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Magnetic smartphone microflow cytometry enables rapid CD4/CD8 T cell quantification

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dc.contributor.authorShin, Hee Sik-
dc.contributor.authorLee, Sung Joo-
dc.contributor.authorKim, Jae In-
dc.contributor.authorKim, Jung Ho-
dc.contributor.authorChoi, Jun Yong-
dc.contributor.authorJeong, Su Jin-
dc.contributor.authorChoi, Sungyoung-
dc.date.accessioned2026-01-22T02:30:51Z-
dc.date.available2026-01-22T02:30:51Z-
dc.date.created2026-01-16-
dc.date.issued2026-01-
dc.identifier.issn1473-0197-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/210133-
dc.description.abstractAccurate enumeration of CD4+ and CD8+ T lymphocytes is essential for HIV management, yet conventional flow cytometry remains largely inaccessible in resource-limited settings. Current point-of-care testing (POCT) approaches, including lateral flow assays and fluorescence-based imaging methods, offer improved accessibility but typically compromise accuracy and yield semi-quantitative results. Here, we present a magnetic-activated smartphone microflow cytometry (MACC) platform that enables rapid, highly accessible, and fully quantitative T lymphocyte counting at the POCT. MACC integrates microfluidic immunomagnetic cell separation with smartphone-based bright-field imaging, providing high-sensitivity, highly accessible analysis without requiring sophisticated laboratory equipment or fluorescent labels. A degassing-driven microfluidic pumping mechanism ensures stable microflow generation for reliable continuous analysis, while smartphone imaging enables clear differentiation of targeted lymphocytes from non-lymphocytes. The complete assay, including magnetic bead labeling, chip operation, hands-on procedures, and automated cell-counting analysis, is completed within 24 min. Validation with HIV-infected patient samples demonstrated strong concordance between MACC and conventional flow cytometry for CD4+ and CD8+ counts as well as CD4/CD8 ratio measurements, with minimal bias. By combining high accessibility, cost-effectiveness, and ease of operation, MACC represents a promising alternative to traditional methods, facilitating decentralized HIV monitoring and expanding diagnostic accessibility in resource-limited settings.-
dc.languageEnglish-
dc.publisherRoyal Society of Chemistry-
dc.relation.isPartOfLAB ON A CHIP-
dc.relation.isPartOfLAB ON A CHIP-
dc.subject.MESHCD4-Positive T-Lymphocytes* / cytology-
dc.subject.MESHCD8-Positive T-Lymphocytes* / cytology-
dc.subject.MESHFlow Cytometry* / instrumentation-
dc.subject.MESHHIV Infections / immunology-
dc.subject.MESHHumans-
dc.subject.MESHImmunomagnetic Separation / instrumentation-
dc.subject.MESHLab-On-A-Chip Devices*-
dc.subject.MESHMagnetic Phenomena-
dc.subject.MESHMicrofluidic Analytical Techniques* / instrumentation-
dc.subject.MESHSmartphone*-
dc.titleMagnetic smartphone microflow cytometry enables rapid CD4/CD8 T cell quantification-
dc.typeArticle-
dc.contributor.googleauthorShin, Hee Sik-
dc.contributor.googleauthorLee, Sung Joo-
dc.contributor.googleauthorKim, Jae In-
dc.contributor.googleauthorKim, Jung Ho-
dc.contributor.googleauthorChoi, Jun Yong-
dc.contributor.googleauthorJeong, Su Jin-
dc.contributor.googleauthorChoi, Sungyoung-
dc.identifier.doi10.1039/d5lc00801h-
dc.relation.journalcodeJ02148-
dc.identifier.eissn1473-0189-
dc.identifier.pmid41416687-
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2026/lc/d5lc00801h-
dc.contributor.affiliatedAuthorKim, Jae In-
dc.contributor.affiliatedAuthorKim, Jung Ho-
dc.contributor.affiliatedAuthorChoi, Jun Yong-
dc.contributor.affiliatedAuthorJeong, Su Jin-
dc.identifier.scopusid2-s2.0-105025106328-
dc.identifier.wosid001642499400001-
dc.citation.volume26-
dc.citation.number2-
dc.citation.startPage437-
dc.citation.endPage447-
dc.identifier.bibliographicCitationLAB ON A CHIP, Vol.26(2) : 437-447, 2026-01-
dc.identifier.rimsid91029-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordPlusDEVICE-
dc.subject.keywordPlusTECHNOLOGIES-
dc.subject.keywordPlusPERFORMANCE-
dc.type.docTypeArticle; Early Access-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryInstruments & Instrumentation-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaInstruments & Instrumentation-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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