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dc.contributor.authorHu, Shang-Hsiuen_US
dc.contributor.authorTsai, Chia-Huien_US
dc.contributor.authorLiao, Chen-Fuen_US
dc.contributor.authorLiu, Dean-Moen_US
dc.contributor.authorChen, San-Yuanen_US
dc.date.accessioned2014-12-08T15:10:46Z-
dc.date.available2014-12-08T15:10:46Z-
dc.date.issued2008-10-21en_US
dc.identifier.issn0743-7463en_US
dc.identifier.urihttp://dx.doi.org/10.1021/la801138een_US
dc.identifier.urihttp://hdl.handle.net/11536/8239-
dc.description.abstractIn this study, a magnetic-sensitive microcapsule was prepared using Fe3O4/poly(allylamine) (Fe3O4/PAH) polyelectrolyte to construct the shell. Structural integrity, microstructural evolution, and corresponding release behaviors of fluorescence dyes and doxorubicin were systematically investigated. Experimental observations showed that the presence of the magnetic nanoparticles in the shell structure allowed the shell structure to evolve from nanocavity development to final rupture of the shell under a given magnetic stimulus of different time durations. Such a microstructural evolution of the magnetic sensitive shell structure explained a corresponding variation of the drug release profile, from relatively slow release to burst-like behavior at different stages of stimulus. It has proposed that the presence of magnetic nanoparticles produced heat, due to magnetic energy dissipation (as Brown and Neel relaxations), and mechanical vibration and motion that induced stress development in the thin shell. Both mechanisms significantly accelerated the relaxation of the shell structure, causing such a microstructural evolution. With such a controllable microstructural evolution of the magnetic-sensitive shell structure, active substances can be well-regulated in a manageable manner with a designable profile according to the time duration under magnetic field. A cell culture study also indicated that the magnetic-sensitive microcapsules allowed a rapid uptake by the A549 cell line, a cancerous cell line, suggesting that the magnetic-sensitive microcapsule with controllable rupturing behavior of the shell offers a potential and effective drug carrier for anticancer applications.en_US
dc.language.isoen_USen_US
dc.titleControlled Rupture of Magnetic Polyelectrolyte Microcapsules for Drug Deliveryen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/la801138een_US
dc.identifier.journalLANGMUIRen_US
dc.citation.volume24en_US
dc.citation.issue20en_US
dc.citation.spage11811en_US
dc.citation.epage11818en_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:000260049300066-
dc.citation.woscount115-
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