Dual enzyme-like Co-FeSe 2 nanoflowers with GSH degradation capability for NIR II-enhanced catalytic tumor therapy.
Jingge ZhangEnna HaDanyang LiShuqing HeLuyang WangShaolong KuangJunqing HuPublished in: Journal of materials chemistry. B (2023)
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 FeSe 2 (Co-FeSe 2 ) nanozymes by a simple wet chemistry method. Co-FeSe 2 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-FeSe 2 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.
Keyphrases
- cell death
- reactive oxygen species
- fluorescent probe
- crystal structure
- photodynamic therapy
- cell cycle arrest
- dna damage
- oxidative stress
- quantum dots
- mental health
- endothelial cells
- drug release
- stem cells
- cancer therapy
- cell proliferation
- radiation therapy
- mass spectrometry
- high resolution
- endoplasmic reticulum stress
- highly efficient
- bone marrow
- metal organic framework
- transcription factor
- gold nanoparticles