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基于芯片上心脏模型的高通量心脏功能评估及其在药物筛选中的应用

High-Content Assessment of Cardiac Function Using Heart-on-a-Chip Devices as Drug Screening Model.

机构信息

Institute of Biomaterials and Biomedical Engineering, University of Toronto, Toronto, ON, Canada.

Department of Chemical Engineering and Applied Chemistry, University of Toronto, Toronto, ON, Canada.

出版信息

Stem Cell Rev Rep. 2017 Jun;13(3):335-346. doi: 10.1007/s12015-017-9736-2.

Abstract

Drug discovery and development continues to be a challenge to the pharmaceutical industry despite great advances in cell and molecular biology that allow for the design of better targeted therapeutics. Many potential drug compounds fail during the clinical trial due to inefficacy and toxicity that were not predicted during preclinical stages. The fundamental problem lies with the use of traditional drug screening models that still largely rely on the use of cell lines or animal cell monolayers, which leads to lack of predictive power of human tissue and organ response to the drug candidates. More physiologically relevant systems are therefore critical in relieving the burden of high failure rates. Emerging knowledge and techniques in tissue engineering and microfabrication have enabled the development of micro-engineered systems - collectively known as organs-on-chips - that may lead to a paradigm shift in preclinical drug screening assays. In this review we explore the technological advances and challenges in the development of heart-on-a-chip models, by addressing current assessment methods for drug-induced cardiotoxicity and providing a perspective on the modifications that should be implemented to realize the full potential of this system.

摘要

尽管细胞和分子生物学取得了巨大进展,使得设计更好的靶向治疗药物成为可能,但药物发现和开发仍然是制药行业面临的挑战。许多潜在的药物化合物在临床试验中失败,原因是在临床前阶段没有预测到无效性和毒性。根本问题在于使用传统的药物筛选模型,这些模型仍然在很大程度上依赖于细胞系或动物细胞单层的使用,这导致对候选药物的人体组织和器官反应的预测能力不足。因此,更符合生理的系统对于减轻高失败率的负担至关重要。组织工程和微制造领域的新兴知识和技术使微工程系统的发展成为可能——这些系统统称为“芯片上器官”——这可能会导致临床前药物筛选检测的范式转变。在这篇综述中,我们探讨了心脏芯片模型发展中的技术进步和挑战,通过解决当前用于评估药物诱导的心脏毒性的方法,并提供了对应该实施的修改的观点,以实现该系统的全部潜力。

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