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DOI: 10.3791/64265-v
Shane Rui Zhao1,2, Gema Mondéjar-Parreño1,2, Dong Li1,2, Mengcheng Shen1,2, Joseph C. Wu1,2,3
1Stanford Cardiovascular Institute,Stanford University School of Medicine, 2Division of Cardiovascular Medicine, Department of Medicine,Stanford University School of Medicine, 3Department of Radiology,Stanford University School of Medicine
Please note that some of the translations on this page are AI generated. Click here for the English version.
Human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) are a reliable model for assessing cardiac safety during drug development. This article details methodologies for evaluating the contractility and electrophysiology of hiPSC-CMs.
人诱导的多能干细胞来源的心肌细胞(hiPSC-CMs)已成为药物诱导的心脏毒性筛查和疾病建模的有前途的 体外 模型。在这里,我们详细介绍了用于测量hiPSC-CMs的收缩力和电生理学的方案。
心脏安全性评估是药物开发过程中的关键组成部分。人iPSC来源的心肌细胞已被证明是一种可靠、高效和基于人类的临床前心脏安全性评估模型。我们已经建立了全面研究人iPSC来源心肌细胞功能特征的方法,这些方法具有非常重要的疾病建模,药物诱导的心脏毒性筛查和精准医学。
越来越多地将人iPSC来源的心肌细胞纳入标准的临床前安全性评估过程,有可能提高候选化合物毒性预测的准确性。首先培养人iPSC来源的心肌细胞至少10天,然后再进行测量。打开温度控制器并将其设置为 37 摄氏度。
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