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dc.contributor.authorEades, Jason
dc.contributor.authorAudiffred, Julianne F.
dc.contributor.authorFincher, Micah
dc.contributor.authorChoi, Jin-Woo
dc.contributor.authorSoper, Steven A.
dc.contributor.authorMonroe, William Todd
dc.date.accessioned2023-05-09T18:34:08Z
dc.date.available2023-05-09T18:34:08Z
dc.date.issued2023-01-22
dc.identifier.citationEades, J.; Audiffred, J.F.; Fincher, M.; Choi, J.-W.; Soper, S.A.; Monroe, W.T. A Simple Micromilled Microfluidic Impedance Cytometer with Vertical Parallel Electrodes for Cell Viability Analysis. Micromachines 2023, 14, 283. https://doi.org/10.3390/mi14020283en_US
dc.identifier.urihttps://hdl.handle.net/1808/34147
dc.description.abstractMicrofluidic impedance cytometry has been demonstrated as an effective platform for single cell analysis, taking advantage of microfabricated features and dielectric cell sensing methods. In this study, we present a simple microfluidic device to improve the sensitivity, accuracy, and throughput of single suspension cell viability analysis using vertical sidewall electrodes fabricated by a widely accessible negative manufacturing method. A microchannel milled through a 75 µm platinum wire, which was embedded into poly-methyl-methacrylate (PMMA), created a pair of parallel vertical sidewall platinum electrodes. Jurkat cells were interrogated in a custom low-conductivity buffer (1.2 ± 0.04 mS/cm) to reduce current leakage and increase device sensitivity. Confirmed by live/dead staining and electron microscopy, a single optimum excitation frequency of 2 MHz was identified at which live and dead cells were discriminated based on the disruption in the cell membrane associated with cell death. At this frequency, live cells were found to exhibit changes in the impedance phase with no appreciable change in magnitude, while dead cells displayed the opposite behavior. Correlated with video microscopy, a computational algorithm was created that could identify cell detection events and determine cell viability status by application of a mathematical correlation method.en_US
dc.publisherMDPIen_US
dc.rights© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.en_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectSingle cellen_US
dc.subjectMicrofluidic impedance cytometryen_US
dc.subjectImpedance spectroscopyen_US
dc.subjectMicromillingen_US
dc.subjectVertical electrodesen_US
dc.subjectSidewall electrodesen_US
dc.titleA Simple Micromilled Microfluidic Impedance Cytometer with Vertical Parallel Electrodes for Cell Viability Analysisen_US
dc.typeArticleen_US
kusw.kuauthorSoper, Steven A.
kusw.kudepartmentCenter of Biomodular Multiscale Systems for Precision Medicineen_US
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.3390/mi14020283en_US
dc.identifier.orcidhttps://orcid.org/0000-0001-6364-1604en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-9210-9681en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-8292-7058en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-7889-3799en_US
kusw.oaversionScholarly/refereed, publisher versionen_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.identifier.pmidPMC9959585en_US
dc.rights.accessrightsopenAccessen_US


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© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.
Except where otherwise noted, this item's license is described as: © 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.