Nickel uptake in leafy greens from contaminated soil: an investigation into phytoavailability and health risk assessment using in vitro digestion model.

Nickel (Ni) is a toxic metal that not only pollutes the environment but also causes harmful impacts on plant growth and human health. Therefore, it is crucial to assess the relationship between the phytoavailability of Ni in soil and its accumulation in edible and non-edible parts of vegetables. A pot experiment was conducted to investigate Ni uptake in three different leafy vegetables, spinach (Spinacia oleracea L.), lettuce (Lactuca sativa L.), and fenugreek (Trigonella foenum-graecum L.), grown in soil artificially contaminated with Ni at three different treatment levels (100 mg kg-1, 200 mg kg-1, and 300 mg kg-1). The potential dietary toxicity of these vegetables in humans was examined by using an in vitro digestion model. The lowest and highest chlorophyll contents were detected in lettuce at 300 mg kg-1 of Ni concentration and in control plants of spinach. Their values were 34.16 ± 3.01 (SPAD unit) and 53 ± 3.7673 (SPAD unit), respectively. Among the three vegetables, lettuce and spinach at 300 mg kg-1 exhibited the highest accumulation of Ni, with 43 mg kg-1 in edible parts and 182 mg kg-1 in non-edible parts. Furthermore, health risk index (HRI) values were found to be > 1 for lettuce and fenugreek at Ni concentrations of 200 and 300 mg kg-1 for both children and adults. The average bioaccessibility of Ni in lettuce, fenugreek, and spinach during the gastrointestinal phase was 32-23%, 24-10%, and 45-37%, respectively, at a Ni concentration of 300 mg kg-1. All three vegetables grown on Ni-contaminated soil may potentially contribute to food chain toxicity. The HRI values being > 1 suggest that these vegetables are unsafe for consumption. Monitoring of Ni concentration in leafy vegetables is essential to minimize human health risks associated with food chain contamination.

Assessment and computational bioevaluation of heavy metals from selected cosmetic products.

Heavy metal toxicity in environment has been an increasing issue for last decades, though now the attention has diverted to presence of heavy metals in cosmetic products. The aim of this study was to determine the concentration of selected heavy metals in cosmetic products (lipsticks and foundations) using ICP-OES. Health risk assessment was done by using hazard quotient (HQ) and hazard index (HI). HQ for lipsticks was below the safe limit (HQ = < 1) while for foundations it exceeded the safe limit (HQ = >1). Mostly, mercury (Hg) and iron (Fe) were found to be exceeding the permissible limit, the allowed limits are Hg, 1 ppm; Fe, 10 ppm; Cd, 0.3 ppm; and Cr, 1 ppm. Iron was found to be highest in lipsticks (123.86 ± 1.05 ppm) as well as in foundations (34.52 ± 0.08 ppm). Health risk assessment was done by using hazard quotient (HQ) and hazard index (HI). HQ for lipsticks was below the safe limit (HQ = < 1) while for foundations it exceeded the safe limit (HQ = >1). To understand the binding pattern of heavy metals to skin targets, molecular docking studies were carried out. This revealed the potentially harmful behavior of these heavy metals on the skin. This will provide new direction for the structural changes of consistence and activity of macromolecules in our body. Research proved that prolonged use of cosmetic products containing heavy metals can be harmful and sometimes fatal to human life as these heavy metals can penetrate through the skin and target the skin enzymes, disrupting their normal function leading to various skin related issues such as dermatitis (itching, redness, burning) hence the monitoring of cosmetic products is necessary for safety of human being.

Microbeads in personal care products sold in Pakistan: extraction, quantification, characterization, and buoyancy analysis.

