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Self‐expandable tubular collagen implants

Collagen has been extensively used as a biomaterial, yet for tubular organ repair, synthetic polymers or metals (e.g., stents) are typically used. In this study, we report a novel type of tubular implant solely consisting of type I collagen, suitable to self‐expand in case of minimal invasive implan...

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Autores principales: Versteegden, Luuk R.M., ter Meer, Marja, Lomme, Roger M.L.M., van der Vliet, J. Adam, Schultze Kool, Leo J., van Kuppevelt, Toin H., Daamen, Willeke F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032829/
https://www.ncbi.nlm.nih.gov/pubmed/29704312
http://dx.doi.org/10.1002/term.2685
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author Versteegden, Luuk R.M.
ter Meer, Marja
Lomme, Roger M.L.M.
van der Vliet, J. Adam
Schultze Kool, Leo J.
van Kuppevelt, Toin H.
Daamen, Willeke F.
author_facet Versteegden, Luuk R.M.
ter Meer, Marja
Lomme, Roger M.L.M.
van der Vliet, J. Adam
Schultze Kool, Leo J.
van Kuppevelt, Toin H.
Daamen, Willeke F.
author_sort Versteegden, Luuk R.M.
collection PubMed
description Collagen has been extensively used as a biomaterial, yet for tubular organ repair, synthetic polymers or metals (e.g., stents) are typically used. In this study, we report a novel type of tubular implant solely consisting of type I collagen, suitable to self‐expand in case of minimal invasive implantation. Potential benefits of this collagen scaffold over conventional materials include improved endothelialization, biodegradation over time, and possibilities to add bioactive components to the scaffold, such as anticoagulants. Implants were prepared by compression of porous scaffolds consisting of fibrillar type I collagen (1.0–2.0% (w/v)). By applying carbodiimide cross‐linking to the compressed scaffolds in their opened position, entropy‐driven shape memory was induced. The scaffolds were subsequently crimped and dried around a guidewire. Upon exposure to water, crimped scaffolds deployed within 15–60 s (depending on the collagen concentration used), thereby returning to the original opened form. The scaffolds were cytocompatible as assessed by cell culture with human primary vascular endothelial and smooth muscle cells. Compression force required to compress the open scaffolds increased with collagen content from 16 to 32 mN for 1.0% to 2.0% (w/v) collagen scaffolds. In conclusion, we report the first self‐expandable tubular implant consisting of solely type I collagen that may have potential as a biological vascular implant.
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spelling pubmed-60328292018-07-12 Self‐expandable tubular collagen implants Versteegden, Luuk R.M. ter Meer, Marja Lomme, Roger M.L.M. van der Vliet, J. Adam Schultze Kool, Leo J. van Kuppevelt, Toin H. Daamen, Willeke F. J Tissue Eng Regen Med Short Communication Collagen has been extensively used as a biomaterial, yet for tubular organ repair, synthetic polymers or metals (e.g., stents) are typically used. In this study, we report a novel type of tubular implant solely consisting of type I collagen, suitable to self‐expand in case of minimal invasive implantation. Potential benefits of this collagen scaffold over conventional materials include improved endothelialization, biodegradation over time, and possibilities to add bioactive components to the scaffold, such as anticoagulants. Implants were prepared by compression of porous scaffolds consisting of fibrillar type I collagen (1.0–2.0% (w/v)). By applying carbodiimide cross‐linking to the compressed scaffolds in their opened position, entropy‐driven shape memory was induced. The scaffolds were subsequently crimped and dried around a guidewire. Upon exposure to water, crimped scaffolds deployed within 15–60 s (depending on the collagen concentration used), thereby returning to the original opened form. The scaffolds were cytocompatible as assessed by cell culture with human primary vascular endothelial and smooth muscle cells. Compression force required to compress the open scaffolds increased with collagen content from 16 to 32 mN for 1.0% to 2.0% (w/v) collagen scaffolds. In conclusion, we report the first self‐expandable tubular implant consisting of solely type I collagen that may have potential as a biological vascular implant. John Wiley and Sons Inc. 2018-05-15 2018-06 /pmc/articles/PMC6032829/ /pubmed/29704312 http://dx.doi.org/10.1002/term.2685 Text en © 2018 The Authors. Journal of Tissue Engineering and Regenerative Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Versteegden, Luuk R.M.
ter Meer, Marja
Lomme, Roger M.L.M.
van der Vliet, J. Adam
Schultze Kool, Leo J.
van Kuppevelt, Toin H.
Daamen, Willeke F.
Self‐expandable tubular collagen implants
title Self‐expandable tubular collagen implants
title_full Self‐expandable tubular collagen implants
title_fullStr Self‐expandable tubular collagen implants
title_full_unstemmed Self‐expandable tubular collagen implants
title_short Self‐expandable tubular collagen implants
title_sort self‐expandable tubular collagen implants
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032829/
https://www.ncbi.nlm.nih.gov/pubmed/29704312
http://dx.doi.org/10.1002/term.2685
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