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Related Concept Videos

Flow Cytometry01:23

Flow Cytometry

12.9K
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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Related Experiment Video

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Simultaneous Assessment of Kinship, Division Number, and Phenotype via Flow Cytometry for Hematopoietic Stem and Progenitor Cells
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Cell streak imaging cytometry for rare cell detection.

Joshua Balsam1, Hugh Alan Bruck2, Avraham Rasooly3

  • 1Division of Biology, Office of Science and Engineering, FDA, Silver Spring, MD 20993, United States; University of Maryland, College Park, MD 20742, United States.

Biosensors & Bioelectronics
|September 13, 2014
PubMed
Summary
This summary is machine-generated.

This study introduces a novel imaging flow cytometer with streak imaging for sensitive rare cell detection. The device accurately quantifies rare cells in large volumes, showing promise for clinical diagnostics.

Keywords:
Flow cytometryImage enhancementRare cellsResource-poor settingsWide-field imagingmHealth

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Area of Science:

  • Biomedical Engineering
  • Cell Biology
  • Medical Diagnostics

Background:

  • Detection of rare cells, like circulating tumor cells, is crucial for clinical applications.
  • Current methods face limitations in sensitivity and data management for detecting very low cell concentrations.

Purpose of the Study:

  • To develop a highly sensitive imaging flow cytometer with streak imaging capability for rare cell detection.
  • To improve data management and throughput for rare cell analysis.

Main Methods:

  • Developed a streak mode imaging flow cytometer utilizing low-speed video to capture fluorescently labeled cells.
  • Integrated a "wide" high-throughput flow cell for analyzing large sample volumes (up to 20 mL/min).
  • Enhanced image signal-to-noise ratio using background subtraction, pixel binning, and CMOS color channel selection.

Main Results:

  • Successfully detected rare cells at concentrations of 1 cell/mL and 0.1 cell/mL in buffer with high accuracy.
  • Demonstrated accurate detection of rare cells spiked in whole blood at 10 cells/mL.
  • Achieved an average measurement of 0.91 cell/mL for a target of 1 cell/mL and 0.083 cell/mL for a target of 0.1 cell/mL.

Conclusions:

  • The developed streak mode imaging flow cytometer offers high sensitivity and accuracy for rare cell detection.
  • The system's high throughput and enhanced imaging capabilities enable analysis of large sample volumes.
  • The device's simplicity and low cost present opportunities for expanded clinical diagnostics, particularly in resource-limited settings.