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  • A label-free and high-throughput separation of neuron and glial cells using an inertial microfluidic platform

    Author(s)
    Jin, Tiantian
    Yan, Sheng
    Zhang, Jun
    Yuan, Dan
    Huang, Xu-Feng
    Li, Weihua
    Griffith University Author(s)
    Zhang, Jun
    Year published
    2016
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    Abstract
    While neurons and glial cells both play significant roles in the development and therapy of schizophrenia, their specific contributions are difficult to differentiate because the methods used to separate neurons and glial cells are ineffective and inefficient. In this study, we reported a high-throughput microfluidic platform based on the inertial microfluidic technique to rapidly and continuously separate neurons and glial cells from dissected brain tissues. The optimal working condition for an inertial biochip was investigated and evaluated by measuring its separation under different flow rates. Purified and enriched neurons ...
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    While neurons and glial cells both play significant roles in the development and therapy of schizophrenia, their specific contributions are difficult to differentiate because the methods used to separate neurons and glial cells are ineffective and inefficient. In this study, we reported a high-throughput microfluidic platform based on the inertial microfluidic technique to rapidly and continuously separate neurons and glial cells from dissected brain tissues. The optimal working condition for an inertial biochip was investigated and evaluated by measuring its separation under different flow rates. Purified and enriched neurons in a primary neuron culture were verified by confocal immunofluorescence imaging, and neurons performed neurite growth after separation, indicating the feasibility and biocompatibility of an inertial separation. Phencyclidine disturbed the neuroplasticity and neuron metabolism in the separated and the unseparated neurons, with no significant difference. Apart from isolating the neurons, purified and enriched viable glial cells were collected simultaneously. This work demonstrates that an inertial microchip can provide a label-free, high throughput, and harmless tool to separate neurological primary cells.
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    Journal Title
    Biomicrofluidics
    Volume
    10
    Issue
    3
    DOI
    https://doi.org/10.1063/1.4949770
    Subject
    Classical physics
    Other engineering
    Nanotechnology
    Science & Technology
    Life Sciences & Biomedicine
    Physical Sciences
    Biochemical Research Methods
    Biophysics
    Publication URI
    http://hdl.handle.net/10072/407497
    Collection
    • Journal articles

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