Morphing in nature and beyond: a review of natural and synthetic shape-changing materials and mechanisms

Shape-changing materials open an entirely new solution space for a wide range of disciplines: from architecture that responds to the environment and medical devices that unpack inside the body, to passive sensors and novel robotic actuators. While synthetic shape-changing materials are still in their infancy, studies of biological morphing materials have revealed key paradigms and features which underlie efficient natural shape-change. Here, we review some of these insights and how they have been, or may be, translated to artificial solutions. We focus on soft matter due to its prevalence in nature, compatibility with users and potential for novel design. Initially, we review examples of natural shape-changing materials—skeletal muscle, tendons and plant tissues—and compare with synthetic examples with similar methods of operation. Stimuli to motion are outlined in general principle, with examples of their use and potential in manufactured systems. Anisotropy is identified as a crucial element in directing shape-change to fulfil designed tasks, and some manufacturing routes to its achievement are highlighted. We conclude with potential directions for future work, including the simultaneous development of materials and manufacturing techniques and the hierarchical combination of effects at multiple length scales.</p

Magnetically Controllable Polymer Nanotubes from a Cyclized Crosslinker for Site-Specific Delivery of Doxorubicin

Externally controlled site specific drug delivery could potentially provide a means of reducing drug related side effects whilst maintaining, or perhaps increasing therapeutic efficiency. The aim of this work was to develop a nanoscale drug carrier, which could be loaded with an anti-cancer drug and be directed by an external magnetic field. Using a single, commercially available monomer and a simple one-pot reaction process, a polymer was synthesized and crosslinked within the pores of an anodized aluminum oxide template. These polymer nanotubes (PNT) could be functionalized with iron oxide nanoparticles for magnetic manipulation, without affecting the large internal pore, or inherent low toxicity. Using an external magnetic field the nanotubes could be regionally concentrated, leaving areas devoid of nanotubes. Lastly, doxorubicin could be loaded to the PNTs, causing increased toxicity towards neuroblastoma cells, rendering a platform technology now ready for adaptation with different nanoparticles, degradable pre-polymers, and various therapeutics

Effects of Au nanoparticles on thermoresponsive genipin-crosslinked gelatin hydrogels

Gold gelatin hydrogel nanocomposites crosslinked with genipin have been prepared, and the effect of citrate capped Au nanoparticles (NPs) as nanofillers in the crosslinking and swelling of gelatin and release of a model drug (methylene blue) from gelatin nanocomposites have been investigated. The citrate-capped Au NPs prevented the crosslinking reaction between the gelatin and genipin and resulted in less crosslinked hydrogels. Although less crosslinked, the Au gelatin nanocomposites swelled less than the unfilled crosslinked gelatin. The gelatin composites were optically active and thermo-sensitive in a temperature range acceptable for living cells. In vitro release studies demonstrated that the irradiation of the composite gels with monochromatic green light (10532 nm, 100 mW) increases the release of the encapsulated methylene blue, most likely due to the photothermal effect of Au nanoparticles. This opens the possibility to explore the application of these nanocomposites as carriers in remotely controlled light-triggered drug release