Strunk Till, Joshi Arundhati, Moeinkhah Mahta, Renzelmann Timon, Dierker Lea, Grotheer Dietmar, Graupner Nina, Müssig Jörg, Brüggemann Dorothea
Institute for Biophysics, University of Bremen, Otto-Hahn-Allee 1, 28359 Bremen, Germany.
Hochschule Bremen - City University of Applied Sciences, Neustadtswall 30, 28199 Bremen, Germany.
ACS Appl Bio Mater. 2024 Sep 16;7(9):6186-6200. doi: 10.1021/acsabm.4c00761. Epub 2024 Sep 3.
Self-assembled fibrinogen nanofibers are promising candidates for skin tissue engineering due to their biocompatibility and ability to mimic the native blood clot architecture. Here, we studied the structure-property relationship and degradation of rehydrated fibrinogen nanofibers prepared by salt-induced self-assembly, focusing on the effect of scaffold layering, cross-linking time and freeze-drying. Optimal fiber stability was achieved with cross-linking by formaldehyde (FA) vapor, while treatment with liquid aldehydes, genipin, EDC, and transglutaminase failed to preserve the nanofibrous architecture upon rehydration. Scaffold layering did not significantly influence the mechanical properties but changed the scaffold architecture, with bulk fiber scaffolds being more compact than layered scaffolds. Freeze-drying maintained the mechanical properties and interconnected pore network with average pore diameters around 20 μm, which will enhance the storage stability of self-assembled fibrinogen scaffolds. Varying cross-linking times altered the scaffold mechanics without affecting the swelling behavior, indicating that scaffold hydration can be controlled independently of the mechanical characteristics. Cross-linking times of 240 min increased scaffold stiffness and decreased elongation, while 30 min resulted in mechanical properties similar to native skin. Cross-linking for 120 min was found to reduce scaffold degradation by various enzymes in comparison to 60 min. Overall, after 35 days of incubation, plasmin and a combination of urokinase and plasminogen exhibited the strongest degradative effect, with nanofibers being more susceptible to enzymatic degradation than planar fibrinogen due to their higher specific surface area. Based on these results, self-assembled fibrinogen fiber scaffolds show great potential for future applications in soft tissue engineering that require controlled structure-function relationships and degradation characteristics.
自组装纤维蛋白原纳米纤维因其生物相容性以及模拟天然血凝块结构的能力,成为皮肤组织工程中很有前景的候选材料。在此,我们研究了通过盐诱导自组装制备的复水纤维蛋白原纳米纤维的结构-性能关系及降解情况,重点关注支架分层、交联时间和冷冻干燥的影响。用甲醛(FA)蒸汽交联可实现最佳的纤维稳定性,而用液体醛类、京尼平、1-乙基-3-(3-二甲氨基丙基)碳二亚胺(EDC)和转谷氨酰胺酶处理后,复水时无法保持纳米纤维结构。支架分层对机械性能影响不显著,但改变了支架结构,整体纤维支架比分层支架更致密。冷冻干燥保持了机械性能和相互连通的孔隙网络,平均孔径约为20μm,这将提高自组装纤维蛋白原支架的储存稳定性。不同的交联时间改变了支架力学性能,而不影响溶胀行为,表明支架水合作用可独立于机械特性进行控制。交联240分钟可增加支架刚度并降低伸长率,而交联30分钟则产生与天然皮肤相似的机械性能。与交联60分钟相比,发现交联120分钟可减少支架被各种酶的降解。总体而言,孵育35天后,纤溶酶以及尿激酶和纤溶酶原的组合表现出最强的降解作用,由于纳米纤维具有更高的比表面积,它们比平面纤维蛋白原更容易受到酶解降解。基于这些结果,自组装纤维蛋白原纤维支架在需要可控的结构-功能关系和降解特性的软组织工程未来应用中显示出巨大潜力。