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In vivo evaluation of a regenerative approach to nasal dorsum augmentation with a polycaprolactone-based implant

BACKGROUND: Alternative techniques for nasal dorsum augmentation are of paramount importance in reconstructive and plastic surgery. In contrast to autologous cartilage grafts, tissue-engineered grafts can be created de novo and yield low–none donor site morbidity as compared to autologous grafts lik...

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Autores principales: Wiggenhauser, Paul S., Balmayor, Elizabeth R., Rotter, Nicole, Schantz, Jan T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6348657/
https://www.ncbi.nlm.nih.gov/pubmed/30691516
http://dx.doi.org/10.1186/s40001-019-0364-y
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author Wiggenhauser, Paul S.
Balmayor, Elizabeth R.
Rotter, Nicole
Schantz, Jan T.
author_facet Wiggenhauser, Paul S.
Balmayor, Elizabeth R.
Rotter, Nicole
Schantz, Jan T.
author_sort Wiggenhauser, Paul S.
collection PubMed
description BACKGROUND: Alternative techniques for nasal dorsum augmentation are of paramount importance in reconstructive and plastic surgery. In contrast to autologous cartilage grafts, tissue-engineered grafts can be created de novo and yield low–none donor site morbidity as compared to autologous grafts like rib or ear cartilage. To address this demand, this study investigated the in vivo regenerative potential of polycaprolactone-based implants as an alternative to autologous cartilage grafting during rhinoplasty. METHODS: Implants were placed at the nasal dorsum in two groups of minipigs and kept in situ for 2 and 6 months, respectively. Subsequently, the implants were harvested and examined by histology (hematoxylin–eosin, alcian blue, and safranin O) and immunostaining (collagen I and collagen II). Further analysis was performed to measure diameter and distance of polycaprolactone struts. RESULTS: Histological examination revealed a persistent formation of connective tissue with some spots resembling a cartilaginous-like matrix after 6 months. In such areas, cells of chondrocyte appearance could be identified. There was a significant decrease in strut diameter but a non-significant difference in strut distance. CONCLUSION: Our results indicated that the investigated polycaprolactone-based implants have shown a regenerative and stable nasal dorsum augmentation after 6 months in vivo. Thus, we believe that customized polycaprolactone-based implants could become an alternative technique for nasal dorsum augmentation without the need for autologous cartilage grafts.
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spelling pubmed-63486572019-01-31 In vivo evaluation of a regenerative approach to nasal dorsum augmentation with a polycaprolactone-based implant Wiggenhauser, Paul S. Balmayor, Elizabeth R. Rotter, Nicole Schantz, Jan T. Eur J Med Res Research BACKGROUND: Alternative techniques for nasal dorsum augmentation are of paramount importance in reconstructive and plastic surgery. In contrast to autologous cartilage grafts, tissue-engineered grafts can be created de novo and yield low–none donor site morbidity as compared to autologous grafts like rib or ear cartilage. To address this demand, this study investigated the in vivo regenerative potential of polycaprolactone-based implants as an alternative to autologous cartilage grafting during rhinoplasty. METHODS: Implants were placed at the nasal dorsum in two groups of minipigs and kept in situ for 2 and 6 months, respectively. Subsequently, the implants were harvested and examined by histology (hematoxylin–eosin, alcian blue, and safranin O) and immunostaining (collagen I and collagen II). Further analysis was performed to measure diameter and distance of polycaprolactone struts. RESULTS: Histological examination revealed a persistent formation of connective tissue with some spots resembling a cartilaginous-like matrix after 6 months. In such areas, cells of chondrocyte appearance could be identified. There was a significant decrease in strut diameter but a non-significant difference in strut distance. CONCLUSION: Our results indicated that the investigated polycaprolactone-based implants have shown a regenerative and stable nasal dorsum augmentation after 6 months in vivo. Thus, we believe that customized polycaprolactone-based implants could become an alternative technique for nasal dorsum augmentation without the need for autologous cartilage grafts. BioMed Central 2019-01-28 /pmc/articles/PMC6348657/ /pubmed/30691516 http://dx.doi.org/10.1186/s40001-019-0364-y Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Wiggenhauser, Paul S.
Balmayor, Elizabeth R.
Rotter, Nicole
Schantz, Jan T.
In vivo evaluation of a regenerative approach to nasal dorsum augmentation with a polycaprolactone-based implant
title In vivo evaluation of a regenerative approach to nasal dorsum augmentation with a polycaprolactone-based implant
title_full In vivo evaluation of a regenerative approach to nasal dorsum augmentation with a polycaprolactone-based implant
title_fullStr In vivo evaluation of a regenerative approach to nasal dorsum augmentation with a polycaprolactone-based implant
title_full_unstemmed In vivo evaluation of a regenerative approach to nasal dorsum augmentation with a polycaprolactone-based implant
title_short In vivo evaluation of a regenerative approach to nasal dorsum augmentation with a polycaprolactone-based implant
title_sort in vivo evaluation of a regenerative approach to nasal dorsum augmentation with a polycaprolactone-based implant
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6348657/
https://www.ncbi.nlm.nih.gov/pubmed/30691516
http://dx.doi.org/10.1186/s40001-019-0364-y
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