Our expert for hiPSC-derived cardiac cells, as well as cell-based assays & services for drug safety and efficacy screenings
Human iPSC-derived cardiomyocytes in combination with the CardioExcyte 96 system enables detailed detection of potential cardioactive and proarrhythmic effects of test compounds on the contractility and electrophysiology of cardiomyocytes in a 96-well plate format.
This combination provides a highly relevant in vitro assay platform to study the cardiac safety profile of compounds during drug development.
You can find a step-by-step description on how to combine Pluricyte® Cardiomyocytes with the CardioExcyte 96 system in our User Guide.
Case studies assessed the effects of cardioactive compounds on the electrophysiology (i.e. extracellular field potential, EFP) and impedance of Pluricyte Cardiomyocytes using the CardioExcyte 96 system. They showed expected pharmacological responses in a reproducible manner, which could be readily detected with the CardioExcyte 96 system.
Pharmacological response of Pluricyte Cardiomyocytes to nifedipine
The L-type calcium channel blocker, nifedipine, induced a concentration-dependent decrease in impedance peak-amplitude (left) and in field potential duration (right) in Pluricyte Cardiomyocytes.
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