Blending chitosan-g-poly(caprolactone) with poly(caprolactone) by electrospinning to produce functional fiber mats for tissue engineering applications

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dc.identifier.uri http://dx.doi.org/10.15488/10156
dc.identifier.uri https://www.repo.uni-hannover.de/handle/123456789/10228
dc.contributor.author de Cassan, D.
dc.contributor.author Becker, A.
dc.contributor.author Glasmacher, B.
dc.contributor.author Roger, Y.
dc.contributor.author Hoffmann, A.
dc.contributor.author Gengenbach, T.R.
dc.contributor.author Easton, C.D.
dc.contributor.author Hänsch, R.
dc.contributor.author Menzel, H.
dc.date.accessioned 2020-11-03T09:48:31Z
dc.date.available 2020-11-03T09:48:31Z
dc.date.issued 2019
dc.identifier.citation de Cassan, D.; Becker, A.; Glasmacher, B.; Roger, Y.; Hoffmann, A. et al.: Blending chitosan-g-poly(caprolactone) with poly(caprolactone) by electrospinning to produce functional fiber mats for tissue engineering applications. In: Journal of Applied Polymer Science (2019), 48650. DOI: https://doi.org/10.1002/app.48650
dc.description.abstract Use of electrospun fiber mats for tissue engineering applications has become increasingly prominent. One of the most important polymers in research, poly(ε-caprolactone) (PCL), however, lacks biological performance, easy access to modifications and cellular recognition sites. To improve these properties and to enable further modifications, PCL was blended with chitosan grafted with PCL (CS-g-PCL) and subsequently processed via electrospinning. In this way, chitosan was enriched at the fiber's surface presenting cationic amino groups. The fiber mats were analyzed by various techniques such as scanning electron microscopy (SEM), confocal laser scanning microscopy (CLSM), and X-ray photoelectron spectroscopy (XPS). Furthermore, analyzing thermal properties and crystallinity, showed that an increased content of CS-g-PCL in blend composition leads to a higher overall crystallinity in produced fiber mats. Blending CS-g-PCL into PCL significantly increased initial cellular attachment and proliferation as well as cell vitality, while maintaining adequate mechanical properties, fiber diameter, and interstitial volume. As proof of principle for easy access to further modification, fluorescently labeled alginate (Alg-FA) was attached to the fiber's surface and verified by CLSM. Hence, blending CS-g-PCL with PCL can overcome an inherent weakness of PCL and create bioactive implants for tissue engineering applications. © 2019 The Authors. Journal of Applied Polymer Science published by Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019, 137, 48650. © 2019 The Authors. Journal of Applied Polymer Science published by Wiley Periodicals, Inc. eng
dc.language.iso eng
dc.publisher Chichester : John Wiley and Sons Ltd
dc.relation.ispartofseries Journal of Applied Polymer Science (2019)
dc.rights CC BY-NC 4.0 Unported
dc.rights.uri https://creativecommons.org/licenses/by-nc/4.0/
dc.subject Blend eng
dc.subject cell compatibility eng
dc.subject chitosan eng
dc.subject electrospinning eng
dc.subject polycaprolacton eng
dc.subject surface enrichment eng
dc.subject X-ray photoelectron spectroscopy eng
dc.subject Biomechanics eng
dc.subject Blending eng
dc.subject Chitosan eng
dc.subject Crystallinity eng
dc.subject Electrospinning eng
dc.subject Fibers eng
dc.subject Photoelectrons eng
dc.subject Photons eng
dc.subject Polymeric implants eng
dc.subject Scanning electron microscopy eng
dc.subject Tissue eng
dc.subject X ray photoelectron spectroscopy eng
dc.subject Biological performance eng
dc.subject Cell compatibility eng
dc.subject Cellular attachments eng
dc.subject Confocal laser scanning microscopy eng
dc.subject Poly (epsiloncaprolactone) eng
dc.subject polycaprolacton eng
dc.subject Surface enrichment eng
dc.subject Tissue engineering applications eng
dc.subject Tissue engineering eng
dc.subject.ddc 540 | Chemie ger
dc.title Blending chitosan-g-poly(caprolactone) with poly(caprolactone) by electrospinning to produce functional fiber mats for tissue engineering applications
dc.type Article
dc.type Text
dc.relation.issn 0021-8995
dc.relation.doi https://doi.org/10.1002/app.48650
dc.bibliographicCitation.issue 18
dc.bibliographicCitation.volume 137
dc.bibliographicCitation.firstPage 48650
dc.description.version publishedVersion
tib.accessRights frei zug�nglich


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