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Thiol–Ene Cross-linking of Poly(ethylene glycol) within High Internal Phase Emulsions: Degradable Hydrophilic PolyHIPEs for Controlled Drug Release
[Image: see text] Macroporous polymer monoliths prepared from high internal phase emulsions (HIPEs) can be found in various biomedical applications. While typically water-in-oil HIPEs are applied for polyHIPE preparation, they are not suitable for hydrophilic polyHIPE preparation. Herein, direct oil...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8619294/ https://www.ncbi.nlm.nih.gov/pubmed/34840351 http://dx.doi.org/10.1021/acs.macromol.1c01240 |
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author | Hobiger, Viola Zahoranova, Anna Baudis, Stefan Liska, Robert Krajnc, Peter |
author_facet | Hobiger, Viola Zahoranova, Anna Baudis, Stefan Liska, Robert Krajnc, Peter |
author_sort | Hobiger, Viola |
collection | PubMed |
description | [Image: see text] Macroporous polymer monoliths prepared from high internal phase emulsions (HIPEs) can be found in various biomedical applications. While typically water-in-oil HIPEs are applied for polyHIPE preparation, they are not suitable for hydrophilic polyHIPE preparation. Herein, direct oil-in-water emulsions based on water-soluble poly(ethylene glycol)diacrylate or poly(ethylene glycol)dimethacrylate were developed. Furthermore, the incorporation of a hydrophilic water-miscible thiol, ethoxylated trimethylolpropane tris(3-mercaptopropionate) (ETTMP) was reported for the first time within thiol–ene polyHIPEs. Due to the transparency of the emulsions, rapid curing via photopolymerization was feasible. The average pore diameters of the resulting polyHIPEs ranged between 1.2 and 3.6 μm, and porosity of up to 90% was achieved. The water uptake of the materials reached up to 1000% by weight. Drug loading and release were demonstrated, employing salicylic acid as a model drug. Porous profile and biodegradability add to the usefulness of the material for biomedical applications. |
format | Online Article Text |
id | pubmed-8619294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-86192942021-11-26 Thiol–Ene Cross-linking of Poly(ethylene glycol) within High Internal Phase Emulsions: Degradable Hydrophilic PolyHIPEs for Controlled Drug Release Hobiger, Viola Zahoranova, Anna Baudis, Stefan Liska, Robert Krajnc, Peter Macromolecules [Image: see text] Macroporous polymer monoliths prepared from high internal phase emulsions (HIPEs) can be found in various biomedical applications. While typically water-in-oil HIPEs are applied for polyHIPE preparation, they are not suitable for hydrophilic polyHIPE preparation. Herein, direct oil-in-water emulsions based on water-soluble poly(ethylene glycol)diacrylate or poly(ethylene glycol)dimethacrylate were developed. Furthermore, the incorporation of a hydrophilic water-miscible thiol, ethoxylated trimethylolpropane tris(3-mercaptopropionate) (ETTMP) was reported for the first time within thiol–ene polyHIPEs. Due to the transparency of the emulsions, rapid curing via photopolymerization was feasible. The average pore diameters of the resulting polyHIPEs ranged between 1.2 and 3.6 μm, and porosity of up to 90% was achieved. The water uptake of the materials reached up to 1000% by weight. Drug loading and release were demonstrated, employing salicylic acid as a model drug. Porous profile and biodegradability add to the usefulness of the material for biomedical applications. American Chemical Society 2021-11-08 2021-11-23 /pmc/articles/PMC8619294/ /pubmed/34840351 http://dx.doi.org/10.1021/acs.macromol.1c01240 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Hobiger, Viola Zahoranova, Anna Baudis, Stefan Liska, Robert Krajnc, Peter Thiol–Ene Cross-linking of Poly(ethylene glycol) within High Internal Phase Emulsions: Degradable Hydrophilic PolyHIPEs for Controlled Drug Release |
title | Thiol–Ene Cross-linking of Poly(ethylene glycol)
within High Internal Phase Emulsions: Degradable Hydrophilic PolyHIPEs
for Controlled Drug Release |
title_full | Thiol–Ene Cross-linking of Poly(ethylene glycol)
within High Internal Phase Emulsions: Degradable Hydrophilic PolyHIPEs
for Controlled Drug Release |
title_fullStr | Thiol–Ene Cross-linking of Poly(ethylene glycol)
within High Internal Phase Emulsions: Degradable Hydrophilic PolyHIPEs
for Controlled Drug Release |
title_full_unstemmed | Thiol–Ene Cross-linking of Poly(ethylene glycol)
within High Internal Phase Emulsions: Degradable Hydrophilic PolyHIPEs
for Controlled Drug Release |
title_short | Thiol–Ene Cross-linking of Poly(ethylene glycol)
within High Internal Phase Emulsions: Degradable Hydrophilic PolyHIPEs
for Controlled Drug Release |
title_sort | thiol–ene cross-linking of poly(ethylene glycol)
within high internal phase emulsions: degradable hydrophilic polyhipes
for controlled drug release |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8619294/ https://www.ncbi.nlm.nih.gov/pubmed/34840351 http://dx.doi.org/10.1021/acs.macromol.1c01240 |
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