Nagiah Naveen, El Khoury Raven, Othman Mahmoud H, Akimoto Jun, Ito Yoshihiro, Roberson David A, Joddar Binata
Inspired Materials & Stem-Cell Based Tissue Engineering Laboratory, Department of Metallurgical, Materials, and Biomedical Engineering, M201 Engineering, The University of Texas at El Paso, El Paso, Texas 79968, United States.
Nano Medical Engineering Laboratory, RIKEN Cluster for Pioneering Research, Wako, Saitama 351-0198, Japan.
ACS Omega. 2022 Apr 13;7(16):13894-13905. doi: 10.1021/acsomega.2c00271. eCollection 2022 Apr 26.
In this study, three types of electrospun scaffolds, including furfuryl-gelatin (f-gelatin) alone, f-gelatin with polycaprolactone (PCL) in a 1:1 ratio, and coaxial scaffolds with PCL (core) and f-gelatin (sheath), were developed for tissue engineering applications. Scaffolds were developed through single nozzle electrospinning and coaxial electrospinning, respectively, to serve as scaffolds for cardiac tissue engineering. Uniform fibrous structures were revealed in the scaffolds with significantly varying average fiber diameters of 760 ± 80 nm (f-gelatin), 420 ± 110 nm [f-gelatin and PCL (1:1)], and 810 ± 60 nm (coaxial f-gelatin > PCL) via scanning electron microscopy. The distinction between the core and the sheath of the fibers of the coaxial f-gelatin > PCL electrospun fibrous scaffolds was revealed by transmission electron microscopy. Thermal analysis and Fourier transformed infrared (FTIR) spectroscopy revealed no interactions between the polymers in the blended electrospun scaffolds. The varied blending methods led to significant differences in the elastic moduli of the electrospun scaffolds with the coaxial f-gelatin > PCL revealing the highest elastic modulus of all scaffolds (164 ± 3.85 kPa). All scaffolds exhibited excellent biocompatibility by supporting the adhesion and proliferation of human AC16 cardiomyocytes cells. The biocompatibility of the coaxial f-gelatin > PCL scaffolds with superior elastic modulus was assessed further through adhesion and functionality of human-induced pluripotent stem cell (hiPSC)-derived cardiomyocytes, thereby demonstrating the potential of the coaxially spun scaffolds as an ideal platform for developing cardiac tissue-on-a-chip models. Our results demonstrate a facile approach to produce visible light cross-linkable, hybrid, biodegradable nanofibrous scaffold biomaterials, which can serve as platforms for cardiac tissue engineered models.
在本研究中,开发了三种类型的电纺支架,包括单独的糠醇 - 明胶(f - 明胶)、糠醇 - 明胶与聚己内酯(PCL)以1:1比例混合的支架以及以PCL为芯、f - 明胶为鞘的同轴支架,用于组织工程应用。分别通过单喷嘴电纺和同轴电纺来制备支架,以用作心脏组织工程的支架。通过扫描电子显微镜观察发现,支架呈现出均匀的纤维结构,平均纤维直径差异显著,分别为760 ± 80 nm(f - 明胶)、420 ± 110 nm [f - 明胶与PCL(1:1)]和810 ± 60 nm(同轴f - 明胶>PCL)。通过透射电子显微镜揭示了同轴f - 明胶>PCL电纺纤维支架纤维的芯和鞘之间的差异。热分析和傅里叶变换红外(FTIR)光谱表明,在混合电纺支架中的聚合物之间没有相互作用。不同的混合方法导致电纺支架的弹性模量存在显著差异,同轴f - 明胶>PCL的弹性模量在所有支架中最高(164 ± 3.85 kPa)。所有支架通过支持人AC16心肌细胞的黏附和增殖表现出优异的生物相容性。通过人诱导多能干细胞(hiPSC)来源的心肌细胞的黏附和功能进一步评估了具有优异弹性模量的同轴f - 明胶>PCL支架的生物相容性,从而证明了同轴纺丝支架作为开发心脏芯片组织模型的理想平台的潜力。我们的结果展示了一种简便的方法来制备可见光可交联、混合、可生物降解的纳米纤维支架生物材料,其可作为心脏组织工程模型的平台。