Please use this identifier to cite or link to this item: https://doi.org/10.1007/s10856-011-4397-1
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dc.titleMesoporous silica nanoparticle-functionalized poly(methyl methacrylate)-based bone cement for effective antibiotics delivery
dc.contributor.authorShen, S.-C.
dc.contributor.authorNg, W.K.
dc.contributor.authorShi, Z.
dc.contributor.authorChia, L.
dc.contributor.authorNeoh, K.G.
dc.contributor.authorTan, R.B.H.
dc.date.accessioned2014-10-09T06:53:10Z
dc.date.available2014-10-09T06:53:10Z
dc.date.issued2011-10
dc.identifier.citationShen, S.-C., Ng, W.K., Shi, Z., Chia, L., Neoh, K.G., Tan, R.B.H. (2011-10). Mesoporous silica nanoparticle-functionalized poly(methyl methacrylate)-based bone cement for effective antibiotics delivery. Journal of Materials Science: Materials in Medicine 22 (10) : 2283-2292. ScholarBank@NUS Repository. https://doi.org/10.1007/s10856-011-4397-1
dc.identifier.issn09574530
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/89385
dc.description.abstractPoly(methyl methacrylate)-based bone cements are functionalized with mesoporous silica nanoparticles (MSN) to enable a highly efficient and sustained release of antibiotics to reduce the risk of post-operative joint infection. To overcome the limited drug release of 5% for only 1 day with the current commercial-grade bone cements, a 8 wt% MSN-formulated bone cement is able to increase the drug release efficiency by 14-fold and sustain the release for up to 80 days. The loaded MSN is suggested to build up an effective network of rod-shaped silica particles with uniformly arranged nanoporous channels, which is responsible for the effective drug diffusion and extend time-release to the external surfaces. MSN has no detrimental effect on the critical weight-bearing bending modulus and compression strength of bone cement. In vitro assay test results show a much sustained antibacterial effect and low cytotoxicity of MSN demonstrating the potential applicability of MSN-formulated bone cement. © Springer Science+Business Media, LLC 2011.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1007/s10856-011-4397-1
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1007/s10856-011-4397-1
dc.description.sourcetitleJournal of Materials Science: Materials in Medicine
dc.description.volume22
dc.description.issue10
dc.description.page2283-2292
dc.description.codenJSMME
dc.identifier.isiut000295712600014
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