Melody Cai‐Syaun WuJack Hau‐Ting WeiRicky Yu‐Syun FanEng Zhi SimKen‐Tye YongTianxun GongKien Voon Kong2024-11-292024-11-292024-10-18https://scholars.lib.ntu.edu.tw/handle/123456789/723398BODIPY analogs are promising photosensitizers for molecular phototherapy; however, they exhibit high dark cytotoxicity and limited singlet oxygen generation capacity. In this study, we developed self-assembled core-shell nanophotosensitizers by linking a bipyridine group to BODIPY (Bpy-BODIPY) and promoting J-aggregation on gold nanourchins. This design enhances photostability and reduces the energy gap between the lowest singlet excited state and the lower triplet state, facilitating efficient singlet oxygen production. We characterized these nanophotosensitizers using UV-visible spectroscopy, transmission electron microscopy (TEM), surface-enhanced Raman spectroscopy (SERS) and dynamic light scattering (DLS), which confirmed the formation of the desired core-shell structure and J-aggregates. Notably, Bpy-BODIPY@Au significantly suppresses tau protein aggregation and enhances neuroprotective action, even in the presence of a phosphatase inhibitor. This work broadens the application of BODIPY chemistry to nanoagents for neuroprotective therapy.enBODIPYGold nanoparticlesPhotosensitizersSinglet oxygenTau proteinjournal article10.1002/cbic.202400562