Atomic Absorption Spectrometer Research Articles

Efficient biosorption of Zn(II), Cd(II), and Pb(II) by Aspergillus brasiliensis in industrial wastewater coupled with electrochemical monitoring via sensor enhanced with modified silver nanoparticles.

This work investigates the use of Aspergillus brasiliensis, this particular species of Aspergillus, as a biosorbent for the first time. It is employed to biosorption Zn(II), Cd(II), and Pb(II) and combines the biosorption experiments with electrochemical measurements for in situ analysis. For the experiments, a batch system was employed with the dead biomass. In order to determine the biosorption capacity, the impact of several operational parameters was examined, including pH, temperature, agitation speed, contact time, and initial metal concentration, and the optimum values were 5, 30°C, 150rpm, 2h, and 150ppm, respectively. Using 0.2g biomass in 100mL solution, the maximal uptake of Zn(II), Cd(II), and Pb(II) at ideal conditions was determined to be 33.67, 24.51, and 36.76, respectively. The Langmuir and Freundlich isotherm model was studied for the biosorption process. An electrochemical sensor using nanomaterials is designed and constructed to monitor the concentration of these metals. The silver nanoparticles functionalized with thiosemicarbazide and 6-mercaptohexanoic acid (mercaptohexanoylhydrazinecarbothioamide-coated silver nanoparticles, MHHC-AgNPs) linked to the carboxylated multi-walled carbon nanotubes (MWCNTs) were utilized for glassy carbon electrode modification (MHHC-AgNPs/MWCNTs/GCE). The concentration range of Zn(II) is 0.7-173µg/L, Cd(II) is 1.18-293µg/L, and Pb(II) is 2.17-540µg/L. The detection limits for Zn(II), Cd(II), and Pb(II) are 0.036µg/L, 0.15µg/L, and 0.16µg/L, respectively. Under optimized conditions, these results were obtained using the differential pulse anodic stripping voltammetry method (DPASV). The successful detection of Zn(II), Cd(II), and Pb(II) was achieved by effectively preventing interference from other common ions. It was effectively employed for measuring ions in industrial wastewater, and the results obtained aligned with those acquired from an atomic absorption spectrometer (AAS). Thus, Aspergillus brasiliensis species, along with this electrochemical sensor, can be used to remediate and monitor environmental pollution, Zn(II), Cd(II), and Pb(II), successfully.

Effect of Contact Time on the Sorption of Metal Ions Associated with Produced Water on Pulverized Oyster Shell (OS) as Adsorbent

The aim of this research is to investigate Metal ion sorption potentials of pulverized Oyster Shell as adsorbent in produced water from selected flow stations in the Niger Delta region of Nigeria. Produced water samples were collected from six (6) different oil drilling installations (CC7T, CC8T, WELL 2 GSS, WELL 8 TEB, AZUZUAMA ST 1, AZUZUAMA ST 2) around the Niger Delta area of Nigeria. The waste oyster shell was collected in Akpan-Andem Market in Uyo, Akwa-Ibom State and processed using well established protocols. Atomic Absorption Spectrometer (AAS) was used to determine selected metals’ Nickel (Ni), Cobalt (Co), Copper (Cu), Iron (Fe), Lead (Pb), Calcium (Ca) and Potassium (K) concentrations. The obtained values for Nickel ranged from 0.076mg/l at AZUZU-AMA ST1 flow station to 2.882 mg/l at WELL2-GSS flow station with average value of 0.745 mg/l. The obtained value for Cobalt ranged from ˂0.001 mg/l at CC-8T and CC-7T to 0.277 mg/l at AZUZUAMA ST1. Values obtained for Cu, Fe, Pb, Ca, and K ranged between: 0.195 mg/l at WELL2-GSS to 0.449 mg/l at AZUZU-AMA ST1; 2.785 mg/l to 89.279mg/l; ˂0.001 mg/l to 0.483 mg/l; 16.217 mg/l to 92.714 mg/l and 96.386 mg/l to 105.416 mg/l respectively. Generally, the amount of metal ions absorbed/adsorbed onto pulverized Oyster shell (OS) increased swiftly within 2 hours and slowly with further increase of contact time and then tended to be stable. For pulverized Oyster shell adsorbent, the adsorption/absorption capacity decreases with the increasing contact time. The adsorbent (OS) isn’t good material for removal of Calcium and Cobalt in produced water but was very effective adsorbent for Ni, Fe, and Pb removal in produced water and less effective for Cu and K removal from produced water. The study underscores the need to further probe outcome of above research at different pH and other relevant variables as well as compares its efficiency with other detoxification technologies like Detoxification by chemical reaction (DCR) technology.

