Thermoresponsive Gels

低临界溶液温度 上临界溶液温度 聚合物 材料科学 色谱中的热响应聚合物 木筏 胶束 药物输送 化学工程 自愈水凝胶 纳米技术 化学物理 聚合 高分子化学 化学 有机化学 水溶液 共聚物 工程类 复合材料 高效液相色谱法 反相色谱法
作者
M. Joan Taylor,Paul Tomlins,Tarsem Sahota
出处
期刊:Gels [Multidisciplinary Digital Publishing Institute]
卷期号:3 (1): 4-4 被引量:152
标识
DOI:10.3390/gels3010004
摘要

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.
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