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Interaction of Human Plasma Proteins with Thin Gelatin-Based Hydrogel Films: A QCM-D and ToF-SIMS Study

[Image: see text] In the fields of surgery and regenerative medicine, it is crucial to understand the interactions of proteins with the biomaterials used as implants. Protein adsorption directly influences cell-material interactions in vivo and, as a result, regulates, for example, cell adhesion on...

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Autores principales: Schönwälder, Sina M. S., Bally, Florence, Heinke, Lars, Azucena, Carlos, Bulut, Özgül D., Heißler, Stefan, Kirschhöfer, Frank, Gebauer, Tim P., Neffe, Axel T., Lendlein, Andreas, Brenner-Weiß, Gerald, Lahann, Jörg, Welle, Alexander, Overhage, Jörg, Wöll, Christof
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215905/
https://www.ncbi.nlm.nih.gov/pubmed/24956040
http://dx.doi.org/10.1021/bm500750v
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author Schönwälder, Sina M. S.
Bally, Florence
Heinke, Lars
Azucena, Carlos
Bulut, Özgül D.
Heißler, Stefan
Kirschhöfer, Frank
Gebauer, Tim P.
Neffe, Axel T.
Lendlein, Andreas
Brenner-Weiß, Gerald
Lahann, Jörg
Welle, Alexander
Overhage, Jörg
Wöll, Christof
author_facet Schönwälder, Sina M. S.
Bally, Florence
Heinke, Lars
Azucena, Carlos
Bulut, Özgül D.
Heißler, Stefan
Kirschhöfer, Frank
Gebauer, Tim P.
Neffe, Axel T.
Lendlein, Andreas
Brenner-Weiß, Gerald
Lahann, Jörg
Welle, Alexander
Overhage, Jörg
Wöll, Christof
author_sort Schönwälder, Sina M. S.
collection PubMed
description [Image: see text] In the fields of surgery and regenerative medicine, it is crucial to understand the interactions of proteins with the biomaterials used as implants. Protein adsorption directly influences cell-material interactions in vivo and, as a result, regulates, for example, cell adhesion on the surface of the implant. Therefore, the development of suitable analytical techniques together with well-defined model systems allowing for the detection, characterization, and quantification of protein adsorbates is essential. In this study, a protocol for the deposition of highly stable, thin gelatin-based films on various substrates has been developed. The hydrogel films were characterized morphologically and chemically. Due to the obtained low thickness of the hydrogel layer, this setup allowed for a quantitative study on the interaction of human proteins (albumin and fibrinogen) with the hydrogel by Quartz Crystal Microbalance with Dissipation Monitoring (QCM-D). This technique enables the determination of adsorbant mass and changes in the shear modulus of the hydrogel layer upon adsorption of human proteins. Furthermore, Secondary Ion Mass Spectrometry and principal component analysis was applied to monitor the changed composition of the topmost adsorbate layer. This approach opens interesting perspectives for a sensitive screening of viscoelastic biomaterials that could be used for regenerative medicine.
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spelling pubmed-42159052015-06-23 Interaction of Human Plasma Proteins with Thin Gelatin-Based Hydrogel Films: A QCM-D and ToF-SIMS Study Schönwälder, Sina M. S. Bally, Florence Heinke, Lars Azucena, Carlos Bulut, Özgül D. Heißler, Stefan Kirschhöfer, Frank Gebauer, Tim P. Neffe, Axel T. Lendlein, Andreas Brenner-Weiß, Gerald Lahann, Jörg Welle, Alexander Overhage, Jörg Wöll, Christof Biomacromolecules [Image: see text] In the fields of surgery and regenerative medicine, it is crucial to understand the interactions of proteins with the biomaterials used as implants. Protein adsorption directly influences cell-material interactions in vivo and, as a result, regulates, for example, cell adhesion on the surface of the implant. Therefore, the development of suitable analytical techniques together with well-defined model systems allowing for the detection, characterization, and quantification of protein adsorbates is essential. In this study, a protocol for the deposition of highly stable, thin gelatin-based films on various substrates has been developed. The hydrogel films were characterized morphologically and chemically. Due to the obtained low thickness of the hydrogel layer, this setup allowed for a quantitative study on the interaction of human proteins (albumin and fibrinogen) with the hydrogel by Quartz Crystal Microbalance with Dissipation Monitoring (QCM-D). This technique enables the determination of adsorbant mass and changes in the shear modulus of the hydrogel layer upon adsorption of human proteins. Furthermore, Secondary Ion Mass Spectrometry and principal component analysis was applied to monitor the changed composition of the topmost adsorbate layer. This approach opens interesting perspectives for a sensitive screening of viscoelastic biomaterials that could be used for regenerative medicine. American Chemical Society 2014-06-23 2014-07-14 /pmc/articles/PMC4215905/ /pubmed/24956040 http://dx.doi.org/10.1021/bm500750v Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Schönwälder, Sina M. S.
Bally, Florence
Heinke, Lars
Azucena, Carlos
Bulut, Özgül D.
Heißler, Stefan
Kirschhöfer, Frank
Gebauer, Tim P.
Neffe, Axel T.
Lendlein, Andreas
Brenner-Weiß, Gerald
Lahann, Jörg
Welle, Alexander
Overhage, Jörg
Wöll, Christof
Interaction of Human Plasma Proteins with Thin Gelatin-Based Hydrogel Films: A QCM-D and ToF-SIMS Study
title Interaction of Human Plasma Proteins with Thin Gelatin-Based Hydrogel Films: A QCM-D and ToF-SIMS Study
title_full Interaction of Human Plasma Proteins with Thin Gelatin-Based Hydrogel Films: A QCM-D and ToF-SIMS Study
title_fullStr Interaction of Human Plasma Proteins with Thin Gelatin-Based Hydrogel Films: A QCM-D and ToF-SIMS Study
title_full_unstemmed Interaction of Human Plasma Proteins with Thin Gelatin-Based Hydrogel Films: A QCM-D and ToF-SIMS Study
title_short Interaction of Human Plasma Proteins with Thin Gelatin-Based Hydrogel Films: A QCM-D and ToF-SIMS Study
title_sort interaction of human plasma proteins with thin gelatin-based hydrogel films: a qcm-d and tof-sims study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215905/
https://www.ncbi.nlm.nih.gov/pubmed/24956040
http://dx.doi.org/10.1021/bm500750v
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