Advanced in vitro cardiac models for drug evaluation: integration of organoids, engineered tissues, and microphysiological systems.

IF 9.9 1区 工程技术 Q1 INSTRUMENTS & INSTRUMENTATION
Young Hyun Kim, Young Hoon Son, Yuri Choi, Min Suk Kim, Sung-Jin Park, Keel Yong Lee
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引用次数: 0

Abstract

In vitro cardiac model systems have rapidly advanced as complementary platforms to conventional two-dimensional (2D) cultures and animal models, which, despite their long-standing contributions, exhibit inherent limitations in predicting human cardiac responses. This review highlights recent progress in biomimetic platforms that more faithfully recapitulate the structure and function of the human myocardium, including engineered three-dimensional (3D) tissues, chambered ventricular constructs, self-organizing cardiac organoids, and microphysiological systems. These models are increasingly being applied as Drug Development Tools (DDTs) for safety pharmacology, efficacy testing, and cardiotoxicity assessment, offering improved predictive performance compared to traditional assays. By incorporating key features, such as three-dimensional tissue architecture, multicellular composition, electromechanical coupling, and physiological loading, these platforms enhance the translational relevance of preclinical studies. Recent innovations include maturation-enhanced organoids, vascularized engineered heart tissues, chamber models with physiological pressure-volume dynamics, and chip-based platforms that enable the real-time assessment of contractility and electrophysiology. Importantly, the integration of immune and vascular components, as well as multi-organ connectivity, further extends their applicability to systemic drug evaluations and disease modeling. Collectively, these advances bridge the gap between reductionist in vitro assays and clinical studies and align with emerging regulatory paradigms that emphasize human-relevant and non-animal testing methods. By enabling mechanistic insights into human cardiogenesis, cardiomyocyte maturation, and patient-specific disease modeling, advanced in vitro cardiac platforms hold great promise for precision pharmacology and regenerative medicine. Overall, in vitro cardiac models represent a transformative paradigm for advancing drug discovery, improving safety predictions, and reducing the reliance on animal testing in cardiovascular research.

用于药物评估的先进体外心脏模型:类器官、工程组织和微生理系统的整合。
体外心脏模型系统已经迅速发展成为传统二维(2D)培养和动物模型的补充平台,尽管它们长期以来做出了贡献,但在预测人类心脏反应方面表现出固有的局限性。这篇综述强调了仿生平台的最新进展,这些平台更真实地概括了人类心肌的结构和功能,包括工程化三维(3D)组织、室室结构、自组织心脏类器官和微生理系统。这些模型越来越多地被用作药物开发工具(DDTs),用于安全性药理学、疗效测试和心脏毒性评估,与传统分析相比,它们提供了更好的预测性能。通过结合三维组织结构、多细胞组成、机电耦合和生理负荷等关键特征,这些平台增强了临床前研究的转化相关性。最近的创新包括成熟增强类器官、血管化工程心脏组织、具有生理压力-体积动力学的腔室模型,以及能够实时评估收缩性和电生理的芯片平台。重要的是,免疫和血管成分的整合,以及多器官的连通性,进一步扩展了它们在系统药物评估和疾病建模中的适用性。总的来说,这些进步弥合了还原论体外试验和临床研究之间的差距,并与强调人类相关和非动物试验方法的新兴监管范式保持一致。通过对人类心脏发生、心肌细胞成熟和患者特异性疾病建模的机制洞察,先进的体外心脏平台在精确药理学和再生医学方面具有很大的前景。总的来说,体外心脏模型代表了一种促进药物发现、提高安全性预测和减少心血管研究中对动物试验依赖的变革性范例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microsystems & Nanoengineering
Microsystems & Nanoengineering Materials Science-Materials Science (miscellaneous)
CiteScore
12.00
自引率
3.80%
发文量
123
审稿时长
20 weeks
期刊介绍: Microsystems & Nanoengineering is a comprehensive online journal that focuses on the field of Micro and Nano Electro Mechanical Systems (MEMS and NEMS). It provides a platform for researchers to share their original research findings and review articles in this area. The journal covers a wide range of topics, from fundamental research to practical applications. Published by Springer Nature, in collaboration with the Aerospace Information Research Institute, Chinese Academy of Sciences, and with the support of the State Key Laboratory of Transducer Technology, it is an esteemed publication in the field. As an open access journal, it offers free access to its content, allowing readers from around the world to benefit from the latest developments in MEMS and NEMS.
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