1.State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, 130012, China
2.Department of Vascular Surgery of China-Japan Union Hospital, Jilin University, Changchun, 130031, China
3.College of Basic Medical Sciences, Jilin University, Changchun, 130021, China
4.Department of Laboratory Animals, College of Animal Sciences, Jilin University, Changchun, 130062, China
5.State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, 130022, China
Zhuo Liu (lzhuo@jlu.edu.cn)
Bing Zhao (zhaob@jlu.edu.cn)
Wei Song (weisong@jlu.edu.cn)
纸质出版日期:2022-10-31,
网络出版日期:2022-09-30,
收稿日期:2022-03-10,
修回日期:2022-08-01,
录用日期:2022-08-23
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SERS monitoring of photoinduced-enhanced oxidative stress amplifier on Au@carbon dots for tumor catalytic therapy[J]. LSA, 2022,11(10):2492-2502.
Li, L. J. et al. SERS monitoring of photoinduced-enhanced oxidative stress amplifier on Au@carbon dots for tumor catalytic therapy. Light: Science & Applications, 11, 2492-2502 (2022).
SERS monitoring of photoinduced-enhanced oxidative stress amplifier on Au@carbon dots for tumor catalytic therapy[J]. LSA, 2022,11(10):2492-2502. DOI: 10.1038/s41377-022-00968-5.
Li, L. J. et al. SERS monitoring of photoinduced-enhanced oxidative stress amplifier on Au@carbon dots for tumor catalytic therapy. Light: Science & Applications, 11, 2492-2502 (2022). DOI: 10.1038/s41377-022-00968-5.
Currently
artificial enzymes-based photodynamic therapy (PDT) is attractive due to its efficient capacity to change the immunosuppressive tumor microenvironment (TME). It is of great significance to study the therapeutic mechanism of novel artificial enzymes in TME through a monitoring strategy and improve the therapeutic effect. In this study
Au@carbon dots (Au@CDs) nanohybrids with a core-shell structure are synthesized
which not only exhibit tunable enzyme-mimicking activity under near-infrared (NIR) light
but also excellent surface-enhanced Raman scattering (SERS) properties. Therefore
Au@CDs show a good capability for monitoring NIR-photoinduced peroxidase-like catalytic processes via a SERS strategy in tumor. Moreover
the Au@CDs deplete glutathione with the cascade catalyzed reactions
thus elevating intratumor oxidative stress amplifying the reactive oxygen species damage based on the NIR-photoinduced enhanced peroxidase and glutathione oxidase-like activities
showing excellent and fast PDT therapeutic effect promoted by photothermal property in 3 min
finally leading to apoptosis in cancer cells. Through SERS monitoring
it is further found that after removing the NIR light source for 33 min
the reactive oxygen species (ROS) activity of the TME is counteracted and eliminated due to the presence of glutathione. This work presents a guidance to rationally design of artificial enzyme for ROS-involved therapeutic strategies and a new spectroscopic tool to evaluate the tumor catalytic therapy.
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