Bioinspired Hybrid Nanostructured PEEK Implant with Enhanced Antibacterial and Anti-inflammatory Synergy.

Implant-associated infections and excessive immune responses are two major postsurgical issues for successful implantation. However, conventional strategies including antibiotic treatment and inflammatory regulation are always compromised due to the comodification of various biochemical agents and instances of functional interference. It is imperative to provide implant surfaces with satisfactory antibacterial and anti-inflammatory properties. Here, a dual-effect nanostructured polyetheretherketone (PEEK) surface (NP@PDA/Zn) with bionic mechano-bactericidal nanopillars and immobilized immunomodulatory Zn2+ is designed. The constructed hybrid nanopillars display remarkable antibacterial performance against Gram-negative and Gram-positive strains through the synergy of physical and chemical bactericidal effects imposed by nanopillars and Zn2+. Meanwhile, the immunoregulatory property is evaluated through the investigation of macrophage polarization both in vitro and in vivo, and the results reveal that NP@PDA/Zn could downregulate the expression of M1-related cytokines and decrease the M1 macrophage recruitment to lower the inflammatory response. Notably, the surface exhibited exceptional biocompatibility with discerning biocidal activity between bacterial and mammalian cells and antioxidant performance that effectively scavenges ROS, minimizing potential cytotoxicity. Taken together, NP@PDA/Zn presents a convenient and promising strategy of combining synergistic bactericidal activity and inflammatory regulation without any mutual interference, which can support the development of multifunctional implant-associated materials.

Bimetallic CoSn nanoparticles anchored on N-doped carbon as antibacterial oxygen reduction catalysts for microbial fuel cells.

Sluggish oxygen reduction reaction (ORR) kinetics and biofilm formation limit the power generation and stability of microbial fuel cells (MFCs). Herein, bimetallic CoSn nanoparticles anchored on ZIF-derived N-doped carbon (CoSn@NC) were designed and synthesized as bifunctional catalysts to accelerate the ORR and improve the antibacterial activity. Sn modulated the electronic structure of bimetallic CoSn by drawing electrons from Co. Electron redistribution of CoSn@NC optimized the O2 adsorption at Co sites for rapid ORR kinetics. The up-shifted d-band center of Co sites reduced the energy barrier of the rate-determining step for *O formation, resulting in efficient catalytic activity. Bimetallic CoSn nanoparticles were beneficial for the four-electron transfer process for more ˙OH species production. Sn2+ and ˙OH synergistically improved the antibacterial activity of CoSn@NC to inhibit the growth of the cathode biofilm and accelerate mass-charge transfer. CoSn@NC demonstrated superior oxygen reduction activity with a half-wave potential of 0.84 V and an onset potential of 0.90 V, respectively. The MFCs assembled with the CoSn@NC cathodic catalyst exhibited an excellent power density of 1380 mW m-2 and long-term stability for 105 h. This work provides a strategy for the design of antibacterial ORR catalysts for improved catalytic activity and long-term stability.

Mechanistic insights into the leaching and environmental safety of arsenic in ceramsite prepared from fly ash.

Utilizing fly ash to prepare ceramsite is a promising way to immobilize heavy metals and recycle industrial solid waste. However, traditional preparation method of fly ash ceramsite has the disadvantages of large ignition loss. Therefore, the present study applied the pressure molding method to enhance solid content and improve the strength of ceramsite. The optimal preparation conditions of ceramsite were suggested as preheating at 450 °C for 25 min followed by sintering at 1050 °C for 30 min. Under such conditions, ceramsite with high compressive strength of 10.8 Mpa, bulk density of 878 kg m-3, and 1-h water absorption of 18.5% was fabricated, in compliance with Chinese standard (GB/T 1743.1-2010). The arsenic leaching concentration from the resulting product was considerably lower than Chinese standard (GB 5085.3-2007). Moreover, arsenic volatilization during ceramsite calcination was insignificant, and the vast majority of arsenic remained in resulting ceramsite. A geochemical speciation model developed for the multiple component system in ceramsite suggested that FeAsO4, Ca5(OH) (AsO4)3, and hydrous ferric oxide adsorption are the primary mechanisms retaining arsenic in ceramsite. Additionally, based on density functional theory calculations and biotoxicity test, the binding site of arsenic atom on mineral components and the environmental safety of ceramsite was determined and evaluated.

