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Thiol-Mediated Chemoselective Strategies for In Situ Formation of Hydrogels

Hydrogels are three-dimensional networks composed of hydrated polymer chains and have been a material of choice for many biomedical applications such as drug delivery, biosensing, and tissue engineering due to their unique biocompatibility, tunable physical characteristics, flexible methods of synth...

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Detalles Bibliográficos
Autor principal: Su, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209259/
https://www.ncbi.nlm.nih.gov/pubmed/30674848
http://dx.doi.org/10.3390/gels4030072
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author Su, Jing
author_facet Su, Jing
author_sort Su, Jing
collection PubMed
description Hydrogels are three-dimensional networks composed of hydrated polymer chains and have been a material of choice for many biomedical applications such as drug delivery, biosensing, and tissue engineering due to their unique biocompatibility, tunable physical characteristics, flexible methods of synthesis, and range of constituents. In many cases, methods for crosslinking polymer precursors to form hydrogels would benefit from being highly selective in order to avoid cross-reactivity with components of biological systems leading to adverse effects. Crosslinking reactions involving the thiol group (SH) offer unique opportunities to construct hydrogel materials of diverse properties under mild conditions. This article reviews and comments on thiol-mediated chemoselective and biocompatible strategies for crosslinking natural and synthetic macromolecules to form injectable hydrogels for applications in drug delivery and cell encapsulation.
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spelling pubmed-62092592019-01-17 Thiol-Mediated Chemoselective Strategies for In Situ Formation of Hydrogels Su, Jing Gels Review Hydrogels are three-dimensional networks composed of hydrated polymer chains and have been a material of choice for many biomedical applications such as drug delivery, biosensing, and tissue engineering due to their unique biocompatibility, tunable physical characteristics, flexible methods of synthesis, and range of constituents. In many cases, methods for crosslinking polymer precursors to form hydrogels would benefit from being highly selective in order to avoid cross-reactivity with components of biological systems leading to adverse effects. Crosslinking reactions involving the thiol group (SH) offer unique opportunities to construct hydrogel materials of diverse properties under mild conditions. This article reviews and comments on thiol-mediated chemoselective and biocompatible strategies for crosslinking natural and synthetic macromolecules to form injectable hydrogels for applications in drug delivery and cell encapsulation. MDPI 2018-09-02 /pmc/articles/PMC6209259/ /pubmed/30674848 http://dx.doi.org/10.3390/gels4030072 Text en © 2018 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Su, Jing
Thiol-Mediated Chemoselective Strategies for In Situ Formation of Hydrogels
title Thiol-Mediated Chemoselective Strategies for In Situ Formation of Hydrogels
title_full Thiol-Mediated Chemoselective Strategies for In Situ Formation of Hydrogels
title_fullStr Thiol-Mediated Chemoselective Strategies for In Situ Formation of Hydrogels
title_full_unstemmed Thiol-Mediated Chemoselective Strategies for In Situ Formation of Hydrogels
title_short Thiol-Mediated Chemoselective Strategies for In Situ Formation of Hydrogels
title_sort thiol-mediated chemoselective strategies for in situ formation of hydrogels
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209259/
https://www.ncbi.nlm.nih.gov/pubmed/30674848
http://dx.doi.org/10.3390/gels4030072
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