Key result
Flexible 4-electrode microelectrode arrays capture high-quality ECGs and reveal site-specific injury currents in preclinical models.
Wearable polymer-based microelectrode arrays can successfully monitor long-term electrophysiological phenotypes in small vertebrate models of heart injury.
Advances preclinical ECG phenotyping in small vertebrate injury models; hypothesis-generating for wearable sensors with no clinical implications yet.
Understanding the regenerative capacity of small vertebrate models has provided new insights into the plasticity of injured myocardium. Here, we demonstrate the application of flexible microelectrode arrays (MEAs) in elucidating electrophysiological phenotypes of zebrafish and neonatal mouse models of heart regeneration. The 4-electrode MEA membranes were designed to detect electrical signals in the aquatic environment. They were micro-fabricated to adhere to the non-planar body surface of zebrafish and neonatal mice. The acquired signals were processed to display an electrocardiogram (ECG) with high signal-to-noise-ratios, and were validated via the use of conventional micro-needle electrodes. The 4-channel MEA provided signal stability and spatial resolution, revealing the site-specific electrical injury currents such as ST-depression in response to ventricular cryo-injury. Thus, our polymer-based and wearable MEA membranes provided electrophysiological insights into long-term conduction phenotypes for small vertebral models of heart injury and regeneration with a translational implication for monitoring cardiac patients.
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Cao et al. (2014) studied Injured myocardium in zebrafish and neonatal mouse models. Flexible microelectrode arrays (MEAs) vs. Conventional micro-needle electrodes was evaluated on Detection of electrical signals (ECG) and site-specific electrical injury currents. Flexible 4-electrode microelectrode arrays successfully acquired high signal-to-noise-ratio ECGs and revealed site-specific electrical injury currents in zebrafish and neonatal mouse models.
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