a 2025

Dual-Organoid Biosensor for Monitoring Cardiac Conduction Disturbances In Vitro

MÁČALA, Jakub; Filip SVĚRÁK; Daniil KABANOV; Šimon VRANA; Deborah BECKEROVÁ et al.

Basic information

Original name

Dual-Organoid Biosensor for Monitoring Cardiac Conduction Disturbances In Vitro

Authors

MÁČALA, Jakub; Filip SVĚRÁK; Daniil KABANOV; Šimon VRANA; Deborah BECKEROVÁ; Jan MÁCHAL; Martin PEŠL; Vladimír ROTREKL and Jan PŘIBYL

Edition

2025

Other information

Language

English

Type of outcome

Konferenční abstrakta

Country of publisher

Czech Republic

Confidentiality degree

is not subject to a state or trade secret

References:

Marked to be transferred to RIV

No

Organization

Středoevropský technologický institut – Repository – Repository

Keywords in English

AFM; cardiomyocytes; arrthytmy; contraction; pluripotent stem cell

Links

EH23_015/0008175, research and development project. LM2023042, research and development project. LUC24105, research and development project. MUNI/G/1125/2022, interní kód Repo.
Changed: 27/2/2026 00:51, RNDr. Daniel Jakubík

Abstract

In the original language

Atomic Force Microscopy (AFM) is traditionally employed as a high-resolution imaging tool to analyze surface morphology and mechanical properties by scanning a sharp tip mounted on a flexible cantilever. Robust feedback system and micromechanical transducers are responsible for the constant adjustment of tip-sample interaction; however, it can be utilized to monitor the contraction dynamics of cardiomyocytes. Moreover, by distinguishing vertical and lateral contractile movements, AFM enables precise differentiation between focal and conductive arrhythmic contractions. This presentation introduces an AFM-based biosensor using a dual-beating human pluripotent stem cell (hPSC)-derived organoid. The high biosensor sensitivity allows detailed analysis of contractile behavior under pharmacological modulation with cardiomodulating drugs. The dual-organoid system enhances model robustness by minimizing variability inherent 19 in single-cell studies, thereby improving its translational relevance for cardiotoxicity assessment.

Files attached