Li Haibing, Zhou Ruijian, Shu Qiang, Xie Mingjun, He Yong
Department of Paediatric Orthopaedics, The Children's Hospital Zhejiang University School of Medicine, Hangzhou 310052, China.
Department of Plastic and Reconstructive Surgery, Zhejiang Provincial People's Hospital, Hangzhou Medical College, Hangzhou 310014, China.
Bioengineering (Basel). 2023 Jan 18;10(2):130. doi: 10.3390/bioengineering10020130.
Gelatin methacryloyl scaffolds with microscale fiber structures own great significance because they can effectively mimic the extracellular matrix environment. Compared with extruding bioprinting, electrospinning technology is more suitable for establishing accurate hydrogel microfibers. However, electrospinning accurate gelatin methacryloyl microfiber remains a big challenge restricted by its bad spinnability. In this paper, polyethylene oxide, which owns promising spinnability, is added into gelatin methacryloyl hydrogel precursor to improve the spinnability of gelatin methacryloyl bioink. A three-dimensional motion platform for electrospinning is designed and built and the spinning process of microfibers under far-electric-field and near-electric-field conditions is systematically studied, respectively. As a result, scaffolds consisted of unordered and ordered microfibers are successfully fabricated under far-electric-field and near-electric field, respectively. In vitro culture experiments of human umbilical vein endothelial cells are carried out using the prepared gelatin methacryloyl microfiber scaffolds. The results show that the cells can easily attach to the microfibers and grow well. Moreover, the gelatin methacryloyl/ polyethylene oxide microfiber scaffold was directly spun on the polycaprolactone mesh scaffold printed by fused modeling printing method. The results showed that the macroscopic ordered and microscopic disordered microfiber scaffold could be successfully established, which could lead to directed cell growth. We believe that this method can effectively solve the problem of hydrogel spinnability and be a powerful tool for various biomedical engineering methods in the future.
具有微米级纤维结构的甲基丙烯酰化明胶支架具有重要意义,因为它们可以有效地模拟细胞外基质环境。与挤出式生物打印相比,静电纺丝技术更适合于制备精确的水凝胶微纤维。然而,精确静电纺丝甲基丙烯酰化明胶微纤维仍然是一个巨大的挑战,因为其可纺性较差。在本文中,将具有良好可纺性的聚环氧乙烷添加到甲基丙烯酰化明胶水凝胶前体中,以提高甲基丙烯酰化明胶生物墨水的可纺性。设计并搭建了一个用于静电纺丝的三维运动平台,并分别系统研究了远电场和近电场条件下微纤维的纺丝过程。结果,分别在远电场和近电场条件下成功制备了由无序和有序微纤维组成的支架。使用制备的甲基丙烯酰化明胶微纤维支架进行了人脐静脉内皮细胞的体外培养实验。结果表明,细胞能够轻松附着在微纤维上并良好生长。此外,将甲基丙烯酰化明胶/聚环氧乙烷微纤维支架直接纺丝在通过熔融成型打印方法打印的聚己内酯网状支架上。结果表明,可以成功建立宏观有序且微观无序的微纤维支架,这可以引导细胞定向生长。我们相信,这种方法可以有效解决水凝胶可纺性问题,并在未来成为各种生物医学工程方法的有力工具。