Properties And Antibacterial Effectiveness Of Metal-ion Doped Borate-based Bioactive Glasses
Abstract
Bioactive glasses (BGs) are physiologically reactive surface biomaterials widely used in biomedical applications and various treatments. Borate bioactive glasses (BBGs) are third-generation BGs, and they exhibit superior biodegradable, bioactive, osteoconductive, antibacterial, and biocompatible properties compared to other types of BGs. Certain concentrations of dopant ions can be incorporated into the chemical structure of BBGs to enhance their biological functionalities and antimicrobial properties. It was demonstrated that those ions play a crucial role in the biological responsiveness in vitro and in vivo once in contact with a physiological environment. The dissolution products of ion-doped BBGs were noted in their ability to stimulate gene expression related to cell differentiation and proliferation, promote angiogenesis, display anti-inflammatory effects, and inhibit bacterial growth within a few hours. Thus, metal-ion-doped BBGs address several limitations encountered by biomedical, tissue engineering, and infection control applications. Considering the research studies on BBGs to date, this review aims to analyze metal-ion-doped BBGs based on their primary antibacterial properties and effectiveness.
Recommended Citation
S. Fakher and D. J. Westenberg, "Properties And Antibacterial Effectiveness Of Metal-ion Doped Borate-based Bioactive Glasses," Future Microbiology, Taylor and Francis Group; Taylor and Francis, Jan 2025.
The definitive version is available at https://doi.org/10.1080/17460913.2025.2470029
Department(s)
Biological Sciences
Second Department
Chemical and Biochemical Engineering
Keywords and Phrases
antibacterial; Borate bioactive glasses; HAP; metal dopant; metal-ion
International Standard Serial Number (ISSN)
1746-0921; 1746-0913
Document Type
Article - Journal
Document Version
Final Version
File Type
text
Language(s)
English
Rights
© 2025 The Authors, All rights reserved.
Creative Commons Licensing
This work is licensed under a Creative Commons Attribution-Noncommercial 4.0 License
Publication Date
01 Jan 2025
PubMed ID
40079871