Cumulative Concentration Research Articles

Deferoxamine-Loaded Chitosan-Based Hydrogel on Bone Implants Showing Enhanced Bond Strength and Pro-Angiogenic Effects.

Angiogenesis is vital for bone fracture healing and plays a significant role in the fate of orthopedic implants. The growth and maintenance of new blood vessels at the fracture site of patients is essential, which promotes the clinical outcome of plasma sprayed Ti (PST) coated orthopedic implants. In order to endow the PST coating with pro-angiogenic effects, deferoxamine-loaded chitosan-based hydrogel was fabricated on the coating surface. Polydopamine-modified chitosan (CS/PDA) hydrogel exhibited enhanced bonding strength to PST coatings as evidenced by scratch test. The deferoxamine-loaded CS/PDA (CS/PDA-DFO) exhibited a sustained drug-release property, and the cumulative concentration of released DFO reached 20.21 μg/mL on day 7. PST-CS/PDA with higher wettability and active group quantity enhanced the viability and adhesion characteristics of human umbilical vein endothelial cells (HUVECs) and upregulated the secretion level of nitric oxide and vascular endothelial growth factor. Moreover, the introduction of DFO in PST-CS/PDA further enhanced the pro-angiogenic effects. Above all, this study offers a novel approach for developing hydrogel coating on orthopedic implants showing enhanced bonding strength and pro-angiogenic effects.

Hierarchical antibiotic delivery system based on calcium phosphate cement/montmorillonite-gentamicin sulfate with drug release pathways

Antibiotic-loaded calcium phosphate cement (CPC) has emerged as a promising biomaterial for drug delivery in orthopedics. However, there are problems such as the burst release of antibiotics, low cumulative release ratio, inappropriate release cycle, inferior mechanical strength, and poor anti-collapse properties. In this research, montmorillonite-gentamicin (MMT-GS) was fabricated by solution intercalation method and served as the drug release pathways in CPC to avoid burst release of GS, achieving promoted cumulative release ratios and a release cycle matched the time of inflammatory response. The results indicated that the highest cumulative release ratio and release concentration of GS in CPC/MMT-GS was 94.1 ± 2.8 % and 1183.05 μg/mL, and the release cycle was up to 504 h. In addition, the hierarchical GS delivery system was divided into three stages, and the kinetics followed the Korsmeyer-Peppas model, the zero-order model, and the diffusion-dissolution model, respectively. Meanwhile, the compressive strength of CPC/MMT-GS was up to 51.33 ± 3.62 MPa. Antibacterial results demonstrated that CPC/MMT-GS exhibited excellent in vitro long-lasting antibacterial properties to E. coli and S. aureus. Furthermore, CPC/MMT-GS promoted osteoblast proliferation and exhibited excellent in vivo histocompatibility. Therefore, CPC/MMT-GS has favorable application prospects in the treatment of bone defects with bacterial infections and inflammatory reactions.

Surface Modification of Hydroxyapatite Coating for Enhanced Antibiotic Therapy

A major strategy to combat implant-associated infections is to develop implant coatings with intrinsic antibacterial activity. Since hydroxyapatite (HAp) coatings and antibiotic administration are commonly used in clinical settings, developing HAp-coated implants with localized antibiotic-releasing properties has attracted popularity. Considering the antibacterial metal species (Ag, Zn, Cu, etc.) in metal–organic frameworks and their drug delivery capacity, in this study, a gentamicin-loaded zeolitic imidazolate framework-8 nanolayer was deposited on a plasma-sprayed HAp coating (HAp/ZIF-8@Gent), which served as a Gent and Zn2+ reservoir. The investigation on the binding interaction between ZIF-8 and HAp indicated that the growth of ZIF-8 was through a Zn2+ seed layer on the HAp coating via an adsorption–replacement mechanism, instead of simple physical adsorption. The HAp/ZIF-8@Gent coating exhibited a sustained drug-release property, and the cumulative concentration of released Gent reached 239.8 ± 7.1 μg/mL on day 8. Compared to the HAp-Zn and HAp/ZIF-8 coatings, the HAp/ZIF-8@Gent coating exhibited significantly higher antibacterial activity against E. coli. This was ascribed to the combined antibacterial effects of Zn2+ and Gent. The cytocompatibility of the HAp/ZIF-8@Gent coating was confirmed via cell proliferation. Above all, the ZIF-8-modified HAp coating with localized delivery of Gent and Zn2+ possessed excellent antibacterial activity and acceptable cytocompatibility, showing potential in mitigating implant-associated infections.

