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A Biomimetic Heparinized Composite Silk-Based Vascular Scaffold with sustained Antithrombogenicity

Autologous grafts, as the gold standard for vascular bypass procedures, associated with several problems that limit their usability, so tissue engineered vessels have been the subject of an increasing number of works. Nevertheless, gathering all of the desired characteristics of vascular scaffolds i...

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Autores principales: Zamani, Masoud, Khafaji, Mona, Naji, Mohammad, Vossoughi, Manouchehr, Alemzadeh, Iran, Haghighipour, Nooshin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493666/
https://www.ncbi.nlm.nih.gov/pubmed/28667291
http://dx.doi.org/10.1038/s41598-017-04510-1
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author Zamani, Masoud
Khafaji, Mona
Naji, Mohammad
Vossoughi, Manouchehr
Alemzadeh, Iran
Haghighipour, Nooshin
author_facet Zamani, Masoud
Khafaji, Mona
Naji, Mohammad
Vossoughi, Manouchehr
Alemzadeh, Iran
Haghighipour, Nooshin
author_sort Zamani, Masoud
collection PubMed
description Autologous grafts, as the gold standard for vascular bypass procedures, associated with several problems that limit their usability, so tissue engineered vessels have been the subject of an increasing number of works. Nevertheless, gathering all of the desired characteristics of vascular scaffolds in the same construct has been a big challenge for scientists. Herein, a composite silk-based vascular scaffold (CSVS) was proposed to consider all the mechanical, structural and biological requirements of a small-diameter vascular scaffold. The scaffold’s lumen composed of braided silk fiber-reinforced silk fibroin (SF) sponge covalently heparinized (H-CSVS) using Hydroxy-Iron Complexes (HICs) as linkers. The highly porous SF external layer with pores above 60 μm was obtained by lyophilization. Silk fibers were fully embedded in scaffold’s wall with no delamination. The H-CSVS exhibited much higher burst pressure and suture retention strength than native vessels while comparable elastic modulus and compliance. H-CSVSs presented milder hemolysis in vitro and significant calcification resistance in subcutaneous implantation compared to non-heparinized ones. The in vitro antithrombogenic activity was sustained for over 12 weeks. The cytocompatibility was approved using endothelial cells (ECs) and vascular smooth muscle cells (SMCs) in vitro. Therefore, H-CSVS demonstrates a promising candidate for engineering of small-diameter vessels.
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spelling pubmed-54936662017-07-05 A Biomimetic Heparinized Composite Silk-Based Vascular Scaffold with sustained Antithrombogenicity Zamani, Masoud Khafaji, Mona Naji, Mohammad Vossoughi, Manouchehr Alemzadeh, Iran Haghighipour, Nooshin Sci Rep Article Autologous grafts, as the gold standard for vascular bypass procedures, associated with several problems that limit their usability, so tissue engineered vessels have been the subject of an increasing number of works. Nevertheless, gathering all of the desired characteristics of vascular scaffolds in the same construct has been a big challenge for scientists. Herein, a composite silk-based vascular scaffold (CSVS) was proposed to consider all the mechanical, structural and biological requirements of a small-diameter vascular scaffold. The scaffold’s lumen composed of braided silk fiber-reinforced silk fibroin (SF) sponge covalently heparinized (H-CSVS) using Hydroxy-Iron Complexes (HICs) as linkers. The highly porous SF external layer with pores above 60 μm was obtained by lyophilization. Silk fibers were fully embedded in scaffold’s wall with no delamination. The H-CSVS exhibited much higher burst pressure and suture retention strength than native vessels while comparable elastic modulus and compliance. H-CSVSs presented milder hemolysis in vitro and significant calcification resistance in subcutaneous implantation compared to non-heparinized ones. The in vitro antithrombogenic activity was sustained for over 12 weeks. The cytocompatibility was approved using endothelial cells (ECs) and vascular smooth muscle cells (SMCs) in vitro. Therefore, H-CSVS demonstrates a promising candidate for engineering of small-diameter vessels. Nature Publishing Group UK 2017-06-30 /pmc/articles/PMC5493666/ /pubmed/28667291 http://dx.doi.org/10.1038/s41598-017-04510-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zamani, Masoud
Khafaji, Mona
Naji, Mohammad
Vossoughi, Manouchehr
Alemzadeh, Iran
Haghighipour, Nooshin
A Biomimetic Heparinized Composite Silk-Based Vascular Scaffold with sustained Antithrombogenicity
title A Biomimetic Heparinized Composite Silk-Based Vascular Scaffold with sustained Antithrombogenicity
title_full A Biomimetic Heparinized Composite Silk-Based Vascular Scaffold with sustained Antithrombogenicity
title_fullStr A Biomimetic Heparinized Composite Silk-Based Vascular Scaffold with sustained Antithrombogenicity
title_full_unstemmed A Biomimetic Heparinized Composite Silk-Based Vascular Scaffold with sustained Antithrombogenicity
title_short A Biomimetic Heparinized Composite Silk-Based Vascular Scaffold with sustained Antithrombogenicity
title_sort biomimetic heparinized composite silk-based vascular scaffold with sustained antithrombogenicity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493666/
https://www.ncbi.nlm.nih.gov/pubmed/28667291
http://dx.doi.org/10.1038/s41598-017-04510-1
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