Monitoring Cell Adhesion on Polycaprolactone-Chitosan Films with Varying Blend Ratios by Quartz Crystal Microbalance with Dissipation

被引:9
作者
Sert, Ayse Buse Ozdabak [1 ]
Bittrich, Eva [2 ]
Uhlmann, Petra [2 ]
Kok, Fatma Nese [1 ]
Kilic, Abdulhalim [1 ]
机构
[1] Istanbul Tech Univ, Dept Mol Biol & Genet, TR-34469 Istanbul, Turkiye
[2] Leibniz Inst Polymerforsch Dresden e V, D-01069 Dresden, Germany
关键词
SUPPORTED LIPID-BILAYERS; QCM-D; PROTEIN ADSORPTION; NANOFIBERS; SURFACES; ELLIPSOMETRY; ATTACHMENT; MORPHOLOGY; SCAFFOLDS; BEHAVIOR;
D O I
10.1021/acsomega.3c01055
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A detailed understanding of the cell adhesion on polymeric surfaces is required to improve the performance of biomaterials. Quartz crystal microbalance with dissipation (QCM-D) as a surface-sensitive technique has the advantage of label-free and real-time monitoring of the cell-polymer interface, providing distinct signal patterns for cell-polymer interactions. In this study, QCM-D was used to monitor human fetal osteoblastic (hFOB) cell adhesion onto polycaprolactone (PCL) and chitosan (CH) homopolymer films as well as their blend films (75:25 and 25:75). Complementary cell culture assays were performed to verify the findings of QCM-D. The thin polymer films were successfully prepared by spin-coating, and relevant properties, i.e., surface morphology, zeta-potential, wettability, film swelling, and fibrinogen adsorption, were characterized. The adsorbed amount of fibrinogen decreased with an increasing percentage of chitosan in the films, which predominantly showed an inverse correlation with surface hydrophilicity. Similarly, the initial cell sedimentation after 1 h resulted in lesser cell deposition as the chitosan ratio increased in the film. Furthermore, the QCM-D signal patterns, which were measured on the homopolymer and blend films during the first 18 h of cell adhesion, also showed an influence of the different interfacial properties. Cells fully spread on pure PCL films and had elongated morphologies as monitored by fluorescence microscopy and scanning electron microscopy (SEM). Corresponding QCM-D signals showed the highest frequency drop and the highest dissipation. Blend films supported cell adhesion but with lower dissipation values than for the PCL film. This could be the result of a higher rigidity of the cell-blend interface because the cells do not pass to the next stages of spreading after secretion of their extracellular matrix (ECM) proteins. Variations in the QCM-D data, which were obtained at the blend films, could be attributed to differences in the morphology of the films. Pure chitosan films showed limited cell adhesion accompanied by low frequency drop and low dissipation.
引用
收藏
页码:17017 / 17027
页数:11
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