Cyclopeptidic photosensitizer prodrugs as proteolytically triggered drug delivery systems of pheophorbide A: part I – self-quenched prodrugs. Issue 11 (14th September 2018)

• Record Type: Journal Article
• Authors: Bouilloux, Jordan; Yuschenko, Oleksandr; Dereka, Bogdan; Boso, Gianluca; Zbinden, Hugo; Vauthey, Eric; Babič, Andréj; Lange, Norbert
• Is Part Of: Photochemical & photobiological sciences. Volume 17:Issue 11(2018)
• Page Start: 1728
• Page End: 1738
• Publication Date: 2018-09-14
• Subjects: Photochemistry -- Periodicals; Photobiology -- Periodicals; 541.35
• DOI: 10.1039/c8pp00317c
• Languages: English
• ISSNs: 1474-905X

Abstract

Abstract : RAFTs bearing multiple copies of pheophorbide A allow perfectly defined photosensitizer prodrugs. Abstract : Herein, we report the synthesis of a new prodrug system consisting of regioselectively addressable functionalized templates bearing multiple pheophorbide A moieties for use in photodynamic therapy. These coupling reactions were achieved using copper-free "click" chemistry, namely a strain-promoted azide–alkyne cycloaddition. This new design was used to obtain well-defined quenched photosensitizer prodrugs with perfect knowledge of the number and position of loaded photosensitizers, providing structures bearing up to six photosentitizers and two PEG chains. These conjugates are ideally quenched in their native state regarding their fluorescence emission (up to 155 ± 28 times less fluorescent for an hexasubstituted conjugate than a monosubstituted non-quenched reference compound) or singlet oxygen production (decreased 8.7-fold in the best case) when excited. After 2 h of proteolytic activation, the fluorescence emission of a tetrasubstituted conjugate was increased 17-fold compared with the initial fluorescence emission.