Stimulus-responsive hydrogels make up an important class of programmable materials for a wide range of biomedical applications. Ultrasound (US) is a stimulus that offers utility because of its ability to permeate tissue and rapidly induce chemical alterations in aqueous media. Here we report on the synthesis and US-mediated disintegration of stimulus-responsive telechelic Dopa-modified polyethylene glycol-based hydrogels. Fe-[PEG-Dopa] hydrogels are formed through Fe-induced cross-linking of four-arm polyethylene glycol-dopamine precursors to produce networks. The relative amounts of H-bonds, coordination bonds, and covalent bonds can be controlled by the [Fe]:[Dopa] molar ratio in precursor solutions. Networks formed from precursors with high [Fe]:[Dopa] ratios create mechanically robust networks (G' = 6880 ± 240 Pa) that are largely impervious to US-mediated disintegration at intensities of ≤43 W/cm. Conversely, lightly cross-linked networks formed through [Fe]:[Dopa] molar ratios of <0.73 are susceptible to rapid disintegration upon exposure to US. Pulsatile US exposure allows temporal control over hydrogel disintegration and programmable self-healing. Sustained US energy can also stabilize hydrogels through the formation of additional cross-links via free radical-mediated coupling of pendant catechols. Taken together, the diverse ranges of mechanical behavior, self-healing capability, and differential susceptibility to ultrasonic disintegration suggest that Fe-[PEG-Dopa] hydrogels yield a class of application-specific stimulus-responsive polymers as smart materials for applications ranging from transient medical implants to matrices for smart drug delivery.

Noble metal nanoparticles loaded smart polymer microgels have gained much attention due to fascinating combination of their properties in a single system. These hybrid systems have been extensively used in biomedicines, photonics, and catalysis. Hybrid microgels are characterized by using various techniques but UV/Vis spectroscopy is an easily available technique for characterization of noble metal nanoparticles loaded microgels. This technique is widely used for determination of size and shape of metal nanoparticles. The tuning of optical properties of noble metal nanoparticles under various stimuli can be studied using UV/Vis spectroscopic method. Time course UV/Vis spectroscopy can also be used to monitor the kinetics of swelling and deswelling of microgels and hybrid microgels. Growth of metal nanoparticles in polymeric network or growth of polymeric network around metal nanoparticle core can be studied by using UV/Vis spectroscopy. This technique can also be used for investigation of various applications of hybrid materials in catalysis, photonics, and sensing. This tutorial review describes the uses of UV/Vis spectroscopy in characterization and catalytic applications of responsive hybrid microgels with respect to recent research progress in this area.

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Applying full cell potential estimation in redox pairs of [PEG-Cat]4 + Mz+ to elucidate contributions of metal ion precursors on hydrogel properties.

Iron–copper bimetallic nanoparticles (Fe-Cu BNPs) were prepared via a green synthesis route. Ixora finlaysoniana has been used in this study as a capping and stabilizing agent in the modification of Fe-Cu BNPs. As-synthesized BNPs were characterized using different techniques including UV/Vis spectrophotometry, FTIR, XRD and SEM. A particle size analyzer and SEM studies indicated the particle size to be in the range of 50–200 nm. In addition, degradation of MB dye in an aqueous system and radical-scavenging potential in a DPPH assay were also examined using BNPs. Methylene blue dye degradation in 17 min was monitored with UV/Vis spectrophotometry, which exhibited the efficiency of Fe-Cu BNPs. Bimetallic nanoparticles were also found to be efficient in neutralizing DPPH free radicals. Furthermore, kinetic studies of both dye degradation and radical scavenging potential are reported in this article. Subsequently, Fe-Cu BNPs synthesized via a green and sustainable method can be employed for dye degradation and free radical-scavenging activities.