Issue 35, 2021

Boosting the photothermal performance of vacancy-rich MoSe2−x nanoflowers for photoacoustic imaging guided tumor chemo-photothermal therapy

Abstract

Due to the relatively low photo-thermal conversion efficiency and poor tumor targeting capacity, phototheranostic nanoagents encounter some challenges in cancer photothermal therapy. To address this problem, in the current research we developed vacancy-rich MoSe2−x (0 ≤ x ≤ 1) nanoflowers (MNFs) with molecular 2-deoxy-D-glucose (2-DG) as the activity target, which could be used as a novel phototheranostic nanoagent in the photoacoustic imaging guided chemo-photothermal synergistic therapy. This selenium-deficient structure endows MNFs with high photothermal conversion efficiency (41.7%) due to the strong localized surface plasmon resonances. Besides, the surface linked 2-DG molecules and the flower-like morphology in the nanoagents promoted the targeting effect (active and passive), thus facilitating the efficient concentration of the nanoagents within the tumor site. Both in vitro and in vivo anti-tumor experiments have demonstrated the high synergistic efficacy promoted by MNFs and complete tumor eradication with lower administration dosages could be achieved. This rational design of nanoparticles not only provided the paradigm of high therapeutic efficacy of a chemo-photothermal protocol for precise cancer theranostics, but also expanded the scope of nanomedical applications using semiconductor-based nanoplatforms through well-defined designing of their microstructures and physiochemical properties.

Graphical abstract: Boosting the photothermal performance of vacancy-rich MoSe2−x nanoflowers for photoacoustic imaging guided tumor chemo-photothermal therapy

Supplementary files

Article information

Article type
Paper
Submitted
24 May 2021
Accepted
21 Jul 2021
First published
27 Jul 2021

Nanoscale, 2021,13, 14960-14972

Boosting the photothermal performance of vacancy-rich MoSe2−x nanoflowers for photoacoustic imaging guided tumor chemo-photothermal therapy

F. Gao, Y. Miao, H. Ma, T. Zhang, H. Fan and L. Zhao, Nanoscale, 2021, 13, 14960 DOI: 10.1039/D1NR03306A

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