Please use this identifier to cite or link to this item: https://doi.org/10.1021/bm3005879
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dc.titleEncapsulation of basic fibroblast growth factor by polyelectrolyte multilayer microcapsules and its controlled release for enhancing cell proliferation
dc.contributor.authorShe, Z.
dc.contributor.authorWang, C.
dc.contributor.authorLi, J.
dc.contributor.authorSukhorukov, G.B.
dc.contributor.authorAntipina, M.N.
dc.date.accessioned2014-06-17T09:43:35Z
dc.date.available2014-06-17T09:43:35Z
dc.date.issued2012-07-09
dc.identifier.citationShe, Z., Wang, C., Li, J., Sukhorukov, G.B., Antipina, M.N. (2012-07-09). Encapsulation of basic fibroblast growth factor by polyelectrolyte multilayer microcapsules and its controlled release for enhancing cell proliferation. Biomacromolecules 13 (7) : 2174-2180. ScholarBank@NUS Repository. https://doi.org/10.1021/bm3005879
dc.identifier.issn15257797
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/67030
dc.description.abstract(Graph Presented) Basic fibroblast growth factor (FGF2) is an important protein for cellular activity and highly vulnerable to environmental conditions. FGF2 protected by heparin and bovine serum albumin was loaded into the microcapsules by a coprecipitation-based layer-by-layer encapsulation method. Low cytotoxic and biodegradable polyelectrolytes dextran sulfate and poly-l-arginine were used for capsule shell assembly. The shell thickness-dependent encapsulation efficiency was measured by enzyme-linked immunosorbent assay. A maximum encapsulation efficiency of 42% could be achieved by microcapsules with a shell thickness of 14 layers. The effects of microcapsule concentration and shell thickness on cytotoxicity, FGF2 release kinetics, and L929 cell proliferation were evaluated in vitro. The advantage of using microcapsules as the carrier for FGF2 controlled release for enhancing L929 cell proliferation was analyzed (Graph Presented). © 2012 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/bm3005879
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentBIOENGINEERING
dc.description.doi10.1021/bm3005879
dc.description.sourcetitleBiomacromolecules
dc.description.volume13
dc.description.issue7
dc.description.page2174-2180
dc.description.codenBOMAF
dc.identifier.isiut000306151700021
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