3B's Research Group-Biomaterials, Biodegradables, and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, Guimarães, Portugal.
Tissue Eng Part A. 2010 Jan;16(1):45-54. doi: 10.1089/ten.TEA.2008.0559.
Spinal cord injury (SCI) represents a significant health and social problem, and therefore it is vital to develop novel strategies that can specifically target it. In this context, the objective of the present work was to develop a new range of three-dimensional (3D) tubular structures aimed at inducing the regeneration within SCI sites. Up to six different 3D tubular structures were initially developed by rapid prototyping: 3D bioplotting-based on a biodegradable blend of starch. These structures were then further complemented by injecting Gellan Gum, a polysaccharide-based hydrogel, in the central area of structures. The mechanical properties of these structures were assessed using dynamic mechanical analysis, under both dry and wet conditions, and their morphologies/porosities were analyzed using micro-computed tomography and scanning electron microscopy. Biological evaluation was carried out to determine their cytotoxicity, using both minimum essential medium (MEM) extraction and MTS tests, as well as by encapsulation of an oligodendrocyte-like cell (M03-13 cell line) within the hydrogel phase. The histomorphometric analysis showed a fully interconnected network of pores with porosity ranging from 70% to 85%. Scaffolds presented compressive modulus ranging from 17.4 to 62.0 MPa and 4.42 to 27.4 MPa under dry and wet conditions, respectively. Cytotoxicity assays revealed that the hybrid starch/poly-epsilon-caprolactone/Gellan Gum scaffolds were noncytotoxic, as they did not cause major alterations on cell morphology, proliferation, and metabolic viability. Moreover, preliminary cell encapsulation assays showed that the hybrid scaffolds could support the in vitro culture of oligodendrocyte-like cells. Finally, preliminary in vivo studies conducted in a hemisection rat SCI model revealed that the above-referred structures were well integrated within the injury and did not trigger chronic inflammatory processes. The results herein presented indicate that these 3D systems might be of use in future SCI regeneration approaches.
脊髓损伤 (SCI) 是一个重大的健康和社会问题,因此开发专门针对它的新策略至关重要。在这种情况下,本工作的目的是开发一系列新的三维 (3D) 管状结构,旨在诱导 SCI 部位的再生。最初通过快速原型制作开发了六种不同的 3D 管状结构:基于可生物降解的淀粉混合物的 3D 生物打印。然后,通过在结构的中心区域注射基于多糖的凝胶糖,进一步补充这些结构。使用动态力学分析评估了这些结构在干燥和潮湿条件下的机械性能,并使用微计算机断层扫描和扫描电子显微镜分析了它们的形态/孔隙率。通过使用最小必需培养基 (MEM) 提取和 MTS 测试以及在水凝胶相中封装少突胶质样细胞 (M03-13 细胞系) 进行了生物评价,以确定其细胞毒性。组织形态计量学分析显示,具有 70%至 85%孔隙率的完全互连的多孔网络。支架在干燥和潮湿条件下的压缩模量分别为 17.4 至 62.0 MPa 和 4.42 至 27.4 MPa。细胞毒性试验表明,混合淀粉/聚己内酯/凝胶糖支架无细胞毒性,因为它们不会对细胞形态、增殖和代谢活力造成重大改变。此外,初步的细胞包封试验表明,混合支架可以支持少突胶质样细胞的体外培养。最后,在半横断大鼠 SCI 模型中进行的初步体内研究表明,上述结构在损伤部位很好地整合在一起,并且不会引发慢性炎症过程。本文介绍的结果表明,这些 3D 系统可能在未来的 SCI 再生方法中得到应用。