Search Results (26)

Background: Associations of antioxidants in prenatal over-the-counter multivitamin-mineral (OTC MVM) supplements with in-utero oxidative stress (OS), antioxidant capacity, and fetal growth are limited. Our objectives were to determine if five fetal ultrasound measurements [biparietal diameter (BPD), head circumference (HC), abdominal circumference (AC), femur length (FL), and estimated fetal weight] were associated with OTC MVM supplements and with minerals, biomarkers of OS, and total antioxidant capacity in amniotic fluid (AF). Methods: For this retrospective study, 176 pregnant women who had undergone age-related amniocentesis for genetic testing were included. Questionnaires recorded prenatal OTC MVM supplementation (yes, no). Ultrasound measurements for early (16–20 weeks) and late (32–36 weeks) gestation were extracted from medical charts. AF concentrations for 15 minerals and trace elements and OS biomarkers in AF [nitric oxide (NO), thiobarbituric acid-reactive substances (TBARS), and ferric-reducing antioxidant power (FRAP)] were measured at 12–20 weeks of gestation. Associations of AF minerals, OS biomarkers, and ultrasound measures were analyzed using multiple linear regressions. Results: Positive associations were observed between AF TBARS and seven AF minerals/elements (calcium, copper, magnesium, nickel, strontium, zinc and iron). At 16–20 weeks, AF copper, nickel, strontium, and selenium were positively associated with BPD, HC, AC, and FL, respectively, NO was positively associated with FL, and FRAP was inversely associated with estimated weight. At 32–36 weeks, calcium was positively associated with BPD and chromium and arsenic were negatively with HC. At 16–20 weeks, higher AF FRAP was inversely associated with FL and this exposure continued to be inversely associated with estimated weight at 32–36 weeks. Conclusions: Concentrations of AF minerals, trace elements and biomarkers of OS and in-utero antioxidant capacity were linked to specific ultrasound measurements at different stages of gestation, suggesting a complex interplay among in utero OS, antioxidant capacity, OTC MVM supplements, and fetal growth. Full article

This paper investigated how increased soil temperatures affect soil mineralogy and major and trace element oxide concentrations and the implications of these effects on the mobility of potentially toxic elements (PTEs) in heat-affected soils amended with sewage sludge. The aim was to determine the efficiency of sewage sludge as an immobilizer of PTEs in heat-affected PTE-contaminated soils. Soil samples were heated to 150 °C, 300 °C, 500 °C, and 750 °C and later amended with stabilized sewage sludge at different rates. The concentrations of arsenic (As), chromium (Cr), cobalt (Co), copper (Cu), lead (Pb), nickel (Ni), and zinc (Zn) in the different geochemical fractions of the soils were determined before heating, after heating, and after sewage sludge application. Increased soil temperatures affected the mineral assemblage and the concentrations of some major and trace element oxides and the degree of weathering of the soils. These changes were, however, insignificant. The segregation of PTEs into the different soil geochemical fractions before and after heating varied. High soil temperatures resulted in an increase in PTE concentrations in the non-residual fractions of the soil (F1, F2, and F3) with a consequent increase in their mobility. The application of sewage sludge to heated and unheated soils reduced PTE concentrations in the F1 and F2 fractions of both soils, whereas it increased PTE concentrations in the F3 and F4 fractions by up to 30% for As and Cu, 20% for Cd, 25% for Co, 60% for Cr and Ni, 50% for Pb, and 55% for Zn. Significant immobilization of the PTEs was observed in the heat-affected soils that received higher amount of sewage sludge. Fire events could increase the mobility of PTEs in soils, but sewage sludge could still effectively immobilize these PTEs, although it needs to be applied at higher application rates. Full article