MedMNIST v2 - A large-scale lightweight benchmark for 2D and 3D biomedical image classification.

We introduce MedMNIST v2, a large-scale MNIST-like dataset collection of standardized biomedical images, including 12 datasets for 2D and 6 datasets for 3D. All images are pre-processed into a small size of 28 × 28 (2D) or 28 × 28 × 28 (3D) with the corresponding classification labels so that no background knowledge is required for users. Covering primary data modalities in biomedical images, MedMNIST v2 is designed to perform classification on lightweight 2D and 3D images with various dataset scales (from 100 to 100,000) and diverse tasks (binary/multi-class, ordinal regression, and multi-label). The resulting dataset, consisting of 708,069 2D images and 9,998 3D images in total, could support numerous research/educational purposes in biomedical image analysis, computer vision, and machine learning. We benchmark several baseline methods on MedMNIST v2, including 2D/3D neural networks and open-source/commercial AutoML tools. The data and code are publicly available at https://medmnist.com/ .

Immobilization of heavy metals in ceramsite prepared using contaminated soils: Effectiveness and potential mechanisms.

Heavy metal contaminated soils pose a serious threat to the environment, and preparing ceramsite using contaminated soils was proposed as an effective method to address this threat in this study. Specifically, two typical soils (i.e., contaminated clay and sandy soil) were mixed with different ratios and calcined at temperature 1000-1200 °C to prepare ceramsite. Special attentions were paid to evaluating the immobilization of heavy metals in ceramsite and identifying the corresponding immobilization mechanisms. Using the leachability of heavy metals from ceramsite as evaluation criteria, the optimum mixing ratio of clay/sandy soil and sintering temperature were determined as 0.6:0.4 and 1200 °C. Moreover, based on the spectroscopic characterizations and thermodynamic calculation, high sintering temperature well facilitated the liquid phases formation, promoting the reactions between heavy metals and aluminosilicates and the valence state conversion of heavy metals. Accordingly, heavy metals were well immobilized in ceramsite by forming thermodynamically stable minerals, being encapsulated in solid matrix, and transforming to valence states with low mobility. The leaching conditions including pH and temperature had minimal effect on the immobilization of heavy metals in ceramsite. In summary, ceramsite prepared by contaminated soils was environmentally friendly and had good potential in engineering application as building materials.

Highly-efficient and easy separation of γ-Fe2O3 selectively adsorbs U(⠥) in waters.

The migration and transformation of uranyl [U (Ⅵ)] ions in the environment are quite dependent on the geological condition in particular with the site enriched in Fe. In this study, the interfacial interaction of U (Ⅵ) ions with maghemite (γ-Fe2O3) particles was studied and the interaction mechanism was explored as well. Batch experiments confirm that γ-Fe2O3 can effectively remove U (Ⅵ) from an aqueous solution within a relatively short reaction time (R% > 92.01% within 3 min) and has a considerable capacity for U (Ⅵ) uptake (qt: 87.35 mg/g). γ-Fe2O3 displays an excellent selectivity for U (Ⅵ) elimination. Results on the effects of natural organic matter such as humic acid (HA) indicated that HA could promote the interfacial interaction between γ-Fe2O3 and U (Ⅵ) under acidic conditions. Compared with other radionuclides (e.g., Sr(Ⅱ) and Cs(Ⅰ)), U (Ⅵ) was more effectively removed by γ-Fe2O3. The U (Ⅵ) removal by γ-Fe2O3 is primarily due to electrostatic interactions and precipitation that result in the long-term retardation of uranium. γ-Fe2O3 not only can fast and selectively adsorb U (Ⅵ) but also can be magnetically recycled, demonstrating that γ-Fe2O3 is a cost-effective and promising material for the clean-up of uranyl ions from radioactive wastewater.

Fabrication, characterization and U(VI) sorption properties of a novel biochar derived from Tribulus terrestris via two different approaches.

