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Related Concept Videos

Overview Of Cell Separation And Isolation01:20

Overview Of Cell Separation And Isolation

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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Related Experiment Video

Updated: May 23, 2026

Microfluidic Buffer Exchange for Interference-free Micro/Nanoparticle Cell Engineering
10:27

Microfluidic Buffer Exchange for Interference-free Micro/Nanoparticle Cell Engineering

Published on: July 10, 2016

Microfluidic sorting of microtissues.

D G Buschke, P Resto, N Schumacher

    Biomicrofluidics
    |April 17, 2012
    PubMed
    Summary
    This summary is machine-generated.

    Researchers developed a novel microfluidic device for sorting large particles, such as embryoid bodies (EBs), enabling high-throughput analysis of 3D cell cultures. This technology efficiently purifies microtissues while maintaining cell viability and function.

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    Microfluidic Device for the Separation of Non-Metastatic (MCF-7) and Non-Tumor (MCF-10A) Breast Cancer Cells Using AC Dielectrophoresis

    Published on: August 11, 2022

    Area of Science:

    • Biotechnology
    • Microfluidics
    • Cell Biology

    Background:

    • Three-dimensional (3D) cell cultures and microtissues are increasingly used to mimic in vitro tissue microenvironments.
    • Flow cytometry advances enable high-throughput analysis of microtissues, but a method for sorting these large particles is lacking.
    • Current limitations hinder the purification of specific cell populations within complex 3D cultures.

    Purpose of the Study:

    • To develop and characterize an accessible microfluidic platform for sorting large particles.
    • To enable high-throughput purification of microtissues based on flow cytometry analysis parameters.
    • To address the need for effective sorting methods in 3D cell culture research.

    Main Methods:

    • A microfluidic-based, electromechanical approach utilizing sheath-less asymmetric curving channels was designed.
    • The device was characterized by analyzing wall shear stress, channel tortuosity, and fluid vorticity.
    • Sorting efficiency and enrichment ratio were evaluated using fluorescently labeled embryoid bodies (EBs).

    Main Results:

    • The microfluidic device achieved a sorting efficiency of 87.3% ± 13.5% for fluorescently labeled EBs.
    • An enrichment ratio of 12.2 ± 8.4 was obtained, demonstrating effective purification.
    • Cell viability, differentiation potential, and long-term function of sorted EBs were preserved.

    Conclusions:

    • The developed microfluidic device offers an effective solution for sorting large particles like microtissues.
    • This technology supports non-invasive, high-throughput analysis and purification of 3D cell cultures.
    • The platform has significant implications for advancing research in tissue engineering and regenerative medicine.