Synthesis of nanotubular oxide on Ti–24Zr–10Nb–2Sn as a drug-releasing system to prevent the growth of Staphylococcus aureus
The aim in the present study was to explore the potential application of titanium nanotubes developed in the Ti–24Zr–10Nb–2Sn alloy, as drug delivery systems to prevent bacterial infections in medical devices. A nanotubular oxide layer was synthesized by electrochemical anodizing on the Ti–24Zr–10Nb...
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Veröffentlicht in: | Chemical papers 2021-06, Vol.75 (6), p.2441-2450 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The aim in the present study was to explore the potential application of titanium nanotubes developed in the Ti–24Zr–10Nb–2Sn alloy, as drug delivery systems to prevent bacterial infections in medical devices. A nanotubular oxide layer was synthesized by electrochemical anodizing on the Ti–24Zr–10Nb–2Sn superelastic alloy and the electrical variables that control the growth at constant potential were determined. Scanning electron microscopy (SEM) showed that the nanostructures show a positive linear growth as a function of the applied potential, the superficial analysis carried out by X-ray photoelectron spectroscopy (XPS) showed different states of valence evidencing the presence of TiO
2
, Nb
2
O
5
, SnO
2,
and ZrO
2
. FTIR spectra confirm the presence of the antibiotic gentamicin in the Ti–24Zr–10Nb–2Sn nanotubes. The developed nanostructures were evaluated in a phosphate buffer solution (PBS) as a controlled release system of antibiotics. It was observed by bacteriological tests that the nanostructured morphology in combination with the chemical composition has bacteriostatic properties; while the release of the antibiotic-loaded inside the nanotubes had a bactericidal effect. The results showed that it is possible to grow and control the morphology of the developed nanostructures on Ti–24Zr–10Nb–2Sn, which can be used for orthopedic purposes to transport and control the local release of molecules like antibiotics at the site of interest and thus prevent postoperative infections.
Graphic abstract |
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ISSN: | 2585-7290 0366-6352 1336-9075 |
DOI: | 10.1007/s11696-020-01495-6 |