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血清和复合制剂制备方法对人心肌诱导多能干细胞(hiPSC-CMs)延迟复极评估的影响。

Effects of Serum and Compound Preparation Methods on Delayed Repolarization Evaluation With Human iPSC-CMs.

机构信息

Division of Systems Biology, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, Arkansas 72079, USA.

Department of Structural Heart Disease, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, China.

出版信息

Toxicol Sci. 2022 Jun 28;188(1):48-61. doi: 10.1093/toxsci/kfac043.

Abstract

Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) have been widely used in the Comprehensive in vitro Proarrhythmia Assay (CiPA). The notable difference of the electrophysiological (EP) responses of hiPSC-CMs in serum and serum-free media (SFM) is puzzling and may impact regulatory decision-making on the cardiac safety of candidate drugs in inducing QT prolongation and torsade de pointes (TdP). In this study, we compared the EP responses of hiPSC-CMs to 10 CiPA compounds and moxifloxacin in serum and SFM; explained the potential reason behind the different EP responses-abiotic compound loss to plastic tubes/plates of hydrophobic compounds prepared in SFM; and investigated the impact of compound preparation methods on drug bioavailability in exposure media, which affects the TdP risk prediction of drugs tested in serum-containing and SFM. For assays to be conducted in SFM, awareness of abiotic compound loss of hydrophobic compounds in serum-free preparations is critical for delay repolarization evaluation and data extrapolation from in vitro to in vivo.

摘要

人诱导多能干细胞衍生的心肌细胞(hiPSC-CMs)已广泛应用于综合体外致心律失常试验(CiPA)。血清和无血清培养基(SFM)中 hiPSC-CMs 的电生理(EP)反应的显著差异令人费解,可能会影响候选药物致 QT 延长和尖端扭转型室性心动过速(TdP)的心脏安全性的监管决策。在这项研究中,我们比较了 hiPSC-CMs 在血清和 SFM 中对 10 种 CiPA 化合物和莫西沙星的 EP 反应;解释了 EP 反应不同的潜在原因——亲脂性化合物在 SFM 中制备时会从塑料管/板中损失非生物化合物;并研究了化合物制备方法对暴露介质中药物生物利用度的影响,这会影响在含血清和 SFM 中进行测试的药物的 TdP 风险预测。对于在 SFM 中进行的测定,需要注意无血清制剂中亲脂性化合物的非生物化合物损失,这对于延迟复极化评估和从体外数据外推至体内至关重要。

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