Crosslinker-Integrated Photocleavable Gelatin-PEG Hydrogel via Bioorthogonal SPAAC Chemistry for UV-Triggered On-Demand Degradation

초록

Light-triggered hydrogel systems offer precise spatiotemporal control over drug release, yet most existing approaches require direct chemical conjugation of a photocleavable linker to the payload, which risks compromising bioactivity and limits applicability to structurally diverse molecules. Here, we report a gelatin-poly(ethylene glycol) (PEG) hybrid hydrogel crosslinked via strain-promoted azide-alkyne cycloaddition (SPAAC) click chemistry, in which an o-nitrobenzyl photocleavable (PC) linker is incorporated into the PEG crosslinker arm rather than conjugated to the drug. Acetylated gelatin-azide (AGA) was synthesized by sequential azide functionalization and amine capping of gelatin, and four-arm PEG-PC-DBCO (4armPEG-PC-DBCO) was prepared by coupling a PC DBCO-PEG4-NHS ester to four-arm PEG amine. Successful incorporation of the azide, DBCO, and o-nitrobenzyl moieties was confirmed by FT-IR spectroscopy, H-1 NMR spectroscopy, and UV-Vis spectrophotometry. Hydrogel formation under physiological conditions (PBS, 37 degrees C) without catalysts or initiators was verified by rheological frequency sweep analysis, which confirmed elastic-dominant behavior (G ' > G ''). Upon irradiation at 365 nm, the crosslinker was cleaved, and rapid network dissolution was observed both macroscopically and by in situ time sweep rheology. This platform enables on-demand, UV-selective hydrogel degradation independently of payload identity, providing a versatile foundation for future controlled drug release applications and dynamic, on-demand degradable scaffolds for tissue engineering.

키워드