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Related Concept Videos

Overview Of Cell Separation And Isolation01:20

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Cell separation was first achieved in 1964 by S. H. Seal, who separated large tumor cells from the smaller blood cells using filtration. Two years later, Pohl and Hawk performed experiments on how cells respond differently to a nonuniform electric field based on the cell type. Such observations were the inception of cell separation methods, which allow isolating a single cell type from a heterogeneous sample.
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Centrifugation is a separation technique based on differences in density or size. It is commonly used to separate solids from aqueous interferents. During centrifugation, the sample is placed in centrifugation tubes and spun at high angular velocity, which allows centrifugal force to act differentially on the different densities or masses of the components. After spinning, the supernatant liquid is decanted. Depending on the specific application, either the pellet or the supernatant is retained...
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Separating Beads and Cells in Multi-channel Microfluidic Devices Using Dielectrophoresis and Laminar Flow
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Blood component separation in straight microfluidic channels.

Lap Man Lee1, Ketan H Bhatt1, Dustin W Haithcock1

  • 1CFD Research Corporation, Huntsville, Alabama 35806, USA.

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|October 19, 2023
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Summary
This summary is machine-generated.

This study presents a novel microfluidic device for rapid blood component separation without dilution or lysis. The passive system achieves high purity for platelets and efficient red blood cell removal, enhancing field diagnostics.

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Area of Science:

  • Biomedical Engineering
  • Microfluidics
  • Hematology

Background:

  • Traditional blood component separation relies on labor-intensive centrifugation.
  • Field and resource-limited blood processing requires advanced, portable technologies.
  • Existing microfluidic methods often necessitate sample pretreatment or exhibit lower efficiency.

Purpose of the Study:

  • To develop a rapid, passive microfluidic device for efficient blood component separation.
  • To improve separation efficiency using integrated fluidic restrictors.
  • To demonstrate versatile operation modes for various blood fractionation applications.

Main Methods:

  • Utilized a small footprint, passive microfluidic channel device.
  • Leveraged margination and inertial focusing effects for separation.
  • Incorporated fluidic restrictors at outlet ports to enhance separation precision.
  • Employed straight microfluidic channels with a high aspect ratio rectangular cross section.

Main Results:

  • Achieved 95.4% platelet purity from human whole blood.
  • Demonstrated 99.9% red blood cell (RBC) removal rate during plasma extraction.
  • Successfully concentrated platelet-rich plasma by 2.6×.
  • Showcased scalable, continuous, and clog-free operation.

Conclusions:

  • The developed microfluidic device offers a versatile and efficient solution for blood component separation.
  • This technology bypasses the need for sample dilution, lysis, or labeling, preserving sample integrity.
  • The system is suitable for integration into multi-step workflows for advanced sample preparation and diagnostics.