Water contamination due to radionuclides is considered a crucial environmental issue. In this study, Tribulus terrestris plant biomass was used as a precursor for obtaining biochar (BC), that was further modified by two different methods using FeCl3 to obtain two different magnetic biochars. Both (one-step biochar, called 1S-BC, and two-steps biochar, called 2S-BC) were studied to investigate their capability for adsorbing/removing uranium (VI) from aqueous solutions. The U(VI) removal efficacy of both biochars was tested for different values of pH, ionic strength, initial concentration of U(VI) and temperature. Experimental adsorption data fitted well to the Freundlich model (achieving as highest value for adsorption capacity KF = 49.56 mg g-1 (mg L-1)-1/n, R2 = 0.99). Thermodynamic studies revealed that adsorption was endothermic, characterized by inner-sphere complexation, and entropy-driven with a relatively increased randomness in the solid-solution interface. X-ray photoelectron spectroscopy (XPS) revealed that U(VI) sorption took place by surface complexation between U(VI) and oxygen containing functional groups on both biochars. Five consecutive regeneration cycles verified an excellent reusability for 1S-BC. The overall results allow to conclude that the FeCl3 modification of the biochar obtained from Tribulus terrestris plant biomass could give an efficient alternative adsorbent for U(VI) removal in a variety of environmental conditions, promoting protection of the environment and human health, as well as facilitating resource utilization and sustainable management of the materials studied.

Graphene oxide functionalized with nano hydroxyapatite for the efficient removal of U(VI) from aqueous solution.

Water contamination caused by radionuclides is a major environmental issue. Uranium (U) belongs to the actinide group of elements. Hexavalent uranium (U(VI)) is radioactively and chemically harmful and highly mobile in the environment and wastewater stream. Therefore, developing highly efficient materials for minimizing the environmental impact of U(VI) is essential. To achieve this goal, we successfully synthesized a novel material, namely graphene oxide (GO)/hydroxyapatite (HAP), by directly assembling GO and HAP through a facile hydrothermal method, which exhibits effective U(VI) removal and immobilization. The GO/HAP composite has an outstanding sorption capacity for U(VI) (i.e., 373.00 mg/g) within 5 min at a pH of 3.0. The parameters from thermodynamic analysis indicated that the GO/HAP composite absorbed U(VI) through a process of spontaneous and exothermic adsorption. XPS, XRD, and FT-IR results revealed that the composite's phosphate group was mainly responsible for U(VI) retention and incorporation. The GO/HAP composite's enhanced U(VI) sorption capacity is most likely ascribed to the synergistic effect after functionalizing with nano HAP. The current findings may greatly facilitate the creation of rational design strategies to develop highly efficient materials that can treat radioactive wastewater.

The influence of particle size and natural organic matter on U(VI) retention by natural sand: Parameterization and mechanism study.

Contamination caused by radionuclides such as uranium (U) has become an increasingly serious environmental problem. The unique and diverse features of uranyl ions (U(VI)) remarkably dominate their mobility and environmental impact on the ecosystem. Understanding the sorption behavior and fate of aqueous U(VI) ions on natural mineral(s) such as quartz sand (a typical type of crystalline silica (SiO2)) particles is essential for unraveling many environmental issues. In this work, the sorption of uranyl ions by various particle size quartz sands under different reaction conditions was thoroughly investigated. The quartz sand with an average particle size of 3.588 µm exhibited an excellent sorption performance for the removal of aqueous U(VI) ions at pH 5.0. The sorption rate increased as the dosage of sorbent increased. The sorption rate descends with the rise of the initial U(VI) concentration while its sorption amount is reversed. The elevation of temperature impeded the U(VI) sorption. Humic acid (a typical natural organic matter) showed significant impacts on U(VI) removal. Ions of Ca2+, CO32- and K+ remarkably inhibited the U(VI) sorption, while PO43- ions significantly promoted the U(VI) sorption. The pseudo second-order kinetic model could fit well with the experimental sorption data. The U(VI) sorption is mainly chemisorption and it is an exothermic process. After sorption, the surface of used quartz sand became much smooth and XPS signals of U(VI) were detected, evidencing the success of the removal of aqueous U(VI). The outcomes of this study highlighted both solution pH and natural organic matters played critical roles on U(VI) removal by sand particles. This study further enhances our comprehension from the molecular-scale process manipulating U(VI) sorption behavior at the mineral-aqueous interface.

Glycyrrhetinic acid alleviates hepatic inflammation injury in viral hepatitis disease via a HMGB1-TLR4 signaling pathway.