Human health risk of exposure to potentially toxic metals (PTMS) in indoor settled dusts from selected worship centres (WCS)

The study aimed to determine the concentration of potentially toxic metals (PTMs) and the health risk of exposure to indoor dust from worship centres in Abeokuta, Nigeria. Twenty-four (24) dust samples were collected from various corners of selected worship centres. One (1) gram of the sieved dust was digested using aqua regia. PTM analyses were done using an Atomic Absorption Spectrometer (AAS). The result revealed the presence of Iron (Fe)> Zinc (Zn)>Manganese (Mn)> Lead (Pb) > Copper (Cu) >Nickel (Ni) > Cadmium (Cd) (1050; 81.6; 72.5; 3.304; 2.43; 0.516; 0.076 mg/kg) respectively. The PTMs were within the permissible limit for PTMs in dust stated by UK and Dutch Intervention. Pollution indices revealed Zn as the primary pollutant in the dust. A significant association between Zn, Cu, Ni and Cd while that of Mn and Fe suggest a common origin of anthropogenic and lithogenic sources respectively (p<0.01). Health risk assessment revealed inhalation as the major pathway of PTM exposure with the children population being the most susceptible. Hazard index (HI) values were <1, showing a non-significant non-cancer effect on exposure while the cancer risk estimate shows no carcinogenic risk. Conclusively, the selected worship centres have no PTM concentration of health concern at the time of the investigation. However, regular wet cleaning and close monitoring of the worship centres should be considered.

Mercury contamination of soil and Matricaria chamomilla in selected regions of the Slovak Republic

Abstract Background The aim of our study was to determine the amount of mercury in Chamomile. In certain parts of Slovakia, such as Middle Spiš region in Eastern Slovakia, there has been reports of higher concentration of mercury in the soil. Heavy metals, including mercury, can enter human organism by ingestion. In case of using Chamomile infusions orally there is a risk of administration of mercury into the organism through digestive system. Methods We monitored mercury presence in Chamomile (Matricaria chamomilla) (n = 20) and the soil. We determined the mercury concentration by using the flameless atomic absorption spectrometer - Advanced Mercury Analyzer (AMA-254). Results Chamomile: The lowest concentration was in the roots (0.513 mg.kg-1). The second lowest was in the flower stem samples (1.105 mg.kg-1). The concentration of mercury was higher in the leaves (2.205 mg.kg-1). The highest was measured in the flower (2.541 mg.kg-1). Soil: The mercury content in soil in the entire territory of Slovakia is higher compared to the soil in the world. During our measurements, the concentration of mercury in the soil samples in the territory of Middle Spiš ranged from 100 to 500 mg.kg-1. Conclusions We have to take into account that the quality and contents of the soil are important for the crops, as it will entail their contents. With the knowledge of exceeded norms of mercury content in Slovak soils, it is crucial to monitor the mercury concentration in plants that are harvested there. Key messages • In the examined samples of Chamomile we found mercury, with its highest concentration in flowers and lowest in roots. • In the regions with significant mercury contamination it is crucial to monitor mercury content in harvested plants and to be cautious in regards of their consumption.

Mineral imbalance and cardiovascular disease in animals of the canine (Canidae) and feline (Felidae) families: a study in Russian zoos