An Intermittent Exposure Regime Did Not Alter the Crop Yield and Biomass Responses to an Elevated Ozone Concentration

The intermittent ozone (O3) exposure of crops to alternating high and low concentrations is common in fields, but its impact on crop production has not been thoroughly investigated. In this study, two widely planted and O3-sensitive crops, winter wheat and soybean, were intermittently exposed to elevated O3 concentrations in open-top chambers. The results showed that the winter wheat and soybean yields significantly decreased with O3 exposure (AOT40, cumulative hourly O3 concentration above 40 ppb) (p < 0.001). The relative yield losses were 0.99% per AOT40 for winter wheat and 1.2% per AOT40 for soybean, respectively. The responses of the crop biomasses to elevated O3 concentrations were lower than that of crop yield. Although the O3-induced crop yield and biomass losses under continuous O3 exposure were greater than those under intermittent O3 exposure, the differences were not statistically significant. Therefore, we can conclude that the effects of elevated O3 concentrations on crops are closely related to the exposure dose but not significantly related to the temporal distribution of elevated O3 concentrations. This study improves our understanding of how crop production responds to intermittent O3 exposure.

Biochar accelerated Fenton process for roxarsone oxidation, inorganic arsenic adsorption and simultaneous immobilization of arsenic-iron sludge

Complete remediation of organoarsenics from environmental matrix hits the bottleneck, that is, the sluggish efficiency of oxidative degradation towards organoarsenics and unsatisfying immobilization performance towards generated inorganic arsenic. Herein, we establish a biochar accelerated Fenton (BA-Fenton) process to decontaminate water from roxarsone (ROX). In comparison with Fe2+/H2O2 process (10 μΜ/0.2 mM), the incorporation of 0.5 g L-1 biochar promoted ROX degradation from 48.2% to 98.2% and total arsenic elimination from 67.6% to 97.3%, respectively. In BA-Fenton process, •OH as the dominant reactive oxygen species (ROS), exhibited a cumulative concentration of 0.42 mM, three times higher than that in classical Fenton process. Crucially, the presence of biochar in Fenton process significantly enhanced the stability of arsenic-iron sludge, whereas the secondary leaching of total arsenic decreased from 433.8 μg-As L-1 to 13.9 μg-As L-1, meeting the prescribed environmental quality standards for surface water in China (50 μg-As L-1, GB 3838-2002). Mechanistic studies unveiled ROX remediation mechanism by BA-Fenton process, highlighting the dual functionality of biochar. On one hand, biochar efficiently reduced Fe3+ to Fe2+ with a rate constant of 0.225 min-1, overcoming the rate-determining step of classical Fenton process for •OH production, consequently promoting the transformation of ROX to As(V). On the other hand, molecular spectroscopy analysis elucidated that in-situ formed As(V) was adsorbed by ferric hydroxides with the formation of arsenic-iron sludge. Subsequently, biochar immobilized arsenic-iron sludge through hydrogen bonds, electrostatic attraction and surface complexation. Furthermore, real water studies demonstrated the effective remediation of organoarsenics by BA-Fenton process in tap water, lake water and chicken manure leachate. This “Two Birds with One Stone” strategy with low-cost, environmental-friendly and sustainable biochar holds great promise for the ultimate disposal of industrial wastewater containing organoarsenics.

Measurement report: Atmospheric ice nuclei in the Changbai Mountains (2623 m a.s.l.) in northeastern Asia

