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dc.contributor.authorHsu, Wei-Liangen_US
dc.contributor.authorLee, Mon-Juanen_US
dc.contributor.authorLee, Weien_US
dc.date.accessioned2019-12-13T01:10:02Z-
dc.date.available2019-12-13T01:10:02Z-
dc.date.issued2019-10-01en_US
dc.identifier.issn2156-7085en_US
dc.identifier.urihttp://dx.doi.org/10.1364/BOE.10.004987en_US
dc.identifier.urihttp://hdl.handle.net/11536/153099-
dc.description.abstractThe fundamental principle of liquid-crystal (LC)-based biosensing is the sensitive response of LC orientation to external stimuli. Biomolecules such as proteins or DNAs immobilized on the glass substrate of a LC cell are detected through disrupting the LC alignment and, in turn, altering the birefringence, resulting in changes in the optical texture that can be readily observed under a polarizing optical microscope. With an additional weak electric field across a sandwiched LC cell, we demonstrate in this study a novel label-free biodetection technique with amplified signal and improved detection limit. By applying the binarization analysis as the quantitative approach, the increase in the light leakage area in the optical texture of LCs with increasing amount of biomolecules can be quantitated with a bright-area-ratio (BAR)-versus-concentration curve. The reported biosensing technique exploits both the optical and electrical properties of LCs and is potentially applicable to other LC-based rapid screening and bioassays. (C) 2019 Optical Society of America under the terms of the OSA Open Access Publishing Agreementen_US
dc.language.isoen_USen_US
dc.titleElectric-field-assisted signal amplification for label-free liquid-crystal-based detection of biomoleculesen_US
dc.typeArticleen_US
dc.identifier.doi10.1364/BOE.10.004987en_US
dc.identifier.journalBIOMEDICAL OPTICS EXPRESSen_US
dc.citation.volume10en_US
dc.citation.issue10en_US
dc.citation.spage4987en_US
dc.citation.epage4998en_US
dc.contributor.department影像與生醫光電研究所zh_TW
dc.contributor.departmentInstitute of Imaging and Biomedical Photonicsen_US
dc.identifier.wosnumberWOS:000488614300006en_US
dc.citation.woscount0en_US
Appears in Collections:Articles