Wang Jing, Zhang Huixue, Qu Yueyang, Yang Yang, Xu Shuhui, Ji Zhenni, Wang Yuxiu, Zhang Xiuli, Luo Yong
State Key Laboratory of Fine Chemicals, Department of Pharmaceutical Engineering, School of Chemical Engineering, Dalian University of Technology, #2, Linggong Road, Dalian, 116024, Liaoning Province, China.
Jiangsu Key Laboratory of Neuropsychiatric Disease and College of Pharmaceutical Science, Suzhou Medical College, Soochow University, #199, Renai Road, Suzhou, 215127, Jiangsu Province, China.
Microsyst Nanoeng. 2025 May 14;11(1):89. doi: 10.1038/s41378-025-00933-3.
Physiological supporting systems, such as the vascular network and excretion system, are crucial for the effective functioning of organs. This study demonstrates that when a body-on-a-chip microdevice is coupled with miniaturized physiological support systems, it can create a multi-organ microphysiological system capable of more accurately mimicking the physiological complexity of a body, thereby offering potential for preclinical drug testing. To exemplify this concept, we have developed a model system comprising 18 types of microtissues interconnected by a vascular network that replicates the in vivo blood distribution among the organs. Furthermore, this system includes an excretory system with a micro-stirrer that ensures elimination efficiency akin to in vivo conditions. Our findings indicate that this system can: (1) survive and function for almost two months; (2) achieve two-compartment pharmacokinetics of a drug; (3) investigate the dynamic relationship between the tissue distribution and toxicity of a drug; (4) establish the multimorbidity model and evaluate the effectiveness of polypharmacy, challenging tasks with traditional animal models; (5) reduce animal usage in drug evaluations. Notably, features from points (2) to (4) are capabilities not achievable by other in vitro models. The strategy proposed in this study can also be applied to the development of multi-organ microphysiological systems that mimic the physiological complexity of human organs or the entire body.
诸如血管网络和排泄系统等生理支持系统对于器官的有效运作至关重要。本研究表明,当芯片上人体微器件与小型化生理支持系统相结合时,它可以创建一个能够更准确模拟人体生理复杂性的多器官微生理系统,从而为临床前药物测试提供了潜力。为了例证这一概念,我们开发了一个模型系统,该系统由18种通过血管网络相互连接的微组织组成,该血管网络可复制体内器官间的血液分布。此外,该系统还包括一个带有微型搅拌器的排泄系统,以确保排泄效率与体内条件相似。我们的研究结果表明,该系统能够:(1)存活并发挥功能近两个月;(2)实现药物的双室药代动力学;(3)研究药物的组织分布与毒性之间的动态关系;(4)建立多种疾病并存模型并评估联合用药的有效性,而这些都是传统动物模型难以完成的任务;(5)减少药物评估中的动物使用量。值得注意的是,从第(2)点到第(4)点所提及的功能是其他体外模型无法实现的。本研究中提出的策略也可应用于开发模拟人体器官或整个身体生理复杂性的多器官微生理系统。