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Random copolymer hydrogels of methacrylic acid (MAA) and JV-isopropylacrylamide (NIPAAm) were synthesized by free-radical polymerization in the presence of a cross-linking agent. The gels were characterized for their temperature-and pH-responsive behavior by equilibrium swelling experiments, differential scanning calorimetry, and thermal mechanical analysis. Depending upon composition, the gels showed sharp swelling transitions with small changes in temperature or pH, with initial time-dependent response reaching equilibrium on a time scale of hours.

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This paper reviews the design and development of magnetothermally-triggered drug delivery systems, whereby magnetic nanoparticles are combined with thermally-activated materials. By combining superparamagnetic nanoparticles with lower critical solution temperature (LCST) polymers, an alternating current (AC) magnetic field can be used to trigger localized heating in vivo, which in turn causes a phase change in the host polymer to allow diffusion and release of drugs. The use of magnetic nanoparticles for biomedical applications is reviewed, as well as the design of thermally-activated polymeric systems. Current research on externally-triggered delivery is highlighted, with a focus on the design and challenges in developing magnetothermally-activated systems.

The room temperature ionic liquid, 1-butyl-3-methylimidazolium hexafluorophosphate, [C4mim][PF6] was found to be an efficient plasticizer for poly(methyl methacrylate), prepared by in situ radical polymerization in the ionic liquid medium; the polymers have physical characteristics comparable with those containing traditional plasticizers and retain greater thermal stability.

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