Abstract. Atmospheric ice nucleation plays an important role in modulating the global hydrological cycle and atmospheric radiation balance. To date, few comprehensive field observations of ice nuclei have been carried out at high-altitude sites, which are close to the height of mixed-phase cloud formation. In this study, we measured the concentration of ice-nucleating particles (INPs) in the immersion freezing mode at the summit of the Changbai Mountains (2623 m above sea level), northeast Asia, in summer 2021. The cumulative number concentration of INPs varied from 1.6 × 10−3 to 78.3 L−1 over the temperature range of −5.5 to −29.0 °C. Proteinaceous-based biological materials accounted for the majority of INPs, with the proportion of biological INPs (bio-INPs) exceeding 67 % across the entire freezing-temperature range, with this proportion even exceeding 90 % above −13.0 °C. At freezing temperatures ranging from −11.0 to −8.0 °C, bio-INPs were found to significantly correlate with wind speed (r = 0.5–0.8, p < 0.05) and Ca2+ (r = 0.6–0.9), and good but not significant correlation was found with isoprene (r = 0.6–0.7) and its oxidation products (isoprene × O3) (r = 0.7), suggesting that biological aerosols may attach to or mix with soil dust and contribute to INPs. During the daytime, bio-INPs showed a positive correlation with the planetary boundary layer (PBL) height at freezing temperatures ranging from −22.0 to −19.5 °C (r > 0.7, p < 0.05), with the valley breezes from southern mountainous regions also influencing the concentration of INPs. Moreover, the long-distance transport of air mass from the Japan Sea and South Korea significantly contributed to the high concentrations of bio-INPs. Our study emphasizes the important role of biological sources of INPs in the high-altitude atmosphere of northeastern Asia and the significant contribution of long-range transport to the INP concentrations in this region.

Trace organic contaminants in lake waters: Occurrence and environmental risk assessment at the national scale in Canada

Numerous contaminants are produced and used daily, a significant fraction ultimately finding their way into natural waters. However, data on their distribution in lakes is lacking. To address this gap, the presence of 54 trace organic contaminants (TrOCs), representative of various human activities, was investigated in the surface water of 290 lakes across Canada. These lakes ranged from remote to highly impacted by human activities. In 88% of the sampled lakes, contaminants were detected, with up to 28 detections in a single lake. The compounds most frequently encountered were atrazine, cotinine, and deethylatrazine, each of which was present in more than a third of the lakes. The range of detected concentrations was from 0.23 ng/L to about 2200 ng/L for individual compounds, while the maximum cumulative concentration exceeded 8100 ng/L in a single lake. A risk assessment based on effect concentrations for three aquatic species (Pimephales promelas, Daphnia magna, and Tetrahymena pyriformis) was conducted, revealing that 6% of lakes exhibited a high potential risk for at least one species. In 59% of lakes, some contaminants with potential sub-lethal effects were detected, with the detection of up to 17 TrOCs with potential impacts. The results of this work provide the first reference point for monitoring the evolution of contamination in Canadian lakes by TrOCs. They demonstrate that a high proportion of the sampled lakes bear an environmentally relevant anthropogenic chemical footprint.

Enhanced degradation of enoxacin using ferrihydrite-catalyzed heterogeneous photo-Fenton process

The ferrihydrite-catalyzed heterogeneous photo-Fenton reaction shows great potential for environmental remediation of fluoroquinolone (FQs) antibiotics. The degradation of enoxacin, a model of FQ antibiotics, was studied by a batch experiment and theoretical calculation. The results revealed that the degradation efficiency of enoxacin reached 89.7% at pH 3. The hydroxyl radical (∙OH) had a significant impact on the degradation process, with a cumulative concentration of 43.9 μmol L−1 at pH 3. Photogenerated holes and electrons participated in the generation of ∙OH. Eleven degradation products of enoxacin were identified, with the main degradation pathways being defluorination, quinolone ring and piperazine ring cleavage and oxidation. These findings indicate that the ferrihydrite-catalyzed photo-Fenton process is a valid way for treating water contaminated with FQ antibiotics.

Numerical analysis and improvement strategy of particulate matter concentration in underground subway stations

Particulate matter (PM) is an important air pollutant in subway systems. Exposure to high PM concentrations poses a threat to human health and raises concerns. Piston effect can provide the outdoor fresh air to subway stations through station exits, but it also brings PM from tunnels to platforms when the train enters the station. In this paper, a transient numerical model is developed according to an actual subway station and validated by field tests. The model is used to investigate PM10 concentration at platform induced by train movement. The cumulative PM10 concentration at platform in one day is calculated according to the train schedule. Platform screen door (PSD) with adjustable vents is studied to control the PM10 level at platform and energy saving in 27 cities of five climatic zones in China are discussed. The results show that adjustable vent height should be less than 0.70 m to ensure that PM10 concentrations at platform can be maintained at an acceptable level and the requirement of fresh air can be met. Moreover, energy consumption can be reduced by more than 70 % in different cities compared with the conventional mechanical ventilation system. The optimized adjustable vent can provide an important reference for improving indoor air quality (IAQ) and saving energy consumption of ventilation systems in underground facilities.

