Turning Polysaccharides into Injectable and Rapid Self-Healing Antibacterial Hydrogels for Antibacterial Treatment and Bacterial-Infected Wound Healing.

Great efforts have been devoted to the development of novel and multifunctional wound dressing materials to meet the different needs of wound healing. Herein, we covalently grafted quaternary ammonium groups (QAGs) containing 12-carbon straight-chain alkanes to the dextran polymer skeleton. We then oxidized the resulting product into oxidized quaternized dextran (OQD). The obtained OQD polymer is rich in antibacterial QAGs and aldehyde groups. It can react with glycol chitosan (GC) via the Schiff-base reaction to form a multifunctional GC@OQD hydrogel with good self-healing behavior, hemostasis, injectability, inherent superior antibacterial activity, biocompatibility, and excellent promotion of healing of methicillin-resistant Staphylococcus aureus (MRSA)-infected wounds. The biosafe and nontoxic GC@OQD hydrogel with a three-dimensional porous network structure possesses an excellent swelling rate and water retention capacity. It can be used for hemostasis and treating irregular wounds. The designed GC@OQD hydrogel with inherent antibacterial activity possesses good antibacterial efficacy on both S. aureus (Gram-positive bacteria) and Escherichia coli (Gram-negative bacteria), as well as MRSA bacteria, with antibacterial activity greater than 99%. It can be used for the treatment of wounds infected by MRSA and significantly promotes the healing of wounds. Thus, the multifunctional antibacterial GC@OQD hydrogel has the potential to be applied in clinical practice as a wound dressing.

Antioxidant and antibacterial hydrogel formed by protocatechualdehyde-ferric iron complex and aminopolysaccharide for infected wound healing.

To better treat bacteria-infected wounds and promote healing, new wound dressings must be developed. In this study, we obtained PA@Fe by chelating iron trivalent ions (Fe3+) with protocatechualdehyde (PA), which has a catechol structure. Subsequently, we reacted it with ethylene glycol chitosan (GC) via a Schiff base reaction and loaded vancomycin to obtain an antibacterial Gel@Van hydrogel with a photothermal response. The as-prepared Gel@Van hydrogel exhibited good injectability, self-healing, hemostasis, photothermal stability, biocompatibility, and antioxidant and antibacterial properties. Moreover, Gel@Van hydrogel achieved highly synergistic antibacterial efficacy through photothermal and antibiotic sterilization. In a mouse skin-damaged infection model, Gel@Van hydrogel had a strong ability to promote the healing of methicillin-resistant Staphylococcus aureus (MRSA)-infected wounds, indicating the great potential application value of Gel@Van hydrogel in the field of treating and promoting the healing of infected wounds.

Contaminated soil remediation with nano-FeS loaded lignin hydrogel: A novel strategy to produce safe rice grains while reducing cadmium in paddy field.

Cadmium (Cd) contamination in agricultural soil has been an elevated concern due to the high health risks associated with the transfer through the soil-food chain, particularly in the case of rice. Recently, there has numerous researches on the use of nanoparticle-loaded materials for heavy metal-polluted soil remediation, resulting in favorable outcomes. However, there has been limited research focus on the field-scale application and recovery. This study was aimed to validate the Cd reduction effect of the nano-FeS loaded lignin hydrogel composites (FHC) in mildly polluted paddies, and to propose a field-scale application method. Hence, a multi-site field experiment was conducted in southern China. After the application for 94-103 days, the FHC exhibited a high integrity and elasticity, with a recovery rate of 91.90%. The single-round remediation led to decreases of 0.42-31.72% in soil Cd content and 1.52-49.11% in grain Cd content. Additionally, this remediation technique did not adversely impact rice production. Consequently, applying FHC in the field was demonstrated to be an innovative, efficient, and promising remediation technology. Simultaneously, a strategy was proposed for reducing Cd levels while cultivating rice in mildly polluted fields using the FHC.

Surface-wettable nonenzymatic fiber-optic sensor for selective detection of hydrogen peroxide.

