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dc.contributor.authorHsiao, Meng-Hsuanen_US
dc.contributor.authorLarsson, Mikaelen_US
dc.contributor.authorLarsson, Anetteen_US
dc.contributor.authorEvenbratt, Hanneen_US
dc.contributor.authorChen, Ying-Yuen_US
dc.contributor.authorChen, You-Yinen_US
dc.contributor.authorLiu, Dean-Moen_US
dc.date.accessioned2014-12-08T15:24:19Z-
dc.date.available2014-12-08T15:24:19Z-
dc.date.issued2012-08-10en_US
dc.identifier.issn0168-3659en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.jconrel.2012.05.038en_US
dc.identifier.urihttp://hdl.handle.net/11536/16906-
dc.description.abstractThermo-gelling injectable nanogels, with no burst release of loaded drug, were prepared by a simple route by combining self assembled nanocapsules of amphiphilically modified chitosan with glycerophosphate di-sodium salt and glycerol. The potential as a depot drug delivery system was demonstrated in vivo through the therapeutic effect of ethosuximide (ESM) loaded nanogels, suppressing spike wave discharges (SWDs) in Long Evan rat model. Simultaneously clearance of gels from the site of administration was monitored non-invasively using MRI. The gel structure was characterized using TEM and SEM, confirming the gels to be an assembly of nanocapsules and using two-photon microscopy to visualize the network structure. In vitro drug release studies using ESM revealed that the nanogels exhibited extended, mostly Fickian release. Finally, all investigated formulations displayed excellent cytotoxicity data determined by MTT assay using human retinal pigmented epithelium cells. All presented properties are highly desirable for injectable depot gels for drug delivery. (c) 2012 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectAmphiphilic chitosanen_US
dc.subjectDrug deliveryen_US
dc.subjectNano capsulesen_US
dc.subjectThermo responsiveen_US
dc.subjectIn vivoen_US
dc.titleDesign and characterization of a novel amphiphilic chitosan nanocapsule-based thermo-gelling biogel with sustained in vivo release of the hydrophilic anti-epilepsy drug ethosuximideen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.jconrel.2012.05.038en_US
dc.identifier.journalJOURNAL OF CONTROLLED RELEASEen_US
dc.citation.volume161en_US
dc.citation.issue3en_US
dc.citation.spage942en_US
dc.citation.epage948en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000308077000028-
dc.citation.woscount11-
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