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Here, we describe a new photoelectrochemical imaging method termed light-addressable square wave voltammetry (LASWV). It measures local SWV currents at an unstructured electrolyte/insulator/semiconductor (EIS) field-effect substrate by illuminating and addressing the substrate with an intensity-constant laser. Due to the continuous generation of charge carriers in the light-irradiated semiconductor, the drift and diffusion of photoinjected carriers within the semiconductor bulk would slow down the equilibrium processes of charge and discharge in one potential pulse cycle. Therefore, even though SWV is sampled at the end of the direct and reverse pulses to reject capacitive currents, in our approach, photoinduced capacitive current can still be detected as an effective sensory signal. The obtained current-potential (I-V) curve shows a typical shape corresponding to the accumulation, depletion, and inversion regions of field-effect devices. We demonstrated that LASWV can be used as a field-effect chemical sensor to measure the solution pH and monitor enzymatic reactions. More importantly, since the charge carriers are only generated in the illuminated area, the laser spot in the device can be used as a virtual probe to record local electrochemical properties such as impedance with microresolution.

The robust cell-in-shell structure is highly desirable for endowing living cells with an artificial exoskeleton to defend them from many environmental factors such as osmotic pressure, shear force, heat, UV radiation, and enzymes. Cell encapsulation has shown potential applications in many fields and attracted increasing interest. However, the influences of the precursors on the cell viability during the shell formation process are not clear and seldom investigated. Here, zinc nitrite, zinc acetate and zinc sulfate were applied individually to synthesize zeolitic imidazolate framework-8 (ZIF-8) shells on living cells. All the zinc salt precursors could convert to a ZIF-8 layer on the living cell surface. The zinc salts and organic ligand did not exhibit obvious toxicity to yeast cells when applied individually. However, dead cells were observed during the living cell encapsulation process using different zinc precursors. Compared with zinc nitrate and zinc acetate, ZIF-8 formed by zinc sulfate led to a higher percentage of cell death, especially under high concentrations of zinc sulfate. Cell division was suppressed by the ZIF-8 shell but restored fully upon shell removal by EDTA solution or pH 4.0 buffer. Escherichia coli (E. coli) cells showed a lower percentage of cell death, indicating excellent tolerance to the ZIF-8 encapsulation process. This work illustrates the cell toxicity during the formation of ZIF-8 cell shells by different zinc salts and engineering of the cell growth by MOF coating, which could provide a foundation for further quantitative analysis and potential applications in biomedicine and bioengineering.

Cellulose nanocrystal (CNC) composite filter papers were fabricated by a facile method, which consists of the bleaching and hydrolysis of fibers, and drop coating of filter papers with CNC solution. The filter properties of the composite filter papers were applied for the removal of bacteria from aqueous solutions. Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) were used to evaluate the bacteria removal performance of the CNC composite filter papers. It is indicated that the nanopores formed by nanoscale rod-like crystals contribute to the bacteria removal capacity of porous CNC nanocomposite filter papers. Overlapped five layers of the CNC composite filter papers displayed a rapid (0.12 L/min) and highly efficient removal (remove rate at ~ 100%) of bacteria from aqueous solutions. Due to their advantages of convenient preparation, sustainable materials and low cost, the CNC composite filter papers have promising prospects and potential applications in many fields concerning bacteria removal and water purification.

How to obtain sufficient functional olfactory receptors and coupled to transducers with high efficiency are crucial to biomimetic olfactory-based biosensors. In this study, a cell-free expression system was employed to prepare functional olfactory receptors that were utilized as sensitive elements for biomimetic olfactory receptor-based biosensors. A nematode olfactory receptor, ODR-10, was used as a model of olfactory receptors and expressed in Escherichia coli (E. coli) cell-free expression system. To improve the coupling efficiency and obtain the on-chip purification, a His6-tag was expressed as a fusion to ODR-10, which makes the expressed ODR-10 capable of selectively binding to the sensor surface modified with anti-His6-tag aptamers. Electrolyte-insulator-semiconductor (EIS) sensors were utilized as the transducer to measure the capacitance changes induced by the ODR-10 responding to its natural ligand, diacetyl. The results show that ODR-10 was successfully expressed using E. coli cell-free expression system and the expression could be promoted by adding 0.5% Brij58 as the detergent. Capacitance measurement results indicate that this olfactory receptor-based biosensor can detect diacetyl with high specificity and sensitivity. Concentration-dependent linear response to diacetyl ranging from 0.01 nM to 1 nM was obtained. The detection limit was as low as 0.01 nM. All the results demonstrated that the cell-free expression system provides a new approach for the preparation of functional olfactory receptors, which have great potential to be applied in biomimetic sensors towards chemical sensing.

