硫氧还蛋白还原酶
活性氧
光动力疗法
聚集诱导发射
光敏剂
部分
化学
荧光
硫氧还蛋白
癌细胞
光热治疗
组合化学
纳米技术
生物物理学
生物化学
材料科学
癌症
酶
光化学
生物
立体化学
有机化学
物理
量子力学
遗传学
作者
Hang Zou,Jing Zhang,Chang-Meng Wu,Benzhao He,Yubing Hu,Herman H. Y. Sung,Ryan T. K. Kwok,Jacky W. Y. Lam,Lei Zheng,Ben Zhong Tang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2021-05-03
卷期号:15 (5): 9176-9185
被引量:48
标识
DOI:10.1021/acsnano.1c02882
摘要
Gold complexes have been recognized as potential anticancer agents against various kinds of diseases due to their inherent suppressions of antioxidant thioredoxin reductase (TrxR) activity. Herein, a powerful aggregation-induced emission luminogen (AIEgen), TBP-Au, was designed and synthesized by integrating an anticancer Au(I) moiety with an AIE-active photosensitizer (TBP), in which both the production and consumption routes of reactive oxygen species (ROS) were elaborately considered simultaneously to boost the anticancer efficacy. It has been demonstrated that TBP-Au could realize superior two-photon fluorescence imaging in tumor tissues with high resolution and deep penetration as well as long-term imaging in live animals due to its AIE property. In addition, the introduction of a special Au(I) moiety could tune the organelle specificity and efficiently facilitate the ROS-determined photodynamic therapy (PDT). More impressively, TBP-Au could efficiently eliminate cancer cells under light irradiation through the preconceived synergetic approaches from the PDT and the effective suppression of TrxR, demonstrating that TBP-Au holds great potential for precise cancer theranostics.
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