Microbeads used in personal care products (PCPs) as an exfoliating agent or as a sorbent phase for delivering active ingredients are the most common sources of microplastics. The release of these plastic microbeads into aquatic environments has raised significant concerns due to their direct availability for ingestion by organisms upon entering the recipient waters. In this study, twelve personal care products (PCPs; 5 face washes and 7 scrubs) were analyzed for microbead content, size, polymer type, and buoyant behavior. Among the face washes, the highest microbead content (i.e., 11 ± 1.2 mg/g) was found in Neutrogena (NS), while the lowest was found in Nivea (NI) with 0.33 ± 0 mg/g. In case of scrubs, Cool and Cool (CL) contained a higher concentration of microbeads (i.e., 57.08±14.15 mg/g) and a lower concentration was found in Yong Chin (YC) (i.e., 10.5±1.5 mg/g). The sizes of microbeads ranged from 3.14 ± 0 to 747 ± 313 µm, and most of the isolated microbeads showed negative buoyant behavior in both freshwater and seawater. The FTIR spectra showed that the microbeads were mainly composed of ethyl-vinyl acetate (66.66%), high-density polyethylene (16.66%), polyethylene terephthalate (8.3%), and nitrile (8.3%). The presence of plastic microbeads in PCPs highlights the need to regulate their use as an exfoliating agent and to raise public awareness to prevent the discharge of these persistent and potentially harmful elements into the environment.

Impacts of stormwater pipe materials and pipe repairs on stormwater quality: a review.

The water quality implications of transferring stormwater through pipes composed of concrete (new and used), polyvinyl chloride (PVC), galvanized corrugated steel (GCS), high-density polyethylene (HDPE), and pipes subjected to cured in place pipe (CIPP) and spray in place pipe (SIPP) trenchless repair technologies on stormwater quality are reviewed. Studies involve either the use of flowing water or an immersion experimental design, with data showing contact with pipe materials can affect stormwater quality parameters including pH, electrical conductivity (EC), and concentrations of minerals, metals, and organic constituents, e.g. styrene. 'In-transport' changes in pH (1-3 units), EC (2-3-fold), bicarbonate (3-44-fold), and calcium (2-17-fold) in stormwaters were reported following exposure to concrete pipes. Differences between the use of synthetic and field-collected stormwater were identified, e.g. turbidity levels in field-collected stormwater reduced on passage through all pipe types, compared to synthetic water where levels of turbidity on exposure to concrete and cement-based SIPP increased slightly. Transfer through PVC and HDPE pipes had minimal effects on physicochemical parameters, whereas exposure to galvanized corrugated steel pipes led to increases in EC, Zn, and Pb. Though limited data was available, the use of CIPP repairs and associated waste condensate generated during thermal curing and/or incomplete curing of resins was identified to release organic contaminants of concerns (e.g. styrene, vinylic monomers, dibutyl phthalate (DBP), diethyl phthalate (DEP), and benzaldehyde). The implications of findings for both future research and stakeholders with responsibility for reducing diffuse pollution loads to receiving waters are considered.

Microplastic pollution in the surface water and sediments from Kallar Kahar wetland, Pakistan: occurrence, distribution, and characterization by ATR-FTIR.

This study reports the distribution of microplastics in surface water and sediments collected from Kallar Kahar wetland, Punjab, Pakistan, which is a game reserve and hosts migratory birds during winter season. Microplastics were extracted using density separation and wet oxidation method. The microplastics identification was done under a stereo-microscope, and their polymer compositions were characterized using an attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy. The average abundance of microplastics in water and sediment samples was 88 ± 14.5 items/L and 5720 ± 2580 items/kg, respectively. The dominant shape groups of microplastics in water were fiber (58.7%), irregular fragments (32.4%), and beads (8.7%) with dominant colors as transparent > black > yellow ≈ white > red > green > pink > blue. Similar distribution in sediments was found, i.e., fiber (61.2%), irregular fragments (28.4%), and beads (10.3%) with dominant colors as transparent > pink > white > red ≈ black > blue > brown > green ≈ yellow. The ATR-FTIR spectra of visible microplastics were identified to be polypropylene (PP), high density polyethylene (HDPE), ethylene vinyl acetate (EVA), low density polyethylene (LDPE), nitrile, polymethyl methacrylate (PMMA), latex, and polyethylene terephthalate (PETE). In the study area, recreational activities, improper waste disposal, and runoff from catchment areas are the main reasons for the contamination of microplastics in the Lake. The pollution load can be minimized by taking measures such as creating awareness, promotion of ecotourism, and reducing plastic use.

Experimental Calculations of Metals Content in Skin-Whitening Creams and Theoretical Investigation for Their Biological Effect Against Tyrosinase Enzyme.

