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The in vivo blood compatibility of bio-inspired small diameter vascular graft: effect of submicron longitudinally aligned topography
BACKGROUND: Cardiovascular disease is the leading cause of deaths worldwide and the arterial reconstructive surgery remains the treatment of choice. Although large diameter vascular grafts have been widely used in clinical practices, there is an urgent need to develop a small diameter vascular graft...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850682/ https://www.ncbi.nlm.nih.gov/pubmed/24083888 http://dx.doi.org/10.1186/1471-2261-13-79 |
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author | Liu, Ruiming Qin, Yuansen Wang, Huijin Zhao, Yong Hu, Zuojun Wang, Shenming |
author_facet | Liu, Ruiming Qin, Yuansen Wang, Huijin Zhao, Yong Hu, Zuojun Wang, Shenming |
author_sort | Liu, Ruiming |
collection | PubMed |
description | BACKGROUND: Cardiovascular disease is the leading cause of deaths worldwide and the arterial reconstructive surgery remains the treatment of choice. Although large diameter vascular grafts have been widely used in clinical practices, there is an urgent need to develop a small diameter vascular graft with enhanced blood compatibility. Herein, we fabricated a small diameter vascular graft with submicron longitudinally aligned topography, which mimicked the tunica intima of the native arterial vessels and were tested in Sprague–Dawley (SD) rats. METHODS: Vascular grafts with aligned and smooth topography were prepared by electrospinning and were connected to the abdominal aorta of the SD rats to evaluate their blood compatibility. Graft patency and platelet adhesion were evaluated by color Doppler ultrasound and immunofluorescence respectively. RESULTS: We observed a significant higher patency rate (p = 0.021) and less thrombus formation in vascular graft with aligned topography than vascular graft with smooth topography. However, no significant difference between the adhesion rates on both vascular grafts (smooth/aligned: 0.35‰/0.12‰, p > 0.05) was observed. Moreover, both vascular grafts had few adherent activated platelets on the luminal surface. CONCLUSION: Bionic vascular graft showed enhanced blood compatibility due to the effect of surface topography. Therefore, it has considerable potential for using in clinical application. |
format | Online Article Text |
id | pubmed-3850682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38506822013-12-16 The in vivo blood compatibility of bio-inspired small diameter vascular graft: effect of submicron longitudinally aligned topography Liu, Ruiming Qin, Yuansen Wang, Huijin Zhao, Yong Hu, Zuojun Wang, Shenming BMC Cardiovasc Disord Research Article BACKGROUND: Cardiovascular disease is the leading cause of deaths worldwide and the arterial reconstructive surgery remains the treatment of choice. Although large diameter vascular grafts have been widely used in clinical practices, there is an urgent need to develop a small diameter vascular graft with enhanced blood compatibility. Herein, we fabricated a small diameter vascular graft with submicron longitudinally aligned topography, which mimicked the tunica intima of the native arterial vessels and were tested in Sprague–Dawley (SD) rats. METHODS: Vascular grafts with aligned and smooth topography were prepared by electrospinning and were connected to the abdominal aorta of the SD rats to evaluate their blood compatibility. Graft patency and platelet adhesion were evaluated by color Doppler ultrasound and immunofluorescence respectively. RESULTS: We observed a significant higher patency rate (p = 0.021) and less thrombus formation in vascular graft with aligned topography than vascular graft with smooth topography. However, no significant difference between the adhesion rates on both vascular grafts (smooth/aligned: 0.35‰/0.12‰, p > 0.05) was observed. Moreover, both vascular grafts had few adherent activated platelets on the luminal surface. CONCLUSION: Bionic vascular graft showed enhanced blood compatibility due to the effect of surface topography. Therefore, it has considerable potential for using in clinical application. BioMed Central 2013-10-01 /pmc/articles/PMC3850682/ /pubmed/24083888 http://dx.doi.org/10.1186/1471-2261-13-79 Text en Copyright © 2013 Liu 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 Liu, Ruiming Qin, Yuansen Wang, Huijin Zhao, Yong Hu, Zuojun Wang, Shenming The in vivo blood compatibility of bio-inspired small diameter vascular graft: effect of submicron longitudinally aligned topography |
title | The in vivo blood compatibility of bio-inspired small diameter vascular graft: effect of submicron longitudinally aligned topography |
title_full | The in vivo blood compatibility of bio-inspired small diameter vascular graft: effect of submicron longitudinally aligned topography |
title_fullStr | The in vivo blood compatibility of bio-inspired small diameter vascular graft: effect of submicron longitudinally aligned topography |
title_full_unstemmed | The in vivo blood compatibility of bio-inspired small diameter vascular graft: effect of submicron longitudinally aligned topography |
title_short | The in vivo blood compatibility of bio-inspired small diameter vascular graft: effect of submicron longitudinally aligned topography |
title_sort | in vivo blood compatibility of bio-inspired small diameter vascular graft: effect of submicron longitudinally aligned topography |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850682/ https://www.ncbi.nlm.nih.gov/pubmed/24083888 http://dx.doi.org/10.1186/1471-2261-13-79 |
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