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Modular Small Diameter Vascular Grafts with Bioactive Functionalities

We report the fabrication of a novel type of artificial small diameter blood vessels, termed biomimetic tissue-engineered blood vessels (bTEBV), with a modular composition. They are composed of a hydrogel scaffold consisting of two negatively charged natural polymers, alginate and a modified chitosa...

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Published in:PloS one 2015-07, Vol.10 (7), p.e0133632
Main Authors: Neufurth, Meik, Wang, Xiaohong, Tolba, Emad, Dorweiler, Bernhard, Schröder, Heinz C, Link, Thorben, Diehl-Seifert, Bärbel, Müller, Werner E G
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cited_by cdi_FETCH-LOGICAL-c692t-1dc99dd64cfa7952254fd2a962af987f12158a1f5b00bba760289da1810034693
cites cdi_FETCH-LOGICAL-c692t-1dc99dd64cfa7952254fd2a962af987f12158a1f5b00bba760289da1810034693
container_end_page
container_issue 7
container_start_page e0133632
container_title PloS one
container_volume 10
creator Neufurth, Meik
Wang, Xiaohong
Tolba, Emad
Dorweiler, Bernhard
Schröder, Heinz C
Link, Thorben
Diehl-Seifert, Bärbel
Müller, Werner E G
description We report the fabrication of a novel type of artificial small diameter blood vessels, termed biomimetic tissue-engineered blood vessels (bTEBV), with a modular composition. They are composed of a hydrogel scaffold consisting of two negatively charged natural polymers, alginate and a modified chitosan, N,O-carboxymethyl chitosan (N,O-CMC). Into this biologically inert scaffold two biofunctionally active biopolymers are embedded, inorganic polyphosphate (polyP) and silica, as well as gelatin which exposes the cell recognition signal, Arg-Gly-Asp (RGD). These materials can be hardened by exposure to Ca(2+) through formation of Ca(2+) bridges between the polyanions, alginate, N,O-CMC, and polyP (alginate-Ca(2+)-N,O-CMC-polyP). The bTEBV are formed by pressing the hydrogel through an extruder into a hardening solution, containing Ca(2+). In this universal scaffold of the bTEBV biomaterial, polycations such as poly(L-Lys), poly(D-Lys) or a His/Gly-tagged RGD peptide (three RGD units) were incorporated, which promote the adhesion of endothelial cells to the vessel surface. The mechanical properties of the biopolymer material (alginate-Ca(2+)-N,O-CMC-polyP-silica) revealed a hardness (elastic modulus) of 475 kPa even after a short incubation period in CaCl2 solution. The material of the artificial vascular grafts (bTEBVs with an outer size 6 mm and 1.8 mm, and an inner diameter 4 mm and 0.8 mm, respectively) turned out to be durable in 4-week pulsatile flow experiments at an alternating pressure between 25 and 100 mbar (18.7 and 75.0 mm Hg). The burst pressure of the larger (smaller) vessels was 850 mbar (145 mbar). Incorporation of polycationic poly(L-Lys), poly(D-Lys), and especially the His/Gly-tagged RGD peptide, markedly increased the adhesion of human, umbilical vein/vascular endothelial cells, EA.HY926 cells, to the surface of the hydrogel. No significant effect of the polyP samples on the clotting of human plasma is measured. We propose that the metabolically degradable polymeric scaffold bTEBV is a promising biomaterial for future prosthetic vascular grafts.
