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Fabrication of 3D Cardiac Microtissue Arrays using Human iPSC-Derived Cardiomyocytes, Cardiac Fibroblasts, and Endothelial Cells
Published on: March 14, 2021
A simulation study evaluating the performance of high-density electrode arrays on myocardial tissue
1Electrical and Computer Engineering Department, University of Vermont, Burlington 05405-0156, USA. eason@emba.uvm.edu
High-density electrode arrays for cellular activation detection do not significantly distort tissue wavefronts. Findings suggest that electrode spacing ratio (SR) below 2.0 is viable for electrophysiological studies.
Area of Science:
- Electrophysiology
- Biomedical Engineering
- Computational Neuroscience
Background:
- High-density multielectrode arrays (MEAs) are crucial for detecting cellular activation.
- Increasing electrode density challenges fundamental assumptions of activation mapping regarding electrode separation and interference.
- The point-like assumption of electrodes may be invalidated by dense MEAs.
Purpose of the Study:
- To directly test the assumptions of activation mapping for high-density electrode arrays.
- To evaluate the impact of electrode width and spacing ratio (SR) on signal detection.
- To analyze wavefront propagation and activation timing in the presence of dense MEAs.
Main Methods:
- Utilized a finite element model incorporating modified Fitzhugh-Nagumo kinetics.
- Represented electrodes as isopotential surfaces with varying widths and spacing ratios (SR).
- Simulated the detection of cellular activation by a single electrode from a passing wavefront.
Main Results:
- High-density arrays did not cause significant wavefront curvature or alter activation timing.
- Signal strength and crosstalk are influenced by the interaction between wavefronts and induced electrode sources.
- Sensitivity analysis confirmed generalizability across various physiological conditions.
Conclusions:
- Current electrode array designs with large spacing relative to diameter may be overly conservative.
- Electrode arrays with a spacing ratio (SR) less than 2.0 can perform successfully in electrophysiological studies.
- Dense MEAs can reliably detect cellular activation without compromising fundamental mapping assumptions.
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