Self-Assembled BODIPY@Au Core-Shell Structures for Durable Neuroprotective Phototherapy.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Melody Cai-Syaun Wu, Jack Hau-Ting Wei, Ricky Yu-Syun Fan, Eng Zhi Sim, Ken-Tye Yong, Tianxun Gong, Kien Voon Kong
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引用次数: 0

Abstract

BODIPY 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.

用于持久神经保护光疗的自组装 BODIPY@Au 核壳结构。
BODIPY 类似物是很有希望用于分子光疗的光敏剂;然而,它们表现出较高的暗细胞毒性和有限的单线态氧生成能力。在这项研究中,我们开发了自组装核壳纳米光敏剂,方法是在 BODIPY 上连接一个联吡啶基团(Bpy-BODIPY),并促进 J 在纳米金上聚集。这种设计提高了光稳定性,并缩小了最低单线激发态与较低三线态之间的能隙,从而促进了单线态氧的高效产生。值得注意的是,即使在磷酸酶抑制剂存在的情况下,Bpy-BODIPY@Au 也能显著抑制 tau 蛋白的聚集并增强神经保护作用。这项工作拓宽了 BODIPY 化学在神经保护疗法纳米试剂方面的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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