Key result
Multielectrode array technology using human induced pluripotent stem cell-derived cardiomyocytes provides a facile in vitro screen for compound-induced effects on cardiac electrophysiology.
The use of hiPSC-CMs with MEA technology provides a viable in vitro human cardiomyocyte model for routine preclinical screening of compound-induced cardiotoxicity.
May aid preclinical cardiotoxicity screening in drug development; leaves open clinical outcome correlation.
Cardiotoxicity is a leading cause of compound attrition during drug development. Preclinical models used to assess the risk for compound-induced effects on cardiac electrophysiology largely rely on animals that can differ in terms of sensitivity and specificity to the targeted clinical response. There is currently no in vitro human cardiomyocyte model for routine preclinical compound screening, as adult human cardiac tissue is unsuitable for such screening. The commercial availability of human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) makes possible the development of assays for assessing compound-induced effects on cardiac function in a human cardiomyocyte-like model. Using multielectrode array (MEA) technology with hiPSC-CMs provides a facile screen for compound-induced effects on cardiac electrophysiology. The MEA data generated from hiPSC-CMs correlate well with the results of conventional preclinical assays and clinical findings. Described in this unit is a technique for measuring extracellular field potentials from hiPSC-CMs using MEA technology to screen for compound-induced effects on cardiac electrophysiology.
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Kate Harris (2015) studied Cardiotoxicity. Multielectrode array (MEA) technology with hiPSC-CMs was evaluated on Compound-induced effects on cardiac electrophysiology. Multielectrode array technology using human induced pluripotent stem cell-derived cardiomyocytes provides a facile in vitro screen for compound-induced effects on cardiac electrophysiology.
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