Drozdov A D, Christiansen J deClaville
Department of Materials and Production, Aalborg University Fibigerstraede 16 Aalborg 9220 Denmark
RSC Adv. 2020 Nov 24;10(70):42718-42732. doi: 10.1039/d0ra08619c. eCollection 2020 Nov 23.
Thermo-responsive (TR) hydrogels with a lower critical solution temperature swell strongly at temperatures below their volume phase transition temperature and collapse above . Biomedical application of these materials requires tuning the critical temperature in a rather wide interval. A facile method for modulation of is to polymerize the basic monomers with hydrophilic or hydrophobic comonomers. Although the effectiveness of this method has been confirmed by experimental data, molar fractions of comonomers necessary for fine tuning of in macroscopic gels and microgels are unknown. A simple model is developed for the equilibrium swelling of TR copolymer gels. Its adjustable parameters are found by fitting swelling diagrams on several macro- and microgels with -isopropylacrylamide as a basic monomer. Good agreement is demonstrated between the experimental swelling curves and results of numerical analysis. An explicit expression is derived for the volume phase transition temperature as a function of molar fraction of comonomers. The ability of this relation to predict the critical temperature is confirmed by comparison with observations.
具有较低临界溶液温度的热响应(TR)水凝胶在低于其体积相变温度时会强烈溶胀,而在高于该温度时会塌陷。这些材料的生物医学应用需要在相当宽的温度区间内调节临界温度。一种调节临界温度的简便方法是将基本单体与亲水性或疏水性共聚单体聚合。尽管该方法的有效性已得到实验数据的证实,但在宏观凝胶和微凝胶中精确调节临界温度所需的共聚单体摩尔分数尚不清楚。本文建立了一个用于TR共聚物凝胶平衡溶胀的简单模型。通过拟合以N-异丙基丙烯酰胺为基本单体的几种宏观和微观凝胶的溶胀图,确定了其可调参数。实验溶胀曲线与数值分析结果之间显示出良好的一致性。推导了体积相变温度作为共聚单体摩尔分数函数的显式表达式。通过与实验观察结果比较,证实了该关系式预测临界温度的能力。