期刊
PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS
卷 197, 期 9, 页码 964-972出版社
TAYLOR & FRANCIS LTD
DOI: 10.1080/10426507.2022.2049267
关键词
Silica; nanoparticle; modification; drug delivery; antibacterial material
资金
- Canakkale Onsekiz Mart University [FYL-2019-3106]
In this study, monodispersed silica nanoparticles were synthesized and modified to achieve drug release and antibacterial properties. The modified nanoparticles exhibited controlled drug release behavior and showed antibacterial activity against various bacteria.
In this study, monodispersed silica nanoparticles were synthesized using the Stober method. The synthesized nanoparticles underwent a range of surface modifications and were converted to nanoparticles with drug release and antibacterial features. For modification, firstly -NH2 groups were created on the silica nanoparticle surface using (3-Aminopropyl)triethoxysilane (APTES). In the second stage, hexachlorocyclotriphosphazene (Phz) molecules were bound to the silica nanoparticle surfaces due to these amino groups. In the final stage of modification, the chloride groups in the hexachlorocyclotriphosphazene structure were modified with trimethoprim (TMP) and nanoparticles with antibacterial properties were obtained. The modified silica nanoparticles were characterized with scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), Fourier transform infrared spectroscopy (FT-IR), Transmission Electron Microscopy (TEM), and Thermogravimetric analysis (TGA). The silica-based nanoparticles were used for release of rhodamine 6G, chosen as a model drug. As a result of the drug release studies, the modified silica nanoparticles were found to abide by the Korsmeyer-Peppas low power model and non-Fickian release mechanism as release model. Additionally, nanoparticles both loaded and not loaded with the model drug were determined to have antibacterial properties against Escherichia coli, Bacillus subtilis, and Staphylococcus aureus bacteria.
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