: 4.774