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bioRxiv · 10.1101/2020.07.28.224006

A Portable Impedance Microflow Cytometer for Measuring Cellular Response to Hypoxia

Dieujus, D.·Qiang, Y.·Du, E.
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Abstract

This paper presents the development and testing of a low-cost, portable microflow cytometer based on electrical impedance sensing, for single cell analysis under controlled oxygen microenvironment. The cytometer system is based on an AD5933 impedance analyzer chip, a microfluidic chip, and an Arduino microcontroller operated by a custom Android application. A representative case study on human red blood cells (RBCs) affected by sickle cell disease is conducted to demonstrate the capability of the cytometry system. Equivalent circuit model of a suspending biological cell is used to interpret the electrical impedance of single flowing RBCs. In normal blood, cytoplasmic resistance and membrane capacitance do not change significantly with the change in oxygen tension. In contrast, RBCs affected by sickle cell disease show that upon hypoxia treatment, the cytoplasmic resistance decrease from 11.6 M{Omega} to 23.4 M{Omega}, and membrane capacitance decrease from 1.1 pF to 0.8 pF. Strong correlations are identified between the changes in these subcellular electrical components of single cells and the cell sickling process induced by hypoxia treatment. The representative results reported in this paper suggest that single cell electrical impedance can be used as a sensitive biophysical marker for quantifying cellular response to change in oxygen concentration. The developed flow cytometry system and the methodology can also be extended to analysis of cellular response to hypoxia in other cell types. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=124 SRC="FIGDIR/small/224006v1_ufig1.gif" ALT="Figure 1"> View larger version (38K): org.highwire.dtl.DTLVardef@147f903org.highwire.dtl.DTLVardef@2d4c35org.highwire.dtl.DTLVardef@1e63b0dorg.highwire.dtl.DTLVardef@2eeb0c_HPS_FORMAT_FIGEXP M_FIG C_FIG

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Dieujus, D., Qiang, Y., Du, E.. 2020-07-29. A Portable Impedance Microflow Cytometer for Measuring Cellular Response to Hypoxia. https://doi.org/10.1101/2020.07.28.224006

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