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用于病理生理研究和药物筛选的仿生心脏微系统。

Biomimetic cardiac microsystems for pathophysiological studies and drug screens.

作者信息

Lee Joohyung, Razu Md Enayet, Wang Xinmei, Lacerda Carla, Kim Jungkyu Jay

机构信息

Department of Mechanical Engineering, Texas Tech University, Lubbock, TX, USA.

Department of Chemical Engineering, Texas Tech University, Lubbock, TX, USA.

出版信息

J Lab Autom. 2015 Apr;20(2):96-106. doi: 10.1177/2211068214560903. Epub 2014 Dec 18.

Abstract

Microfabricated organs-on-chips consist of tissue-engineered 3D in vitro models, which rely on engineering design and provide the physiological context of human organs. Recently, significant effort has been devoted to the creation of a biomimetic cardiac system by using microfabrication techniques. By applying allometric scaling laws, microengineered cardiac systems simulating arterial flow, pulse properties, and architectural environments have been implemented, allowing high-throughput pathophysiological experiments and drug screens. In this review, we illustrate the recent trends in cardiac microsystems with emphasis on cardiac pumping and valving functions. We report problems and solutions brought to light by existing organs-on-chip models and discuss future directions of the field. We also describe the needs and desired design features that will enable the control of mechanical, electrical, and chemical environments to generate functional in vitro cardiac disease models.

摘要

微制造的芯片器官由组织工程化的三维体外模型组成,这些模型依赖于工程设计并提供人体器官的生理环境。最近,人们投入了大量精力利用微制造技术创建仿生心脏系统。通过应用异速生长比例定律,已经实现了模拟动脉血流、脉搏特性和结构环境的微工程心脏系统,从而能够进行高通量病理生理实验和药物筛选。在这篇综述中,我们阐述了心脏微系统的最新趋势,重点是心脏泵血和瓣膜功能。我们报告了现有芯片器官模型所揭示的问题及解决方案,并讨论了该领域的未来方向。我们还描述了能够控制机械、电和化学环境以生成功能性体外心脏病模型的需求和理想设计特征。

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