用于药物开发的体外仿生心脏平台

Sungwoo Cho, S. Ko
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引用次数: 0

摘要

新药开发目前非常昂贵且耗时。此外,一些经过动物和临床试验批准的药物由于不良反应而被撤销批准。大约30%的此类药物有心脏副作用。传统的基于细胞的药物毒性试验是在与体内环境完全不同的条件下进行的,并且由于物种之间的差异,用于药物评价的动物试验具有局限性。因此,研究人员越来越关注开发能够克服这些限制的模型,以实现准确的药物毒性测试。本文概述了体外仿生心脏平台,如心脏类器官、三维生物打印和心脏芯片设备,并描述了它们的优点、局限性和未来前景。开发和使用有效的心脏仿生模型可以通过提供更具体的药物代谢信息和降低药物开发后期的失败率,有助于开发替代动物试验的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biomimetic in vitro heart platforms for drug development
New drug development is currently very expensive and time-consuming. In addition, some drugs that are approved after animal and clinical trials have their approval revoked because of adverse effects. About 30% of such drugs have heart side effects. Conventional cell-based drug toxicity tests are performed under conditions entirely different from the in vivo environment, and animal testing for drug evaluation has limitations because of differences between species. Therefore, researchers are increasingly focusing on developing models that can overcome these limitations to enable accurate drug toxicity tests. This review outlines biomimetic in vitro heart platforms, such as heart organoids, 3-dimensional bioprinting, and heart-on-a-chip devices, and describes their advantages, limitations, future perspectives. The development and use of effective cardiac biomimetic models could contribute to the development of alternatives to animal testing by providing more specific information on drug metabolism and reducing the rate of failure in later stages of drug development.
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