A micro-nanostructure-based surface-modified fiber-optic sensor has been developed herein to selectively detect hydrogen peroxide (H2O2). In our design, phenylboronic ester-modified polymers were used as a modified cladding medium that allows chemo-optic transduction. Sensing is mechanistically based on oxidation and subsequent hydrolysis of the phenylboronic ester-modified polymer, which modulates hydrophobic properties of fiber-optic devices, which was confirmed during characterization of the chemical functional group and hydrophobicity of the active sensing material. This work illustrates a useful strategy of exploiting principles of chemical modifications to design surface-wettable fiber-optic sensing devices for detecting reactive species of broad relevance to biological and environmental analyses.

Selective Doping to Controllably Tailor Maximum Unit-Cell-Volume Change of Intercalating Li+ -Storage Materials: A Case Study of γ Phase Li3 VO4.

Capacity decay of an intercalating Li+ -storage material is mainly due to the its particle microcracks from stress-causing volume change. To extend its cycle life, its unit-cell-volume change has to be minimized as much as possible. Here, based on a γ-Li3 VO4 model material, the authors explore selective doping as a general strategy to controllably tailor its maximum unit-cell-volume change, then clarify the relationship between its crystal-structure openness and maximum unit-cell-volume change, and finally demonstrate the superiority of "zero-strain" materials within 25-60 °C (especially at 60 °C). With increasing the large-sized Ge4+ dopant, the unit-cell volume of γ-Li3+ x Gex V1- x O4 becomes larger and its crystal structure becomes looser, resulting in the decrease of its maximum unit-cell-volume change. In contrast, the doping with small-sized Si4+ shows a reverse trend. The tailoring reveals that γ-Li3.09 Ge0.09 V0.91 O4 owns the smallest maximum unit-cell-volume change of 0.016% in the research field of intercalating Li+ -storage materials. Consequently, γ-Li3.09 Ge0.09 V0.91 O4 nanowires exhibit excellent cycling stability at 25/60 °C with 94.8%/111.5% capacity-retention percentages after 1800/1500 cycles at 2 A g-1 . This material further shows large reversible capacities, proper working potentials, and high rate capability at both temperatures, fully demonstrating its great application potential in long-life lithium-ion batteries.

Visualizing nitroreductase activity in living cells and tissues under hypoxia and hepatic inflammation.

Detecting nitroreductase (NTR) activity in hypoxic cells and tissues in situ represents an important step toward accurate delineation of hypoxic disease loci. However, it remains challenging to develop fluorescent probes with the necessary attributes of selectivity, sensitivity, precise targeting and aqueous solubility. Herein, two kinds of fluorescent probes (NNP and cRGD-NNP) built on a 2-nitroimidazole sensing platform were synthesized for the detection of NTR activity in cell and in vivo models of hypoxia. In the presence of NADH, NNP displayed high selectivity for NTR, a strong fluorescence enhancement (108 fold), and a low detection limit (3.6 ng mL-1). Benefiting from the hydrophilic structure and tumor-targeting properties of the cRGD cyclopeptide group, the probe cRGD-NNP efficiently detected NTR activity in MCF cancer cells under hypoxia. In addition, the liposome-encapsulated probe was successfully applied to visualize NTR during liver inflammation in mice.

Partially Reduced Titanium Niobium Oxide: A High-Performance Lithium-Storage Material in a Broad Temperature Range.

The existing electrode materials for lithium-ion batteries (LIBs) generally suffer from poor rate capability at low temperatures, severely limiting their applications in winter and cold climate area. Here, partially reduced TiNb24 O62 (PR-TNO) are reported that demonstrates excellent electrochemical performance in a broad temperature range, notably at low temperatures. Its crystal structure is similar to that of Ti2 Nb10 O29 upon partial reduction in H2 . The titanium and niobium ions in PR-TNO enable multielectron transfer, safe operation, and high Coulombic efficiencies. Benefiting from the increased electronic conductivity of the partially reduced phase and its robust crystal structure with a large interlayer spacing, PR-TNO shows fast electron and Li+ transport, small volume change associated with Li+ storage, and notable capacitive behavior, resulting in good electrochemical performance even at very low temperatures. At -20 °C, a large reversible capacity of 313 mAh g-1 is obtained at 0.1C, reaching 83.3% of that at 25 °C. At 5C, high rate capability (58.3% of that at 0.5C) is achieved, only slightly lower than that at 25 °C (60.7%). Furthermore, PR-TNO demonstrates excellent cyclic stability with 99.2% of the initial capacity after 1680 cycles, confirming its excellent suitability for low-temperature LIBs.

