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Microinstrumentation for Brain Organoids.

Devan Patel1, Saniya Shetty2, Chris Acha1

  • 1Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD, 21218, USA.

Advanced Healthcare Materials
|January 13, 2024
PubMed
Summary
This summary is machine-generated.

New 3D microinstrumentation is crucial for brain organoid research, overcoming limitations of traditional 2D tools. This enables advanced brain organoid-machine interfaces for neuroscience and drug discovery.

Keywords:
microfluidicsmicrophysiological systemsneuromodulationneuromorphic computingorganoid intelligence

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Area of Science:

  • Neuroscience
  • Biotechnology
  • Bioengineering

Background:

  • Brain organoids, 3D stem cell aggregates, mimic human brain structures and functions.
  • They offer advanced models for developmental biology, neuroscience, toxicology, and computer engineering, surpassing limitations of traditional 2D cell cultures and animal studies.
  • Existing microinstrumentation, often 2D-based, faces challenges interfacing with 3D brain organoids.

Purpose of the Study:

  • To review conventional planar approaches and emerging 3D microinstrumentation for brain organoid research.
  • To highlight the necessity of developing new instrumentation compatible with 3D organoid formats and live cell culture.
  • To discuss advancements enabling robust organoid culture and reliable 3D spatiotemporal information transfer.

Main Methods:

  • Survey of recently developed microinstrumentation for organoid-machine interfaces.
  • Discussion of 3D printed and curved microfluidics.
  • Review of 3D optical techniques, buckling/self-folding microelectrode arrays (MEAs), 3D electrochemical interfaces, and 3D magnetic/acoustic technologies.

Main Results:

  • Emerging 3D microinstrumentation shows promise for overcoming 2D limitations in brain organoid research.
  • Technologies discussed include advanced microfluidics, optical methods, MEAs, electrochemical sensors, and magnetic/acoustic systems.
  • These innovations facilitate two-way information transfer with brain organoids.

Conclusions:

  • There is a critical need for novel 3D microinstrumentation to advance brain organoid research.
  • Developing scalable, 3D-compatible tools is essential for robust organoid culture and reliable spatiotemporal data acquisition.
  • Future work should focus on addressing challenges for seamless organoid-machine interfacing.