Composite Polymer Hydrogels with high and Reversible Elongation under Magnetic Stimuli

The field of soft actuators is dominated by elastomers that experience mechanical deformations in response to external stimuli. In this context, magnetic stimuli attract considerable interest because of their easy application, tunability, fast response, remote actuation, and safe penetration in biological environments. Since very recently, research interests in the field are being redirected towards hydrogels, which could virtually replace elastomers, overcoming their limitations and expanding the field of application of soft actuators. The mechanical actuation of hydrogels is a nascent field full of challenges, such as achieving reliable and significant responsiveness. Here we demonstrate that the combination of a physical polymer hydrogel with a dispersed phase consisting of clusters of magnetic particles, results in magnetic hydrogel composites that exhibit high and reversible elongation in response to magnetic stimuli. Our analyses show that this response is strongly dependent on the matrix elasticity, the concentration of magnetic particles, and the particle distribution within the network of polymer nanofibres. Our strategy for the maximization of the response of magnetic hydrogels should be a catalyst for the development of novel applications of composite hydrogels, such as a valve remotely actuated by a magnetic field that we also present here as a proof-of-concept. © 2021 The Author(s).Dr. Mariusz Barczak is acknowledged for help with SEM imaging of iron particles. Ms. Laura Quesada de la Torre is acknowledged for help with design of graphical abstract. This study was supported by project FIS2017-85954-R (Ministerio de Economía, Industria y Competitividad, MINECO, and Agencia Estatal de Investigación, AEI, Spain, cofunded by Fondo Europeo de Desarrollo Regional, FEDER, European Union ). CGV acknowledges financial support by Ministerio de Ciencia, Innovación y Universidades and University of Granada, Spain, for her FPU17/00491 grant. AZ thanks the Russian Science Foundation, project 20-12-00031, for the financial support. LRA thanks the Spanish State Research Agency (Spanish Ministry of Science and Innovation ) through Juan de la Cierva Incorporacion Fellowship ( IJC2018-037951-I ). Funding for open access charge: Universidad de Granada / CBUA

In situ real-time monitoring of the mechanism of self-assembly of short peptide supramolecular polymers

Making use of the combination of multiparametric Fluorescence Lifetime Imaging Microscopy (FLIM) and single-molecule Fluorescence Lifetime Correlation Spectroscopy (FLCS), we have been able to study for the early stages of the fluorenylmethyloxycarbonyl-diphenylalanine (Fmoc-FF) self-assembly process with single-molecule resolution, the kinetics of fiber formation, the packaging of the peptides within the fibers and the capacity of the peptides to reassemble after disruption (self-healing) in the presence of different metallic cations. Other techniques such as FTIR, TEM, DSC and DFT calculations support our findings. The impact that the mechanism of self-assembly has on the physical (rigidity and self-healing) properties of the resulting gels have also been evaluated by rheology. Calcium ions are able to promote the self-assembly of Fmoc-FF faster and more efficiently, forming more rigid hydrogels than do cesium ions. The reasons behind this effect may be explained by the different capacities that these two cations have to coordinate with the peptide, modulate its hydrophobicity and stabilize the water-solute interphase. These findings shed light on the impact that small changes have on the process of self-assembly and can help to understand the influence of the environmental conditions on the in vivo uncontrolled self-assembly of certain proteins