促心律失常
电穿孔
细胞内
电生理学
生物医学工程
电极
心脏毒性
计算机科学
材料科学
医学
药品
药理学
化学
生物
内科学
细胞生物学
基因
物理化学
化疗
生物化学
作者
Zeinab Jahed,Yang Yang,Ching‐Ting Tsai,Ethan Foster,Allister F. McGuire,Huaxiao Yang,Aofei Liu,Csaba Forró,Zen Yan,Xin Jian Jiang,Mingtao Zhao,Wei Zhang,Xiao Li,Thomas L. Li,Annalisa Pawlosky,Joseph C. Wu,Bianxiao Cui
标识
DOI:10.1038/s41467-022-29726-2
摘要
Abstract Drug-induced cardiotoxicity arises primarily when a compound alters the electrophysiological properties of cardiomyocytes. Features of intracellular action potentials (iAPs) are powerful biomarkers that predict proarrhythmic risks. In the last decade, a number of vertical nanoelectrodes have been demonstrated to achieve parallel and minimally-invasive iAP recordings. However, the large variability in success rate and signal strength have hindered nanoelectrodes from being broadly adopted for proarrhythmia drug assessment. In this work, we develop vertically-aligned nanocrown electrodes that are mechanically robust and achieve > 99% success rates in obtaining intracellular access through electroporation. We validate the accuracy of nanocrown electrode recordings by simultaneous patch clamp recording from the same cell. Finally, we demonstrate that nanocrown electrodes enable prolonged iAP recording for continual monitoring of the same cells upon the sequential addition of four incremental drug doses. Our technology development provides an advancement towards establishing an iAP screening assay for preclinical evaluation of drug-induced arrhythmogenicity.
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