Carboxylated Hexagonal Boron Nitride/Graphene Configuration for Electrosynthesis of High‐Concentration Neutral Hydrogen Peroxide

AbstractThe electrosynthesis of hydrogen peroxide (H2O2) via two‐electron (2e−) oxygen (O2) reduction reaction (ORR) has great potential to replace the traditional energy‐intensive anthraquinone process, but the design of low‐cost and highly active and selective catalysts is greatly challenging for the long‐term H2O2 production under industrial relevant current density, especially under neutral electrolytes. To address this issue, this work constructed a carboxylated hexagonal boron nitride/graphene (h‐BN/G) heterojunction on the commercial activated carbon through the coupling of B, N co‐doping with surface oxygen groups functionalization. The champion catalyst exhibited a high 2e− ORR selectivity (>95 %), production rate (up to 13.4 mol g−1 h−1), and Faradaic efficiency (FE, >95 %). The long‐term H2O2 production under the high current density of 100 mA cm−2 caused the cumulative concentration as high as 2.1 wt %. The combination of in situ Raman spectra and theoretical calculation indicated that the carboxylated h‐BN/G configuration promotes the adsorption of O2 and the stabilization of the key intermediates, allowing a low energy barrier for the rate‐determining step of HOOH* release from the active site and thus improving the 2e− ORR performance. The fast dye degradation by using this electrochemical synthesized H2O2 further illustrated the promising practical application.

Carboxylated Hexagonal Boron Nitride/Graphene Configuration for Electrosynthesis of High-Concentration Neutral Hydrogen Peroxide.

The electrosynthesis of hydrogen peroxide (H2 O2 ) via two-electron (2e- ) oxygen (O2 ) reduction reaction (ORR) has great potential to replace the traditional energy-intensive anthraquinone process, but the design of low-cost and highly active and selective catalysts is greatly challenging for the long-term H2 O2 production under industrial relevant current density, especially under neutral electrolytes. To address this issue, this work constructed a carboxylated hexagonal boron nitride/graphene (h-BN/G) heterojunction on the commercial activated carbon through the coupling of B, N co-doping with surface oxygen groups functionalization. The champion catalyst exhibited a high 2e- ORR selectivity (>95 %), production rate (up to 13.4 mol g-1 h-1 ), and Faradaic efficiency (FE, >95 %). The long-term H2 O2 production under the high current density of 100 mA cm-2 caused the cumulative concentration as high as 2.1 wt %. The combination of in situ Raman spectra and theoretical calculation indicated that the carboxylated h-BN/G configuration promotes the adsorption of O2 and the stabilization of the key intermediates, allowing a low energy barrier for the rate-determining step of HOOH* release from the active site and thus improving the 2e- ORR performance. The fast dye degradation by using this electrochemical synthesized H2 O2 further illustrated the promising practical application.

Introducing the novel concept of cumulative concentration roses for studying the transport of ultrafine particles from an airport to adjacent residential areas

Abstract. Airports are often surrounded by urban residential areas, which is both a motivation and challenge for studying their potential impact on local air quality. Airports are a relevant source of ultrafine particles (UFPs), which can pose a risk to human health due to their small size (particle diameter Dp≤100 nm). However, in urban environments, UFPs originate from a multitude of biogenic and anthropogenic sources. Here, we investigate UFPs in close proximity to an airport to disentangle their impact on local air quality from other urban sources. We present observations and analyses of airborne UFP concentrations and size distributions determined at two sites in close proximity to Munich Airport. Therefore, two novel measurement stations were established north and south of the airport but were neither situated on the axis of prevailing wind directions nor impacted by fly overs. This set-up allowed us to explore a mainly advection-driven distribution of UFPs into the most populated adjacent residential areas. The observation period covered a full year from August 2021 to July 2022. We analysed the data set in three steps. (1) First, we derived UFP concentration roses using the wind data as reported at 10 m height at the airport to represent the local wind field. An increase in particle number concentrations and a shift of the modal maximum towards smaller mobility diameters became evident for wind directions, including those approaching from the airport. During the airport's operation hours during the daytime, median particle number concentrations were 2.2- and 1.6-fold compared to nighttime at the northern station and the southern station. However, our data had a high variability, and the direction-based analysis was uncertain due to other potential UFP sources in the surroundings and the assumption of a homogeneous, local wind field. (2) Next, we derived concentration roses employing the airflow observations from the two measuring stations at 5.3 m height. While the annual concentration rose in principle yielded the same conclusions as the first analysis step, a significant seasonal and diurnal variability of UFPs and wind became evident. The influencing factors were likely other urban local UFP sources, an increased surface roughness due to green vegetation, and the atmospheric boundary layer development. (3) In order to assess the possible advection of UFPs from the direction of Munich Airport relative to all other directions over the course of the year, we calculated cumulative concentration roses with both local- and site-scale wind data. Under the assumption of a homogeneous local wind field, the fraction of all UFPs sampled in airflows approaching from the airport's direction was 21 % (N322) and 40 % (S229). Considering a local background, the range of UFP advection from Munich Airport to the adjacent residential areas was up to 10 % in the north and 14 % in the south. It has to be noted that these values highlight the relative magnitude of the maximum impact of the airport on local air quality as they do not distinguish between UFP sources from the airport and other measuring sites. Additionally, they integrate over a time period during which the airport did not reach its full capacity compared to pre-COVID-19 times.