doi_str_mv 10.1371/journal.pone.0133632
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They are composed of a hydrogel scaffold consisting of two negatively charged natural polymers, alginate and a modified chitosan, N,O-carboxymethyl chitosan (N,O-CMC). Into this biologically inert scaffold two biofunctionally active biopolymers are embedded, inorganic polyphosphate (polyP) and silica, as well as gelatin which exposes the cell recognition signal, Arg-Gly-Asp (RGD). These materials can be hardened by exposure to Ca(2+) through formation of Ca(2+) bridges between the polyanions, alginate, N,O-CMC, and polyP (alginate-Ca(2+)-N,O-CMC-polyP). The bTEBV are formed by pressing the hydrogel through an extruder into a hardening solution, containing Ca(2+). In this universal scaffold of the bTEBV biomaterial, polycations such as poly(L-Lys), poly(D-Lys) or a His/Gly-tagged RGD peptide (three RGD units) were incorporated, which promote the adhesion of endothelial cells to the vessel surface. 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Medical Complete (Alumni)</collection><collection>https://resources.nclive.org/materials</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest advanced technologies &amp; aerospace journals</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials science collection</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Neufurth, Meik</au><au>Wang, Xiaohong</au><au>Tolba, Emad</au><au>Dorweiler, Bernhard</au><au>Schröder, Heinz C</au><au>Link, Thorben</au><au>Diehl-Seifert, Bärbel</au><au>Müller, Werner E G</au><au>Zhao, Feng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modular Small Diameter Vascular Grafts with Bioactive Functionalities</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2015-07-23</date><risdate>2015</risdate><volume>10</volume><issue>7</issue><spage>e0133632</spage><pages>e0133632-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>We report the fabrication of a novel type of artificial small diameter blood vessels, termed biomimetic tissue-engineered blood vessels (bTEBV), with a modular composition. They are composed of a hydrogel scaffold consisting of two negatively charged natural polymers, alginate and a modified chitosan, N,O-carboxymethyl chitosan (N,O-CMC). Into this biologically inert scaffold two biofunctionally active biopolymers are embedded, inorganic polyphosphate (polyP) and silica, as well as gelatin which exposes the cell recognition signal, Arg-Gly-Asp (RGD). These materials can be hardened by exposure to Ca(2+) through formation of Ca(2+) bridges between the polyanions, alginate, N,O-CMC, and polyP (alginate-Ca(2+)-N,O-CMC-polyP). The bTEBV are formed by pressing the hydrogel through an extruder into a hardening solution, containing Ca(2+). In this universal scaffold of the bTEBV biomaterial, polycations such as poly(L-Lys), poly(D-Lys) or a His/Gly-tagged RGD peptide (three RGD units) were incorporated, which promote the adhesion of endothelial cells to the vessel surface. The mechanical properties of the biopolymer material (alginate-Ca(2+)-N,O-CMC-polyP-silica) revealed a hardness (elastic modulus) of 475 kPa even after a short incubation period in CaCl2 solution. The material of the artificial vascular grafts (bTEBVs with an outer size 6 mm and 1.8 mm, and an inner diameter 4 mm and 0.8 mm, respectively) turned out to be durable in 4-week pulsatile flow experiments at an alternating pressure between 25 and 100 mbar (18.7 and 75.0 mm Hg). The burst pressure of the larger (smaller) vessels was 850 mbar (145 mbar). Incorporation of polycationic poly(L-Lys), poly(D-Lys), and especially the His/Gly-tagged RGD peptide, markedly increased the adhesion of human, umbilical vein/vascular endothelial cells, EA.HY926 cells, to the surface of the hydrogel. No significant effect of the polyP samples on the clotting of human plasma is measured. We propose that the metabolically degradable polymeric scaffold bTEBV is a promising biomaterial for future prosthetic vascular grafts.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26204529</pmid><doi>10.1371/journal.pone.0133632</doi><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1932-6203
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issn 1932-6203
1932-6203
language eng
recordid cdi_plos_journals_1698387557
source Access via ProQuest (Open Access); PubMed Central
subjects Absorbable Implants
Adhesion
Alginates - chemistry
Alginic acid
Biocompatible Materials - chemistry
Biological products
Biomaterials
Biomedical materials
Biomimetics
Biopolymers
Blood
Blood Coagulation - drug effects
Blood plasma
Blood Vessel Prosthesis
Blood vessels
Calcium alginate
Calcium chloride
Calcium Chloride - pharmacology
Cell adhesion & migration
Cell Line, Transformed
Cell recognition
Chitosan
Chitosan - chemistry
Clotting
Collagen
Elastic Modulus
Endothelial cells
Endothelial Cells - cytology
Fabrication
Gelatin
Gene expression
Glucuronic Acid - chemistry
Grafting
Grafts
Hardening
Hemodialysis
Hexuronic Acids - chemistry
Human Umbilical Vein Endothelial Cells - cytology
Humans
Hydrogels
Hydrogels - chemistry
Kinases
Materials Testing
Mechanical properties
Mercury
Modular engineering
Modulus of elasticity
Natural polymers
Oligopeptides - pharmacology
Organ transplantation
Peptides
Physiology
Polyanions
Polycations
Polyethylene terephthalate
Polymers
Polyphosphates - chemistry
Pressure
Prostheses
Prostheses and implants
Silica
Silica gel
Silicon Dioxide
Stem cells
Tensile Strength
Thrombosis
Tissue Engineering
Tissue Scaffolds
Transplants & implants
Umbilical vein
Vascular Grafting
Vascular surgery
title Modular Small Diameter Vascular Grafts with Bioactive Functionalities
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