Spray drying induced engineering a hierarchical reduced graphene oxide supported heterogeneous Tin dioxide and Zinc oxide for Lithium-ion storage.

In this work, a hierarchical reduced graphene oxide (RGO) supportive matrix consisting of both larger two-dimensional RGO sheets and smaller three-dimensional RGO spheres was engineered with ZnO and SnO2 nanoparticles immobilized. The ZnO and SnO2 nanocrystals with controlled size were in sequence engineered on the surface of the RGO sheets during the deoxygenation of graphene oxide sample (GO), where the zinc-containing ZIF-8 sample and metal tin foil were used as precursors for ZnO and SnO2, respectively. After a spray drying treatment and calcination, the final ZnO@SnO2/RGO-H sample was obtained, which delivered an outstanding specific capacity of 982 mAh·g-1 under a high current density of 1000 mA·g-1 after 450 cycles. Benefitting from the unique hierarchical structure, the mechanical strength, ionic and electric conductivities of the ZnO@SnO2/RGO-H sample have been simultaneously promoted. The joint contributions from pseudocapacitive and battery behaviors in lithium-ion storage processes bring in both large specific capacity and good rate capability. The industrially mature spray drying method for synthesizing RGO based hierarchical products can be further developed for wider applications.

Ethylenediamine grafted to graphene oxide@Fe3O4 for chromium(VI) decontamination: Performance, modelling, and fractional factorial design.

A method for grafting ethylenediamine to a magnetic graphene oxide composite (EDA-GO@Fe3O4) was developed for Cr(VI) decontamination. The physicochemical properties of EDA-GO@Fe3O4 were characterized using HRTEM, EDS, FT-IR, TG-DSC, and XPS. The effects of pH, sorbent dose, foreign anions, time, Cr(VI) concentration, and temperature on decontamination process were studied. The solution pH can largely affect the decontamination process. The pseudo-second-order model is suitable for being applied to fit the adsorption processes of Cr(VI) with GO@Fe3O4 and EDA-GO@Fe3O4. The intra-particle diffusion is not the rate-controlling step. Isotherm experimental data can be described using the Freundlich model. The effects of multiple factors on the Cr(VI) decontamination was investigated by a 25-1 fractional factorial design (FFD). The adsorption process can significantly be affected by the main effects of A (pH), B (Cr(VI) concentration), and E (Adsorbent dose). The combined factors of AB (pH × Cr(VI) concentration), AE (pH × Adsorbent dose), and BC (Cr(VI) concentration × Temperature) had larger effects than other factors on Cr(VI) removal. These results indicated that EDA-GO@Fe3O4 is a potential and suitable candidate for treatment of heavy metal wastewater.

Decontamination of tetracycline by thiourea-dioxide-reduced magnetic graphene oxide: Effects of pH, ionic strength, and humic acid concentration.

Thiourea-dioxide-reduced magnetic graphene oxide (TDMGO) was successfully prepared as an efficient adsorbent for the removal of tetracycline (TC) from aqueous solutions via strong adsorptive interactions. The composite was characterized by SEM, TEM, EDS, TGA, FT-IR, XPS, XRD and VSM. The effects of variables such as the pH, TC concentration, and temperature were successfully analyzed. The kinetics and isothermal parameters were described well by pseudo-second-order and Langmuir isotherm models, respectively, and the maximum adsorption capacity (qm) of TDMGO for TC calculated from the Langmuir isotherm was 1233mg/g at 313K. The removal of TC onto TDMGO, as indicated by the thermodynamic parameters, was spontaneous and endothermic. The removal performance was slightly affected by the solution pH. The presence of NaCl in the solution facilitated TC adsorption, and the optimum adsorption capacity was obtained when the NaCl concentration was >0.001M. The adsorption capacity decreased slightly with increasing humic acid concentration. In addition, the adsorbent could be regenerated and reused. Based on these results, TDMGO is a promising adsorbent for the efficient removal of TC antibiotics from aquatic environments for pollution treatment.