It is important to consider the full spectrum of complex interactions between mineral elements and biologically active substances to evaluate the development of cardiovascular disease (CVD) in animals, in addition to the classical physiological approach. This study aimed to assess changes in mineral element levels in wild and exotic animals in relation to their cardiovascular diseases. A total of 171 animals, including 128 healthy and 43 sick animals from three Russian zoos, were sampled and analyzed. For the first time, species from the canine (nine) and feline (seven) families from Moscow, Ivanovo, and Yaroslavl zoos in the Central Federal District of Russia were selected. A total of 108 samples from canines and 63 samples from feline animals were collected. Mineral element measurements were conducted on 1026 samples via a "Kvant-2A" atomic absorption spectrometer from Russia. Correlation and regression analyses were performed. CVDs were found in 10.1% of the studied animals, with a high percentage of heart muscle pathologies noted (25.8% of all CVDs). Iron (Fe) accumulated in canine and feline fur at approximately 208 and 203 mg/kg, with variations of 72.8% and 80.9%, respectively. A significant decrease in Fe and an increase in cadmium (Cd) during CVD were observed (correlations r = 0.25 and r = 0.16, respectively). The dysregulation of Fe homeostasis, increased absorption, and accumulation of Fe in the reticuloendothelial system are discussed. Finally, the mineral elements absorbed by canine and feline fur can be ranked in descending order: Fe > Zn > Cu > Pb > Cd > As.

Effect of Pregnancy on Mercury Concentration in the Body of Free-living Small Rodents.

Relatively little information exists on the effects of mercury on terrestrial wildlife populations. We analyzed 38 free-living small rodent females (Myodes glareolus, Microtus agrestris, and Apodemus flavicolis), of which 11 were pregnant, for total mercury concentrations in combined liver and kidney samples. Using a single-purpose atomic absorption spectrometer for mercury determination, the measured mercury values ranged from 0.006 to 0.079 mg/kg. Pregnant females had significantly (P<0.041) higher mercury levels in liver and kidney than did nonpregnant females. Our results suggest that during mercury biomonitoring studies it is necessary to consider the pregnancy of the analyzed animals.

Assessment of Some Heavy Elements in Selected Fruits from the Markets of Anbar Governorate: Implications for Human Health

Eating fruit can be a useful way to enhance health and reduce the risk of many diseases. At the same time, if this fruit exceeds the permissible limit, it can be a source of diseases dangerous to human health. Therefore, this issue presents a complex and multifaceted challenge. The current study aims to assess the concentration of certain heavy metals (chromium, iron, nickel, copper, manganese) in the pulp and peels of selected fruits from the markets of Anbar Governorate, Iraq. Ten types of fruits were selected (quince, fig, orange, apple, banana, mango, watermelon, carrot, pomegranate, kiwi) and compared with internationally permissible limits. The concentrations were measured using an atomic absorption spectrometer. The results indicated the concentration of some metals exceeding limits of the international standard. For instance, it was noted that the concentration of Ni in the peels very high and the samples that exceeded the international limit were; A2 – B2 – C2 – K2 – M2 – P2 – S2 where samples had 6.548, 3, 3.645, 3.323, 17.516, 4.290 and 5.258 mg/L of Ni. In the pulp, nickel was found at high concentrations exceeding the international limits in samples (A1 - B1 - C1 - K1 - M1 - O1 - P1 - S1), with concentrations of (23.645 - 3.968 - 6.226 - 13.645 - 2.355 - 8.806 - 19.129) mg/L. The highest Ni was found in apple pulp at 23 mg/L while the lowest concentration of Ni was found in orange peel and fig pulp at 0.097 mg/L.

Heavy Metals Analysis of Breweries Effluent used in Soil Cultivated with Glycine Max (L.) Merr. Accessions with Biochar Augmentation