D-limonene nanoemulsion as skin permeation enhancer for curcumin prepared by ultrasonic emulsification

d-limonene nanoemulsion (NE) previously showed satisfactory potential for storage stability and might be a safety carrier for transdermal drug delivery systems (TDDSs). Curcumin has been widely studied for health promotion, food safety, and functions. This study evaluated the application of d-limonene NE carrier for curcumin embedding and the transdermal absorption effect. Results revealed that the droplet size of curcumin NE affected the cumulative concentration of transdermal absorption following the descending order of hydrophilic-lipophilic balance (HLB) 11 > 8 > 5 > 3 > microemulsion (p < 0.05). The droplet size was also correlated with the steady-state flux of transdermal absorption by permeability and was twice as high for HLB value 11 (84.3 nm) and HLB value 3 (384.7 nm). In addition, the cumulative concentration of HLB 11 (57.13 %) was nearly double higher than that of HLB 3 (26.29 %) (p < 0.05). The developed d-limonene-encapsulated curcumin NE has a macroscopic bioactivity, which can be retarded release by encapsulating the bioactive source, enabling it to be biomimetic simply. Therefore, the study has important implications for forming and designing encapsulated bioactive TDDS. All these findings suggested that d-limonene NE could function as a carrier for TDDS in food/cosmetic products.

Leukemia risk assessment of exposure to low-levels of benzene based on the linearized multistage model.

To assess leukemia risk in occupational populations exposed to low levels of benzene. Leukemia incidence data from the Chinese Benzene Cohort Study were fitted using the Linearized multistage (LMS) model. Individual benzene exposure levels, urinary S-phenylmercapturic acid (S-PMA) and trans, trans-muconic acid (t, t-MA) were measured among 98 benzene-exposed workers from factories in China. Subjects were categorized into four groups by rounding the quartiles of cumulative benzene concentrations (< 3, 3-5, 5-12, ≥12 mg/m3·year, respectively). The risk of benzene-induced leukemia was assessed using the LMS model, and the results were validated using the EPA model and the Singapore semi-quantitative risk assessment model. The leukemia risks showed a positive correlation with increasing cumulative concentration in the four exposure groups (excess leukemia risks were 4.34, 4.37, 4.44 and 5.52 × 10-4, respectively; Ptrend < 0.0001) indicated by the LMS model. We also found that the estimated leukemia risk using urinary t, t-MA in the LMS model was more similar to those estimated by airborne benzene compared to S-PMA. The leukemia risk estimated by the LMS model was consistent with both the Singapore semi-quantitative risk assessment model at all concentrations and the EPA model at high concentrations (5-12, ≥12 mg/m3·year), while exceeding the EPA model at low concentrations (< 3 and 3-5 mg/m3·year). However, in all four benzene-exposed groups, the leukemia risks estimated by these three models exceeded the lowest acceptable limit for carcinogenic risk set by the EPA at 1 × 10-6. This study demonstrates the utility of the LMS model derived from the Chinese benzene cohort in assessing leukemia risk associated with low-level benzene exposure, and suggests that leukemia risk may occur at cumulative concentrations below 3 mg/m3·year.