Objective: The study aims to assess the overall safety of cultured tilapias in Jeddah City, Saudi Arabia by assessing the impact of infection and anthropogenic pollution on farmed tilapias based on fish sex, body weight, length, and heavy metals contamination. Materials and methods: A total of 111 fish were collected from an aquaculture farm in Hada Al-Sham, Jeddah, Saudi Arabia. Physicochemical parameters of water from the culture system were evaluated. Both ecto- and endoparasites were checked. Haematological, biochemical and histopathological investigations were evaluated. In addition, heavy metals, namely, cadmium (Cd), chromium (Cr), copper (Cu), nickel (Ni), lead (Pb), and zinc (Zn) were evaluated in different fish tissues and water samples from the aquaculture system. Results: The study revealed stressed aquaculture system. Tilapias were infested by both ectoparasites including Trichodina, Icthyophthirius multifiliis, Dactylogrus, and Cichlidogyrus, and endoparasites as Icthyophonus hoferi, the nematode Capillaria and coccidian protozoa. The study showed that male tilapias had greater infestation rates than females and longer and heavier male fish tended to be more susceptible to Dactylogyrus infection. Infected fish showed altered biochemical markers with subsequent increases in inflammatory and oxidative stress markers. The post-mortem lesion in the skin, gill lamellae, intestine, spleen, and liver showed significant pathological remarks. All investigated fish tissues revealed higher rates of heavy metals bioaccumulation compared to the surrounding waters. On the other hand, infected Nile tilapia tissues showed higher rate of metals accumulation compared to non-infected ones. Metals accumulated at a higher rate in the liver followed by kidney, intestine, gills, and muscles, respectively. Conclusions: This study is recognized as the first to address the food safety of farmed tilapias in Jeddah, Saudi Arabia. The results emphasized a significant relation between parasites and heavy metal in disrupting fish defense systems and harming fish’s physiological homeostasis and the histological state of tissues. The parasitized and polluted farmed fish pose health risk to humans due to possible zoonosis from parasitic infections and its subsequent bacterial infections with long-term exposure to toxic chemicals. Addressing the need for a combination of improved aquaculture practices, and stringent regulatory oversight. Full article

In order to understand the distribution, occurrence forms, and influencing factors of chromium (Cr), nickel (Ni), and copper (Cu) in soil aggregates, a five-step extraction method was used to determine their forms in soil aggregates of different sizes in a mountainous area of northern Hebei Province. The ecological risk was evaluated using the geo-accumulation index (I_geo) and primary and secondary comparison value method (RSP). Redundancy analysis (RDA) was used to identify the main factors affecting the distribution and morphology of Cr, Ni, and Cu in soil. The results showed that in vertical distribution, Cr, Ni, and Cu were concentrated in the surface soil, but there was no clear relationship between soil depth and heavy metal content. The distribution characteristics revealed that Cr, Ni, and Cu in soils mainly existed in relatively stable Fe-Mn oxides and residue states, and their morphology in aggregates did not vary considerably with particle size. Furthermore, the RSP results showed that the pollution risk of Cr, Ni, and Cu was higher, with Cr and Ni posing the highest risk in the 0.5–1 mm and 1–2 mm particle size ranges. The RDA results showed that available phosphorus and soil organic matter (SOM) were the main factors that caused the characteristic difference of 1–2 mm aggregate components. Additionally, hydrolyzed nitrogen, cation exchange capacity (CEC), and calcium exchange have positive effects on the residual state of Cr. For Ni, SOM, CEC and exchangeable calcium have positive effects on the binding state of Fe and Mn oxides and carbonate. For Cu, CEC and exchangeable calcium are the key factors that cause the morphological differences of aggregates. Based on the above results, a theoretical basis has been provided for the prevention and control of pollution in the subsequent research area. Full article

In this study, we optimized the traditional composition of AISI 8630 steel and evaluated its corrosion resistance through a series of tests. We conducted corrosion tests in a 3.5% NaCl solution and performed a 720 h fixed-load tensile test in accordance with the NACE TM-0177-2016 standard to assess sulfide stress corrosion cracking (SSCC). To analyze the corrosion products and the structure of the corrosion film, we employed X-ray diffraction and transmission electron microscopy. The corrosion rate, characteristics of the corrosion products, structure of the corrosion film, and corrosion resistance mechanism of the material were investigated. The results indicate that the optimized AISI 8630 material demonstrates excellent corrosion resistance. After 720 h of exposure, the primary corrosion products were identified as chromium oxide, copper sulfide, iron oxide, and iron–nickel sulfide. The corrosion film exhibited a three-layer structure: the innermost layer with a thickness of 200–300 nm contained higher concentrations of alloying elements and formed a dense, cohesive rust layer that hindered the diffusion of oxygen and chloride ions, thus enhancing corrosion resistance. The middle layer was thicker and less rich in alloying elements, while the outer layer, approximately 300–400 nm thick, was relatively loose. Full article

