Synthesis of novel nanostructured bredigite-amoxicillin scaffolds for bone defect treatment: cytocompatibility and antibacterial activity

Bone infections in human beings are an essentially destructive problem with crucial clinical and economic effects; thus, incorporation of antibiotics such as amoxicillin (AMX) into the scaffold was developed as an effective treatment for bone infections. In this respect, we develop new nanostructure...

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Main Authors: Rad, H. R. Bakhsheshi, Hamzah, E., Abbasizadeh, N., Najafinezhad, A., Kashefian, M.
Format: Article
Published: Springer New York LLC 2018
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Online Access:http://eprints.utm.my/id/eprint/85582/
http://dx.doi.org/10.1007/s10971-018-4606-1
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Institution: Universiti Teknologi Malaysia
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spelling my.utm.855822020-06-30T08:53:56Z http://eprints.utm.my/id/eprint/85582/ Synthesis of novel nanostructured bredigite-amoxicillin scaffolds for bone defect treatment: cytocompatibility and antibacterial activity Rad, H. R. Bakhsheshi Hamzah, E. Abbasizadeh, N. Najafinezhad, A. Kashefian, M. TJ Mechanical engineering and machinery Bone infections in human beings are an essentially destructive problem with crucial clinical and economic effects; thus, incorporation of antibiotics such as amoxicillin (AMX) into the scaffold was developed as an effective treatment for bone infections. In this respect, we develop new nanostructured bredigite (Bre; Ca7MgSi4O16)–amoxicillin (AMX; α-amino-hydroxybenzyl-penicillin) scaffolds containing different concentrations of amoxicillin (0, 3, 5, and 10%) by using space holder method to assure bactericidal properties. The result depicted that the Bre–AMX scaffolds possess porosity of 80–82% with high compressive strength of 1.2–1.4 MPa and controlled antibiotic release for prevention of infection. Bre–(3–10%)AMX scaffolds were able to destroy Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) bacteria, as well as effectively inhibit the growth of bacterial cells; in addition, the antibacterial activity of the AMX-loaded scaffolds augmented with the increase of the AMX concentration. Sustained drug release was detected from Bre–AMX scaffolds accompanied by initial burst release of 20% for 8 h, followed by a sustained release, which is favorable for bone infection treatment. These new Bre–(3–5%)AMX scaffolds possess excellent mechanical properties and antibacterial activity with no cytotoxicity suggested as an appropriate alternative for bone infection treatment. Springer New York LLC 2018-04 Article PeerReviewed Rad, H. R. Bakhsheshi and Hamzah, E. and Abbasizadeh, N. and Najafinezhad, A. and Kashefian, M. (2018) Synthesis of novel nanostructured bredigite-amoxicillin scaffolds for bone defect treatment: cytocompatibility and antibacterial activity. Journal of Sol-Gel Science and Technology, 86 (1). pp. 83-93. ISSN 0928-0707 http://dx.doi.org/10.1007/s10971-018-4606-1
institution Universiti Teknologi Malaysia
building UTM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Malaysia
content_source UTM Institutional Repository
url_provider http://eprints.utm.my/
topic TJ Mechanical engineering and machinery
spellingShingle TJ Mechanical engineering and machinery
Rad, H. R. Bakhsheshi
Hamzah, E.
Abbasizadeh, N.
Najafinezhad, A.
Kashefian, M.
Synthesis of novel nanostructured bredigite-amoxicillin scaffolds for bone defect treatment: cytocompatibility and antibacterial activity
description Bone infections in human beings are an essentially destructive problem with crucial clinical and economic effects; thus, incorporation of antibiotics such as amoxicillin (AMX) into the scaffold was developed as an effective treatment for bone infections. In this respect, we develop new nanostructured bredigite (Bre; Ca7MgSi4O16)–amoxicillin (AMX; α-amino-hydroxybenzyl-penicillin) scaffolds containing different concentrations of amoxicillin (0, 3, 5, and 10%) by using space holder method to assure bactericidal properties. The result depicted that the Bre–AMX scaffolds possess porosity of 80–82% with high compressive strength of 1.2–1.4 MPa and controlled antibiotic release for prevention of infection. Bre–(3–10%)AMX scaffolds were able to destroy Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) bacteria, as well as effectively inhibit the growth of bacterial cells; in addition, the antibacterial activity of the AMX-loaded scaffolds augmented with the increase of the AMX concentration. Sustained drug release was detected from Bre–AMX scaffolds accompanied by initial burst release of 20% for 8 h, followed by a sustained release, which is favorable for bone infection treatment. These new Bre–(3–5%)AMX scaffolds possess excellent mechanical properties and antibacterial activity with no cytotoxicity suggested as an appropriate alternative for bone infection treatment.
format Article
author Rad, H. R. Bakhsheshi
Hamzah, E.
Abbasizadeh, N.
Najafinezhad, A.
Kashefian, M.
author_facet Rad, H. R. Bakhsheshi
Hamzah, E.
Abbasizadeh, N.
Najafinezhad, A.
Kashefian, M.
author_sort Rad, H. R. Bakhsheshi
title Synthesis of novel nanostructured bredigite-amoxicillin scaffolds for bone defect treatment: cytocompatibility and antibacterial activity
title_short Synthesis of novel nanostructured bredigite-amoxicillin scaffolds for bone defect treatment: cytocompatibility and antibacterial activity
title_full Synthesis of novel nanostructured bredigite-amoxicillin scaffolds for bone defect treatment: cytocompatibility and antibacterial activity
title_fullStr Synthesis of novel nanostructured bredigite-amoxicillin scaffolds for bone defect treatment: cytocompatibility and antibacterial activity
title_full_unstemmed Synthesis of novel nanostructured bredigite-amoxicillin scaffolds for bone defect treatment: cytocompatibility and antibacterial activity
title_sort synthesis of novel nanostructured bredigite-amoxicillin scaffolds for bone defect treatment: cytocompatibility and antibacterial activity
publisher Springer New York LLC
publishDate 2018
url http://eprints.utm.my/id/eprint/85582/
http://dx.doi.org/10.1007/s10971-018-4606-1
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