Derivation of threshold values for the sulfur nutritional status of European silver fir from a cumulative concentration distribution

AbstractFor European silver fir (Abies alba (Mill)), reliable threshold values for the sulfur nutritional status are not available. Because European silver fir is an important coniferous tree species in Central Europe and due to the fact that by reduced S emissions, S is becoming a more and more critical nutrient this knowledge gap should be closed. From the interpretation of the cumulative distribution of sulfur concentrations in first‐year needles, the respective threshold values for the range of normal nutrition as well as the threshold for deficiency could be derived. When knowing these thresholds also the range of harmonic nutrition, which is the range for the optimal relation of two nutrients, could be calculated. As compared to the very few literature data available and compared to the respective values of the two most important European conifers Norway spruce (Picea abies) and Scots pine (Pinus sylvestris), the values derived for S nutrition of European silver fir are very reasonable. With respect to the S nutritional thresholds, European silver fir is very close to the values of the other two conifers, whereas the harmonic range of S in relation to N is a bit shifted to higher values indicating that European silver fir has a slightly higher demand for S (in relation to N). There is a certain time lag between the reduction of SO2 emissions in Europe and the reduction of S concentrations in needles, suggesting that S stored in the soil during periods of high emissions is relevant for S nutrition of trees for a longer period of time.

Pesticide pollution in argentine drinking water: A call to ensure safe access

The application of pesticides in Argentina has been on the rise since 2000. However, the monitoring of pesticides in drinking water lacks regular updates. This research study analysed 53 pesticides and degradation products to evaluate their presence in drinking water. The most frequently detected pesticides in drinking water were atrazine, metolachlor, imidacloprid, hydroxyatrazine, imazethapyr and 2.4D. During the sample collection period, 25% of the soil was planted with winter crops, while just under 50% was allocated to summer crops, especially corn and soybeans. The correlation between the pesticides used in these crops and those found in drinking water was significant/notable. As a matter of fact, the individual concentration of pesticides in drinking water [25] exceeded the European limit in 8.7% and 17.6% of the samples collected from public and private water supplies, respectively, while the cumulative concentration of pesticides in drinking water exceeded the limit in 4.3% and 13.9% of the samples from public and private supplies, respectively. Based on these findings, we recommend/propose the inclusion of pesticides within the regulatory framework that governs the quality control of drinking water to guarantee the protection of public health and progressively reduce the use of pesticides in the Argentine agricultural system. Adopting these measures will contribute to ensuring the safety and sustainability of drinking water sources for the population.

Exposure levels and health implications of fungicides, neonicotinoid insecticides, triazine herbicides and their associated metabolites in pregnant women and men

Exposure to pesticides can pose a series of advance effects on human health. However, the exposure levels and health implications of the current use pesticides and their metabolites in both men and pregnant women remain unclear. In this study, an analytical method was developed to quantify fungicides, neonicotinoid insecticides, triazine herbicides, and their metabolites in the human serum. Fifty of the 73 target pesticides and metabolites were detected in the human serum of men and pregnant women from Wuxi, China, which included 11 triazine herbicides and metabolites, 17 neonicotinoid insecticides and metabolites, and 22 fungicides. Fungicides had the highest cumulative concentration (49.5 ng/mL), followed by neonicotinoid insecticides and metabolites (6.38 ng/mL), and triazine herbicides and metabolites (5.10 ng/mL). Moreover, the estimated daily intake (EDI) of fungicides was 10.4 and 12.7 times higher than that of triazine herbicides (included their metabolites) and neonicotinoid insecticides (included their metabolites), respectively. Of the three categories of pesticides, exposure to fungicides contributed to the highest exposure risk within the hazard quotient in the range of 5.1 × 10−3-0.17. Correlation analysis revealed that the pesticide exposure levels in human serum were correlated with their maximum residue levels in vegetables and fruits. Pesticide exposure has also been correlated with the weight and Body Mass Index (BMI) of humans based on structural equation modeling. This study provides new insights into the exposure of men and pregnant women to a cocktail of fungicides, neonicotinoid insecticides, triazine herbicides and their metabolites.

Porous N-Doped Carbon Decorated with Atomically Dispersed Independent Dual Metal Sites from Energetic Zeolite Imidazolate Frameworks as Bidirectional Catalysts for Lithium-Sulfur Batteries.

