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Updated: May 24, 2025

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Automated Microfluidic Blood Lysis Protocol for Enrichment of Circulating Nucleated Cells
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Dielectrophoretic Microfluidic Designs for Precision Cell Enrichments and Highly Viable Label-Free Bacteria Recovery
Dean E Thomas1, Kyle S Kinskie1, Kyle M Brown1
1CytoRecovery, Inc., Blacksburg, VA 24060, USA.
Micromachines
|March 6, 2025
Summary
This study developed label-free microfluidic devices for isolating E. coli bacteria from blood. CytoChip B effectively recovered over 98% of bacteria, enabling early infection detection.
Area of Science:
- Biomedical Engineering
- Microfluidics
- Cellular Biology
Background:
- Cellular analysis of biological samples faces challenges in cell sorting and recovery.
- Label-free microfluidics offer a promising solution for complex sample processing.
- Escherichia coli (E. coli) infections are a significant global health concern.
Purpose of the Study:
- To investigate label-free microfluidic device designs for enriching E. coli from whole human blood.
- To evaluate device performance in terms of throughput, scalability, precision, and recovery viability.
- To mimic infection workflows for early pathogen detection.
Main Methods:
- Utilized dielectrophoresis (DEP) for particle manipulation and cell sorting.
- Compared two microfluidic designs: CytoChip D (continuous flow) and CytoChip B (batch or continuous).
- Assessed recovery rates and purity of E. coli from spiked whole human blood samples.
Main Results:
- CytoChip D showed potential for high throughput but failed in effective bacteria recovery.
- CytoChip B achieved over 98% purity recovery of E. coli, even at ultra-low concentrations (<100 CFU/mL).
- Demonstrated feasibility for processing and recovering low bacterial concentrations for downstream applications.
Conclusions:
- CytoChip B is a viable technology for high-purity recovery of E. coli from blood.
- This method supports downstream analysis, bacterial culture, and drug testing for infection diagnostics.
- Future work will focus on scaling CytoChip B for increased sample volume processing.