Beer production has promulgated the prevalence of heavy metal contamination in the environment (soil and water bodies). The magnitude of breweries wastewater-effluent effect discharged on soil and its effect on crop quality in terms of growth and physiology must therefore be investigated. This study aims to assess the level of seven heavy metals (HM) (lead (Pb), nickel (Ni), chromium (Cr), copper (Cu), cadmium (Cd), zinc (Zn) and iron (Fe)) in breweries wastewater-effluent and its effect on the growth of Glycine max accessions (TGM-3990, TGM-1348, TGM-1732, TGM-2175 and TGM-928) as well as the influence of biochar soil amendment in the induction of HM tolerance in G. max. Effluent properties were analyzed using the A1 portable TDS/EC meter. HM in the wastewater-effluent was determined using Atomic Absorption Spectrometer (AAS). The experiment was set up in a complete block design. 3 seeds G. max accessions were planted in 7kg of sterilized soil (control, effluent and biochar treatments). Growth parameters were taken using standard methods, while the total photosynthetic pigments (TPP) were determined using the atLeaf chlorophyll meter. The wastewater-effluent recorded an electrical conductivity (EC) of 928µS/cm, total dissolved solids (TDS) (464ppm), Temperature (31.9-32.6°C) and pH (5.37). Results for HM concentration showed; Pb (0.20mg/L), Ni (&lt;0.001mg/L), Cr (0.03mg/L), Cu (&lt;0.001mg/L), Cd (&lt;0.001mg/L), Zn (&lt;0.001mg/L) and Fe (8.74mg/L). The trend shows that Fe˃Pb˃Cr˃Cd˃Cu˃Ni˃Zn. Cr, Cd, Cu, Ni and Zn were significantly below the World Health Organization (WHO) and Waste Water Forum (WWF) permissible limit, while Fe and Pb significantly higher. G. max accessions TGM-928 (80%) and TGM-3990 (80%) had better germination percentage (GP), TGM-1348 (60%) had the lowest GP, while TGM-2175 recorded no germination in all treatments. At 6 weeks after planting (WAP), it was observed that irrigation of G. max accessions with breweries wastewater-effluent significantly (p=0.001) stimulated growth parameters such as shoot length for TGM-3990 which recorded; Treatment=19.53±0.94cm; Control=17.10±0.67cm; Biochar=40.83±1.01cm) while TGM-1732 had the highest shoot growth (T=38.57±1.53cm; C=25.00±0.00cm; B=82.33±5.70cm) when compared to their controls. TGM-3990 (T=32.20mg/kg, C=34.10mg/kg, 43.30mg/kg) recorded the least TPP contents, while TGM-928 (T=51.00mg/kg, C=45.60mg/kg, B=43.50mg/kg) recorded the highest TPP in all treatments. Amelioration of soil with biochar significantly (p=0.001) stimulated growth above the effluent treatment and control. Similar trend was observed for leaf area, petiole length, leaf number, stem girth and internode length. This study has shown that breweries effluent has the potential of growth enhancement in G. max cultivation and in combination biochar application reduces the need for additional fertilizer application.

Mobilization mechanisms and spatial distribution of arsenic in groundwater of western Bangladesh: Evaluating water quality and health risk using EWQI and Monte Carlo simulation

Arsenic (As) contamination in groundwater is emerging as a significant global concern, posing serious risks to the safety of drinking water and public health. To understand the release mechanisms, mobilization processes, spatial distribution, and probabilistic health risks of As in western Bangladesh, forty-seven samples were collected and analyzed using an atomic absorption spectrometer (AAS). The As concentrations in groundwater ranged from 1.97 to 697.4 μg L⁻1 (mean: 229.9), significantly exceeding recommended levels. The dominant hydrochemistry of As-enriched groundwater was Ca–Mg–HCO₃, with the primary sources of arsenic in groundwater being the dissolution of arsenic-bearing minerals in sediment and the recharge of aquifers from the Ganges River Basin. The assessment using the Entropy Water Quality Index revealed that the groundwater is unsuitable for drinking, with 89.36% (n = 42) of the samples surpassing the WHO's limit for arsenic. Rock-water interactions, including calcite dissolution and silicate weathering within the confined aquifer, predominantly influenced hydrochemical properties. The significant relationships among Fe, Mn, and As indicate that the reductive dissolution of FeOOH and/or MnOOH considerably contributes to the release of As from sediment into groundwater. Geochemical modeling analysis revealed that siderite and rhodochrosite precipitate into aquifer solids, suggesting a weak to moderate relationship among As, Fe, and Mn. The long residence time of groundwater, combined with the presence of a clayey aquitard, likely controls the mobilization of arsenic in the aquifer. For the first time, Monte Carlo simulations have been used in arsenic-prone areas to assess the severity of arsenic contamination in western Bangladesh. The analysis indicates that out of 100,000 people, 10 may develop cancer as a result of drinking arsenic-contaminated water, with children being more susceptible than adults.

Functionalization of Ti3C2 MXene with Diethylenetriamine for a Column-Based Solid-Phase Extraction of Heavy Metals.