Lithium-sulfur (Li-S) batteries have ultrahigh theoretical specific capacity and energy density, which are considered to be very promising energy storage devices. However, the slow redox kinetics of polysulfides are the main reason for the rapid capacity decay of Li-S batteries. A reasonable electrocatalyst for the Li-S battery should reduce the reaction barrier and accelerate the reaction kinetics of the bidirectional catalytic conversion of lithium polysulfides (LiPSs), thereby reducing the cumulative concentration of LiPSs in the electrolyte. In this report, porous N-doped carbon nanofibers decorated with independent dual metal sites as catalysts for Li-S batteries were fabricated in one step using a fusion-foaming method. Experimental and theoretical analyses demonstrate that the synergistic effect of independent dual metal sites provides strong LiPS affinity, improved electronic conductivity, and enhanced redox kinetics of polysulfides. Therefore, the assembled Li-S battery exhibits high rate performance (discharge specific capacity of 771 mA h g-1 at 2C) and excellent cycle stability (capacity decay rate of 0.51% after 1000 cycles at 1C).

Analytical model for organic contaminant transport in a cut-off wall and aquifer dual-domain system considering barrier arrangements

This paper presents an analytical study of organic contaminants transport in a cut-off wall and aquifer dual-domain system, considering the effects of the inlet boundary conditions and cut-off structural arrangements. The comprehensive sensitivity analysis of parameters focusing on the breakthrough time, attenuation time and cumulative concentration are presented using the Monte Carlo simulation and Sobol global method. The simplified constant inlet boundary condition can lead to an excessively conservative prediction of the contaminant breakthrough compared to the ‘finite mass’ and ‘decaying source’ boundary conditions. The cut-off wall hydraulic performance can be enhanced by reducing the contaminant's head loss, shape factor, half-life and cut-off wall hydraulic conductivity while increasing the retardation factor. The contaminant's half-life can largely influence the maximum contaminant concentration, attenuation time and breakthrough time. For example, the maximum contaminant concentrations for T1/2 = 1.4 years and T1/2 = 100 years are 13 and 123 times greater than that for T1/2 = 0.1 year, respectively. The influence of the variation of shape factor on the breakthrough curve should be taken into consideration. Altering the structural arrangement of the cut-off wall to accommodate a smaller shape factor increases the contaminant breakthrough time. The proposed solution allows the analysis of a cut-off wall and aquifer system with different inlet boundary conditions and structural arrangements of the cut-off wall.

The combined use of erythropoietin and iron preparations for the management of postpartum anemia: a systematic review and meta-analysis

INTRODUCTION: There are limited data on the effectiveness of erythropoietin in combination with oral ferrotherapy for the management of postpartum anemia. OBJECTIVE: To evaluate the efficacy of erythropoietin in combination with oral iron compared with oral ferrotherapy in puerperas with postpartum haemorrhage. MATERIALS AND METHODS: MEDLINE, Scopus, EBSCOhost and 5 other databases (January 1980 to February 2023) were searched for articles on the use of oral iron in combination with and without erythropoietin for the treatment of post-hemorrhagic anemia in puerperas. Primary outcomes: hemoglobin level, hemoglobin increase, hematocrit, number of blood transfusions, secondary outcomes: ferritin level, serum iron, lactation capacity. The analysis was carried out in accordance with the PRISMA guidelines, 2020. RESULTS: 4 studies were analyzed, 198 women were included. When using erythropoietin in combination with oral ferrotherapy, the cumulative value of the increase in hemoglobin concentration after 5 days, 2 weeks of treatment was significantly higher compared with the control group (mean difference [MD]: 11.83 g/L, 95% CI 4.43–19.23; р = 0.002, MD 10.13 g/L, 95% CI 4.97–15.29; р = 0.0001), respectively. The cumulative mean hemoglobin concentration after 40 days of treatment was significantly higher in the erythropoietin group (MD 11.00 g/L, 95% CI 1.70–20.30; р = 0.02). The cumulative mean hematocrit after 2 weeks of treatment was significantly higher in the erythropoietin group (MD 3.35 %, 95% CI 0.31–6.39; р = 0.03). The use of erythropoietin in combination with oral iron reduces the likelihood of blood transfusion (relative risk 0.12, 95% CI 0.02–0.95; р = 0.04). CONCLUSIONS: A faster hematological response was shown with the combined use of erythropoietin with oral ferrotherapy compared with monotherapy with iron preparations in the management of postpartum anemia. Further studies with sufficient sample sizes are required.