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dc.contributor.authorLin, Yung-Shengen_US
dc.contributor.authorHuang, Keng-Shiangen_US
dc.contributor.authorYang, Chih-Huien_US
dc.contributor.authorWang, Chih-Yuen_US
dc.contributor.authorYang, Yuh-Shyongen_US
dc.contributor.authorHsu, Hsiang-Chenen_US
dc.contributor.authorLiao, Yu-Juen_US
dc.contributor.authorTsai, Chia-Wenen_US
dc.date.accessioned2014-12-08T15:23:22Z-
dc.date.available2014-12-08T15:23:22Z-
dc.date.issued2012-03-28en_US
dc.identifier.issn1932-6203en_US
dc.identifier.urihttp://dx.doi.org/e33184en_US
dc.identifier.urihttp://hdl.handle.net/11536/16363-
dc.description.abstractThis study demonstrated the fabrication of alginate microfibers using a modular microfluidic system for magnetic-responsive controlled drug release and cell culture. A novel two-dimensional fluid-focusing technique with multi-inlets and junctions was used to spatiotemporally control the continuous laminar flow of alginate solutions. The diameter of the manufactured microfibers, which ranged from 211 mm to 364 mm, could be well controlled by changing the flow rate of the continuous phase. While the model drug, diclofenac, was encapsulated into microfibers, the drug release profile exhibited the characteristic of a proper and steady release. Furthermore, the diclofenac release kinetics from the magnetic iron oxide-loaded microfibers could be controlled externally, allowing for a rapid drug release by applying a magnetic force. In addition, the successful culture of glioblastoma multiforme cells in the microfibers demonstrated a good structural integrity and environment to grow cells that could be applied in drug screening for targeting cancer cells. The proposed microfluidic system has the advantages of ease of fabrication, simplicity, and a fast and low-cost process that is capable of generating functional microfibers with the potential for biomedical applications, such as drug controlled release and cell culture.en_US
dc.language.isoen_USen_US
dc.titleMicrofluidic Synthesis of Microfibers for Magnetic-Responsive Controlled Drug Release and Cell Cultureen_US
dc.typeArticleen_US
dc.identifier.doie33184en_US
dc.identifier.journalPLOS ONEen_US
dc.citation.volume7en_US
dc.citation.issue3en_US
dc.citation.epageen_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000304489000017-
dc.citation.woscount14-
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