Microfluidic platforms for monitoring cardiomyocyte electromechanical activity

Abstract Cardiovascular diseases account for ~40% of global deaths annually. This situation has revealed the urgent need for the investigation and development of corresponding drugs for pathogenesis due to the complexity of research methods and detection techniques. An in vitro cardiomyocyte model i...

Full description

Saved in:
Bibliographic Details
Main Authors: Wei Wang, Weiguang Su, Junlei Han, Wei Song, Xinyu Li, Chonghai Xu, Yu Sun, Li Wang
Format: Article
Language:English
Published: Nature Publishing Group 2025-01-01
Series:Microsystems & Nanoengineering
Online Access:https://doi.org/10.1038/s41378-024-00751-z
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1841544492421742592
author Wei Wang
Weiguang Su
Junlei Han
Wei Song
Xinyu Li
Chonghai Xu
Yu Sun
Li Wang
author_facet Wei Wang
Weiguang Su
Junlei Han
Wei Song
Xinyu Li
Chonghai Xu
Yu Sun
Li Wang
author_sort Wei Wang
collection DOAJ
description Abstract Cardiovascular diseases account for ~40% of global deaths annually. This situation has revealed the urgent need for the investigation and development of corresponding drugs for pathogenesis due to the complexity of research methods and detection techniques. An in vitro cardiomyocyte model is commonly used for cardiac drug screening and disease modeling since it can respond to microphysiological environmental variations through mechanoelectric feedback. Microfluidic platforms are capable of accurate fluid control and integration with analysis and detection techniques. Therefore, various microfluidic platforms (i.e., heart-on-a-chip) have been applied for the reconstruction of the physiological environment and detection of signals from cardiomyocytes. They have demonstrated advantages in mimicking the cardiovascular structure and function in vitro and in monitoring electromechanical signals. This review presents a summary of the methods and technologies used to monitor the contractility and electrophysiological signals of cardiomyocytes within microfluidic platforms. Then, applications in common cardiac drug screening and cardiovascular disease modeling are presented, followed by design strategies for enhancing physiology studies. Finally, we discuss prospects in the tissue engineering and sensing techniques of microfluidic platforms.
format Article
id doaj-art-1d8c7e736a3a4202b6442e950be71d04
institution Kabale University
issn 2055-7434
language English
publishDate 2025-01-01
publisher Nature Publishing Group
record_format Article
series Microsystems & Nanoengineering
spelling doaj-art-1d8c7e736a3a4202b6442e950be71d042025-01-12T12:27:53ZengNature Publishing GroupMicrosystems & Nanoengineering2055-74342025-01-0111112210.1038/s41378-024-00751-zMicrofluidic platforms for monitoring cardiomyocyte electromechanical activityWei Wang0Weiguang Su1Junlei Han2Wei Song3Xinyu Li4Chonghai Xu5Yu Sun6Li Wang7School of Mechanical Engineering, Qilu University of Technology (Shandong Academy of Sciences)School of Mechanical Engineering, Qilu University of Technology (Shandong Academy of Sciences)School of Mechanical Engineering, Qilu University of Technology (Shandong Academy of Sciences)Department of Minimally Invasive Comprehensive Treatment of Cancer, Shandong Provincial Hospital Affiliated to Shandong First Medical UniversityDepartment of Minimally Invasive Comprehensive Treatment of Cancer, Shandong Provincial Hospital Affiliated to Shandong First Medical UniversitySchool of Mechanical Engineering, Qilu University of Technology (Shandong Academy of Sciences)Department of Mechanical and Industrial Engineering, University of TorontoSchool of Mechanical Engineering, Qilu University of Technology (Shandong Academy of Sciences)Abstract Cardiovascular diseases account for ~40% of global deaths annually. This situation has revealed the urgent need for the investigation and development of corresponding drugs for pathogenesis due to the complexity of research methods and detection techniques. An in vitro cardiomyocyte model is commonly used for cardiac drug screening and disease modeling since it can respond to microphysiological environmental variations through mechanoelectric feedback. Microfluidic platforms are capable of accurate fluid control and integration with analysis and detection techniques. Therefore, various microfluidic platforms (i.e., heart-on-a-chip) have been applied for the reconstruction of the physiological environment and detection of signals from cardiomyocytes. They have demonstrated advantages in mimicking the cardiovascular structure and function in vitro and in monitoring electromechanical signals. This review presents a summary of the methods and technologies used to monitor the contractility and electrophysiological signals of cardiomyocytes within microfluidic platforms. Then, applications in common cardiac drug screening and cardiovascular disease modeling are presented, followed by design strategies for enhancing physiology studies. Finally, we discuss prospects in the tissue engineering and sensing techniques of microfluidic platforms.https://doi.org/10.1038/s41378-024-00751-z
spellingShingle Wei Wang
Weiguang Su
Junlei Han
Wei Song
Xinyu Li
Chonghai Xu
Yu Sun
Li Wang
Microfluidic platforms for monitoring cardiomyocyte electromechanical activity
Microsystems & Nanoengineering
title Microfluidic platforms for monitoring cardiomyocyte electromechanical activity
title_full Microfluidic platforms for monitoring cardiomyocyte electromechanical activity
title_fullStr Microfluidic platforms for monitoring cardiomyocyte electromechanical activity
title_full_unstemmed Microfluidic platforms for monitoring cardiomyocyte electromechanical activity
title_short Microfluidic platforms for monitoring cardiomyocyte electromechanical activity
title_sort microfluidic platforms for monitoring cardiomyocyte electromechanical activity
url https://doi.org/10.1038/s41378-024-00751-z
work_keys_str_mv AT weiwang microfluidicplatformsformonitoringcardiomyocyteelectromechanicalactivity
AT weiguangsu microfluidicplatformsformonitoringcardiomyocyteelectromechanicalactivity
AT junleihan microfluidicplatformsformonitoringcardiomyocyteelectromechanicalactivity
AT weisong microfluidicplatformsformonitoringcardiomyocyteelectromechanicalactivity
AT xinyuli microfluidicplatformsformonitoringcardiomyocyteelectromechanicalactivity
AT chonghaixu microfluidicplatformsformonitoringcardiomyocyteelectromechanicalactivity
AT yusun microfluidicplatformsformonitoringcardiomyocyteelectromechanicalactivity
AT liwang microfluidicplatformsformonitoringcardiomyocyteelectromechanicalactivity