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Origami paper-based sample preconcentration using sequentially driven ion concentration polarization

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dc.contributor.authorLee, J.-
dc.contributor.authorYoo, Y.K.-
dc.contributor.authorLee, D.-
dc.contributor.authorKim, C.-
dc.contributor.authorKim, K.H.-
dc.contributor.authorLee, S.-
dc.contributor.authorKwak, S.-
dc.contributor.authorKang, J.Y.-
dc.contributor.authorKim, H.-
dc.contributor.authorYoon, D.S.-
dc.contributor.authorHur, D.-
dc.contributor.authorLee, J.H.-
dc.date.accessioned2021-12-03T09:41:34Z-
dc.date.available2021-12-03T09:41:34Z-
dc.date.created2021-08-31-
dc.date.issued2021-03-07-
dc.identifier.issn1473-0197-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/129090-
dc.description.abstractIon concentration polarization (ICP) is one of the preconcentration techniques which can acquire a high preconcentration factor. Still, the main hurdles of ICP are its instability and low efficiency under physiological conditions with high ionic strength and abundant biomolecules. Here, we suggested a sequentially driven ICP process, which enhanced the electrokinetic force required for preconcentration, enabling enrichment of highly ionic raw samples without increasing the electric field. We acquired a 13-fold preconcentration factor (PF) in human serum using a paper-based origami structure consisting of multiple layers for three-dimensional sequential ICP (3D seq-ICP). Moreover, we demonstrated a paper-based enzyme-linked immunosorbent assay (ELISA) by 3D seq-ICP using tau protein, showing a 6-fold increase in ELISA signals. © The Royal Society of Chemistry 2021.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherRoyal Society of Chemistry-
dc.titleOrigami paper-based sample preconcentration using sequentially driven ion concentration polarization-
dc.typeArticle-
dc.contributor.affiliatedAuthorYoon, D.S.-
dc.identifier.doi10.1039/d0lc01032d-
dc.identifier.scopusid2-s2.0-85102289214-
dc.identifier.wosid000626710700002-
dc.identifier.bibliographicCitationLab on a Chip, v.21, no.5, pp.867 - 874-
dc.relation.isPartOfLab on a Chip-
dc.citation.titleLab on a Chip-
dc.citation.volume21-
dc.citation.number5-
dc.citation.startPage867-
dc.citation.endPage874-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaInstruments & Instrumentation-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryInstruments & Instrumentation-
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