posted on 2021-05-03, 16:41authored byHang Zou, Jing Zhang, Changmeng Wu, Benzhao He, Yubing Hu, Herman H. Y. Sung, Ryan T. K. Kwok, Jacky W. Y. Lam, Lei Zheng, Ben Zhong Tang
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.