Graphene oxide and its magnetic nanoparticle-based composites are a well-known tool to remove heavy metals from wastewater. Unfortunately, one of the major issues in handling such small particles consists of their difficult removal from treated wastewater (even when their magnetic properties are exploited), due to their very small diameter. One possible way to overcome this problem is to embed them in a macroscopic biopolymer matrix, such as alginate or chitosan beads. In this way, the adsorbent becomes easier to handle and can be used to build, for example, a packed column, as in a traditional industrial adsorber. In this work, the removal performances of two different embedded magnetic nanocomposite adsorbents (MNAs) are discussed. The first type of MNA is based on ferrite magnetic nanoparticles (MNPs) generated by coprecipitation using iron(II/III) salts and ammonium hydroxide, while the second is based on a 2D material composed of MNP-decorated graphene oxide. Both MNAs were embedded in cross-linked alginate beads and used to treat artificial water contaminated with chromium(III), nickel(II), and copper(II) in different concentrations. The yield of removal and differences between MNAs and non-embedded magnetic nanomaterials are also discussed. From the results, it was found that the time to reach the adsorption equilibrium is higher when compared to that of the nanomaterials only, due to the lower surface/volume ratio of the beads, but the adsorption capacity is higher, due to the additional interaction with alginate. Full article

Human exposure to acute and chronic levels of heavy metal ions are linked with various health issues, including reduced children’s intelligence quotients, developmental challenges, cancers, hypertension, immune system compromises, cytotoxicity, oxidative cellular damage, and neurological disorders, among other health challenges. The potential environmental HMI contaminations, the biomagnification of heavy metal ions along food chains, and the associated risk factors of heavy metal ions on public health safety are a global concern of top priority. Hence, developing low-cost analytical protocols capable of rapid, selective, sensitive, and accurate detection of heavy metal ions in environmental samples and consumable products is of global public health interest. Conventional flame atomic absorption spectroscopy, graphite furnace atomic absorption spectroscopy, atomic emission spectroscopy, inductively coupled plasma–optical emission spectroscopy, inductively coupled plasma–mass spectroscopy, X-ray diffractometry, and X-ray fluorescence have been well-developed for HMIs and trace element analysis with excellent but varying degrees of sensitivity, selectivity, and accuracy. In addition to high instrumental running and maintenance costs and specialized personnel training, these instruments are not portable, limiting their practicality for on-demand, in situ, field study, or point-of-need HMI detection. Increases in the use of electrochemical and colorimetric techniques for heavy metal ion detections arise because of portable instrumentation, high sensitivity and selectivity, cost-effectiveness, small size requirements, rapidity, and visual detection of colorimetric nanosensors that facilitate on-demand, in situ, and field heavy metal ion detections. This review highlights the new approach to low-cost, rapid, selective, sensitive, and accurate detection of heavy metal ions in ecosystems (soil, water, air) and consumable products. Specifically, the review highlights low-cost, portable, and recent advances in smartphone-operated screen-printed electrodes (SPEs), plastic chip SPES, and carbon fiber paper-based nanosensors for environmental heavy metal ion detection. In addition, the review highlights recent advances in colorimetric nanosensors for heavy metal ion detection requirements. The review provides the advantages of electrochemical and optical nanosensors over the conventional methods of HMI analyses. The review further provides in-depth coverage of the detection of arsenic (As), cadmium (Cd), chromium (Cr), copper (Cu), mercury (Hg), manganese (Mn), nickel (Ni), lead (Pb), and zinc (Zn) ions in the ecosystem, with emphasis on environmental and biological samples. In addition, the review discusses the advantages and challenges of the current electrochemical and colorimetric nanosensors protocol for heavy metal ion detection. It provides insight into the future directions in the use of the electrochemical and colorimetric nanosensors protocol for heavy metal ion detection. Full article

