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The theranostic nanoagent Mo2C for multi-modal imaging-guided cancer synergistic phototherapyElectronic supplementary information (ESI) available: STEM image and EDX spectra, H&E staining, hematological data, calculation of singlet oxygen quantum yield and photothermal conversion efficiency, cytotoxicity tests, in vitroPA and CT imaging results, and biodegradation tests. See DOI: 10.1039/c9bm00239a

Authors :
ZhangEqual contribution from Q. Zhang, Qun
Huang., W. C.
Huang, Weicheng
Yang, Chunyu
Wang, Fei
Song, Chuanqi
Gao, Yan
Qiu, Yunfeng
Yan, Mei
Yang, Bin
Guo, Chongshen
Source :
Biomaterials Science; 2019, Vol. 7 Issue: 7 p2729-2739, 11p
Publication Year :
2019

Abstract

Multifunctional theranostic platforms, especially single component-based platforms, enable both cancer treatment and real-time imaging as well as enhance the efficiency of treatment. In this study, 50 nm Mo2C nanospheres were explored as a “one-for-all” theranostic agent. The light-harvesting of Mo2C covered the entire near infrared region, and NIR irradiation concurrently triggered hyperthermia and reactive oxygen species (ROS) production; thus, synergistic outcomes of photothermal and photodynamic therapy could be realized. Both in vitroand in vivoexperiments have confirmed the superiority of the synergistic phototherapy in killing cancer cells and removing solid tumors; moreover, Mo2C proposed herein has been proven to be applicable as a photoacoustic imaging and CT imaging contrast agent for in vivotumor depiction; furthermore, Mo2C demonstrates excellent biocompatibility, showing minimal hematotoxicity and tissue toxicity. A theoretical simulation performed by density functional theory revealed that the metallic character and the interband/intraband transition of Mo2C accounted for its broad photoabsorption. The antitumor mechanism of Mo2C was investigated on a solid tumor by B-mode ultrasonography (US) and magnetic resonance imaging (MRI), revealing a typical liquefactive necrosis process; hence, herein, the dual-imaging guided phototherapy was efficiently mediated by Mo2C.

Details

Language :
English
ISSN :
20474830 and 20474849
Volume :
7
Issue :
7
Database :
Supplemental Index
Journal :
Biomaterials Science
Publication Type :
Periodical
Accession number :
ejs50413173
Full Text :
https://doi.org/10.1039/c9bm00239a