The demand for skin-whitening creams (SWCs) has increased rapidly worldwide due to sharp rise in product advertisements in the media and the growing awareness. Metals are present either as impurities or added intentionally in creams and may have toxic effects on users. The present study was carried out to determine the content of metals such as mercury (Hg), cadmium (Cd), lead (Pb), arsenic (As), chromium (Cr), nickel (Ni), cobalt (Co), copper (Cu), zinc (Zn), and iron (Fe) in fifteen skin-whitening creams marketed at local shops in Islamabad, Pakistan. The concentrations of metals were analyzed by inductive coupled plasma-optical emission spectrometer (ICP-OES) after digestion with a mixture of HNO3, HCl, and H2O2. The skin-whitening creams were found to have metal concentrations in parts per million (ppm) in the following range: Hg (1.0-18,210 ppm), Co (0.1992-1.9931 ppm), Cr (1.0453-2.7455 ppm), Cu (0.6987-0.1997 ppm), Fe (8.8868-28.6213 ppm), Ni (0.7487-1.5958 ppm), Pb (0.2997-4.7287 ppm), and Zn (7819.2-39,696.7 ppm). As and Cd were not detected in any of the fifteen skin-whitening creams. Only one cream (L'Oréal Paris White Perfect) was found in safe limits defined by the Food and Drug Administration for cosmetics. In order to elucidate the mechanism of lower production of melanin in presence of heavy metals, a molecular docking study was carried out by using Molecular Operating Environment (MOE) software. A good correlation was observed between experimental findings and molecular docking studies.

Comparative Study of Protective Effect of Cimetidine and Verapamil on Paracetamol-Induced Hepatotoxicity in Mice.

Paracetamol, chemically known as acetaminophen, if taken in higher doses has hepatotoxic potential. Cimetidine by inhibiting the cytochromal enzymes and reducing the production of the toxic metabolite can reduce the hepatotoxic potential while Verapamil can act as a hepatoprotective by maintaining calcium homeostasis. The present study was conducted to study the hepatoprotective activity of Cimetidine and Verapamil against the toxicity induced by paracetamol. In addition to the group receiving only distilled water or 300 mg/kg paracetamol additional groups were added treated with 150 mg/kg Cimetidine and Verapamil alone or both. The Liver function tests and histopathology revealed hepatotoxicity in the group receiving paracetamol (PCM) while normal parameters were observed in the groups receiving Cimetidine and Verapamil. Our results strongly suggested that Cimetidine and Verapamil possess hepatoprotective potential against paracetamol induced hepatotoxicity.

A review on the potential uses of red mud as amendment for pollution control in environmental media.

Red mud is a solid waste of bauxite processing by Bayer process which involves caustic digestion of Al-containing mineral for alumina production. The global inventory of red mud waste reached an estimated amount of 4 billion tons in 2015, increasing at an approximate rate of 120 million tons per year. Therefore, its management is becoming a global environmental issue for the protection of environment, and the need for awareness in this regard is becoming crucial. Although red mud is not considered as a hazardous material in many countries, its high alkalinity and fine particle size may pose significant environmental threat, and it is found to be an interesting material for environmental remediation purposes due to rich iron content. This paper provides a review of possible remedial applications of red mud in various environmental compartments. Modification of red mud creates novel opportunities for cost-effective and efficient removal of metal ions, inorganic anions, dyes, and phenols from wastewater and acid mine drainage. Re-vegetation of red mud disposal sites, treatment of metal-contaminated acidic soils presents the usefulness of this material but less research has been done so far to investigate its use in the stabilization of polluted sediments. On the other hand, leaching and eco-toxicological tests have also revealed that red mud does not pose high toxicity to the environment making it suitable for the treatment of contaminated media. Nevertheless, neutralization of red mud is recommended for its safe disposal and secure application in any environmental media.

Capping of marine sediments with valuable industrial by-products: Evaluation of inorganic pollutants immobilization.

