Dual enzyme-like Co–FeSe2 nanoflowers with GSH degradation capability for NIR II-enhanced catalytic tumor therapy

Nanozymes mediated catalytic therapy can produce toxic reactive oxygen species (ROS) and destroy the metabolic balance of tumor cells, providing a new direction for cancer treatment. However, the catalytic efficiency of a single nanozyme is limited by the complexity of the tumor microenvironment (hy...

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Veröffentlicht in:Journal of materials chemistry. B, Materials for biology and medicine Materials for biology and medicine, 2023-05, Vol.11 (19), p.4274-4286
Hauptverfasser: Zhang, Jingge, Enna Ha, Li, Danyang, He, Shuqing, Wang, Luyang, Kuang, Shaolong, Hu, Junqing
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container_end_page 4286
container_issue 19
container_start_page 4274
container_title Journal of materials chemistry. B, Materials for biology and medicine
container_volume 11
creator Zhang, Jingge
Enna Ha
Li, Danyang
He, Shuqing
Wang, Luyang
Kuang, Shaolong
Hu, Junqing
description Nanozymes mediated catalytic therapy can produce toxic reactive oxygen species (ROS) and destroy the metabolic balance of tumor cells, providing a new direction for cancer treatment. However, the catalytic efficiency of a single nanozyme is limited by the complexity of the tumor microenvironment (hypoxia, GSH overexpression, etc.). In order to overcome these problems, we designed flower-like Co-doped FeSe2 (Co–FeSe2) nanozymes by a simple wet chemistry method. Co–FeSe2 nanozymes not only exhibit high POD and OXD-mimicking activities for facile kinetics, but also effectively consume over-expressed glutathione (GSH), inhibiting the consumption of generated ROS and destroying the metabolic balance of the tumor microenvironment. These catalytic reactions trigger cell death through apoptosis and ferroptosis dual pathways. More importantly, under the NIR II laser irradiation, the catalytic activities of Co–FeSe2 nanozymes are boosted, confirming the photothermal and catalytic synergistic tumor therapy. This study takes advantage of self-cascading engineering that offers new ideas for designing efficient redox nanozymes and promoting their clinical translation.
doi_str_mv 10.1039/d3tb00220a
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source Royal Society Of Chemistry Journals
subjects Apoptosis
Cancer therapies
Cell death
Ferroptosis
Glutathione
Hypoxia
Irradiation
Metabolism
Reactive oxygen species
Therapy
Tumor cells
Tumor microenvironment
Tumors
title Dual enzyme-like Co–FeSe2 nanoflowers with GSH degradation capability for NIR II-enhanced catalytic tumor therapy
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