Wearable multi-channel microelectrode membranes for elucidating electrophysiological phenotypes of injured myocardium
Author(s) -
Hung Cao,
Fei Yu,
Yu Zhao,
Xiaoxiao Zhang,
Joyce Tai,
Juhyun Lee,
Ali Darehzereshki,
Malcolm Bersohn,
ChingLing Lien,
C. Neil,
YuChong Tai,
Tzung K. Hsiai
Publication year - 2014
Publication title -
integrative biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.853
H-Index - 70
eISSN - 1757-9708
pISSN - 1757-9694
DOI - 10.1039/c4ib00052h
Subject(s) - electrophysiology , microelectrode , zebrafish , regeneration (biology) , cardiac electrophysiology , biomedical engineering , multielectrode array , wearable computer , membrane , neuroscience , biology , materials science , electrode , medicine , microbiology and biotechnology , chemistry , computer science , biochemistry , genetics , gene , embedded system
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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