3D Spatiotemporal Electrophysiology of Cardiac Organoids Using Shell Microelectrode Arrays

Cardiac organoids have emerged as powerful platforms for modeling human heart development and disease. However, traditional 2D microelectrode arrays (MEAs) are limited to planar recordings and fail to capture the 3D propagation of electrical signals. Here, programmable, shape-adaptive, organoid-encapsulating shell MEAs are presented as a technology that enables comprehensive 3D electrophysiological mapping. These on-chip-fabricated devices feature customizable geometries and electrode layouts tailored to an organoid's unique morphology. Shell MEAs generate high-resolution 3D isochrone and conduction velocity maps, unveiling long-term spatiotemporal field potential dynamics in spontaneously beating organoids. Furthermore, they integrate multiple modalities, such as calcium imaging to corroborate electrophysiological findings and pharmacological screening to assess organoid responses to isoproterenol, E-4031, and serotonin. This platform represents a significant advance in bioelectronic interfaces, enabling high-content 3D spatiotemporal functional analysis for cardiac disease modeling and pharmacological testing.

Authors

Institutions

Publication Details

Journal
Advanced Materials
Published
2025-10-07
DOI
https://doi.org/10.1002/adma.202506793
Citations
4
Primary Topic
Neuroscience and Neural Engineering
Type
article
Field-Weighted Citation Impact
3.64
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

3D Spatiotemporal Electrophysiology of Cardiac Organoids Using Shell Microelectrode Arrays

Hanwen Wang, David H. Gracias, Deok‐Ho Kim, Soo Jin Choi et al.
4 citations
Advanced Materials
Neuroscience and Neural Engineering
3.64
article

3D Spatiotemporal Electrophysiology of Cardiac Organoids Using Shell Microelectrode Arrays

Hanwen Wang, David H. Gracias, Deok‐Ho Kim, Soo Jin Choi, Derosh George, Z. Liu, Feiyu Yang
article en
4 citations

Abstract

Cardiac organoids have emerged as powerful platforms for modeling human heart development and disease. However, traditional 2D microelectrode arrays (MEAs) are limited to planar recordings and fail to capture the 3D propagation of electrical signals. Here, programmable, shape-adaptive, organoid-encapsulating shell MEAs are presented as a technology that enables comprehensive 3D electrophysiological mapping. These on-chip-fabricated devices feature customizable geometries and electrode layouts tailored to an organoid's unique morphology. Shell MEAs generate high-resolution 3D isochrone and conduction velocity maps, unveiling long-term spatiotemporal field potential dynamics in spontaneously beating organoids. Furthermore, they integrate multiple modalities, such as calcium imaging to corroborate electrophysiological findings and pharmacological screening to assess organoid responses to isoproterenol, E-4031, and serotonin. This platform represents a significant advance in bioelectronic interfaces, enabling high-content 3D spatiotemporal functional analysis for cardiac disease modeling and pharmacological testing.

Advanced MaterialsVol. 38(2)
Johns Hopkins University (US), Johns Hopkins Medicine (US), Sidney Kimmel Comprehensive Cancer Center (US), University of Baltimore (US)
Openalex Percentile: Top 6%
Neuroscience and Neural Engineering
3.64
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.