Soil contaminated with petroleum substances is classified as hazardous, i.e., particularly harmful to the proper functioning of environmental ecosystems. It is therefore necessary to take measures to restore the homeostasis and ecological potential of degraded areas. The study aim was to determine the impact of bentonite, compost, and calcium oxide (CaO) on trace element content in the maize grown on diesel oil (DO)-contaminated soil. Increasing doses of the petroleum substance increased the accumulation of chromium (Cr), lead (Pb), copper (Cu), nickel (Ni), manganese (Mn), cobalt (Co), and cadmium (Cd) in maize. The largest increases were found for Cu (by 76%), Co (by 73%), and Pb (by 42%). All soil amendments proved useful for in situ stabilization of anthropogenically transformed soils. Bentonite reduced Cr (by 94%), Cu (by 84%), and Mn content (by 53%), while compost reduced the contents of Cu (by 75%), Mn (by 44%), and iron (Fe—by 29%) in maize. CaO significantly reduced the levels of Cr (by 94%), Cu (by 84%), Ni (by 66%), Mn (by 32%), Co (by 72%), zinc (Zn—by 30%), and Cd (by 22%) in maize. The effects of compost and bentonite on maize chemical composition were smaller than that achieved with CaO, and the direction of changes in elements content depended on the DO dose and the element type. Full article

In recent years, during industrial development, the expanding discharge of harmful metallic ions from different industrial wastes (such as arsenic, barium, cadmium, chromium, copper, lead, mercury, nickel, selenium, silver, or zinc) into different water bodies has caused serious concern, with one of the problematic elements being represented by selenium (Se) ions. Selenium represents an essential microelement for human life and plays a vital role in human metabolism. In the human body, this element acts as a powerful antioxidant, being able to reduce the risk of the development of some cancers. Selenium is distributed in the environment in the form of selenate (SeO₄^2–) and selenite (SeO₃^2–), which are the result of natural/anthropogenic activities. Experimental data proved that both forms present some toxicity. In this context, in the last decade, only several studies regarding selenium’s removal from aqueous solutions have been conducted. Therefore, in the present study, we aim to use the sol–gel synthesis method to prepare a nanocomposite adsorbent material starting from sodium fluoride, silica, and iron oxide matrices (SiO₂/Fe(acac)₃/NaF), and to further test it for selenite adsorption. After preparation, the adsorbent material was characterized by scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX). The mechanism associated with the selenium adsorption process has been established based on kinetic, thermodynamic, and equilibrium studies. Pseudo second order is the kinetic model that best describes the obtained experimental data. Also, from the intraparticle diffusion study, it was observed that with increasing temperature the value of the diffusion constant, K_diff, also increases. Sips isotherm was found to best describe the experimental data obtained, the maximum adsorption capacity being ~6.00 mg Se(IV) per g of adsorbent material. From a thermodynamic point of view, parameters such as ΔG⁰, ΔH⁰, and ΔS⁰ were evaluated, proving that the process studied is a physical one. Full article

Petroleum-derived substances have become the factor adversely affecting the soil quality and, also, crop production. However, the ability to immobilise contaminants is limited in anthropogenically altered soils. Therefore, a study was undertaken to evaluate the effects of soil contamination with diesel oil (0, 2.5, 5 and 10 cm³ kg⁻¹) on the contents of trace elements in the soil and determine the suitability of different neutralising materials (compost, bentonite and calcium oxide) for the in situ stabilisation of soil contaminated with this petroleum derivative. In the soil contaminated with the highest dose of diesel oil (10 cm³ kg⁻¹), a decrease in chromium, zinc and cobalt and an increase in the total nickel, iron and cadmium concentrations were found in the series without the addition of neutralising materials. Remediation with compost and mineral materials contributed to a significant reduction of nickel and iron, as well as cobalt, in soil (calcium oxide only). All materials used contributed to an increase in cadmium, chromium, manganese and copper in the soil. The above-mentioned materials (most notably calcium oxide) can be successfully used to reduce the effect of diesel oil on the contents of some trace elements in soil. Full article

