Please use this identifier to cite or link to this item: https://doi.org/10.1117/12.621763
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dc.titleTowards an ideal polymer scaffold for tendon/ligament tissue engineering
dc.contributor.authorSahoo, S.
dc.contributor.authorOuyang, H.W.
dc.contributor.authorGoh, J.C.-H.
dc.contributor.authorTay, T.-E.
dc.contributor.authorToh, S.L.
dc.date.accessioned2014-10-07T09:15:51Z
dc.date.available2014-10-07T09:15:51Z
dc.date.issued2005
dc.identifier.citationSahoo, S., Ouyang, H.W., Goh, J.C.-H., Tay, T.-E., Toh, S.L. (2005). Towards an ideal polymer scaffold for tendon/ligament tissue engineering. Proceedings of SPIE - The International Society for Optical Engineering 5852 PART II : 658-664. ScholarBank@NUS Repository. https://doi.org/10.1117/12.621763
dc.identifier.issn0277786X
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/86099
dc.description.abstractTissue engineering holds promise in treating injured tendons and ligaments by replacing the injured tissues with "engineered tissues" with identical mechanical and functional characteristics. A biocompatible, biodegradable, porous scaffold with optimized architecture, sufficient surface area for cell attachment, growth and proliferation, favorable mechanical properties, and suitable degradation rate is a pre-requisite to achieve success with this approach. Knitted poly(lactide-co-glycolide) (PLGA) scaffolds comprising of microfibers of 25 micron diameter were coated with PLGA nanofibers on their surfaces by electrospinning technique. A cell suspension of pig bone marrow stromal cells (BMSC) was seeded on the scaffolds by pipetting, and the cell-scaffold constructs were cultured in a CO2 incubator, at 37°C for 1-2 weeks. The "engineered tissues" were then assessed for cell attachment and proliferation, tissue formation, and mechanical properties. Nanofibers, of diameter 300-900 nm, were spread randomly over the knitted scaffold. The reduction in pore-size from about 1 mm (in the knitted scaffold) to a few micrometers (in the nano-microscaffold) allowed cell seeding by direct pipetting, and eliminated the need of a cell-delivery system like fibrin gel. BMSCs were seen to attach and proliferate well on the nano-microscaffold, producing abundant extracellular matrix. Mechanical testing revealed that the cell-seeded nano-microscaffolds possessed slightly higher values of failure load, elastic-region stiffness and toe-region stiffness, than the unseeded scaffolds. The combination of superior mechanical strength and integrity of knitted microfibers, with the large surface area and improved hydrophilicity of the electrospun nanofibers facilitated cell attachment and new tissue formation. This holds promise in tissue engineering of tendon/ligament.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1117/12.621763
dc.sourceScopus
dc.subjectElectrospinning
dc.subjectLigament
dc.subjectNanofiber
dc.subjectPLGA
dc.subjectTendon
dc.subjectTissue engineering
dc.typeConference Paper
dc.contributor.departmentBIOENGINEERING
dc.contributor.departmentORTHOPAEDIC SURGERY
dc.contributor.departmentMECHANICAL ENGINEERING
dc.description.doi10.1117/12.621763
dc.description.sourcetitleProceedings of SPIE - The International Society for Optical Engineering
dc.description.volume5852 PART II
dc.description.page658-664
dc.description.codenPSISD
dc.identifier.isiut000229932000105
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