Various human disorders are cured by the use of licorice, a key ingredient of herbal remedies. Glycyrrhizic acid (GL), a triterpenoid glycoside, is the aqueous extract from licorice root. Glycyrrhetinic acid (GA) has been reported to be a major bioactive hydrolysis product of GL and has been regarded as an anti-inflammatory agent for the treatment of a variety of inflammatory diseases, including hepatitis. However, the mechanism by which GA inhibits viral hepatic inflammatory injury is not completely understood. In this study, we found that, by consecutively treating mice with a traditional herbal recipe, licorice plays an important role in the detoxification of mice. We also employed a murine hepatitis virus (MHV) infection model to illustrate that GA treatment inhibited activation of hepatic inflammatory responses by blocking high-mobility group box 1 (HMGB1) cytokine activity. Furthermore, decreased HMGB1 levels and downstream signaling triggered by injection of a neutralizing HMGB1 antibody or TLR4 gene deficiency, also significantly protected against MHV-induced severe hepatic injury. Thus, our findings characterize GA as a hepatoprotective therapy agent in hepatic infectious disease not only by suppressing HMGB1 release and blocking HMGB1 cytokine activity, but also via an underlying viral-induced HMGB1-TLR4 immunological regulation axis that occurs during the cytokine storm. The present study provides a new therapy strategy for the treatment of acute viral hepatitis in the clinical setting.

[Nitrogen and phosphorus composition in urban runoff from the new development area in Beijing].

Stormwater runoff samples were collected from two impervious roof and road of the new development area in Beijing, during three rainfall events in an attempt to characterize the urban runoff and determine nitrogen and phosphorus composition. The outcomes are expected to offer the practical guidance in sources control of urban runoff pollution. The results indicated that the stormwater runoff from the studied area presented a strong first flush for all monitored events and constituents. Eighty percent of the total pollutant loads were transported by the first 10 mm flow volume for roof runoff, whereas 80% of the total pollutant loads were discharged by the first 15 mm flow volume for road runoff. Average EMCs of TSS, COD, TN, NH4(+) -N, NO3(-) -N and TP for roof runoff were 50.2 mg x L(-1), 81.7 mg x L(-1), 6.07 mg x L(-1), 2.94 mg x L(-1), 1.05 mg x L(-1), and 0.11 mg x L(-1), respectively. Average EMCs of TSS, COD, TN, NH4(+) -N, NO3(-)-N and TP for road runoff were 539.0 mg x L(-1), 276.4 mg x L(-1), 7.00 mg x L(-1), 1.71 mg x L(-1), 1.51 mg x L(-1), and 0.61 mg x L(-1), respectively. Moreover, for the roof runoff, the particle-bound fraction was 20.8% for COD, 12.3% for TN, and 49.7% for TP. For road runoff, the particle-bound fraction was 68.6% for COD, 20.0% for TN, and 73.6% for TP. Nitrogen in roof runoff was predominantly dissolved (87.7%), with ammonia (57.6%) and nitrate (22.5%). Nitrogen in road runoff was also predominantly dissolved (80.0%), with ammonia (42.1%) and nitrate (35.0%). These findings can assist the development of effective source control strategies to immobilize dissolved and particulate-bound nitrogen/phosphorus in urban stormwater.

Treatment of severe Clonorchiasis sinensis by endoscopic nasobiliary drainage and oral praziquantel.

AIM: To assess the therapeutic value of endoscopic nasobiliary drainage (ENBD) and oral praziquantel for severe Clonorchiasis sinensis infection. METHODS: Of the 84 Clonorchiasis sinensis-infected patients enrolled, 58 were treated with ENBD (as observing group, ENBD group), 26 received operations (control group, operation group). Both of the two groups were comparable in terms of patient's age, body mass index. Before and one week after treatment, the average diameters of common bile ducts were measured by ultrasound, and serum bilirubin, ALP, gamma-GT and ALT were detected by biochemical methods. After ENBD or operation, the patients took praziquantel for two days. RESULTS: Compared with the patients in operation group, ENBD patients in ENBD group had higher recovery rates of abdominal pain and fever as well as jaundice, quicker remission, smaller trauma, fewer complications and lower cost. CONCLUSION: ENBD combined with oral praziquantel is an effective and safe method for the treatment of severe Clonorchiasis sinensis.