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Fabrication of Ti3C2 MXene Microelectrode Arrays for In Vivo Neural Recording
Published on: February 12, 2020
Surface-Engineered Titanium Carbide MXenzyme Boosts ROS-Scavenging and Anti-Inflammation Activities for Inflammatory
Shuying He1, Jingnan Qiu1, Heqing Tao1
1Department of Gastroenterology, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, Guangdong, China.
This study introduces novel nanoparticles (TTCM) that reduce oxidative stress and inflammation, effectively treating inflammatory bowel disease (IBD) in mice by rebalancing immune cells and strengthening the gut barrier.
Area of Science:
- Biomedical Engineering
- Immunology
- Nanotechnology
Background:
- Inflammatory bowel disease (IBD) involves chronic intestinal inflammation linked to M1/M2 macrophage imbalance.
- Reactive oxygen species (ROS) and mitochondrial dysfunction exacerbate IBD severity.
Purpose of the Study:
- To develop a novel ROS-scavenging nanocarrier system for IBD treatment.
- To modulate macrophage polarization from pro-inflammatory M1 to anti-inflammatory M2 phenotypes.
Main Methods:
- Synthesized titanium carbide (Ti3C2) and mannose-modified trimethyl chitosan to form TTCM nanoparticles.
- Evaluated TTCM biocompatibility, stability in gastrointestinal fluids, and in vitro effects on ROS, mitochondrial potential, and inflammatory pathways.
- Assessed TTCM efficacy in a dextran sulfate sodium (DSS)-induced acute colitis mouse model.
Main Results:
- TTCM nanoparticles demonstrated excellent biocompatibility and stability.
- In vitro studies showed TTCM reduced ROS, restored mitochondrial function, increased SOD activity, and suppressed the TLR4/NF-κB pathway, promoting M1 to M2 macrophage repolarization.
- TTCM enhanced antioxidant efficacy and intestinal barrier function.
- In vivo experiments confirmed TTCM's anti-inflammatory and protective effects, mitigating IBD progression.
Conclusions:
- Oral delivery of ROS-scavenging TTCM nanoparticles shows significant therapeutic potential for IBD.
- This strategy effectively treats IBD by targeting oxidative stress and macrophage imbalance.
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