Thiolated Poly‐ and Oligosaccharide‐Based Hydrogels for Tissue Engineering and Wound Healing

Abstract Due to thiolation of poly‐ and oligosaccharides numerous favorable properties for tissue engineering and wound healing can be introduced. Poly‐ and oligosaccharides can be thiolated via hydroxyl‐to‐thiol conversions or the covalent attachment of sulfhydryl ligands to hydroxyl, carbonic acid...

Full description

Bibliographic Details
Published in:Advanced Functional Materials
Main Authors: Noreen, Sobia, Bernkop‐Schnürch, Andreas
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2023
Subjects:
Online Access:http://dx.doi.org/10.1002/adfm.202310129
https://onlinelibrary.wiley.com/doi/pdf/10.1002/adfm.202310129
id crwiley:10.1002/adfm.202310129
record_format openpolar
spelling crwiley:10.1002/adfm.202310129 2024-06-02T08:05:13+00:00 Thiolated Poly‐ and Oligosaccharide‐Based Hydrogels for Tissue Engineering and Wound Healing Noreen, Sobia Bernkop‐Schnürch, Andreas 2023 http://dx.doi.org/10.1002/adfm.202310129 https://onlinelibrary.wiley.com/doi/pdf/10.1002/adfm.202310129 en eng Wiley http://creativecommons.org/licenses/by-nc/4.0/ Advanced Functional Materials volume 34, issue 4 ISSN 1616-301X 1616-3028 journal-article 2023 crwiley https://doi.org/10.1002/adfm.202310129 2024-05-03T10:45:42Z Abstract Due to thiolation of poly‐ and oligosaccharides numerous favorable properties for tissue engineering and wound healing can be introduced. Poly‐ and oligosaccharides can be thiolated via hydroxyl‐to‐thiol conversions or the covalent attachment of sulfhydryl ligands to hydroxyl, carbonic acid or amino groups on them. Since thiolated poly‐ and oligosaccharides can cross‐link via disulfide bonds, they form stable 3D networks with defined microarchitecture, stiffness, elasticity, and degradability. Furthermore, thiol groups can enhance cell adhesion since cells exhibit cysteine‐rich subdomains on their surface that form disulfide bonds with them. Sulfhydryl groups can also participate in cell signaling pathways favoring various cellular processes like proliferation, migration, spreading, and differentiation that are beneficial for tissue engineering and wound healing. In addition, a controlled release of active ingredients such as growth factors being bound via disulfide bonds to thiolated poly‐ and oligosaccharides can be achieved via thiol/disulfide exchange reactions. Over the last two decades, the number of thiolated poly‐ and oligosaccharides such as thiolated hyaluronic acid and thiolated chitosan used for tissue engineering and wound healing has increased tremendously. Within this review, an overview is provided about the chemistry of thiolated poly‐ and oligosaccharides, their key properties, applications and performance in clinical trials and as marketed products. Article in Journal/Newspaper Carbonic acid Wiley Online Library Advanced Functional Materials
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
description Abstract Due to thiolation of poly‐ and oligosaccharides numerous favorable properties for tissue engineering and wound healing can be introduced. Poly‐ and oligosaccharides can be thiolated via hydroxyl‐to‐thiol conversions or the covalent attachment of sulfhydryl ligands to hydroxyl, carbonic acid or amino groups on them. Since thiolated poly‐ and oligosaccharides can cross‐link via disulfide bonds, they form stable 3D networks with defined microarchitecture, stiffness, elasticity, and degradability. Furthermore, thiol groups can enhance cell adhesion since cells exhibit cysteine‐rich subdomains on their surface that form disulfide bonds with them. Sulfhydryl groups can also participate in cell signaling pathways favoring various cellular processes like proliferation, migration, spreading, and differentiation that are beneficial for tissue engineering and wound healing. In addition, a controlled release of active ingredients such as growth factors being bound via disulfide bonds to thiolated poly‐ and oligosaccharides can be achieved via thiol/disulfide exchange reactions. Over the last two decades, the number of thiolated poly‐ and oligosaccharides such as thiolated hyaluronic acid and thiolated chitosan used for tissue engineering and wound healing has increased tremendously. Within this review, an overview is provided about the chemistry of thiolated poly‐ and oligosaccharides, their key properties, applications and performance in clinical trials and as marketed products.
format Article in Journal/Newspaper
author Noreen, Sobia
Bernkop‐Schnürch, Andreas
spellingShingle Noreen, Sobia
Bernkop‐Schnürch, Andreas
Thiolated Poly‐ and Oligosaccharide‐Based Hydrogels for Tissue Engineering and Wound Healing
author_facet Noreen, Sobia
Bernkop‐Schnürch, Andreas
author_sort Noreen, Sobia
title Thiolated Poly‐ and Oligosaccharide‐Based Hydrogels for Tissue Engineering and Wound Healing
title_short Thiolated Poly‐ and Oligosaccharide‐Based Hydrogels for Tissue Engineering and Wound Healing
title_full Thiolated Poly‐ and Oligosaccharide‐Based Hydrogels for Tissue Engineering and Wound Healing
title_fullStr Thiolated Poly‐ and Oligosaccharide‐Based Hydrogels for Tissue Engineering and Wound Healing
title_full_unstemmed Thiolated Poly‐ and Oligosaccharide‐Based Hydrogels for Tissue Engineering and Wound Healing
title_sort thiolated poly‐ and oligosaccharide‐based hydrogels for tissue engineering and wound healing
publisher Wiley
publishDate 2023
url http://dx.doi.org/10.1002/adfm.202310129
https://onlinelibrary.wiley.com/doi/pdf/10.1002/adfm.202310129
genre Carbonic acid
genre_facet Carbonic acid
op_source Advanced Functional Materials
volume 34, issue 4
ISSN 1616-301X 1616-3028
op_rights http://creativecommons.org/licenses/by-nc/4.0/
op_doi https://doi.org/10.1002/adfm.202310129
container_title Advanced Functional Materials
_version_ 1800749996032655360