Cargando…
Polymeric redox-responsive delivery systems bearing ammonium salts cross-linked via disulfides
A redox-responsive polycationic system was synthesized via copolymerization of N,N-diethylacrylamide (DEAAm) and 2-(dimethylamino)ethyl methacrylate (DMAEMA). N,N’-bis(4-chlorobutanoyl)cystamine was used as disulfide-containing cross-linker to form networks by the quaternization of tertiary amine gr...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778402/ https://www.ncbi.nlm.nih.gov/pubmed/24062825 http://dx.doi.org/10.3762/bjoc.9.189 |
_version_ | 1782285107970703360 |
---|---|
author | Dollendorf, Christian Hetzer, Martin Ritter, Helmut |
author_facet | Dollendorf, Christian Hetzer, Martin Ritter, Helmut |
author_sort | Dollendorf, Christian |
collection | PubMed |
description | A redox-responsive polycationic system was synthesized via copolymerization of N,N-diethylacrylamide (DEAAm) and 2-(dimethylamino)ethyl methacrylate (DMAEMA). N,N’-bis(4-chlorobutanoyl)cystamine was used as disulfide-containing cross-linker to form networks by the quaternization of tertiary amine groups. The insoluble cationic hydrogels become soluble by reduction of disulfide to mercaptanes by use of dithiothreitol (DTT), tris(2-carboxyethyl)phosphine (TCEP) or cysteamine, respectively. The soluble polymeric system can be cross-linked again by using oxygen or hydrogen peroxide under basic conditions. The redox-responsive polymer networks can be used for molecular inclusion and controlled release. As an example, phenolphthalein, methylene blue and reactive orange 16 were included into the network. After treatment with DTT a release of the dye could be recognized. Physical properties of the cross-linked materials, e.g., glass transition temperature (T(g)), swelling behavior and cloud points (T(c)) were investigated. Redox-responsive behavior was further analyzed by rheological measurements. |
format | Online Article Text |
id | pubmed-3778402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-37784022013-09-23 Polymeric redox-responsive delivery systems bearing ammonium salts cross-linked via disulfides Dollendorf, Christian Hetzer, Martin Ritter, Helmut Beilstein J Org Chem Full Research Paper A redox-responsive polycationic system was synthesized via copolymerization of N,N-diethylacrylamide (DEAAm) and 2-(dimethylamino)ethyl methacrylate (DMAEMA). N,N’-bis(4-chlorobutanoyl)cystamine was used as disulfide-containing cross-linker to form networks by the quaternization of tertiary amine groups. The insoluble cationic hydrogels become soluble by reduction of disulfide to mercaptanes by use of dithiothreitol (DTT), tris(2-carboxyethyl)phosphine (TCEP) or cysteamine, respectively. The soluble polymeric system can be cross-linked again by using oxygen or hydrogen peroxide under basic conditions. The redox-responsive polymer networks can be used for molecular inclusion and controlled release. As an example, phenolphthalein, methylene blue and reactive orange 16 were included into the network. After treatment with DTT a release of the dye could be recognized. Physical properties of the cross-linked materials, e.g., glass transition temperature (T(g)), swelling behavior and cloud points (T(c)) were investigated. Redox-responsive behavior was further analyzed by rheological measurements. Beilstein-Institut 2013-08-13 /pmc/articles/PMC3778402/ /pubmed/24062825 http://dx.doi.org/10.3762/bjoc.9.189 Text en Copyright © 2013, Dollendorf et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Dollendorf, Christian Hetzer, Martin Ritter, Helmut Polymeric redox-responsive delivery systems bearing ammonium salts cross-linked via disulfides |
title | Polymeric redox-responsive delivery systems bearing ammonium salts cross-linked via disulfides |
title_full | Polymeric redox-responsive delivery systems bearing ammonium salts cross-linked via disulfides |
title_fullStr | Polymeric redox-responsive delivery systems bearing ammonium salts cross-linked via disulfides |
title_full_unstemmed | Polymeric redox-responsive delivery systems bearing ammonium salts cross-linked via disulfides |
title_short | Polymeric redox-responsive delivery systems bearing ammonium salts cross-linked via disulfides |
title_sort | polymeric redox-responsive delivery systems bearing ammonium salts cross-linked via disulfides |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778402/ https://www.ncbi.nlm.nih.gov/pubmed/24062825 http://dx.doi.org/10.3762/bjoc.9.189 |
work_keys_str_mv | AT dollendorfchristian polymericredoxresponsivedeliverysystemsbearingammoniumsaltscrosslinkedviadisulfides AT hetzermartin polymericredoxresponsivedeliverysystemsbearingammoniumsaltscrosslinkedviadisulfides AT ritterhelmut polymericredoxresponsivedeliverysystemsbearingammoniumsaltscrosslinkedviadisulfides |