In-situ capping of polluted sediment is considered as an inexpensive and effective treatment technology to immobilize contaminants in a short time. In this remediation technique sediments are capped by placing a layer of sand, clean sediment or other materials over sediments in order to mitigate risk. In this study, low cost industrial by products (bauxaline, steel slag, and mixture of the two products) were applied as capping agents. A bench scale laboratory experiment in aquariums was performed to evaluate their effects on Cd, Zn, As, and Cr mobility from an artificially contaminated marine sediment. Without capping, all the contaminants are constantly released with various kinetic depending of mineral oxidation or dissolution or leaching. Nevertheless, release did not exceed 31% of the initial amount of pollutant. Capping sediment with steel slag, bauxaline and their mixture totally captured Cd, Zn, and As. In the case of Cr, only steel slag actively blocked its release. A kinetic model was developed to model As and Cr release, with and without capping. The release times for Cr and As from the sediment were close to 6 days. In the presence of capping agents, the capture time for Cr was found to be 57 days for steel slag, and 7 days for bauxaline. Despite a high capture time, steel slag was the best capping agent since bauxaline matrix was a source of Cr and rapidly released it (release time = 1 day). The results indicated that steel slag and its mixture additive can be used as potential capping materials for the remediation of contaminated sites due to their significant entrapping of Cd, Zn, As, and Cr.

Sediment-bound trace metals in Golfe-Juan Bay, northwestern Mediterranean: Distribution, availability and toxicity.

The concentration, potential mobility, cation exchange capacity and toxicity of eight sediment-bound metals in Golfe-Juan Bay, France were examined. Results revealed significant spatial gradient of metal contamination along Golfe-Juan coast. The distribution and concentration of the metals appear to be influenced by the geochemical properties of the sediment, proximity to anthropogenic sources and general water circulation in the bay. The portion of trace metals found in the exchangeable, carbonate, oxidizable and reducible fractions of the sediment constitute 31%-58% of the total sediment-bound trace metal content, suggesting significant potential for remobilization of metals into the water column. Pb and Ni content of the sediment exceed the limits of the French marine sediment quality. Whole sediment extracts showed acute toxicity to marine rotifers. This study concludes that monitoring and management of sediment-bound trace metals in Golfe-Juan Bay are important so as not to underestimate their availability and risk to the marine ecosystems.

Use of neutralized industrial residue to stabilize trace elements (Cu, Cd, Zn, As, Mo, and Cr) in marine dredged sediment from South-East of France.

Management of marine dredged sediments polluted with trace elements is prime issue in the French Mediterranean coast. The polluted sediments possess ecological threats to surrounding environment on land disposal. Therefore, stabilization of contaminants in multi-contaminated marine dredged sediment is a promising technique. Present study aimed to assess the effect of gypsum neutralized bauxaline(®) (bauxite residue) to decrease the availability of pollutants and inherent toxicity of marine dredged sediment. Bauxaline(®), (alumia industry waste) contains high content of iron oxide but its high alkalinity makes it not suitable for the stabilization of all trace elements from multi-contaminated dredged sediments. In this study, neutralized bauxaline(®) was prepared by mixing bauxaline(®) with 5% of plaster. Experiments were carried out for 3 months to study the effect of 5% and 20% amendment rate on the availability of Cu, Cd, Zn, As, Mo, and Cr. Trace elements concentration, pH, EC and dissolved organic carbon were measured in all leachates. Toxicity of leachates was assessed against marine rotifers Brachionus plicatilis. The Results showed that both treatments have immobilization capacity against different pollutants. Significant stabilization of contaminants (Cu, Cd, Zn) was achieved with 20% application rate whereas As, Mo, and Cr were slightly stabilized. Toxicity results revealed that leachates collected from treated sediment were less toxic than the control sediment. These results suggest that application of neutralized bauxaline(®) to dredged sediment is an effective approach to manage large quantities of dredged sediments as well as bauxite residue itself.

Ex-situ evaluation of bauxite residues as amendment for trace elements stabilization in dredged sediment from Mediterranean Sea: A case study.

Stabilization of marine dredged sediments contaminated with multi-elements is a challenging task in choosing the appropriate sorbent and application dosage. The present study investigates the possibility of using bauxite residues (Bauxaline® and Bauxsol) as amendment for the treatment of contaminated sediment. A pilot scale experiment was conducted for three months to stabilize trace elements in composted contaminated sediment sample using 5% by-product amendment. The results showed that after 3months of treatment, cationic trace elements were effectively immobilized but increased leaching of anionic pollutants was observed. Increased leaching of anionic pollutants could be limited by addition of higher quantities of amendments. The total content of available pollutants decreased in stabilized sediments but this treatment has no effect on the classification of waste. The leachates were then evaluated for acute toxicity using estuarine rotifers Brachionus plicatilis. Bauxite residues can be inexpensive choices for the stabilization of cationic pollutants in dredged sediments.