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Heparanoid hydrogels for cardiovascular tissue regeneration

Includes bibliographical references

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Main Author: Janse van Rensburg, Aliza
Other Authors: Bezuidenhout, Deon
Format: Thesis
Language:English
Published: Division of Biomedical Engineering 2016
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access_status_str Open Access
author Janse van Rensburg, Aliza
author2 Bezuidenhout, Deon
author_browse Bezuidenhout, Deon
Janse van Rensburg, Aliza
author_facet Bezuidenhout, Deon
Janse van Rensburg, Aliza
author_sort Janse van Rensburg, Aliza
collection Thesis
description Includes bibliographical references
format Thesis
id oai:open.uct.ac.za:11427/16695
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:32:39.476Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2016
publishDateRange 2016
publishDateSort 2016
publisher Division of Biomedical Engineering
publisherStr Division of Biomedical Engineering
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/16695 Heparanoid hydrogels for cardiovascular tissue regeneration Janse van Rensburg, Aliza Bezuidenhout, Deon Davies, Neil Biomedical Engineering Includes bibliographical references Heparin (Hep) and heparan sulfate (HS) have been shown to possess anticoagulative properties, inhibit smooth muscle cell proliferation, moderate inflammation and control angiogenesis by stabilization and potentiation of growth factors (GF). These properties are potentially very useful for the treatment of cardiovascular diseases, especially when delivered as injectable hydrogels that can form in situ. This project focused on developing Hep and HS hydrogels for localized GF delivery. Hep and HS were acrylated, characterized and crosslinked with PEG tetra-thiols, either directly (10m% Hep/HS-Ac, Type 1) or by copolymerization with 20PEG8Ac or 20PEG8VS (4m% copolymer; 1.5% Hep/HS-Ac) to form degradable (Type 2D) or non-degradable (Type 2N) gels, respectively. Gelation times, viscoelasticity, swelling, mesh size, Hep/HS elution and activity, as well as GF incorporation and release were studied in vitro. Type 2D gels with covalently incorporated (CI) Hep and GFs were evaluated in vivo as ingrowth matrices in porous polyurethane (PU) scaffolds for healing response in a rat subcutaneous model. 2016-02-02T14:42:02Z 2016-02-02T14:42:02Z 2015 Master Thesis Masters MSc (Med) http://hdl.handle.net/11427/16695 eng application/pdf Division of Biomedical Engineering Faculty of Health Sciences University of Cape Town
spellingShingle Biomedical Engineering
Janse van Rensburg, Aliza
Heparanoid hydrogels for cardiovascular tissue regeneration
thesis_degree_str Master's
title Heparanoid hydrogels for cardiovascular tissue regeneration
title_full Heparanoid hydrogels for cardiovascular tissue regeneration
title_fullStr Heparanoid hydrogels for cardiovascular tissue regeneration
title_full_unstemmed Heparanoid hydrogels for cardiovascular tissue regeneration
title_short Heparanoid hydrogels for cardiovascular tissue regeneration
title_sort heparanoid hydrogels for cardiovascular tissue regeneration
topic Biomedical Engineering
url http://hdl.handle.net/11427/16695
work_keys_str_mv AT jansevanrensburgaliza heparanoidhydrogelsforcardiovasculartissueregeneration