Please use this identifier to cite or link to this item: https://doi.org/10.1002/jbm.a.31854
DC FieldValue
dc.titleStructural stability and bioapplicability assessment of hyaluronic acid-chitosan polyelectrolyte multilayers on titanium substrates
dc.contributor.authorChua, P.H.
dc.contributor.authorNeoh, K.G.
dc.contributor.authorShi, Z.
dc.contributor.authorKang, E.T.
dc.date.accessioned2014-06-17T07:49:23Z
dc.date.available2014-06-17T07:49:23Z
dc.date.issued2008-12-15
dc.identifier.citationChua, P.H., Neoh, K.G., Shi, Z., Kang, E.T. (2008-12-15). Structural stability and bioapplicability assessment of hyaluronic acid-chitosan polyelectrolyte multilayers on titanium substrates. Journal of Biomedical Materials Research - Part A 87 (4) : 1061-1074. ScholarBank@NUS Repository. https://doi.org/10.1002/jbm.a.31854
dc.identifier.issn15493296
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/64622
dc.description.abstractSince bacterial infections associated with implants remain a major cause of their failure, this study investigated the use of polyelectrolyte multilayers (PEMs) comprising hyaluronic acid (HA) and chitosan (CH) to confer antibacterial properties on titanium (Ti). HA and CH were deposited on Ti using the layer-by-layer deposition method. The antibacterial efficacy of the functionalized Ti substrates was assessed using Escherichia coli and Staphylococcus aureus. The number of adherent bacteria on Ti functionalized with HA and CH PEMs was up to an order of magnitude lower than that on the pristine Ti. The effects of chemical crosslinking of the PEMs on the structural stability and antibacterial efficacy were investigated. The chemical crosslinking of the PEMs imparts greater structural stability and preserves the antibacterial properties even after the prolonged immersion in phosphate-buffered saline. The cytotoxicity of the PEMs to osteoblasts was evaluated using the MTT assay. The results showed that the biocompatible and long-lasting antibacterial nature of the functionalized Ti substrates offers great potential for reducing implant-associated infections. © 2008 Wiley Periodicals, Inc.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/jbm.a.31854
dc.sourceScopus
dc.subjectAntibacterial
dc.subjectChitosan
dc.subjectHyaluronic acid
dc.subjectLayer by layer
dc.subjectOsteoblast
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1002/jbm.a.31854
dc.description.sourcetitleJournal of Biomedical Materials Research - Part A
dc.description.volume87
dc.description.issue4
dc.description.page1061-1074
dc.description.codenJBMRC
dc.identifier.isiut000261075600025
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