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

[Image: see text] 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–pol...

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Autores principales: Özdabak Sert, Ayşe Buse, Bittrich, Eva, Uhlmann, Petra, Kok, Fatma Nese, Kılıç, Abdulhalim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10193393/
https://www.ncbi.nlm.nih.gov/pubmed/37214735
http://dx.doi.org/10.1021/acsomega.3c01055
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author Özdabak Sert, Ayşe Buse
Bittrich, Eva
Uhlmann, Petra
Kok, Fatma Nese
Kılıç, Abdulhalim
author_facet Özdabak Sert, Ayşe Buse
Bittrich, Eva
Uhlmann, Petra
Kok, Fatma Nese
Kılıç, Abdulhalim
author_sort Özdabak Sert, Ayşe Buse
collection PubMed
description [Image: see text] 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, ζ-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.
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spelling pubmed-101933932023-05-19 Monitoring Cell Adhesion on Polycaprolactone–Chitosan Films with Varying Blend Ratios by Quartz Crystal Microbalance with Dissipation Özdabak Sert, Ayşe Buse Bittrich, Eva Uhlmann, Petra Kok, Fatma Nese Kılıç, Abdulhalim ACS Omega [Image: see text] 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, ζ-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. American Chemical Society 2023-05-05 /pmc/articles/PMC10193393/ /pubmed/37214735 http://dx.doi.org/10.1021/acsomega.3c01055 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Özdabak Sert, Ayşe Buse
Bittrich, Eva
Uhlmann, Petra
Kok, Fatma Nese
Kılıç, Abdulhalim
Monitoring Cell Adhesion on Polycaprolactone–Chitosan Films with Varying Blend Ratios by Quartz Crystal Microbalance with Dissipation
title Monitoring Cell Adhesion on Polycaprolactone–Chitosan Films with Varying Blend Ratios by Quartz Crystal Microbalance with Dissipation
title_full Monitoring Cell Adhesion on Polycaprolactone–Chitosan Films with Varying Blend Ratios by Quartz Crystal Microbalance with Dissipation
title_fullStr Monitoring Cell Adhesion on Polycaprolactone–Chitosan Films with Varying Blend Ratios by Quartz Crystal Microbalance with Dissipation
title_full_unstemmed Monitoring Cell Adhesion on Polycaprolactone–Chitosan Films with Varying Blend Ratios by Quartz Crystal Microbalance with Dissipation
title_short Monitoring Cell Adhesion on Polycaprolactone–Chitosan Films with Varying Blend Ratios by Quartz Crystal Microbalance with Dissipation
title_sort monitoring cell adhesion on polycaprolactone–chitosan films with varying blend ratios by quartz crystal microbalance with dissipation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10193393/
https://www.ncbi.nlm.nih.gov/pubmed/37214735
http://dx.doi.org/10.1021/acsomega.3c01055
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