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An Assessment of Blood Vessel Remodeling of Nanofibrous Poly(ε-Caprolactone) Vascular Grafts in a Rat Animal Model
The development of an ideal vascular prosthesis represents an important challenge in terms of the treatment of cardiovascular diseases with respect to which new materials are being considered that have produced promising results following testing in animal models. This study focuses on nanofibrous p...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9965469/ https://www.ncbi.nlm.nih.gov/pubmed/36826887 http://dx.doi.org/10.3390/jfb14020088 |
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author | Horakova, Jana Blassova, Tereza Tonar, Zbynek McCarthy, Connor Strnadova, Katerina Lukas, David Mikes, Petr Bowen, Patrick Guillory, Roger Frost, Megan Goldman, Jeremy |
author_facet | Horakova, Jana Blassova, Tereza Tonar, Zbynek McCarthy, Connor Strnadova, Katerina Lukas, David Mikes, Petr Bowen, Patrick Guillory, Roger Frost, Megan Goldman, Jeremy |
author_sort | Horakova, Jana |
collection | PubMed |
description | The development of an ideal vascular prosthesis represents an important challenge in terms of the treatment of cardiovascular diseases with respect to which new materials are being considered that have produced promising results following testing in animal models. This study focuses on nanofibrous polycaprolactone-based grafts assessed by means of histological techniques 10 days and 6 months following suturing as a replacement for the rat aorta. A novel stereological approach for the assessment of cellular distribution within the graft thickness was developed. The cellularization of the thickness of the graft was found to be homogeneous after 10 days and to have changed after 6 months, at which time the majority of cells was discovered in the inner layer where the regeneration of the vessel wall was found to have occurred. Six months following implantation, the endothelialization of the graft lumen was complete, and no vasa vasorum were found to be present. Newly formed tissue resembling native elastic arteries with concentric layers composed of smooth muscle cells, collagen, and elastin was found in the implanted polycaprolactone-based grafts. Moreover, the inner layer of the graft was seen to have developed structural similarities to the regular aortic wall. The grafts appeared to be well tolerated, and no severe adverse reaction was recorded with the exception of one case of cartilaginous metaplasia close to the junctional suture. |
format | Online Article Text |
id | pubmed-9965469 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99654692023-02-26 An Assessment of Blood Vessel Remodeling of Nanofibrous Poly(ε-Caprolactone) Vascular Grafts in a Rat Animal Model Horakova, Jana Blassova, Tereza Tonar, Zbynek McCarthy, Connor Strnadova, Katerina Lukas, David Mikes, Petr Bowen, Patrick Guillory, Roger Frost, Megan Goldman, Jeremy J Funct Biomater Article The development of an ideal vascular prosthesis represents an important challenge in terms of the treatment of cardiovascular diseases with respect to which new materials are being considered that have produced promising results following testing in animal models. This study focuses on nanofibrous polycaprolactone-based grafts assessed by means of histological techniques 10 days and 6 months following suturing as a replacement for the rat aorta. A novel stereological approach for the assessment of cellular distribution within the graft thickness was developed. The cellularization of the thickness of the graft was found to be homogeneous after 10 days and to have changed after 6 months, at which time the majority of cells was discovered in the inner layer where the regeneration of the vessel wall was found to have occurred. Six months following implantation, the endothelialization of the graft lumen was complete, and no vasa vasorum were found to be present. Newly formed tissue resembling native elastic arteries with concentric layers composed of smooth muscle cells, collagen, and elastin was found in the implanted polycaprolactone-based grafts. Moreover, the inner layer of the graft was seen to have developed structural similarities to the regular aortic wall. The grafts appeared to be well tolerated, and no severe adverse reaction was recorded with the exception of one case of cartilaginous metaplasia close to the junctional suture. MDPI 2023-02-03 /pmc/articles/PMC9965469/ /pubmed/36826887 http://dx.doi.org/10.3390/jfb14020088 Text en © 2023 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 Horakova, Jana Blassova, Tereza Tonar, Zbynek McCarthy, Connor Strnadova, Katerina Lukas, David Mikes, Petr Bowen, Patrick Guillory, Roger Frost, Megan Goldman, Jeremy An Assessment of Blood Vessel Remodeling of Nanofibrous Poly(ε-Caprolactone) Vascular Grafts in a Rat Animal Model |
title | An Assessment of Blood Vessel Remodeling of Nanofibrous Poly(ε-Caprolactone) Vascular Grafts in a Rat Animal Model |
title_full | An Assessment of Blood Vessel Remodeling of Nanofibrous Poly(ε-Caprolactone) Vascular Grafts in a Rat Animal Model |
title_fullStr | An Assessment of Blood Vessel Remodeling of Nanofibrous Poly(ε-Caprolactone) Vascular Grafts in a Rat Animal Model |
title_full_unstemmed | An Assessment of Blood Vessel Remodeling of Nanofibrous Poly(ε-Caprolactone) Vascular Grafts in a Rat Animal Model |
title_short | An Assessment of Blood Vessel Remodeling of Nanofibrous Poly(ε-Caprolactone) Vascular Grafts in a Rat Animal Model |
title_sort | assessment of blood vessel remodeling of nanofibrous poly(ε-caprolactone) vascular grafts in a rat animal model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9965469/ https://www.ncbi.nlm.nih.gov/pubmed/36826887 http://dx.doi.org/10.3390/jfb14020088 |
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