Novel Antibacterial and Bioactive Silicate Glass Nanoparticles for Biomedical Applications
Source abstract
Abstract
In this work, the authors propose a new quick sol–gel procedure for bioglass nanoparticles production containing 10% mol of silver (AgBGs). These new AgBGs are characterized by Zeta potential analysis, scanning electron microscopy with X‐ray microanalysis (SEM/EDS), X‐ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and microbiological tests to confirm their bioactive and antibacterial properties. SEM shows that the average particle size is less than 200 nm and EDS confirms the successful incorporation of Ag2O in the bioglass matrix. XRD confirms the amorphous nature of the AgBGs and, after SBF immersion, reveals their bioactive behavior with the presence of crystalline phase of calcium silicate and phosphorus oxide, which are also detected by FTIR analysis. FTIR also confirms the formation of typical siloxane bonds resulting from the condensation of silicate glass. Lastly, it is found that the developed AgBGs has an antibacterial effect against two different types of bacteria, thus demonstrating their ability to reduce the bacterial infection within 16 h.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Bone Tissue Engineering Materials · Facial Trauma and Fracture Management · Medical and Biological Ozone Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
3B's Research Group − Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine. AvePark 4805‐017 Barco Guimarães Portugal
Life and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho 4701‐057 Braga Portugal
References (29)
Show source-provided references
1. 10.1039/b910960a10.1039/b910960a ↗
2. 10.1002/adma.20070318310.1002/adma.200703183 ↗
3. 10.1016/S1359-0286(97)80053-810.1016/S1359-0286(97)80053-8 ↗
4. 10.1007/s10856-006-0432-z10.1007/s10856-006-0432-z ↗
5. 10.1016/j.ceramint.2011.05.15810.1016/j.ceramint.2011.05.158 ↗
6. 10.1146/annurev.micro.50.1.75310.1146/annurev.micro.50.1.753 ↗
7. 10.1023/A:101323152943910.1023/A:1013231529439 ↗
8. 10.1023/A:100881150173410.1023/A:1008811501734 ↗
9. 10.1002/1097-4636(20000905)51:3<484::AID-JBM24>3.0.CO;2-410.1002/1097-4636(20000905)51:3<484::AID-JBM24>3.0.CO;2-4 ↗
10. Crabtree J. H. · Perit. Dial. Int · 2003 · 23 · 36810.1177/089686080302300410 ↗
11. 10.1111/j.1067-1927.2004.012304.x10.1111/j.1067-1927.2004.012304.x ↗
12. 10.1002/mabi.20080005310.1002/mabi.200800053 ↗
13. 10.1016/j.actbio.2014.04.03010.1016/j.actbio.2014.04.030 ↗
14. 10.1016/j.biomaterials.2005.01.03810.1016/j.biomaterials.2005.01.038 ↗
15. 10.1002/1097-4636(20001215)52:4<662::AID-JBM10>3.0.CO;2-310.1002/1097-4636(20001215)52:4<662::AID-JBM10>3.0.CO;2-3 ↗
16. 10.3390/ma904022510.3390/ma9040225 ↗
17. 10.1007/s10973-009-0086-410.1007/s10973-009-0086-4 ↗
18. 10.4028/www.scientific.net/KEM.192-195.59710.4028/www.scientific.net/KEM.192-195.597 ↗
19. 10.1016/j.msec.2011.10.01510.1016/j.msec.2011.10.015 ↗
20. 10.3390/ma606229510.3390/ma6062295 ↗
21. Sambale F. · J. Nanomater · 2015 · 2015 · 9
22. 10.1088/0957-4484/22/49/49401410.1088/0957-4484/22/49/494014 ↗
23. 10.1007/s11051-013-1457-010.1007/s11051-013-1457-0 ↗
24. 10.1039/C6TB00841K10.1039/C6TB00841K ↗
25. 10.1016/j.biomaterials.2006.01.01710.1016/j.biomaterials.2006.01.017 ↗
26. 10.1016/j.ceramint.2011.03.02610.1016/j.ceramint.2011.03.026 ↗
27. 10.1002/(SICI)1097-4636(200007)51:1<80::AID-JBM11>3.0.CO;2-610.1002/(SICI)1097-4636(200007)51:1<80::AID-JBM11>3.0.CO;2-6 ↗
28. 10.1166/jnn.2009.38910.1166/jnn.2009.389 ↗
29. 10.1016/j.resmic.2011.04.00910.1016/j.resmic.2011.04.009 ↗