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Computational Hyperspectral Microflow Cytometry

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dc.contributor.authorYun, Hyo Geun-
dc.contributor.authorCadierno, Yoel Alonso-
dc.contributor.authorKim, Tae Won-
dc.contributor.authorMuñoz-Barrutia, Arrate-
dc.contributor.authorGarica-Gonzalez, Daniel-
dc.contributor.authorChoi, Sungyoung-
dc.date.accessioned2025-03-28T06:00:15Z-
dc.date.available2025-03-28T06:00:15Z-
dc.date.issued2024-07-
dc.identifier.issn1613-6810-
dc.identifier.issn1613-6829-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/206922-
dc.description.abstractMiniaturized flow cytometry has significant potential for portable applications, such as cell-based diagnostics and the monitoring of therapeutic cell manufacturing, however, the performance of current techniques is often limited by the inability to resolve spectrally-overlapping fluorescence labels. Here, the study presents a computational hyperspectral microflow cytometer (CHC) that enables accurate discrimination of spectrally-overlapping fluorophores labeling single cells. CHC employs a dispersive optical element and an optimization algorithm to detect the full fluorescence emission spectrum from flowing cells, with a high spectral resolution of ≈3 nm in the range from 450 to 650 nm. CHC also includes a dedicated microfluidic device that ensures in-focus imaging through viscoelastic sheathless focusing, thereby enhancing the accuracy and reliability of microflow cytometry analysis. The potential of CHC for analyzing T lymphocyte subpopulations and monitoring changes in cell composition during T cell expansion is demonstrated. Overall, CHC represents a major breakthrough in microflow cytometry and can facilitate its use for immune cell monitoring.-
dc.format.extent12-
dc.language영어-
dc.language.isoENG-
dc.publisherWiley - V C H Verlag GmbbH & Co.-
dc.titleComputational Hyperspectral Microflow Cytometry-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.doi10.1002/smll.202400019-
dc.identifier.scopusid2-s2.0-85193616629-
dc.identifier.wosid001227674500001-
dc.identifier.bibliographicCitationSmall, v.20, no.30, pp 1 - 12-
dc.citation.titleSmall-
dc.citation.volume20-
dc.citation.number30-
dc.citation.startPage1-
dc.citation.endPage12-
dc.type.docTypeArticle in press-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.relation.journalWebOfScienceCategoryPhysics, Condensed Matter-
dc.subject.keywordPlusFLOW-CYTOMETRY-
dc.subject.keywordPlusPROGRESS-
dc.subject.keywordAuthorcomputational hyperspectral fluorescence analysis-
dc.subject.keywordAuthormicroflow cytometry-
dc.subject.keywordAuthorsheathless focusing-
dc.subject.keywordAuthorspectral reconstruction-
dc.subject.keywordAuthorT lymphocyte analysis-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1002/smll.202400019-
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