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Related Concept Videos

Flow Cytometry01:23

Flow Cytometry

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The development of flow cytometry techniques began in 1934 with initial attempts by Andrew Moldavan, a bacteriologist who counted the cells in a flowing capillary system. Moldavan pumped cells through a capillary tube focused under a microscope for visualization. The invention of photometry allowed the measurement of differentially-stained cells, and Louis Kamentsky developed the first multiparameter flow cytometer in 1965 to identify and count the cancer cells in cervical tissue specimens.
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An Automated Method to Perform The In Vitro Micronucleus Assay using Multispectral Imaging Flow Cytometry
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Image-based cell-resolved screening assays in flow.

Man Ching Cheung1, Brian McKenna1, Steve S Wang1

  • 1Department of Biomedical Engineering, Boston University, Massachusetts.

Cytometry. Part a : the Journal of the International Society for Analytical Cytology
|December 18, 2014
PubMed
Summary
This summary is machine-generated.

A novel parallel microfluidic cytometer (PMC) enables high-throughput, image-based pharmaceutical screening. This technology offers the statistical power for advanced drug discovery with suspension cells.

Keywords:
HCAhigh-contenthigh-throughputimaginglive-cell assaymicrofluidicreceptor cappingscreening

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Area of Science:

  • Biotechnology
  • Cell Biology
  • Microfluidics

Background:

  • Traditional cell screening methods face limitations in throughput and statistical power.
  • Image-based analysis offers rich cellular information but requires advanced instrumentation.
  • Microfluidic devices provide miniaturized platforms for cell analysis.

Purpose of the Study:

  • To introduce and validate a parallel microfluidic cytometer (PMC) for image-based cell screening.
  • To demonstrate the PMC's capability in analyzing complex cellular events like nuclear translocations and cell capping.
  • To develop and assess a novel classifier for pharmaceutical discovery applications.

Main Methods:

  • Development of a PMC integrating a 1D scanning detector and parallel flow channels.
  • Implementation of multiparameter analysis algorithms for low-pixel-count 1D images.
  • Conducting live- and fixed-cell assays, including NF-kB nuclear translocations and T-cell capping.
  • Development of a multiparametric linear weighted classifier.

Main Results:

  • The PMC successfully performed image-based live- and fixed-cell screening assays.
  • Demonstrated analysis of NF-kB nuclear translocations and T-cell capping.
  • The developed classifier achieved a sufficient Z' factor for pharmaceutical discovery using Jurkat cells.
  • The system shows potential for high-sample-number screening.

Conclusions:

  • The parallel microfluidic cytometer (PMC) is a viable tool for advanced cell-based assays.
  • The PMC offers high throughput and statistical power for pharmaceutical screening.
  • This technology enables new capabilities for image-based drug discovery with suspension samples.