Transition metal carbides, nitrides, and carbonitrides, known as MXenes, are attracting attention for their potential application in trace detection of heavy metals. This study presents diethylenetriamine-functionalized Ti3C2 MXene for trace detection of cadmium and lead ions. Functionalization of Ti3C2 significantly improves the adsorption properties of MXenes by replacing native functional groups with silane moieties that contain three amine groups, offering higher affinity for heavy metals. We demonstrate the efficacy of this material as a solid-phase extractor in column-based solid-phase extraction for heavy metal analysis in various food samples. Diethylenetriamine-functionalized Ti3C2 coupled with the flame atomic absorption spectrometer exhibits exceptional analytical performance. While maintaining a robust stability for 15 adsorption-desorption cycles, the proposed method shows detection limits of 0.09 ng mL-1 for cadmium and 1.7 ng mL-1 for lead, with a linear dynamic range of 0.3-50 ng mL-1 for cadmium and 5-90 ng mL-1 for lead, and relative recoveries of 97.50-101.05 and 98.65-100.80% for cadmium and lead ions, respectively. Additionally, relative standard deviations and enrichment factors were calculated as 0.60-4.70% and 42.3 for cadmium ions and 0.65-1.24% and 44.2 for lead ions.

Phytoremediation potential of seedlings: comparing heavy metal accumulation in Ailanthus, Acer, and Fraxinus species.

This study investigates the phytoremediation potential of non-productive seedlings of Ailanthus altissima, Acer pseudoplatanus, and Fraxinus excelsior for lead, cadmium, and zinc accumulation in contaminated soils of Zanjan Province, an industrial area with significant pollution. The evaluation employed a completely randomized design, with three treatment levels for each element, alongside a control treatment, replicated three times over a two-year period. A total of 810 one-year-old seedlings from the three species were involved in the study. Soil contamination levels, ranging from 0 to 2000mg/kg for lead and zinc and from 0 to 200mg/kg for cadmium, were administered through soil pot irrigation. Sampling of seedling stems and pot soils was conducted in November of 2021 and 2022. The absorption levels of elements in the samples were determined using the dry acid digestion method and an ICP-OES atomic absorption spectrometer. Results indicate species-specific variations in metal absorption, with Ailanthus showing the highest accumulation rates. Findings suggest Ailanthus as a promising candidate for soil improvement in polluted environments, particularly in contaminated soils of Zanjan Province.

Assessment of the Heavy Metal Contaminations of Roadside Soil in Aizawl, Mizoram (India): An In-Depth Analysis Utilising Advanced Scientific Methodologies

The study was conducted to evaluate the heavy metal contamination levels in the roadside soil of Aizawl, Mizoram (India). Twelve sites were sampled monthly from August 2020 to July 2021, and concentrations of copper (Cu), iron (Fe), manganese (Mn), nickel (Ni), lead (Pb), and zinc (Zn) were analyzed using atomic absorption spectrometer. The concentrations of heavy metals at the twelve studied sites varied widely from 0.43-1.06, 20.54-21.21, 2.69-3.41, 0.25-0.54, 0.31-0.49 and 1.35-1.77 for Cu, Fe, Mn, Ni, Pb, and Zn respectively. Pollution assessment tools such as the pollution load index, geo-accumulation index, and enrichment factor indicated moderate pollution levels. The study also observed fluctuations in the contamination levels due to the monsoon rainfall and the COVID-19 pandemic lockdown. Principal component analysis identified vehicular emissions, industrial activities, and atmospheric deposition as the potential sources of heavy metal contamination, with varying patterns observed at each site. While the observed heavy metal concentrations generally met permissible limits, the elevated levels suggested anthropogenic influences. It is crucial to continuously monitor and manage heavy metal contamination to mitigate potential health risks associated with heavy metal exposure.

