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In vivo performance of a novel silk fibroin scaffold for partial meniscal replacement in a sheep model
PURPOSE: Due to the negative effects of meniscectomy, there is a need for an adequate material to replace damaged meniscal tissue. To date, no material tested has been able to replace the meniscus sufficiently. Therefore, a new silk fibroin scaffold was investigated in an in vivo sheep model. METHOD...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661201/ https://www.ncbi.nlm.nih.gov/pubmed/24770350 http://dx.doi.org/10.1007/s00167-014-3009-2 |
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author | Gruchenberg, Katharina Ignatius, Anita Friemert, Benedikt von Lübken, Falk Skaer, Nick Gellynck, Kris Kessler, Oliver Dürselen, Lutz |
author_facet | Gruchenberg, Katharina Ignatius, Anita Friemert, Benedikt von Lübken, Falk Skaer, Nick Gellynck, Kris Kessler, Oliver Dürselen, Lutz |
author_sort | Gruchenberg, Katharina |
collection | PubMed |
description | PURPOSE: Due to the negative effects of meniscectomy, there is a need for an adequate material to replace damaged meniscal tissue. To date, no material tested has been able to replace the meniscus sufficiently. Therefore, a new silk fibroin scaffold was investigated in an in vivo sheep model. METHODS: Partial meniscectomy was carried out to the medial meniscus of 28 sheep, and a scaffold was implanted in 19 menisci (3-month scaffold group, n = 9; 6-month scaffold group, n = 10). In 9 sheep, the defect remained empty (partial meniscectomy group). Sham operation was performed in 9 animals. RESULTS: The silk scaffold was able to withstand the loads experienced during the implantation period. It caused no inflammatory reaction in the joint 6 months postoperatively, and there were no significant differences in cartilage degeneration between the scaffold and sham groups. The compressive properties of the scaffold approached those of meniscal tissue. However, the scaffolds were not always stably fixed in the defect, leading to gapping between implant and host tissue or to total loss of the implant in 3 of 9 cases in each scaffold group. Hence, the fixation technique needs to be improved to achieve a better integration into the host tissue, and the long-term performance of the scaffolds should be further investigated. CONCLUSION: These first in vivo results on a new silk fibroin scaffold provide the basis for further meniscal implant development. Whilst more data are required, there is preliminary evidence of chondroprotective properties, and the compressive properties and biocompatibility are promising. |
format | Online Article Text |
id | pubmed-4661201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-46612012015-12-04 In vivo performance of a novel silk fibroin scaffold for partial meniscal replacement in a sheep model Gruchenberg, Katharina Ignatius, Anita Friemert, Benedikt von Lübken, Falk Skaer, Nick Gellynck, Kris Kessler, Oliver Dürselen, Lutz Knee Surg Sports Traumatol Arthrosc Knee PURPOSE: Due to the negative effects of meniscectomy, there is a need for an adequate material to replace damaged meniscal tissue. To date, no material tested has been able to replace the meniscus sufficiently. Therefore, a new silk fibroin scaffold was investigated in an in vivo sheep model. METHODS: Partial meniscectomy was carried out to the medial meniscus of 28 sheep, and a scaffold was implanted in 19 menisci (3-month scaffold group, n = 9; 6-month scaffold group, n = 10). In 9 sheep, the defect remained empty (partial meniscectomy group). Sham operation was performed in 9 animals. RESULTS: The silk scaffold was able to withstand the loads experienced during the implantation period. It caused no inflammatory reaction in the joint 6 months postoperatively, and there were no significant differences in cartilage degeneration between the scaffold and sham groups. The compressive properties of the scaffold approached those of meniscal tissue. However, the scaffolds were not always stably fixed in the defect, leading to gapping between implant and host tissue or to total loss of the implant in 3 of 9 cases in each scaffold group. Hence, the fixation technique needs to be improved to achieve a better integration into the host tissue, and the long-term performance of the scaffolds should be further investigated. CONCLUSION: These first in vivo results on a new silk fibroin scaffold provide the basis for further meniscal implant development. Whilst more data are required, there is preliminary evidence of chondroprotective properties, and the compressive properties and biocompatibility are promising. Springer Berlin Heidelberg 2014-04-26 2015 /pmc/articles/PMC4661201/ /pubmed/24770350 http://dx.doi.org/10.1007/s00167-014-3009-2 Text en © Springer-Verlag Berlin Heidelberg 2014 |
spellingShingle | Knee Gruchenberg, Katharina Ignatius, Anita Friemert, Benedikt von Lübken, Falk Skaer, Nick Gellynck, Kris Kessler, Oliver Dürselen, Lutz In vivo performance of a novel silk fibroin scaffold for partial meniscal replacement in a sheep model |
title | In vivo performance of a novel silk fibroin scaffold for partial meniscal replacement in a sheep model |
title_full | In vivo performance of a novel silk fibroin scaffold for partial meniscal replacement in a sheep model |
title_fullStr | In vivo performance of a novel silk fibroin scaffold for partial meniscal replacement in a sheep model |
title_full_unstemmed | In vivo performance of a novel silk fibroin scaffold for partial meniscal replacement in a sheep model |
title_short | In vivo performance of a novel silk fibroin scaffold for partial meniscal replacement in a sheep model |
title_sort | in vivo performance of a novel silk fibroin scaffold for partial meniscal replacement in a sheep model |
topic | Knee |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661201/ https://www.ncbi.nlm.nih.gov/pubmed/24770350 http://dx.doi.org/10.1007/s00167-014-3009-2 |
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