Huang Yao, Wang Yixiang, Chen Lingyun, Zhang Lina
Department of Agricultural, Food and Nutritional Science, University of Alberta, Edmonton, AB T6G 2P5, Canada.
J Mater Chem B. 2018 Feb 14;6(6):918-929. doi: 10.1039/c7tb02945d. Epub 2018 Jan 23.
Fiber-shaped cellular architectures have drawn attention due to their structural similarity to the extracellular matrix. For such an application, fibers that are both mechanically robust and biocompatible in the targeted biological environment are required. In this work, a facile method has been developed to prepare mechanically tough reconstituted collagen fibers by extrusion of collagen acetic acid solution into a coagulation bath containing sodium alginate. The structure and morphology of the collagen fiber were studied by XPS, FT-IR, SEM, TEM and DSC. The results indicated that the instant electrostatic interaction and hydrogen bonding between sodium alginate and collagen contributed to the formation of the mechanically strong microfiber, which exhibited a tensile stress and Young's modulus of 313.4 MPa and 5848.5 MPa. During fiber formation, the triple-helix structure of collagen remained undamaged, and self-assembled into closely stacked nanofibrous morphology. In addition, positively charged chitin nanofibers (CNFs) were incorporated into the collagen fiber as reinforcing filler. With increasing CNF concentration, the tensile strength and modulus of the air-dried collagen fiber increased and reached the highest values of 506.6 MPa and 12109.5 MPa at 15 wt% CNFs. The wet strength of the composite fibers was also significantly improved with addition of CNFs, showing mechanical properties (stress and modulus of 47.3 MPa and 988.9 Mpa) comparable to the reported post-crosslinked collagen fibers. Yet, this has been achieved through a physical approach under mild conditions without using toxic chemical crosslinking reagents or causing collagen denaturation, allowing their direct application as promising biomaterials. In vitro tests showed that the addition of CNFs did not induce obvious cytotoxicity of the fibers towards fibroblast cells and the whole composite fibers exhibited a cell viability of >80% for a culture time of up to 72 h. Moreover, the fibroblast alignment on the surface of the fibers was observed by confocal and scanning electron microscope imaging, indicating potential application of the fibers as a cell alignment template in tissue engineering fields for vascular, muscle and neural engineering applications.
纤维状细胞结构因其与细胞外基质的结构相似性而受到关注。对于此类应用,需要在目标生物环境中既具有机械强度又具有生物相容性的纤维。在这项工作中,已开发出一种简便的方法,通过将胶原醋酸溶液挤入含有海藻酸钠的凝固浴中来制备机械坚韧的再生胶原纤维。通过XPS、FT-IR、SEM、TEM和DSC研究了胶原纤维的结构和形态。结果表明,海藻酸钠与胶原之间的即时静电相互作用和氢键有助于形成机械强度高的微纤维,其拉伸应力和杨氏模量分别为313.4 MPa和5848.5 MPa。在纤维形成过程中,胶原的三螺旋结构保持完整,并自组装成紧密堆积的纳米纤维形态。此外,带正电荷的几丁质纳米纤维(CNF)作为增强填料被掺入胶原纤维中。随着CNF浓度的增加,风干胶原纤维的拉伸强度和模量增加,在15 wt% CNF时达到最高值506.6 MPa和12109.5 MPa。添加CNF后,复合纤维的湿强度也显著提高,其机械性能(应力和模量分别为47.3 MPa和988.9 Mpa)与报道的后交联胶原纤维相当。然而,这是通过在温和条件下的物理方法实现的,无需使用有毒的化学交联剂或导致胶原变性,使其能够直接作为有前景的生物材料应用。体外测试表明,添加CNF不会诱导纤维对成纤维细胞产生明显的细胞毒性,并且整个复合纤维在长达72小时的培养时间内表现出>80%的细胞活力。此外,通过共聚焦和扫描电子显微镜成像观察到纤维表面有成纤维细胞排列,表明这些纤维在组织工程领域作为血管、肌肉和神经工程应用的细胞排列模板具有潜在应用价值。