Contamination by potentially toxic metals from urban rivers located in an area covered by the Guarani Aquifer in Southern Brazil

The present study aimed to evaluate the concentration of heavy metals considered globally alarming, such as cadmium (Cd), chromium (Cr), copper (Cu), lead (Pb) and zinc (Zn), in the surface water and in the sediment of urban rivers located in an area covered by the Guarani Aquifer, in Lages, southern Brazil. The water and sediment samples were collected in September and October 2016 in three urban rivers. The quantification of the metals was performed through an atomic absorption spectrometer. The levels of Cd, Cr, Cu, Pb and Zn in the control points (P1 and P7) presented a concentration below the level I proposed by Brazilian legislation 344/2004 of the National Environment Council (CONAMA), while the other points presented concentrations higher and above level I, evidencing an increase of metals in the rivers from upstream to downstream of the urban area of ​​Lages. Cr concentrations above level II proposed by Brazilian legislation at the mouth of the Carahá River were also found, and this value may have adverse effects on aquatic biota. The results show that urban rivers in the area covered by the Guarani Aquifer in Lages have been contaminated by toxic elements associated with anthropogenic activities.

Heavy metals and metalloid contamination and risk evaluation in the surface sediment of the Bakkhali River estuary in Bangladesh

Current state of contamination and subsequent risk of contaminated sediment of a tidal river of Bangladesh was evaluated in the present study. Sediment samples were collected from five locations in the tributary of Bakkhali River estuary during summer (April) and winter (December) season, 2020. Collected samples were processed using standard protocol and the content of heavy metals (Cd, Cr, Cu, Pb and Zn) and metalloid (As), were analyzed by the Flame Atomic Absorption Spectrometer. Sediment contamination was evaluated by pollution load index (PLI), contamination factor (CF), degree of contamination (Cd), potential ecological risk index (PERI), non-carcinogenic and carcinogenic risk (CR) due to the dermal contact of the sediment. Multivariate statistical analysis such as principal component analysis (PCA) and cluster analysis (CA) were also applied to find out the possible sources of the contaminant in the sediment. Results showed the average concentration of As, Cd, Cr, Pb, Cu and Zn was 9.74 ± 3.57, 2.00 ± 0.85, 48.75 ± 8.92, 29.78 ± 8.39, 5.44 ± 2.03 and 56.94 ± 8.57 mg/kg, respectively. Concentration of Cu, Pb and Zn were within the recommended level whereas the concentration of As, Cd and Cr were suppressed the recommended level of WHO and FAO/WHO standards. PLI, CF and Cd revealed considerably low degree of contamination of the sediment. Geo-accumulation index indicated uncontaminated to moderately contaminated condition of the sediment. Although the values of enrichment factor revealed no potential enrichment for most of the metals, Cd showed a minor enrichment during the winter season. Based on the ecological risk assessment, the sediment from all of the sample locations was found to be of moderate to low risk. PCA and CA analysis revealed the origin of contaminants mainly from anthropogenic sources. Although different metals showed non-carcinogenic risk to the inhabitants, cancer risk values for dermal contact (CRderm) were much lower than 10−6 indicating no cancer risk for adult and child. However, the findings also revealed that children were more susceptible to CRderm compared to adults. The present study concluded that long term dermal contact of the sediment of Bakkhali River estuary will be contagious to the people. Therefore, regular monitoring of the estuarine environment is necessary so that contamination does not get worse.

L-cysteine mediated rapid separation of Hg2+ and MeHg+ by anion-exchange HPLC

Owing to the on-going emission of Hg into the global environment, new insight into their bioinorganic chemistry in mammals is urgently required to better understand their adverse health effects and analytical methods to quantify Hg2+ and MeHg+ in environmental samples are needed. Analytical separations can help to address both of these needs. While Hg2+ and MeHg+ have been most frequently separated by cation and reversed-phase (RP) HPLC, we here report on using anion-exchange (AEX) HPLC in conjunction with a flame atomic absorption spectrometer (FAAS) to observe the retention behavior of these mercury species in the pH range 5.0–8.0 using mobile phases comprised of 10 mM l-cysteine (Cys) in 100 mM phosphate buffer. The results obtained for pH 5.0 served as a starting point to develop a rapid HPLC separation for these mercurials. The addition of 5–20 % methanol (MeOH) to this mobile phase revealed that MeOH did not appreciably change the retention of Hg2+, but significantly reduced the retention of MeHg+. A 15 % MeOH-containing mobile phase offered the best compromise between achieving a rapid baseline separation in <400 s at affordable costs. To assess the suitability and robustness of the developed AEX-HPLC separation method for the analysis of environmental samples an inductively coupled plasma atomic emission spectrometer (ICP-AES) was employed as the mercury-specific detector. The developed AEX-HPLC-ICP-AES method allowed to achieve detection limits of 1.5 ppm for Hg2+ and 2.9 ppm for MeHg+ and was successfully applied to analyze wastewater that had been spiked with Hg2+ and MeHg+.