Pol(vinyl chloride) or PVC has functional properties that enable its use in many industrial applications. It suffers from aging, however, in harsh conditions (e.g., elevated temperature or high humidity levels) if oxygen is present. One way to enhance the photostability of PVC is to blend it with additives. Thus, thin films were made by mixing PVC with clotrimazole, and five metal oxide (titanium, copper, cobalt, chromium, and nickel oxides) additives. The metal oxides and clotrimazole were added at concentrations of 0.1 and 0.5% by weight, respectively. The effect of the metal oxide nanoparticles accompanied by clotrimazole on the photodegradation of PVC was then assessed. The results indicated that the additives have a stabilizing effect and protect PVC against photodegradation significantly. The formation of polymeric fragments of small molecular weight containing carbon-carbon double bonds and carbonyl groups was lower in the blends containing metal oxide nanoparticles and clotrimazole than in unblended PVC. Similarly, the decrease in weight was much less for the films blended with additives. Additionally, surface analysis of the irradiated polymeric films showed significantly lower damage in the materials containing additives. The most effective additive in the stabilization of PVC was nickel oxide nanoparticles. The metal oxides are highly alkaline and act as scavengers for the hydrogen chloride produced during the photodegradation of PVC. They additionally act as peroxide decomposers. In contrast, clotrimazole can absorb harmful radiation and act as an ultraviolet absorber due to its heteroatom and aromatic content. Thus, the use of a combination of metal oxide nanoparticles and clotrimazole led to significant improvement in the resistance of PVC toward photodegradation. Full article

Globally, efforts are being made to upgrade and improvise the current wastewater treatment technologies. Industrial wastewater is being generated exponentially, owing to the expansion in chemical industries and civilizations necessitating remediation to prevent further environmental damage and lower associated human risks. In this work, iron oxide nanoparticles (IONPs) have been developed and employed as an efficient nanocatalyst for heavy metal adsorption via the chemical route. The shape, absorbance optical, crystal phase, and magnetization of as-prepared magnetic nanostructures were characterized using XRD (X-ray diffraction), UV-Vis (ultraviolet-visible), HRTEM (High-resolution transmission electron microscopy), FTIR (Fourier transfer infrared spectroscopy), and VSM. Further, the adsorption ability of iron oxide to remove the bulk metallic elements considering cadmium (Cd), lead (Pb), zinc (Zn), chromium (Cr), copper (Cu), and nickel (Ni), present in industrial effluents, were studied. The Maghemite Fe₂O₃ crystal phase having an R-3c group is observed in the XRD results. An identical shape of spherical nanostructures is determined using TEM including ≈21 nm for pure Fe₂O₃. A removal % was studied by using ICP-OES, and showed a Cr (61.2%), Cd (98%), Cu (66%), Ni (64%), Zn (97%), and Pb (98%) removal ability. The application of such monitored nanomaterials to effluent cleaning and sewage discharge emitted via labs and petrochemical industries could be expanded. Full article

Herein, the aqueous extract of Portulaca oleracea has been used as a safe, cheap, eco-friendly, and applicable scale-up method to bio-fabricate copper oxide nanoparticles (CuO-NPs). The character of CuO-NPs were determined using UV-vis spectroscopy, Fourier transform infrared (FT-IR), X-ray diffraction (XRD), Transmission electron microscopy (TEM), Energy dispersive X-ray(EDX), Dynamic light scattering (DLS), and zeta potential. Spherical and crystalline CuO-NPs with a size range of 5–30 nm at a maximum surface plasmon resonance of 275 nm were successfully fabricated. The main components of the green-synthesized particles were Cu and O with weight percentages of 49.92 and 28.45%, respectively. A Zeta-potential value of −24.6 mV was recorded for CuO-NPs, indicating their high stability. The plant-based CuO-NPs showed promising antimicrobial and catalytic activity in a dose-dependent manner. Results showed that the synthesized CuO-NPs had the efficacy to inhibit the growth of pathogens Staphylococcus aureus, Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa, and Candida albicans with low MIC values in the ranges of 6.25–25 µg/mL. The highest decolorization percentages of tanning wastewater were attained under sunlight irradiation conditions at a concentration of 2.0 mg/mL after 200 min with percentages of 88.6 ± 1.5% compared to those which were recorded under dark conditions (70.3 ± 1.2%). The physicochemical parameters of tanning wastewater including total suspended solids (TSS), total dissolved solids (TDS), chemical oxygen demand (COD), biological oxygen demand (BOD), and conductivity under optimum conditions were significantly decreased with percentages of 95.2, 86.7, 91.4, 87.2, and 97.2%, respectively. Interestingly, the heavy metals including cobalt (Co), lead (Pb), nickel (Ni), cadmium (Cd), and chromium (Cr (VI)) decreased with percentages of 73.2, 80.8, 72.4, 64.4, and 91.4%, respectively, after treatment of tanning wastewater with CuO-NPs under optimum conditions. Overall, the plant-synthesized CuO-NPs that have antimicrobial and catalytic activities are considered a promising nano-catalyst and environmentally beneficial to wastewater treatment. Full article

