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Polycaprolactone-Based 3D-Printed Scaffolds as Potential Implant Materials for Tendon-Defect Repair
Chronic tendon ruptures are common disorders in orthopedics. The conventional surgical methods used to treat them often require the support of implants. Due to the non-availability of suitable materials, 3D-printed polycaprolactone (PCL) scaffolds were designed from two different starting materials...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9590089/ https://www.ncbi.nlm.nih.gov/pubmed/36278629 http://dx.doi.org/10.3390/jfb13040160 |
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author | Kempfert, Merle Willbold, Elmar Loewner, Sebastian Blume, Cornelia Pitts, Johannes Menzel, Henning Roger, Yvonne Hoffmann, Andrea Angrisani, Nina Reifenrath, Janin |
author_facet | Kempfert, Merle Willbold, Elmar Loewner, Sebastian Blume, Cornelia Pitts, Johannes Menzel, Henning Roger, Yvonne Hoffmann, Andrea Angrisani, Nina Reifenrath, Janin |
author_sort | Kempfert, Merle |
collection | PubMed |
description | Chronic tendon ruptures are common disorders in orthopedics. The conventional surgical methods used to treat them often require the support of implants. Due to the non-availability of suitable materials, 3D-printed polycaprolactone (PCL) scaffolds were designed from two different starting materials as suitable candidates for tendon-implant applications. For the characterization, mechanical testing was performed. To increase their biocompatibility, the PCL-scaffolds were plasma-treated and coated with fibronectin and collagen I. Cytocompatibility testing was performed using L929 mouse fibroblasts and human-bone-marrow-derived mesenchymal stem cells. The mechanical testing showed that the design adaptions enhanced the mechanical stability. Cell attachment was increased in the plasma-treated specimens compared to the control specimens, although not significantly, in the viability tests. Coating with fibronectin significantly increased the cellular viability compared to the untreated controls. Collagen I treatment showed an increasing trend. The desired cell alignment and spread between the pores of the construct was most prominent on the collagen-I-coated specimens. In conclusion, 3D-printed scaffolds are possible candidates for the development of tendon implants. Enhanced cytocompatibility was achieved through surface modifications. Although adaptions in mechanical strength still require alterations in order to be applied to human-tendon ruptures, we are optimistic that a suitable implant can be designed. |
format | Online Article Text |
id | pubmed-9590089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95900892022-10-25 Polycaprolactone-Based 3D-Printed Scaffolds as Potential Implant Materials for Tendon-Defect Repair Kempfert, Merle Willbold, Elmar Loewner, Sebastian Blume, Cornelia Pitts, Johannes Menzel, Henning Roger, Yvonne Hoffmann, Andrea Angrisani, Nina Reifenrath, Janin J Funct Biomater Article Chronic tendon ruptures are common disorders in orthopedics. The conventional surgical methods used to treat them often require the support of implants. Due to the non-availability of suitable materials, 3D-printed polycaprolactone (PCL) scaffolds were designed from two different starting materials as suitable candidates for tendon-implant applications. For the characterization, mechanical testing was performed. To increase their biocompatibility, the PCL-scaffolds were plasma-treated and coated with fibronectin and collagen I. Cytocompatibility testing was performed using L929 mouse fibroblasts and human-bone-marrow-derived mesenchymal stem cells. The mechanical testing showed that the design adaptions enhanced the mechanical stability. Cell attachment was increased in the plasma-treated specimens compared to the control specimens, although not significantly, in the viability tests. Coating with fibronectin significantly increased the cellular viability compared to the untreated controls. Collagen I treatment showed an increasing trend. The desired cell alignment and spread between the pores of the construct was most prominent on the collagen-I-coated specimens. In conclusion, 3D-printed scaffolds are possible candidates for the development of tendon implants. Enhanced cytocompatibility was achieved through surface modifications. Although adaptions in mechanical strength still require alterations in order to be applied to human-tendon ruptures, we are optimistic that a suitable implant can be designed. MDPI 2022-09-23 /pmc/articles/PMC9590089/ /pubmed/36278629 http://dx.doi.org/10.3390/jfb13040160 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kempfert, Merle Willbold, Elmar Loewner, Sebastian Blume, Cornelia Pitts, Johannes Menzel, Henning Roger, Yvonne Hoffmann, Andrea Angrisani, Nina Reifenrath, Janin Polycaprolactone-Based 3D-Printed Scaffolds as Potential Implant Materials for Tendon-Defect Repair |
title | Polycaprolactone-Based 3D-Printed Scaffolds as Potential Implant Materials for Tendon-Defect Repair |
title_full | Polycaprolactone-Based 3D-Printed Scaffolds as Potential Implant Materials for Tendon-Defect Repair |
title_fullStr | Polycaprolactone-Based 3D-Printed Scaffolds as Potential Implant Materials for Tendon-Defect Repair |
title_full_unstemmed | Polycaprolactone-Based 3D-Printed Scaffolds as Potential Implant Materials for Tendon-Defect Repair |
title_short | Polycaprolactone-Based 3D-Printed Scaffolds as Potential Implant Materials for Tendon-Defect Repair |
title_sort | polycaprolactone-based 3d-printed scaffolds as potential implant materials for tendon-defect repair |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9590089/ https://www.ncbi.nlm.nih.gov/pubmed/36278629 http://dx.doi.org/10.3390/jfb13040160 |
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