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Direct Contraction Force Measurements of Engineered Cardiac Tissue Constructs With Inotropic Drug Exposure
Maria Koivisto1, Milad Mosallaei2, Tarja Toimela1
1FHAIVE (Finnish Hub for Development and Validation of Integrated Approaches), Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Frontiers in Pharmacology
|May 20, 2022
Summary
This study developed a novel system using human cardiac tissue and a piezoelectric sensor to measure heart contractility. The system successfully detected both positive and negative inotropic drug effects, showing potential for drug discovery.
Area of Science:
- Cardiovascular Research
- Biomedical Engineering
- Pharmacology
Background:
- Cardiac contractility is vital for maintaining blood perfusion, and alterations can be fatal.
- Reliable methods for testing drug effects on cardiac contractility are crucial for drug discovery.
- Existing methods may not fully capture the nuances of drug-induced inotropic changes.
Purpose of the Study:
- To develop and validate a novel system for measuring cardiac contraction force.
- To assess the system's capability in detecting drug-induced inotropic effects.
- To evaluate the potential of this system for pharmaceutical research and development.
Main Methods:
- Development of a dual-axis piezoelectric force sensor.
- Creation of human cell-based vascularized cardiac tissue constructs.
- Measurement of cardiac contraction force in response to known inotropic agents.
Main Results:
- The developed system successfully measured cardiac contraction forces.
- Both positive and negative inotropic effects induced by various drugs were detected.
- Dose-dependent responses to inotropic compounds were observed.
Conclusions:
- The cardiac contraction force measurement system, integrating a piezoelectric sensor and human cardiac tissue, is effective.
- This system demonstrates significant potential for evaluating inotropic drug effects in a preclinical setting.
- The technology offers a promising platform for advancing cardiovascular drug discovery.
Keywords:
cardiac tissue modelconformal coatingcontraction forceforce measurementhuman-induced pluripotent stem cell–derived cardiomyocytesin vitro modelinotropic drug
