Microfiber Fabricated via Microfluidic Spinning toward Tissue Engineering Applications.
Lingling TianJingyun MaWei LiXu ZhangXinghua GaoPublished in: Macromolecular bioscience (2023)
Microfibers, a type of long, thin, and flexible material, can be assembled into functional 3D structures by folding, binding, and weaving. As a novel spinning method, combining microfluidic technology and wet spinning, microfluidic spinning technology can precisely control the size, morphology, structure, and composition of the microfibers. Particularly, the process is mild and rapid, which is suitable for preparing microfibers using biocompatible materials and without affecting the viability of cells encapsulated. Furthermore, owing to the controllability of microfluidic spinning, microfibers with well-defined structures (such as hollow structures) will contribute to the exchange of nutrients or guide cell orientation. Thus, this method is often used to fabricate microfibers as cell scaffolds for cell encapsulation or adhesion and can be further applied to biomimetic fibrous tissues. In this review, the focus is on different fiber structures prepared by microfluidic spinning technology, including solid, hollow, and heterogeneous structures, generated from three essential elements: spinning platform, fiber composition, and solidification methods. Furthermore, the application of microfibers is described with different structures in tissue engineering, such as blood vessels, skeletal muscle, bone, nerves, and lung bronchi. Finally, the challenges and future development prospects of microfluidic spinning technology in tissue engineering applications are discussed.
Keyphrases
- tissue engineering
- single cell
- solid state
- high throughput
- circulating tumor cells
- high resolution
- skeletal muscle
- label free
- cell therapy
- gene expression
- induced apoptosis
- type diabetes
- insulin resistance
- mass spectrometry
- cell proliferation
- oxidative stress
- bone marrow
- single molecule
- endoplasmic reticulum stress
- ionic liquid
- drug release
- body composition