Core-shell modified nanofiber mats were used as ion-selective membranes for the first time. Keeping the overall macroscopic size of the sensing element the same as for classical plasticized poly(vinyl chloride) membranes, herein the proposed nanofiber based systems resulted in ultrathin ( less then 10 nm) recognition layers with the total area nearly 3 orders of magnitude larger and the surface to volume ratio close to 7.5 × 107. Thus, for the first time close to 2D potentiometric receptors were obtained. Formation of thin and continuous liquid recognition layers on nanofibers was confirmed by XPS studies. The nanofiber based ion-selective mats used in the classical internal-solution arrangement were characterized with analytical parameters – the slope and detection limit well comparable to those for classical plasticized poly(vinyl chloride) based membranes. Despite the novel arrangement of the ion-selective layer and its nanometric thickness, the reproducibility of the recorded potentials, studied for more than 30 days, was high. Using confocal microscopy it was shown that electrolyte transport through porous nanofibers’ mat phase is the rate limiting step in conditioning of the receptor layer. The estimated electrolyte diffusion coefficients for the nanofiber phase are close to 10-10 cm2 s-1, and thus are orders of magnitude lower compared to values characterizing ion transport through classical poly(vinyl chloride) based membranes. The truly nanostructural character of nanofiber ion-selective mats is visible in chronoamperometric experiments. It was shown that a core-shell nanofiber mat behaves as an array of nanoelectrodes – individual nanofibers. Thus, the novel nanofiber based architecture of ion-selective mats brings also a new quality to the current based electrochemistry of ion-selective sensors.Dielectrophoresis (DEP) is a powerful technique for label-free cell separation in microfluidics. Easily-fabricated DEP separators with low cost and short turnaround time are in extremely high demand in practical applications, especially clinical usage where disposable devices are needed. DEP separators exploiting microelectrodes made of conducting polydimethylsiloxane (PDMS) composites enable the construction of advantageous 3D volumetric electrodes with a simple soft-lithography process. Yet, existing devices incorporating microelectrodes in conducting PDMS generally have their fluidic sidewalls constructed using a different material, and consequently require extra lithography of a sacrificial layer on the semi-finished master for molding the electrode and fluidic sidewalls in separate steps. Here we demonstrate a novel microfluidic DEP separator with a 3D electrode and fluidic structure entirely integrated within silver-PDMS composites. We develop a further simplified one-step molding process with lower cost using a readily-available and reusable SU8 master, eliminating the need for the additional lithography step in existing techniques. The uniquely designed two-layer electrode exhibits a spatially non-uniform electric field that enables cell migration in the vertical direction. The electrode upper layer then offers a harbor-like region for the trapping of the target cells that have drifted upwards, which shelters them from being dragged away by the main flow streams in the lower layer, and thus allows higher operation flow rate. We also optimize the upper layer thickness as a critical dimension for protecting the trapped cells from high drag and show easy widening of our device by elongation of the digits. We demonstrate that the elongated digits involving more parallel flow paths maintain a high capture efficiency of 95.4% for live cells with 85.6% purity in the separation of live/dead HeLa cells. We also investigate the device feasibility in a viability assay for cells post anti-cancer drug treatment.Though carbon matrices could effectively improve the electrical conductivity and accommodate the volume expansion of CuO-based anode materials for lithium ion batteries (LIBs), achieving an optimized utilization ratio of the active CuO component remains a big challenge. In this work, we developed a metal-organic framework (MOF)-derived strategy to synthesize ultrafine CuO nanoparticles embedded in a porous carbon matrix (CuO@C). Benefiting from its unique structure, the resulting CuO@C exhibits a high reversible capacity of 1024 mA h g-1 at 100 mA g-1 after 100 cycles and a long-term cycling stability with a reversible capacity of 613 mA h g-1 at 500 mA g-1 over 700 cycles. The outstanding Li-storage performances can be attributed to its porous carbon matrix and ultrafine CuO nanoparticles with more exposed active sites for electrochemical reactions.3D-Bioprinting has seen a rapid expansion in the last few years, with an increasing number of reported bioinks. Nab-Paclitaxel solubility dmso Alginate is a natural biopolymer that forms hydrogels by ionic cross-linking with calcium ions. Due to its biocompatibility and ease of gelation, it is an ideal ingredient for bioinks. This review focuses on recent advances on bioink formulations based on the combination of alginate with other polysaccharides. In particular, the molecular weight of the alginate and its loading level have an impact on the material’s performance, as well as the loading of the divalent metal salt and its solubility, which affects the cross-linking of the gel. Alginate is often combined with other polysaccharides that can sigificantly modify the properties of the gel, and can optimise alginate for use in different biological applications. It is also possible to combine alginate with sacrificial polymers, which can temporarily reinforce the 3D printed construct, but then be removed at a later stage. Other additives can be formulated into the gels to enhance performance, including nanomaterials that tune rheological properties, peptides to encourage cell adhesion, or growth factors to direct stem cell differentiation. The ease of formulating multiple components into alginate gels gives them considerable potential for further development. In summary, this review will facilitate the identification of different alginate-polysaccharide bioink formulations and their optimal applications, and help inform the design of second generation bioinks, allowing this relatively simple gel system to achieve more sophisticated control over biological processes.