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MULTICHANNEL IMPEDANCE CYTOMETRY DOWNSTREAM OF CELL SEPARATION FOR QUANTIFYING ENRICHMENT OF ACTIVATED MACROPHAGE SUBPOPULATIONS

  • Javad Jarmoshti
  • , Karina Torres-Castro
  • , Li Xiao
  • , Aditya Rane
  • , Armita Salahi
  • , Li Jin
  • , Xudong Li
  • , Federica Caselli
  • , Carlos Honrado
  • , Nathan Swami
  • University of Virginia
  • University of Rome Tor Vergata

Research output: Chapter in Book/Report/Conference proceedingConference contributionpeer-review

Abstract

Cell phenotype-specific microfluidic separation from heterogeneous samples is usually ascertained by imaging fluorescently labeled samples, which is not well suited for phenotypes lacking reliable cell surface markers and for samples utilized in transplant applications for regenerative medicine. The alternate validation method is through off-chip flow cytometry of the collected fractions after fluorescent staining, but this causes dilution of the enriched cell numbers for off-chip analysis. Instead, we present a method for on-chip label-free biophysical cytometry based on single-cell impedance cytometry downstream of cell separation. This is applied for on-chip quantification of the enrichment of activated macrophages by deterministic lateral displacement.

Original languageEnglish
Title of host publicationMicroTAS 2022 - 26th International Conference on Miniaturized Systems for Chemistry and Life Sciences
PublisherChemical and Biological Microsystems Society
Pages109-110
Number of pages2
ISBN (Electronic)9781733419048
StatePublished - 2022
Event26th International Conference on Miniaturized Systems for Chemistry and Life Sciences, MicroTAS 2022 - Hybrid, Hangzhou, China
Duration: Oct 23 2022Oct 27 2022

Publication series

NameMicroTAS 2022 - 26th International Conference on Miniaturized Systems for Chemistry and Life Sciences

Conference

Conference26th International Conference on Miniaturized Systems for Chemistry and Life Sciences, MicroTAS 2022
Country/TerritoryChina
CityHybrid, Hangzhou
Period10/23/2210/27/22

Keywords

  • Activation
  • Deterministic Lateral Displacement
  • Impedance Cytometry
  • Macrophages

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