菁
单线态氧
纳米颗粒
化学
反离子
光化学
光敏剂
生物物理学
纳米技术
氧气
材料科学
离子
有机化学
荧光
物理
量子力学
生物
作者
Yibin Li,Teng Ma,Hao Jiang,Wei Li,Di Tian,Jintao Zhu,Zhong’an Li
出处
期刊:Angewandte Chemie
[Wiley]
日期:2022-03-28
卷期号:61 (24): e202203093-e202203093
被引量:63
标识
DOI:10.1002/anie.202203093
摘要
Abstract Cyanines have been widely used as the photosensitizers (PSs) in the biomedical field, but controlling their molecular aggregates in nanoparticles (NPs) remains a major challenge. Moreover, the impact of aggregate behaviors of cyanines on the photosensitization is still unclear. Herein, the first anionic cyanine PSs based on a tricyanofuran end group have been designed by achieving supramolecular J‐type aggregates in NPs via counterion engineering. Our results indicate that J‐type aggregates in NPs can not only bring significantly red‐shifted emission, negatively charged surface, and high photostability, but also enable a significant 5‐fold increase in singlet oxygen generation efficiency compared to that in the nonaggregate state, providing strong experimental evidence for the superiority of J‐aggregates in enhancing photosensitization. Thus, combined with the mitochondria‐targeting ability, the J‐type aggregate NPs show remarkable in vivo antitumor phototheranostic efficacy, making them have a potential for clinical use.
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