Experimental liver injury with hepatocelluar necrosis and abnormal liver tests is caused by exposure to heavy metals (HMs) like aluminum, arsenic, beryllium, cadmium, chromium, cobalt, copper, iron, lead, mercury, molybdenum, nickel, platinum, thallium, titanium, vanadium, and zinc. As pollutants, HMs disturb the ecosystem, and as these substances are toxic, they may affect the health of humans and animals. HMs are not biodegradable and may be deposited preferentially in the liver. The use of animal models can help identify molecular and mechanistic steps leading to the injury. HMs commonly initiate hepatocellular overproduction of ROS (reactive oxygen species) due to oxidative stress, resulting in covalent binding of radicals to macromolecular proteins or lipids existing in membranes of subcellular organelles. Liver injury is facilitated by iron via the Fenton reaction, providing ROS, and is triggered if protective antioxidant systems are exhausted. Ferroptosis syn pyroptosis was recently introduced as mechanistic concept in explanations of nickel (Ni) liver injury. NiCl₂ causes increased iron deposition in the liver, upregulation of cyclooxygenase 2 (COX-2) protein and mRNA expression levels, downregulation of glutathione eroxidase 4 (GPX4), ferritin heavy chain 1 (FTH1), nuclear receptor coactivator 4 (NCOA4) protein, and mRNA expression levels. Nickel may cause hepatic injury through mitochondrial damage and ferroptosis, defined as mechanism of iron-dependent cell death, similar to glutamate-induced excitotoxicity but likely distinct from apoptosis, necrosis, and autophagy. Under discussion were additional mechanistic concepts of hepatocellular uptake and biliary excretion of mercury in exposed animals. For instance, the organic anion transporter 3 (Oat3) and the multidrug resistance-associated protein 2 (Mrp2) were involved in the hepatic handling of mercury. Mercury treatment modified the expression of Mrp2 and Oat3 as assessed by immunoblotting, partially explaining its impaired biliary excretion. Concomitantly, a decrease in Oat3 abundance in the hepatocyte plasma membranes was observed that limits the hepatic uptake of mercury ions. Most importantly and shown for the first time in liver injury caused by HMs, titanium changed the diversity of gut microbiota and modified their metabolic functions, leading to increased generation of lipopolysaccharides (LPS). As endotoxins, LPS may trigger and perpetuate the liver injury at the level of gut-liver. In sum, mechanistic and molecular steps of experimental liver injury due to HM administration are complex, with ROS as the key promotional compound. However, additional concepts such as iron used in the Fenton reaction, ferroptosis, modification of transporter systems, and endotoxins derived from diversity of intestinal bacteria at the gut-liver level merit further consideration. Full article

In the framework of sustainability, water shortages and water pollution are two important aspects to be considered. Proposing efficient and low-impact technologies is of paramount importance to promote circular economies associated with the use of water in the industrial context, especially in the textile industry. In this work, the application of a set of magnetic nanostructured adsorbents (MNAs) to cleanse metal ions from textile wastewaters was studied and analyzed. MNAs were generated with a low-cost process, involving iron (II/III) salts (e.g., chlorides), sodium or ammonium hydroxide solutions, and graphene oxide, obtained from graphite by a modified Hummers’ method at room temperature. The shape and the size were studied with transmission electron microscopy. Adsorbents were tested with different metal ions (e.g., copper, chromium (III), and nickel). Metal ion concentrations were analyzed by means of inductively coupled plasma optical emission spectroscopy (ICP-OES), and adsorption isotherms were characterized. From the results, the MNAs exhibited the capability of removing metal ions up to a yield of 99% for Cr³⁺, 94.7% for Cu²⁺, and 91.4% for Ni²⁺, along with adsorption loads up to 4.56 mg/g of MNAs. Full article