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dc.contributor.authorChang, Yen-Poen_US
dc.contributor.authorLiu, Kun-Hoen_US
dc.contributor.authorChao, Chih-Shinen_US
dc.contributor.authorChen, San-Yuanen_US
dc.contributor.authorLiu, Dean-Moen_US
dc.date.accessioned2019-04-02T05:58:15Z-
dc.date.available2019-04-02T05:58:15Z-
dc.date.issued2010-09-01en_US
dc.identifier.issn1742-7061en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.actbio.2010.03.009en_US
dc.identifier.urihttp://hdl.handle.net/11536/150012-
dc.description.abstractGd2O3 nanotubes were constructed for the first time by assembling highly crystalline Gd2O3 nanoparticles through the use of combined soft template and sol-gel methods. Amphiphilic block copolymer was used as structure-directing agent and gadolinium isopropoxide as inorganic precursor in non-aqueous solution. The amphiphilic copolymer molecules are known to undergo self-organization above a critical micelle concentration, forming micellular architecture that further provides a structurally ordered active site for the nucleation and growth of Gd monomers. The resulting self-assembly of the Gd2O3 nanocrystals led to the formation of Gd2O3 tubular nanostructure after pyrolytic removal of the template. Transmission electron microscopy analysis indicated a mesoporous channel array along the [1 1 0] direction of the nanotubes where the wall of nanotube is well organized by the assembly of a highly crystalline framework of Gd2O3 nanocrystals. This Gd2O3 nanotube exhibited weak superparamagnetic property and was found to be able to carry and elute a model molecule, i.e. ibuprofen (IBU), in a controllable manner via an external magnetic field. The mechanism of IBU release from the nanotubes with and without the use of magnetic stimulus was proposed. (C) 2010 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectSelf assemblyen_US
dc.subjectGd2O3 Nanotubeen_US
dc.subjectNanocrystalen_US
dc.subjectMagnetic-sensitiveen_US
dc.titleSynthesis and characterization of mesoporous Gd2O3 nanotube and its use as a drug-carrying vehicleen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.actbio.2010.03.009en_US
dc.identifier.journalACTA BIOMATERIALIAen_US
dc.citation.volume6en_US
dc.citation.spage3713en_US
dc.citation.epage3719en_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:000281318400039en_US
dc.citation.woscount9en_US
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