Phenolic, amino acids, and fatty acids profiles and the nutritional properties in the fresh and dried fruits of black rosehip (Rosa pimpinellifolia L.)

Recently, increased attention has been paid to the raw materials of plants as a source of biologically active substances. Black rosehip (Rosa pimpinellifolia L.) fruits could be a good resource for potential functional components in the food, cosmetic and pharmaceutical industries. Also, drying can influence the composition of heat-sensitive phytochemicals. However, less attention is given to comparing black rosehip bioactive compounds particularly compositions of fatty acid, amino acids, and phenolic content in fresh and dried fruits. So in this study, the amino acid constituents (by amino acid analyzer), fatty acids (by GC–MS), mineral elements (by atomic absorption spectrometer), antioxidant (by DPPH) and phenolic compounds (by HPLC) present in fresh and dried fruits of black rosehip naturally grown in Iran were comprehensively investigated. The results showed that dried fruits had a lower level moisture by 51.55%, and a higher level of total phenolic compounds and total sugar by 786.20 mg GAE/100 g and 15.77 g/100 g, respectively. Chlorogenic acid and gallic acid were the major phenolic compounds (109.3 mg/g). Whilst, linoleic acid, oleic acid, and arachidic acid (85.34%) were the most dominant fatty acids. The most dominant amino acids were glutamic acid, phenylalanine, and arginine (29.41 g/100 g). Also, Fe and Mn as micro-elements were the most dominant elements. In general, the results illustrated the potentials and differences of black rosehip fruits grown in the Arasbaran region as promising resources for food sources, pharmaceutics, cosmetics, and breeding programs. Also, these findings confirm that black rosehip fruits contain significant amounts of secondary metabolites that may positively affect human health.

Heavy Metal Pollution Studies of Soil from the Oti-Dompoase Dumpsite in Kumasi

Waste disposal sites contribute a great deal to environmental pollution. The degree of pollution brought on by heavy metal contamination of soil collected from the Oti-Dompoase dump site in Kumasi of Ashanti region, Ghana was investigated in this study. Twelve (12) composite samples of the surface soil were taken in total at 10 cm depth from the dumpsite to conduct metal analysis. The measurement of heavy metal concentration was done utilizing Atomic Absorption Spectrometer, which uses the absorbance at various wavelength of the electromagnetic spectrum to determine the chemical identity of constituents of the sample and their concentrations with the help of standard solutions and Beer-Lambert law. The mean metal concentrations of soil samples were reported and arranged in terms of magnitude as follows: Iron (2,582.21 mg/kg) &gt; Copper (348.50 mg/kg) &gt; Lead (324.85 mg/kg) &gt; Manganese (192.27 mg/kg) &gt; Zinc (146.24 mg/kg) &gt; Cadmium (7.06 mg/kg). Physiochemical properties such as electrical conductivity (EC), pH and organic matter and water content (%) were also investigated using a PHYWE electrical conductivity meter, pH meter and an oven, respectively. Most of the parameters analysed indicated pollution when compared to baseline values, while human exposure levels were within World Health Organization (WHO) standards. Assessments using geo-statistics of different hazard indicators, including pollution load index, contamination factor (CF), and geo-accumulation, all point to heavy metal pollution of the soil samples. Cadmium contamination was very high based on the pollution indices (CF, geo-accumulation, and pollution load) and manganese has the lowest level of pollution. There is limited data on the extent of pollution caused by the Oti-Dompoase dumpsite and this study will serve to fill this knowledge gap and contribute to the Millenium Development Goal seven (7) by providing data on the extent of pollution of soil around the Oti-Dompoase dumpsite and highlight the need for regular monitoring and on-site remediation strategies to safeguard the site to ensure environmental sustainability.

