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To investigate the antibacterial effect, mechanism, and cytotoxicity of Prussian blue/Cerium dioxide (PB/CeO) nanoparticles against Enterococcus faecalis (E. faecalis) and biofilm. PB/CeO nanoparticles were synthesized and characterized. The antibacterial mechanism of nanoparticles was explored through peroxidase (POD) activity assay, hydroxyl radicals (·OH) detection, and measurement of bacterial reactive oxygen species (ROS) and glutathione (GSH)/glutathione disulfide (GSSG) levels. The biocompatibility of PB/CeO was evaluated by Cell Counting Kit-8 (CCK-8) assay and histological examination of the major visceral organs of rats. The antibacterial effect of PB/CeO was assessed using the colony-forming unit (CFU) method. The impact of PB/CeO on E. faecalis biofilm on dentin slices was further observed with CLSM and SEM. ANOVA and t-test were applied for statistical analysis (p < 0.05). PB/CeO demonstrated significant antibacterial activity against E. faecalis, mainly when used with HO, significantly enhancing its antibacterial effect and effectively disrupting E. faecalis biofilms on dentin slices. PB/CeO nanoparticles catalyzed ROS production, disrupting the antioxidant defense system of E. faecalis cells, damaging bacterial cell membranes, and ultimately causing bacterial death. PB/CeO nanoparticles exhibit good biocompatibility at appropriate concentrations in vivo and in vitro. The novel multifunctional nanocomposite shows great antibacterial effects against E. faecalis and its biofilm, with low cytotoxicity and good biocompatibility, offering a novel disinfection strategy for root canal treatment.
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http://dx.doi.org/10.1002/jbm.b.35646 | DOI Listing |
J Biomed Mater Res B Appl Biomater
September 2025
Department of Endodontics, The Affiliated Stomatological Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
To investigate the antibacterial effect, mechanism, and cytotoxicity of Prussian blue/Cerium dioxide (PB/CeO) nanoparticles against Enterococcus faecalis (E. faecalis) and biofilm. PB/CeO nanoparticles were synthesized and characterized.
View Article and Find Full Text PDFSci Rep
August 2025
School of Physical Sciences, Amrita Vishwa Vidyapeetham, Mysuru Campus, Mysuru, 570 026, Karnataka, India.
The rising levels of environmental contamination and oxidative stress disorders have led to a growing demand for multifunctional nanomaterials that possess both biomedical and catalytic importance. CeO nanoparticles (NPs) were synthesized using a green solution combustion method involving Ficus carica F. extract, followed by an evaluation of their structural, biological, and photocatalytic properties.
View Article and Find Full Text PDFAntioxidants (Basel)
May 2025
College of Coastal Agricultural Sciences, Guangdong Ocean University, Zhanjiang 524088, China.
The widespread use of lead (Pb) has led to serious environmental and human health problems worldwide. The application of oxide nanoparticles (CeO NPs) in alleviating abiotic stress in plants has received extensive attention. In this study, 50 mg·L CeO NPs can improve Pb resistance and promote rice growth.
View Article and Find Full Text PDFSensors (Basel)
April 2025
Hunan Engineering Research Center of Water Security Technology and Application, College of Civil Engineering, Hunan University, Changsha 410082, China.
Excessive levels of heavy metal pollutants in the environment pose significant threats to human health and ecosystem stability. Consequently, the accurate and rapid detection of heavy metal ions is critically important. A AgNPs@CeO/Nafion composite was prepared by dispersing nano-ceria (CeO) in a Nafion solution and incorporating silver nanoparticles (AgNPs).
View Article and Find Full Text PDFNeuro Oncol
June 2025
Department of Oncology, McGill University, Montreal, QC, Canada.
Background: Glioblastoma is an aggressive brain cancer with a 5-year survival rate of 5-10%. Current therapeutic options are limited, due in part to drug exclusion by the blood-brain barrier, restricting access of targeted drugs to the tumor. The receptor for the type 1 insulin-like growth factor (IGF-1R) was identified as a therapeutic target in glioblastoma.
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