Development of 6-[ 18 F]fluoro-carbohydrate-based prosthetic groups and their conjugation to peptides via click chemistry

Abstract : This work describes the development of new 6-[18F]fluoro-carbohydrate-based prosthetic groups equipped with an azido arm that are able to participate in copper(I)-catalyzed cycloadditions for 18F labeling of biomolecules under mild conditions. The radiolabeling in high radiochemical yields (up to 68 ± 6%) of these different prosthetic groups is presented. The flexibility of the azido arm introduced on the carbohydrate moieties allows efficient click reactions with different alkyne functionalized peptides such as gluthation or Arg-Gly-Asp derivatives in order to prepare glycopeptides. The radiosyntheses of 18F-labeled glycopeptides proceed in high radiochemical yields (up to 76%) in an automated process with excellent radiochemical purity. The addition of a sugar moiety on peptides should enhance the bioavailability, pharmacokinetic, and in vivo clearance properties of these glycopeptides, compared with the unlabeled native peptide, and these properties are highly favorable for positron emission tomography imaging. A high uptake of 18F-β-gluco-c(RGDfC) is shown by positron emission tomography imaging in a subcutaneous abscess model in the rat, revealing the potential of this tracer to monitor integrin expression as a part of inflammation and/or angiogenesis processes.
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Journal of Labelled Compounds and Radiopharmaceuticals, Wiley-Blackwell, 2015, 59 (2), pp.54 - 62. 〈10.1002/jlcr.3362〉
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Soumis le : lundi 27 mars 2017 - 10:43:32
Dernière modification le : jeudi 22 mars 2018 - 15:49:47

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Charlotte Collet, Fatiha Maskali, Alexandra Clément, Françoise Chrétien, Sylvain Poussier, et al.. Development of 6-[ 18 F]fluoro-carbohydrate-based prosthetic groups and their conjugation to peptides via click chemistry. Journal of Labelled Compounds and Radiopharmaceuticals, Wiley-Blackwell, 2015, 59 (2), pp.54 - 62. 〈10.1002/jlcr.3362〉. 〈hal-01496012〉

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