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The in vivo performance of small-caliber nanofibrous polyurethane vascular grafts

BACKGROUND: In a previous in vitro study, we confirmed that small-caliber nanofibrous polyurethane (PU) vascular grafts have favorable mechanical properties and biocompatibility. In the present study, we examined the in vivo biocompatibility and stability of these grafts. METHODS: Forty-eight adult...

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Autores principales: Hu, Zuo-jun, Li, Zi-lun, Hu, Ling-yu, He, Wei, Liu, Rui-ming, Qin, Yuan-sen, Wang, Shen-ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3523977/
https://www.ncbi.nlm.nih.gov/pubmed/23206536
http://dx.doi.org/10.1186/1471-2261-12-115
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author Hu, Zuo-jun
Li, Zi-lun
Hu, Ling-yu
He, Wei
Liu, Rui-ming
Qin, Yuan-sen
Wang, Shen-ming
author_facet Hu, Zuo-jun
Li, Zi-lun
Hu, Ling-yu
He, Wei
Liu, Rui-ming
Qin, Yuan-sen
Wang, Shen-ming
author_sort Hu, Zuo-jun
collection PubMed
description BACKGROUND: In a previous in vitro study, we confirmed that small-caliber nanofibrous polyurethane (PU) vascular grafts have favorable mechanical properties and biocompatibility. In the present study, we examined the in vivo biocompatibility and stability of these grafts. METHODS: Forty-eight adult male beagle dogs were randomly divided into two groups receiving, respectively, polyurethane (PU) or polytetrafluoroethylene (PTFE) grafts (n = 24 animals / group). Each group was studied at 4, 8, 12, and 24 weeks after graft implantation. Blood flow was analyzed by color Doppler ultrasound and computed tomography angiography. Patency rates were judged by animal survival rates. Coverage with endothelial and smooth muscle cells was characterized by hematoxylin-eosin and immunohistological staining, and scanning electron microscopy (SEM). RESULTS: Patency rates were significantly higher in the PU group (p = 0.02 vs. PTFE group). During the first 8 weeks, endothelial cells gradually formed a continuous layer on the internal surface of PU grafts, whereas coverage of PTFE graft by endothelial cells was inhomogeneous. After 12 weeks, neointimal thickness remained constant in the PU group, while PTFE group showed neointimal hyperplasia. At 24 weeks, some anastomotic sites of PTFE grafts became stenotic (p = 0.013 vs. PU group). Immunohistological staining revealed a continuous coverage by endothelial cells and an orderly arrangement of smooth muscle cells on PU grafts. Further, SEM showed smooth internal surfaces in PU grafts without thrombus or obvious neointimal hyperplasia. CONCLUSIONS: Small-caliber nanofibrous PU vascular grafts facilitate the endothelialization process, prevent excessive neointimal hyperplasia, and improve patency rates.
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spelling pubmed-35239772012-12-18 The in vivo performance of small-caliber nanofibrous polyurethane vascular grafts Hu, Zuo-jun Li, Zi-lun Hu, Ling-yu He, Wei Liu, Rui-ming Qin, Yuan-sen Wang, Shen-ming BMC Cardiovasc Disord Research Article BACKGROUND: In a previous in vitro study, we confirmed that small-caliber nanofibrous polyurethane (PU) vascular grafts have favorable mechanical properties and biocompatibility. In the present study, we examined the in vivo biocompatibility and stability of these grafts. METHODS: Forty-eight adult male beagle dogs were randomly divided into two groups receiving, respectively, polyurethane (PU) or polytetrafluoroethylene (PTFE) grafts (n = 24 animals / group). Each group was studied at 4, 8, 12, and 24 weeks after graft implantation. Blood flow was analyzed by color Doppler ultrasound and computed tomography angiography. Patency rates were judged by animal survival rates. Coverage with endothelial and smooth muscle cells was characterized by hematoxylin-eosin and immunohistological staining, and scanning electron microscopy (SEM). RESULTS: Patency rates were significantly higher in the PU group (p = 0.02 vs. PTFE group). During the first 8 weeks, endothelial cells gradually formed a continuous layer on the internal surface of PU grafts, whereas coverage of PTFE graft by endothelial cells was inhomogeneous. After 12 weeks, neointimal thickness remained constant in the PU group, while PTFE group showed neointimal hyperplasia. At 24 weeks, some anastomotic sites of PTFE grafts became stenotic (p = 0.013 vs. PU group). Immunohistological staining revealed a continuous coverage by endothelial cells and an orderly arrangement of smooth muscle cells on PU grafts. Further, SEM showed smooth internal surfaces in PU grafts without thrombus or obvious neointimal hyperplasia. CONCLUSIONS: Small-caliber nanofibrous PU vascular grafts facilitate the endothelialization process, prevent excessive neointimal hyperplasia, and improve patency rates. BioMed Central 2012-12-03 /pmc/articles/PMC3523977/ /pubmed/23206536 http://dx.doi.org/10.1186/1471-2261-12-115 Text en Copyright ©2012 Hu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hu, Zuo-jun
Li, Zi-lun
Hu, Ling-yu
He, Wei
Liu, Rui-ming
Qin, Yuan-sen
Wang, Shen-ming
The in vivo performance of small-caliber nanofibrous polyurethane vascular grafts
title The in vivo performance of small-caliber nanofibrous polyurethane vascular grafts
title_full The in vivo performance of small-caliber nanofibrous polyurethane vascular grafts
title_fullStr The in vivo performance of small-caliber nanofibrous polyurethane vascular grafts
title_full_unstemmed The in vivo performance of small-caliber nanofibrous polyurethane vascular grafts
title_short The in vivo performance of small-caliber nanofibrous polyurethane vascular grafts
title_sort in vivo performance of small-caliber nanofibrous polyurethane vascular grafts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3523977/
https://www.ncbi.nlm.nih.gov/pubmed/23206536
http://dx.doi.org/10.1186/1471-2261-12-115
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