Emerging Trends in Microfluidic Biomaterials: From Functional Design to Applications

被引:0
作者
Lin, Jiaqi [1 ]
Cui, Lijuan [1 ]
Shi, Xiaokun [1 ]
Wu, Shuping [1 ]
机构
[1] Jiangsu Univ, Inst Polymer Mat, Sch Mat Sci & Engn, Zhenjiang 212013, Peoples R China
基金
中国国家自然科学基金;
关键词
microfluidic technology; microfluidic biomaterials; organ-on-a-chip; 3D bioprinting; medical applications; ON-A-CHIP; ENHANCED ORAL BIOAVAILABILITY; LISTERIA-MONOCYTOGENES; FABRICATION; NANOFIBERS; NANOPARTICLES; INTEGRATION; SEPARATION; SCAFFOLDS; TRANSPORT;
D O I
10.3390/jfb16050166
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The rapid development of microfluidics has driven innovations in material engineering, particularly through its ability to precisely manipulate fluids and cells at microscopic scales. Microfluidic biomaterials, a cutting-edge interdisciplinary field integrating microfluidic technology with biomaterials science, are revolutionizing biomedical research. This review focuses on the functional design and fabrication of organ-on-a-chip (OoAC) platforms via 3D bioprinting, explores the applications of biomaterials in drug delivery, cell culture, and tissue engineering, and evaluates the potential of microfluidic systems in advancing personalized healthcare. We systematically analyze the evolution of microfluidic materials-from silicon and glass to polymers and paper-and highlight the advantages of 3D bioprinting over traditional fabrication methods. Currently, despite significant advances in microfluidics in medicine, challenges in scalability, stability, and clinical translation remain. The future of microfluidic biomaterials will depend on combining 3D bioprinting with dynamic functional design, developing hybrid strategies that combine traditional molds with bio-printed structures, and using artificial intelligence to monitor drug delivery or tissue response in real time. We believe that interdisciplinary collaborations between materials science, micromachining, and clinical medicine will accelerate the translation of organ-on-a-chip platforms into personalized therapies and high-throughput drug screening tools.
引用
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页数:33
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