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Substrate-integrated multielectrode arrays (MEAs) enable multisite, long-term, and label-free sensing and actuation of neuronal electrical signals in reduced cell culture models for network electrophysiology. Conventional, thin-film fabricated passive MEAs typically provide a few tens of electrode sites. New generations of active CMOS-based high-resolution arrays provide the capabilities of simultaneous recordings from thousands of neurons over fields of view of several square millimeters, yet allowing extracellular electrical imaging to be achieved down to the subcellular scale. In turn, such advancement in chip-based electrical readouts can significantly complement recently developed biotechnological and bimolecular techniques for neurobiology applications. Here, we describe (1) a simple method to fabricate passive MEAs and (2) protocols for preparing and growing primary rat hippocampal neuronal cultures and human iPS-derived neurons on MEAs. The aim is to provide reliable protocols for initiating the reader to this technology and for stimulating their further development and experimental use in neurobiology.
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http://dx.doi.org/10.1007/978-1-4939-7792-5_12 | DOI Listing |
Front Toxicol
August 2025
Ncardia Services B.V., Leiden, Netherlands.
Introduction: Efficient preclinical prediction of cardiovascular side effects poses a pivotal challenge for the pharmaceutical industry. Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) are becoming increasingly important in this field due to inaccessibility of human native cardiac tissue. Current preclinical hiPSC-CMs models focus on functional changes such as electrophysiological abnormalities, however other parameters, such as structural toxicity, remain less understood.
View Article and Find Full Text PDFPain Rep
October 2025
Physiology, Pharmacology and Neuroscience, School of Life Sciences, The University of Nottingham, Nottingham, United Kingdom.
Introduction: The dorsal horn (DH) of the spinal cord is physiologically immature at birth. Spinal excitability increases and wide dynamic range (WDR) neurons in lamina V have lowered activation thresholds and larger receptive field sizes.
Objective: The DH is composed of 5 laminae containing diverse interneuronal populations yet our understanding of the physiology of the DH is based on behavioural studies or extrapolation of single cell WDR recordings to the whole network.
Biosens Bioelectron
September 2025
Tianjin Key Laboratory of Life and Health Detection, Life and Health Intelligent Research Institute, Tianjin University of Technology, Tianjin, 300384, PR China. Electronic address:
Wearable sweat sensors offer noninvasive health monitoring through multiplexed biomarker analysis, delivering real-time diagnostics with continuous operational capability. However, chronic cutaneous interface hydration during prolonged monitoring induces adhesive delamination phenomena that manifest as signal attenuation, which fundamentally limits their clinical reliability. To address this challenge, we developed a thermodynamically adaptive polymer interface combining three functional components: mussel-inspired catechol moieties for moisture-tolerant adhesion, hydrophobic acrylates ensuring mechanical stability, and N-isopropylacrylamide enabling thermal responsiveness.
View Article and Find Full Text PDFPLoS One
September 2025
Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Recent advances in three-dimensional (3D) biological brain models in vitro and ex vivo are creating new opportunities to understand the complexity of neural networks but pose the technological challenge of obtaining high-throughput recordings of electrical activity from multiple sites in 3D at high spatiotemporal resolution. This cannot be achieved using planar multi-electrode arrays (MEAs), which contact just one side of the neural structure. Moreover, the specimen adhesion to planar MEAs limits fluid perfusion along with tissue viability and drug application.
View Article and Find Full Text PDFAdv Healthc Mater
September 2025
Singapore Centre for 3D Printing, Nanyang Technological University, Singapore, 639798, Singapore.
Organotypic 3D tissue models require precise electrophysiological interfaces to study function and disease. Multi-electrode arrays (MEAs) are essential for recording and stimulation, yet conventional fabrication methods are costly and time-intensive. This study demonstrates aerosol jet printing (AJP) of gold nanoparticles onto flexible polyimide substrates to produce fully gold, biocompatible MEAs for rapid customization of MEAs.
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