Novel nanostructured baghdadite-vancomycin scaffolds: in-vitro drug release, antibacterial activity and biocompatibility

One of the most important therapeutic and economic concerns regarding surgery, is the occurrence of post-operative infections which leads to an increase in premature failure rate. Therefore, novel nanostructured baghdadite-vancomycin (Ba-Vac) scaffolds were prepared using the space holder method wit...

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Bibliographic Details
Main Authors: Bakhsheshi-Rad, H. R., Hamzah, E., Ismail, A. F., Aziz, M., Hadisi, Z., Kashefian, M., Najafinezhad, A.
Format: Article
Published: Elsevier B.V. 2017
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Online Access:http://eprints.utm.my/id/eprint/76924/
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85027506537&doi=10.1016%2fj.matlet.2017.08.027&partnerID=40&md5=71a3fa43646f552fca485be3e8905b68
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Institution: Universiti Teknologi Malaysia
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Summary:One of the most important therapeutic and economic concerns regarding surgery, is the occurrence of post-operative infections which leads to an increase in premature failure rate. Therefore, novel nanostructured baghdadite-vancomycin (Ba-Vac) scaffolds were prepared using the space holder method with good mechanical properties and controlled drug release to inhibit post-surgery infections. The results showed that the (Ba-Vac) scaffolds were attained with the pore size of 300–400 µm and total porosity of 80–82% with compressive strength of 0.86–0.88 MPa. In drug release profiles, a burst release was observed for 6 h, followed by a sustained release. Ba-Vac scaffolds presented good antibacterial activity toward Staphylococcus aureus (S. aureus). More attachment and spreading of MG-63 osteoblast cells on the Ba and Ba-(1-3 wt%)Vac scaffolds was also observed in comparison with the Ba-5 wt%Vac scaffold. Therefore, the Ba-(1–3 wt%)Vac scaffold is a good candidate for inhibiting post-surgery infections, as well as for bone tissue engineering.