Jeznach Oliwia, Kołbuk Dorota, Reich Tobias, Sajkiewicz Paweł
Institute of Fundamental Technological Research, Polish Academy of Sciences, Pawinskiego 5B, 02-106 Warsaw, Poland.
Department of Chemistry, Johannes Gutenberg University Mainz, Fritz-Strassmann-Weg 2, 55128 Mainz, Germany.
Polymers (Basel). 2022 Oct 4;14(19):4154. doi: 10.3390/polym14194154.
Immobilization of cell adhesive proteins on the scaffold surface has become a widely reported method that can improve the interaction between scaffold and cells. In this study, three nanofibrous scaffolds obtained by electrospinning of poly(caprolactone) (PCL), poly(L-lactide-co-caprolactone) (PLCL) 70:30, or poly(L-lactide) (PLLA) were subjected to chemical immobilization of gelatin based on aminolysis and glutaraldehyde cross-linking, as well as physisorption of gelatin. Two sets of aminolysis conditions were applied to evaluate the impact of amine group content. Based on the results of the colorimetric bicinchoninic acid (BCA) assay, it was shown that the concentration of gelatin on the surface is higher for the chemical modification and increases with the concentration of free NH2 groups. XPS (X-ray photoelectron spectroscopy) analysis confirmed this outcome. On the basis of XPS results, the thickness of the gelatin layer was estimated to be less than 10 nm. Initially, hydrophobic scaffolds are completely wettable after coating with gelatin, and the time of waterdrop absorption was correlated with the surface concentration of gelatin. In the case of all physically and mildly chemically modified samples, the decrease in stress and strain at break was relatively low, contrary to strongly aminolyzed PLCL and PLLA samples. Incubation testing performed on the PCL samples showed that a chemically immobilized gelatin layer is more stable than a physisorbed one; however, even after 90 days, more than 60% of the initial gelatin concentration was still present on the surface of physically modified samples. Mouse fibroblast L929 cell culture on modified samples indicates a positive effect of both physical and chemical modification on cell morphology. In the case of PCL and PLCL, the best morphology, characterized by stretched filopodia, was observed after stronger chemical modification, while for PLLA, there was no significant difference between modified samples. Results of metabolic activity indicate the better effect of chemical immobilization than of physisorption of gelatin.
将细胞黏附蛋白固定在支架表面已成为一种广泛报道的方法,该方法可改善支架与细胞之间的相互作用。在本研究中,通过静电纺丝制备的聚己内酯(PCL)、聚(L-丙交酯-共-己内酯)(PLCL)70:30或聚(L-丙交酯)(PLLA)三种纳米纤维支架,基于氨解和戊二醛交联进行了明胶的化学固定,以及明胶的物理吸附。应用两组氨解条件来评估胺基含量的影响。基于比色双缩脲酸(BCA)测定结果表明,化学修饰后表面明胶浓度更高,且随游离NH2基团浓度增加而增加。X射线光电子能谱(XPS)分析证实了这一结果。基于XPS结果,估计明胶层厚度小于10纳米。最初,疏水支架在用明胶包被后完全可湿润,水滴吸收时间与明胶表面浓度相关。在所有物理和轻度化学修饰的样品中,断裂应力和应变的降低相对较小,这与强烈氨解的PLCL和PLLA样品相反。对PCL样品进行的孵育测试表明,化学固定的明胶层比物理吸附的更稳定;然而,即使在90天后,物理修饰样品表面仍存在超过60%的初始明胶浓度。在修饰样品上进行小鼠成纤维细胞L929细胞培养表明,物理和化学修饰对细胞形态均有积极影响。对于PCL和PLCL,在更强的化学修饰后观察到最佳形态,其特征为伸展的丝状伪足,而对于PLLA,修饰样品之间没有显著差异。代谢活性结果表明,化学固定明胶的效果优于物理吸附。