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dc.contributor.authorTu, Yi-Kaien_US
dc.contributor.authorTsai, Meng-Zheen_US
dc.contributor.authorLee, I-Chinen_US
dc.contributor.authorHsu, Hsin-Yunen_US
dc.contributor.authorHuang, Cheng-Shengen_US
dc.date.accessioned2017-04-21T06:56:04Z-
dc.date.available2017-04-21T06:56:04Z-
dc.date.issued2016en_US
dc.identifier.issn0003-2654en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c6an00023aen_US
dc.identifier.urihttp://hdl.handle.net/11536/133984-
dc.description.abstractWe present an integrated microfluidic system consisting of a label-free biosensor of a guided-mode resonance filter (GMRF) and a microfluidic channel with a micropost filter. The GMRF was fabricated through replica molding using an ultraviolet-curable polymer and a plastic substrate. An array of microposts (a diameter and height of 26.5 and 56 mu m, respectively, and a spacing between 7.5 and 9.5 mu m), fabricated on a silicon substrate through photolithography, was used as the filter. A double-sided tape was used to laminate the GMRF and a microfluidic chip such that the integrated device provides two functions: filtration of the cell debris and quantification of the in-cell protein concentration. By measuring the changes in the resonant wavelength from the GMRF, the detection of beta-actin in an unprocessed lysed cell sample was demonstrated; the cell debris was separated using the micropost filter to prevent false measurement.en_US
dc.language.isoen_USen_US
dc.titleIntegration of a guided-mode resonance filter with microposts for in-cell protein detectionen_US
dc.identifier.doi10.1039/c6an00023aen_US
dc.identifier.journalANALYSTen_US
dc.citation.volume141en_US
dc.citation.issue13en_US
dc.citation.spage4189en_US
dc.citation.epage4195en_US
dc.contributor.department機械工程學系zh_TW
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Mechanical Engineeringen_US
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000378942300030en_US
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