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
标识
DOI:10.1002/anie.202203093
摘要
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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