Zhou Liangbin, Huang Jingjing, Li Cun, Gu Qi, Li Gang, Li Zhong Alan, Xu Jiankun, Zhou Jie, Tuan Rocky S
Department of Biomedical Engineering, Faculty of Engineering, The Chinese University of Hong Kong, Hong Kong SAR, China; Center for Neuromusculoskeletal Restorative Medicine, Hong Kong Science and Technology Park, Hong Kong SAR, China; Musculoskeletal Research Laboratory, Department of Orthopaedics and Traumatology, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China; Innovative Orthopaedic Biomaterials and Drug Translational Research Laboratory, Li Ka Shing Institute of Health Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China.
Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Med. 2025 Apr 11;6(4):100667. doi: 10.1016/j.medj.2025.100667.
Organoids and organs-on-chips (OoCs) are rapidly evolving technologies for creating miniature human tissue models. They can mimic complex physiological functions and pathological conditions, offering more realistic platforms for disease modeling, drug screening, precision medicine, and regenerative therapies. The passing of the FDA Modernization Act 2.0 has reduced animal testing requirements for drug trials, marking a significant milestone in using advanced in vitro models such as organoids and OoCs for therapeutic discovery. Apart from technical and ethical challenges, regulatory issues persist in ensuring the reliability, scientificity, and applicability of these models in drug development. This perspective explores the concept, advancements, pros and cons, and applications of organoids and OoCs, particularly in drug research and development. It also examines global regulatory agencies' policies and actions on using these models in drug evaluation, aiming to guide industry standard setting and advance regulatory science.
类器官和芯片上器官(OoC)是用于创建微型人体组织模型的快速发展的技术。它们可以模拟复杂的生理功能和病理状况,为疾病建模、药物筛选、精准医学和再生疗法提供更现实的平台。《美国食品药品监督管理局2.0现代化法案》的通过减少了药物试验的动物试验要求,这标志着在使用类器官和OoC等先进体外模型进行治疗发现方面的一个重要里程碑。除了技术和伦理挑战外,在确保这些模型在药物开发中的可靠性、科学性和适用性方面,监管问题依然存在。本观点探讨了类器官和OoC的概念、进展、优缺点及应用,特别是在药物研发方面。它还审视了全球监管机构在药物评估中使用这些模型的政策和行动,旨在指导行业标准制定并推动监管科学发展。
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