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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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Related Experiment Video

Updated: Apr 4, 2026

Fluorescence-activated Cell Sorting for Purification of Plasmacytoid Dendritic Cells from the Mouse Bone Marrow
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Acoustofluidic Fluorescence Activated Cell Sorter.

Ahmad Ahsan Nawaz1,2, Yuchao Chen1, Nitesh Nama1

  • 1Department of Engineering Science and Mechanics, The Pennsylvania State University , University Park, Pennsylvania 16802, United States.

Analytical Chemistry
|September 3, 2015
PubMed
Summary
This summary is machine-generated.

This study introduces an acoustofluidic fluorescence activated cell sorting (FACS) device for high-throughput cell isolation. The novel chip integrates cell focusing and sorting, achieving high purity and cell viability for biological applications.

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Assembly and Operation of an Acoustofluidic Device for Enhanced Delivery of Molecular Compounds to Cells
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Area of Science:

  • Biotechnology
  • Microfluidics
  • Cell Biology

Background:

  • Selective cell isolation is critical for biological research and clinical diagnostics.
  • Existing cell sorting methods face limitations in throughput, resolution, or complexity.

Purpose of the Study:

  • To develop an integrated acoustofluidic fluorescence activated cell sorting (FACS) device.
  • To achieve on-demand, high-throughput, and high-resolution cell detection and sorting on a single chip.

Main Methods:

  • Utilized microfluidic drifting for precise 3D cell focusing.
  • Employed standing surface acoustic waves (SSAW) for triggered, on-demand cell sorting.
  • Integrated laser interrogation and acoustic sorting on a single microfluidic chip.

Main Results:

  • Demonstrated continuous isolation of fluorescently labeled HeLa cells with high purity (92.3 ± 3.39%).
  • Achieved a high throughput of approximately 1200 events/s.
  • Maintained high post-sort cell viability (99.18%), indicating biocompatibility.

Conclusions:

  • The integrated acoustofluidic FACS device enables efficient, high-purity cell sorting.
  • The technology offers a promising platform for developing portable, user-friendly FACS instruments.
  • This device has significant potential for diverse biological studies and clinical applications.