A spectrophotometric analysis of copper and zinc released from stainless steel brackets coated with a combination of copper oxide and zinc oxide nanoparticles in artificial saliva

Nanocoating stainless steel orthodontic brackets with a combination of copper and zinc oxide nanoparticles might alter the quantity of ions released from them in saliva. The purpose of the study was to evaluate the quantity of copper and zinc ions released from stainless steel brackets coated with a combination of copper oxide and zinc oxide. Stainless steel orthodontic brackets (Ormco Mini -Diamond series 0.22” slot, MBT prescription) (ORMCO CORP Glendora, California, USA) (n= 15 in each group) were coated with nanoparticles of copper oxide (Group I) , zinc oxide (Group II) and a combination of copper oxide –zinc oxide (Group III) nanoparticles using a spray pyrolysis method . The quantity of copper and zinc ions released from these three groups of brackets, when stored in artificial saliva and intubated at 37 C was evaluated at 24hrs, 7th day, 14th day and 28th day using an atomic absorption spectrometer. The three groups of coated brackets released significantly more copper and zinc ions than the uncoated brackets. The copper oxide nanocoated and zinc oxide nano coated stainless steel orthodontic brackets released more copper and zinc ions when compared to the copper oxide - zinc oxide combination nanocoated orthodontic brackets and uncoated brackets. The highest surge of ion release was noted at the 7th day in all the three coated groups for both the ions evaluated. Brackets coated with a combination of copper oxide and zinc oxide nanoparticles demonstrated reduced levels of copper and zinc ion release in artificial saliva when compared to copper oxide nanocoated brackets and zinc oxide nanocoated brackets..

Health Risk Assessment of Toxic Metal(loids) Consumed Through Plant-Based Anti-diabetic Therapeutics Collected in the Northern Divisional City of Rajshahi, Bangladesh.

The present study investigates human health risks upon consumption of herbal medicines in terms of ten toxic metalloids in 20 plant-based anti-diabetic therapeutics. The analysis of metalloids was determined by an atomic absorption spectrometer after microwave-assisted digestion. The computation of hazard quotients (HQ) and hazard indexes (HI) of metalloids leads to the assessment of non-carcinogenic health risks. Carcinogenic risk was assessed based on cancer slope factor (CSF) and chronic daily intake (CDI) values. Comparison with WHO regulatory cut-off points for each metalloid: seven samples for Mn, 12 samples for Hg, three samples for Cu, eight samples for Ni, four samples for Cd, two samples for Pb, one sample for Cr, and eight samples for Zn are unsafe to consume. Non-carcinogenic human health risk is predicted for Mn in seven samples, Fe in one sample, Hg in ten samples, Cu in three samples, Ni in one sample, and Pb in two samples. HI values greater than 1 predict non-carcinogenic health risk in thirteen samples. Incremental lifetime cancer risk (ILCR) remains for As (inorganic) in 12 samples, Cr (+ 6) in one sample, and Pb in no samples. To guarantee consumer safety, the implementation of strict monitoring is suggested.

Health Risk Assessment of Metal Contamination in Four Green Leafy Vegetables from Various Open Markets in Benghazi

This study analysed aluminium, essential metals (chromium, manganese, iron, nickel, copper and zinc), and toxic metals (lead and cadmium) in green leafy vegetables (arugula, mint, parsley, and spinach) obtained from various markets in Benghazi city. A flame Atomic Absorption Spectrometer was used to determine the metal contents. Hazard quotient (HQ) and hazard index (HI) calculations were employed to assess non-carcinogenic and carcinogenic risks associated with the metals in the vegetables. Results showed that aluminium was detected in only 50% of the samples. All vegetable samples contained manganese, iron, copper and zinc within the ranges of 1.072-6.87mg, 26.71-298.4mg, 1.00-3.45mg and 3.61-9.33mg per 1kg of vegetable dry weight, respectively. Nickel and chromium were found in 33% and 50% of the samples, respectively. Cadmium and lead were present in all samples except for two spinach and two parsley samples. The levels of essential metals in the samples were below the maximum allowable limits set by FAO-WHO regulations. However, the contents of nickel, cadmium and lead in some vegetable samples exceeded the maximum limits. The metal contents in the collected vegetables were mostly lower than reported results from previous international studies. The HQ and HI values for the analysed metals were all below unity, suggesting that the consumption of these selected vegetables as part of a daily diet poses no threat to human health.