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Review

微流控血脑屏障器官芯片系统的构建及评估应用

王玉珍a, 常亚冉a,b,*, 郭广生a, 汪夏燕a,*   

  1. a北京工业大学 化学与生命科学学院化学系 材料循环低碳再生全国重点实验室 环境安全与生物效应卓越中心 北京 100124;
    b北京大学 材料科学与工程学院 北京 100871
  • 投稿日期:2025-11-24
  • 通讯作者: *E-mail: yaranchang@pku.edu.cn; xiayanwang@bjut.edu.cn
  • 作者简介:王玉珍, 就读于北京工业大学化学与生命科学学院, 2023级化学专业硕士. 主要研究方向为血脑屏障芯片构建及应用. 常亚冉, 博士, 北京大学材料科学与工程学院博士后, 2024年毕业于北京工业大学, 获得工学博士学位, 主要研究方向为微流控芯片的构建与应用. 郭广生, 博士, 北京工业大学化学与生命科学学院教授, 国务院特殊津贴获得者、北京市首批战略科技人才. 研究方向包括微流控芯片系统的构建与应用、微纳尺度分离分析和新型微纳分析仪器研制等. 汪夏燕, 博士, 北京工业大学化学与生命科学学院教授, 国家杰出青年科学基金获得者、国家“万人计划”科技创新领军人才、国务院特殊津贴获得者、北京市优秀教师. 研究方向包括微流控芯片系统的构建与应用、微纳尺度分离分析、单细胞分析和新型微纳分析仪器研制等.
  • 基金资助:
    国家自然科学基金((Nos. 22327805, 22476223)和北京市卓越青年科学家项目(BJJWZYJH01201910005017)资助.

Construction and Evaluation of Microfluidic Blood-Brain Barrier Organ-on-Chips System

Wang Yuzhena, Chang Yarana,b,*, Guo Guangshenga, Wang Xiayana,*   

  1. aCenter of Excellence for Environmental Safety and Biological Effects, State Key Laboratory of Materials Low-Carbon Recycling, Department of Chemistry, College of Chemistry and Life Science, Beijing University of Technology, Beijing 100124, China;
    bSchool of Materials Science and Technology, Peking University, Beijing 100871, China
  • Received:2025-11-24
  • Supported by:
    National Natural Science Foundation of China (Nos. 22327805, 22476223) and the Beijing Outstanding Young Scientist Program (BJJWZYJH01201910005017).

The blood-brain barrier (BBB) serves as a crucial physiological structure that maintains homeostasis within the central nervous system. While its highly selective permeability protects the brain from exogenous substances, it also hinders the delivery of therapeutic agents. The current understanding of the physiological functions of the BBB remains relatively limited, primarily due to the absence of reliable in vitro models capable of accurately replicating its complex architecture and functionality. In recent years, microfluidic technology has emerged as a pivotal platform for developing highly biomimetic BBB models, capitalizing on its distinctive advantages in microscale fluid manipulation, establishment of multicellular co-culture systems, and reconstruction of physiologically relevant microenvironments. This review systematically summarizes recent advances in microfluidic BBB-on-a-chip systems, with particular focus on three key aspects: chip design configurations, fluid driving mechanisms, and cellular source selection. In terms of chip architecture, the discussion encompasses various structural designs, including sandwich-structured design, parallel channel design, three-dimensional tubular design, and angiogenic design. Regarding fluid propulsion methods, the analysis covers both pump-driven systems and gravity-driven approaches. The examination of cellular sources includes immortalized cell lines, primary cell isolates, and stem cell-derived endothelial populations. Furthermore, the review comprehensively outlines established methodologies for evaluating barrier integrity and function. These assessment techniques include measuring transendothelial electrical resistance, performing permeability assays with molecular tracers, and analyzing the expression of tight junction proteins and specialized transporters. The review concludes by addressing the current challenges confronting microfluidic BBB technology and proposing strategic directions for future development. These perspectives include enhancing model biomimicry through the incorporation of additional neurovascular unit components, promoting technical standardization to ensure experimental reproducibility and comparability, developing personalized diagnostic and therapeutic models through integration of patient-specific cells, and exploring innovative applications through synergistic combination with artificial intelligence technologies. This comprehensive analysis aims to provide valuable guidance for researchers working at the intersection of biomedical engineering, neuroscience, and pharmaceutical development.

Key words: microfluidics, organ-on-a-chip, blood-brain barrier, BBB organ-on-chips, in vitro models