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Liquid crystalline hydrogels are an attractive class of soft materials to direct charge transport, mechanical actuation, and cell migration. When such systems contain supramolecular polymers, it is possible in principle to easily shear align nanoscale structures and create bulk anisotropic properties. However, reproducibly fabricating and patterning aligned supramolecular domains in 3D hydrogels remains a challenge using conventional fabrication techniques. Here, a method is reported for 3D printing of ionically crosslinked liquid crystalline hydrogels from aqueous supramolecular polymer inks. Using a combination of experimental techniques and molecular dynamics simulations, it is found that pH and salt concentration govern intermolecular interactions among the self-assembled structures where lower charge densities on the supramolecular polymers and higher charge screening from the electrolyte result in higher viscosity inks. Enhanced hierarchical interactions among assemblies in high viscosity inks increase the printability and ultimately lead to greater nanoscale alignment in extruded macroscopic filaments when using small nozzle diameters and fast print speeds. The use of this approach is demonstrated to create materials with anisotropic ionic and electronic charge transport as well as scaffolds that trigger the macroscopic alignment of cells due to the synergy of supramolecular self-assembly and additive manufacturing.Colloidal assembly at fluid interfaces has a great potential for the bottom-up fabrication of novel structured materials. However, challenges remain in realizing controllable and tunable assembly of particles into diverse structures. Herein, the capillary assembly of magnetic ellipsoidal Janus particles at a fluid-fluid interface is reported. Depending on their tilt angle, that is, the angle the particle main axis forms with the fluid interface, these particles deform the interface and generate capillary dipoles or hexapoles. Driven by capillary interactions, multiple particles thus assemble into chain-, hexagonal-lattice-, and ring-like structures, which can be actively controlled by applying an external magnetic field. selleck compound A field-strength phase diagram is predicted in which various structures are present as stable states. Owing to the diversity, controllability, and tunability of assembled structures, magnetic ellipsoidal Janus particles at fluid interfaces could therefore serve as versatile building blocks for novel materials.With increasing demand for grid-scale energy storage, potassium-ion batteries (PIBs) have emerged as promising complements or alternatives to commercial lithium-ion batteries owing to the low cost, natural abundance of potassium resources, the low standard reduction potential of potassium, and fascinating K+ transport kinetics in the electrolyte. However, the low energy density and unstable cycle life of cathode materials hamper their practical application. Therefore, cathode materials with high capacities, high redox potentials, and good structural stability are required with the advancement toward next-generation PIBs. To this end, understanding the structure-dependent intercalation electrochemistry and recognizing the existing issues relating to cathode materials are indispensable prerequisites. This review summarizes the recent advances of PIB cathode materials, including metal hexacyanometalates, layered metal oxides, polyanionic frameworks, and organic compounds, with an emphasis on the structural advantages of the K+ intercalation reaction. Moreover, major current challenges with corresponding strategies for each category of cathode materials are highlighted. Finally, future research directions and perspectives are presented to accelerate the development of PIBs and facilitate commercial applications. It is believed that this review will provide practical guidance for researchers engaged in developing next-generation advanced PIB cathode materials.In this study, we report first time in India on the morphology, ultra-architectural pattern of the chorion in the egg and egg hair (setae). Further, physico-chemical characterizations of egg hairs (setae) were studied in the new invasive pest, fall armyworm, Spodoptera frugiperda. The egg is dome shaped with flattened base and curves upward to a broadly rounded point at the apex. HR-SEM micrographs revealed the surface ultrastructure of eggs chorion and shows structural elements of a marked rosette of petals surround the micropyle followed by micropylar rosette region around the micropyle plate. There was a small single micropylar opening along with 9 micropylar rosette cells and 13 micropylar rosette zones present near to the micropylar pit. In the egg the first order ribs were absent, but around 58-60 numbers of second order ribs were present. All the ventral and lateral cells of the eggs are connected by 19-22 cross striae and not forming a grid pattern, but joints with the longitudinal ribs at several of angles and totally 1,277-1,495 convex cells present at the egg's surface. The physico-chemical characteristics of egg hairs were studied using Fourier transform infrared (FT-IR) and thermogravimetric analysis (TGA) analysis. TGA results show that three weight losses occurred at 142, 418, and 880°C, respectively. FT-IR confirms the presence of amides, sulfoxide, and nitro compounds in egg hairs (setae).Osteosarcoma (OS) is a malignant bone neoplasm, mostly occurring in pediatric patients. OS is characterized by a highly aggressive and metastatically active tumor. Chemotherapy followed by surgical excision is the treatment of choice but is often associated with both chemoresistance and relapse. Hence, it is important to develop further understanding of OS pathogenesis and identify potential therapeutic targets. Both the signal transducer and activator of transcription 3 (STAT3) and mammalian target of rapamycin (mTOR) have been implicated in OS pathogenesis. Crosstalk between mTOR and STAT3 signaling has been shown to regulate hypoxia-induced angiogenesis in other diseases. In this study, we determined using OS cell lines if there is a crosstalk between these two pathways and how that impacts sensitivity to treatment with Rapamycin. OS cell lines exhibited differential sensitivity to mTOR inhibitor Rapamycin. Evaluation of phosphorylated STAT3 showed that in Rapamycin-sensitive 143B cells, the inhibitor decreased phosphorylation of STAT3 at Y705, but not at S727 whereas, in Rapamycin-resistant U2OS cells, the inhibitor decreased S727 phosphorylation but not Y705.