The decomposition of hydrogen peroxide was determined in the neutral solution of ZIF-67 crystals. The fast decomposition of H2O2 can be observed by naked eyes in seconds after mixing the reactants. A crumpled surface was observed for ZIF-67 crystals after the decomposition reaction. The decomposition reaction was found to follow the first-order kinetics. Temperature-dependent studies calculated that the activation energy was 37 kJ mol−1. Based on the obtained results, a possible mechanism was proposed.

The tumor immune microenvironment (TIME) is comprised of a complex milieu that contributes to stunting antitumor immune responses by restricting T cells to accumulate in the vicinity of the tumor. Nanomedicine-based strategies are being proposed as a salvage effort to reinvigorate antitumor immunity. Various strategies, however, often fail to unleash the antitumor immune response because of the paucity of appropriate therapeutic targets in the complex TIME, invigorating a fervor of investigation into mechanisms underlying the TIME to resist nanomedicines. In this review article, effective nano/biomaterial-based delivery and TIME normalization approaches that promote T cell-mediated antitumor immune response will be discussed, with a focus on emerging preclinical and clinical strategies for immune normalization. Based on currently available evidence, it seems as if the ultimate success of cancer immunotherapy and nanomedicine hinges on the capacity to normalize the TIME. Here, how nanomedicines target immunosuppressive cells and signaling pathways to broaden the impact of cancer immunotherapy are explored. Acquisition of the urgently needed knowledge of nanomedicine-mediated immune normalization will guide researchers and scientists towards clinical applications of cancer immunotherapy.

A new photoelectrochemical imaging method termed scanning electrochemical photometric sensor (SEPS) is proposed in this work. It was derived from light-addressable potentiometric sensor (LAPS) and scanning photoinduced impedance microscopy (SPIM) using a front-side laser illumination at a field-effect structure. When the laser beam scans across the sensor substrate, local photocurrent changes at inversion due to the light absorption of analytes can be recorded. It will be shown that SEPS could be used for label-free living cell imaging with micro-resolution as well as real-time quantitative absorption analysis, which would broaden the applications of traditional LAPS/SPIM from potentiometric/impedance measurements to local optical analysis.

A miniaturized platform combining integrated microelectrode (IME) and functional nucleic acids was developed for homogeneous label-free electrochemical biosensing. IME was constructed with a carbon fiber microelectrode and a platinum wire in a θ type glass tube as a two-electrode system for electrochemical monitoring at microliter level. A newly reported G-triplex/methylene blue (G3/MB) complex was used as the signal generator in the homogeneous label-free electrochemical biosensor. G3 has strong affinity with MB and it can cause significant decrease of the diffusion current of MB after binding. Melamine was chosen as the model target. Since melamine can interact with nucleobase thymine (T) to form T-melamine-T structure through complementary hydrogen bonds, a single-strand functional DNA hairpin structure with poly T and G3 elaborately blocked via base pairing was designed. The presence of melamine can trigger the conformation switching of the DNA hairpin to release the G3. The released G3 combined with MB could therefore change the diffusion current, leading to a simple and rapid detection of melamine. The combination of functional DNA hairpin as target recognition element, G3/MB as signal generator, and IME as transducer provided a "Mix and Measure" miniaturized platform for the construction of homogeneous label-free electrochemical biosensors.

UV irradiation is a threat to the living cells which could damage the DNA and lead to the death of cells. In this study, delaminated Ti3C2Tx flake was applied as a novel UV-protective material for living cells. Compared with naked yeasts, the cell viability of coated yeasts could be obviously increased after exposing to the UV light. Besides yeasts, this material could be applied in the protection of mammalian cell under UV irradiation. Thus, the delaminated MXene flake has potential applications in cells storage, cell transportation, and UV-resistant fields.

Following the publication of the original article [1], it was reported that the accession number given in the ‘Data accessibility’ declaration, GSE65696, is incorrect.