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Thermoresponsive Gels
Thermoresponsive gelling materials constructed from natural and synthetic polymers can be used to provide triggered action and therefore customised products such as drug delivery and regenerative medicine types as well as for other industries. Some materials give Arrhenius-type viscosity changes bas...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318636/ https://www.ncbi.nlm.nih.gov/pubmed/30920501 http://dx.doi.org/10.3390/gels3010004 |
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author | Taylor, M. Joan Tomlins, Paul Sahota, Tarsem S. |
author_facet | Taylor, M. Joan Tomlins, Paul Sahota, Tarsem S. |
author_sort | Taylor, M. Joan |
collection | PubMed |
description | Thermoresponsive gelling materials constructed from natural and synthetic polymers can be used to provide triggered action and therefore customised products such as drug delivery and regenerative medicine types as well as for other industries. Some materials give Arrhenius-type viscosity changes based on coil to globule transitions. Others produce more counterintuitive responses to temperature change because of agglomeration induced by enthalpic or entropic drivers. Extensive covalent crosslinking superimposes complexity of response and the upper and lower critical solution temperatures can translate to critical volume temperatures for these swellable but insoluble gels. Their structure and volume response confer advantages for actuation though they lack robustness. Dynamic covalent bonding has created an intermediate category where shape moulding and self-healing variants are useful for several platforms. Developing synthesis methodology—for example, Reversible Addition Fragmentation chain Transfer (RAFT) and Atomic Transfer Radical Polymerisation (ATRP)—provides an almost infinite range of materials that can be used for many of these gelling systems. For those that self-assemble into micelle systems that can gel, the upper and lower critical solution temperatures (UCST and LCST) are analogous to those for simpler dispersible polymers. However, the tuned hydrophobic-hydrophilic balance plus the introduction of additional pH-sensitivity and, for instance, thermochromic response, open the potential for coupled mechanisms to create complex drug targeting effects at the cellular level. |
format | Online Article Text |
id | pubmed-6318636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63186362019-01-17 Thermoresponsive Gels Taylor, M. Joan Tomlins, Paul Sahota, Tarsem S. Gels Review Thermoresponsive gelling materials constructed from natural and synthetic polymers can be used to provide triggered action and therefore customised products such as drug delivery and regenerative medicine types as well as for other industries. Some materials give Arrhenius-type viscosity changes based on coil to globule transitions. Others produce more counterintuitive responses to temperature change because of agglomeration induced by enthalpic or entropic drivers. Extensive covalent crosslinking superimposes complexity of response and the upper and lower critical solution temperatures can translate to critical volume temperatures for these swellable but insoluble gels. Their structure and volume response confer advantages for actuation though they lack robustness. Dynamic covalent bonding has created an intermediate category where shape moulding and self-healing variants are useful for several platforms. Developing synthesis methodology—for example, Reversible Addition Fragmentation chain Transfer (RAFT) and Atomic Transfer Radical Polymerisation (ATRP)—provides an almost infinite range of materials that can be used for many of these gelling systems. For those that self-assemble into micelle systems that can gel, the upper and lower critical solution temperatures (UCST and LCST) are analogous to those for simpler dispersible polymers. However, the tuned hydrophobic-hydrophilic balance plus the introduction of additional pH-sensitivity and, for instance, thermochromic response, open the potential for coupled mechanisms to create complex drug targeting effects at the cellular level. MDPI 2017-01-10 /pmc/articles/PMC6318636/ /pubmed/30920501 http://dx.doi.org/10.3390/gels3010004 Text en © 2017 by the authors. 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 Taylor, M. Joan Tomlins, Paul Sahota, Tarsem S. Thermoresponsive Gels |
title | Thermoresponsive Gels |
title_full | Thermoresponsive Gels |
title_fullStr | Thermoresponsive Gels |
title_full_unstemmed | Thermoresponsive Gels |
title_short | Thermoresponsive Gels |
title_sort | thermoresponsive gels |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318636/ https://www.ncbi.nlm.nih.gov/pubmed/30920501 http://dx.doi.org/10.3390/gels3010004 |
work_keys_str_mv | AT taylormjoan thermoresponsivegels AT tomlinspaul thermoresponsivegels AT sahotatarsems thermoresponsivegels |