Microinstrumentation for Brain Organoids

Author:

Patel Devan1,Shetty Saniya2,Acha Chris1,Pantoja Itzy E. Morales3ORCID,Zhao Alice4,George Derosh1ORCID,Gracias David H.15678ORCID

Affiliation:

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

2. Department of Biomedical Engineering Johns Hopkins University Baltimore MD 21218 USA

3. Center for Alternatives to Animal Testing (CAAT) Department of Environmental Health and Engineering Bloomberg School of Public Health, Johns Hopkins University Baltimore MD 21205 USA

4. Department of Biology Johns Hopkins University Baltimore MD 21218 USA

5. Department of Chemistry Johns Hopkins University Baltimore MD 21218 USA

6. Department of Materials Science and Engineering Johns Hopkins University Baltimore MD 21218 USA

7. Department of Oncology Johns Hopkins University School of Medicine Baltimore MD 21205 USA

8. Laboratory for Computational Sensing and Robotics (LCSR) Johns Hopkins University Baltimore MD 21218 USA

Abstract

AbstractBrain organoids are three‐dimensional aggregates of self‐organized differentiated stem cells that mimic the structure and function of human brain regions. Organoids bridge the gaps between conventional drug screening models such as planar mammalian cell culture, animal studies, and clinical trials. They can revolutionize the fields of developmental biology, neuroscience, toxicology, and computer engineering. Conventional microinstrumentation for conventional cellular engineering, such as planar microfluidic chips; microelectrode arrays (MEAs); and optical, magnetic, and acoustic techniques, has limitations when applied to three‐dimensional (3D) organoids, primarily due to their limits with inherently two‐dimensional geometry and interfacing. Hence, there is an urgent need to develop new instrumentation compatible with live cell culture techniques and with scalable 3D formats relevant to organoids. This review discusses conventional planar approaches and emerging 3D microinstrumentation necessary for advanced organoid–machine interfaces. Specifically, this article surveys recently developed microinstrumentation, including 3D printed and curved microfluidics, 3D and fast‐scan optical techniques, buckling and self‐folding MEAs, 3D interfaces for electrochemical measurements, and 3D spatially controllable magnetic and acoustic technologies relevant to two‐way information transfer with brain organoids. This article highlights key challenges that must be addressed for robust organoid culture and reliable 3D spatiotemporal information transfer.

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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