The next stage of development for optically active surgical adjuncts must address practical constraints whilst minimizing risks of adverse effects. Exploiting the technology's full potential also requires improvements in the usefulness of imagery equipment.

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Point-of-care medical devices offer the potential for rapid biomarker detection and reporting of medical conditions, thereby bypassing the requirements for offline clinical laboratory facilities in many cases. Label-free electrochemical techniques are suitable for use in handheld diagnostic devices due the inherent electronic detection modality and low requirement for processing reagents. While electrochemical impedance sensing is widely used in tissue analysis such as body composition measurement, its use in point-of-care patient testing is yet to be widely adopted. Here we have considered a number of issues currently limiting the translation of electrochemical impedance sensing into clinical biosensor devices. Specifically, we have addressed the current requirement for these sensors to be connected to an external processor by applying a minimum number of frequencies required for optimized biomarker detection, and subsequently delivering analytics within the measurement device. The POISED-5 device was evaluated using a sensor for the ovarian cancer biomarker cancer antigen 125 (CA125), demonstrating performance comparable to standard laboratory equipment, with direct interpretation of response signal amplitude substituting traditional impedance component calculation and model fitting.

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Before the viability of a cell formulation can be assessed for implementation in commercial sodium ion batteries, processes applied in cell production should be validated and optimized. This review summarizes the steps performed in constructing sodium ion (Na‐ion) cells at research scale, highlighting parameters and techniques that are likely to impact measured cycling performance. Consistent process‐structure‐performance links have been established for typical lithium‐ion (Li‐ion) cells, which can guide hypotheses to test in Na‐ion cells. Liquid electrolyte viscosity, sequence of mixing electrode slurries, rate of drying electrodes and cycling characteristics of formation were found critical to the reported capacity of laboratory cells. Based on the observed importance of processing to battery performance outcomes, the current focus on novel materials in Na‐ion research should be balanced with deeper investigation into mechanistic changes of cell components during and after production, to better inform future designs of these promising batteries.

This work aimed to answer fundamental questions about the optimal processing and formulation of hard carbon electrodes typical of those anticipated in commercial sodium-ion cells. Procedurally simple tests were proposed to compare the effects of slurry mixing energy and conductive additives on the morphology of and conductive networks in electrodes made with hard carbons from two different manufacturers. Long-range and short-range electronic conductivity was quantified with high repeatability for samples of each hard carbon electrode produced on different days. The most significant changes induced by mixing energy were observed in the electrodes produced without conductive additives, which was found to relate to post-processing particle size. Hard carbon from one source was pulverized by high energy mixing, replacing the electronic effect of conductive additives while increasing pore tortuosity and impedance. These findings recommend evaluating the dry electrode through-resistance as a complement to quantifying pre-cycling impedance to validate mixing protocol and the application of conductive additives in hard carbon electrodes. These procedures can also serve as reliable low-cost methods for quality control at early stages of sodium-ion anode manufacturing.