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dc.contributor.authorYu, Chun-Kangen_US
dc.contributor.authorHu, Kan-Hungen_US
dc.contributor.authorWang, Shing-Hoaen_US
dc.contributor.authorHsu, Todden_US
dc.contributor.authorTsai, Huei-Tingen_US
dc.contributor.authorChen, Chien-Chonen_US
dc.contributor.authorLiu, Shiu-Meien_US
dc.contributor.authorLin, Tai-Yuanen_US
dc.contributor.authorChen, Chin-Hsingen_US
dc.date.accessioned2014-12-08T15:37:34Z-
dc.date.available2014-12-08T15:37:34Z-
dc.date.issued2011-02-01en_US
dc.identifier.issn0947-8396en_US
dc.identifier.urihttp://dx.doi.org/10.1007/s00339-010-5968-6en_US
dc.identifier.urihttp://hdl.handle.net/11536/25828-
dc.description.abstractThe use of titanium dioxide (TiO(2)) in photodynamic therapy for the treatment of cancer cells has been proposed following studies of cultured cancer cells. In this work, an ordered channel array of anodic titanium oxide (ATO) was fabricated by anodizing titanium foil. The ATO layer of nanotubes with diameters of 100 nm was made in NH(4)F electrolyte by anodization. The photocatalytic effect of ATO was examined on various culture media by ultraviolet A (UV-A) (366 nm) irradiation. After UV-A irradiation of the ATO layer, redox potential of Tris-HCl buffer (pH 7.5) and dilute acrylamide solution increased instantaneously. The redox potential of the serum-containing RPMI1640 medium also increased dramatically, while that of serum-containing MEM and DMEM media increased slightly. The UVA-induced high redox potential was correlated with the greater ability to break down plasmid DNA strands. These phenomena suggest that a culture medium, such as RPMI1640, with a greater ability to produce free radical may be associated with a stronger photocatalytic effect of ATO on cultured cancer cells reported previously.en_US
dc.language.isoen_USen_US
dc.titlePhotocatalytic effect of anodic titanium oxide nanotubes on various cell culture mediaen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s00339-010-5968-6en_US
dc.identifier.journalAPPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSINGen_US
dc.citation.volume102en_US
dc.citation.issue2en_US
dc.citation.spage271en_US
dc.citation.epage274en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000286828000004-
dc.citation.woscount3-
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