Coupled Plasma Atomic Emission Spectrometry Research Articles

Chemical characterization of baby food consumed in Italy.

In this study, a total of 30 elements (essential and non-essential or toxic) were determined in 25 foods consumed in Italy by children aged 0-6 months and produced in Europe. Inductively Coupled Plasma-Atomic Emission Spectrometry and Inductively Coupled Plasma-Mass Spectrometry were used as measurement techniques for the elements of interest. The estimated intakes for one-year-old infants were compared with risk estimators and nutritional requirements. Data indicate that commercially available baby food in Italy provides an excellent contribution for Mn, Cu, Fe, Zn, Ca, K, and P, covering up to approximately 70% of the adequate intake (AI) for an infant aged 6-12 months. The intake of detectable toxic elements was always below the safety limit: even the most concentrated toxic elements never exceeded about 86% of the Provisional Tolerable Weekly Intake (PTWI). This result indicates that the analyzed baby food is of good quality and does not pose risks to children's health.

Development of a technique for X-ray fluorescence analysis of zinc-aluminum-magnesium alloys

A technique for X-ray fluorescence spectral analysis of zinc-aluminum- magnesium alloys has been developed, which allows the determination of Mg, Al, Pb, Si, Cu, Mn, Fe, Ni content in the alloy. The effect of the sample preparation method on the linearity of calibration graphs is revealed. The conditions for determining the main alloying (Al, Mg) and impurity (Pb, Fe, Cu, Si, Mn, Ni) elements by X-ray fluorescence spectrometry were studied. It is proposed to use the correction of the matrix effect by selecting alpha coefficients for the intensity of X- ray radiation with subsequent automatic conversion of the function into a linear form. Calibration graphs for determination of the elements in the corresponding ranges, i.e., Mg (0.00019 – 5.04%), Al (0.0002 – 12.4%), Pb (0.0012 – 2.07%), Si (0.0005 – 0.12%), Cu (0.0006 – 5.95%), Mn (0.0004 – 0.00524%), Fe (0.0009 – 0.41%), Ni (0.0009 – 0.27%), were obtained using standard reference samples and production samples of the alloys, the chemical composition of which was previously determined by inductively coupled plasma atomic emission spectrometry (ICP-AES). The correctness of the developed methodology was confirmed by analysis of standard samples and comparative analysis of the obtained results using the Student’s t-test.

Influence of Hybrid Surface Modification on Biocompatibility and Physicochemical Properties of Ti-6Al-4V ELI Titanium.

Titanium-based materials are the most widely used materials in biomedical applications. However, according to literature findings, the degradation products of titanium have been associated with potential allergic reactions, inflammation, and bone resorption. The corrosion process of Ti-6Al-4V in the human body environment may be exacerbated by factors such as reduced pH levels and elevated concentrations of chloride compounds. Coatings made of biopolymers are gaining attention as they offer numerous advantages for enhancing implant functionality, including improved biocompatibility, bioactivity, wettability, drug release, and antibacterial activity. This study analyzes the physicochemical and electrochemical behavior of the Ti-6Al-4V ELI alloy subjected to PCL and PCL/TiO2 deposition by the electrospinning method. To characterize the polymer-based layer, tests of chemical and phase composition, as well as surface morphology investigations, were performed. Wetting angle tests were conducted as part of assessing the physicochemical properties. The samples were subjected to corrosion behavior analysis, which included open circuit potential measurements, potentiodynamic tests, and the electrochemical impedance spectroscopy method. Additionally, the quantification of released ions post the potentiodynamic test was carried out using the inductively coupled plasma atomic emission spectrometry (ICP-AES) method. Cytotoxicity tests were also performed. It was found that surface modification by depositing a polymer-based layer on the titanium substrate material using the electrospinning method provides improved corrosion behavior, and the samples exhibit non-toxic properties.

Exploring the significance of potassium homeostasis in copper ion binding to human αB-Crystallin

αB-Crystallin (αB-Cry) is a small heat shock protein known for its protective role, with an adaptable structure that responds to environmental changes through oligomeric dynamics. Cu(II) ions are crucial for cellular processes but excessive amounts are linked to diseases like cataracts and neurodegeneration. This study investigated how optimal and detrimental Cu(II) concentrations affect αB-Cry oligomers and their chaperone activity, within the potassium-regulated ionic-strength environment. Techniques including isothermal titration calorimetry, differential scanning calorimetry, fluorescence spectroscopy, inductively coupled plasma atomic emission spectroscopy, cyclic voltammetry, dynamic light scattering, circular dichroism, and MTT assay were employed and complemented by computational methods. Results showed that potassium ions affected αB-Cry's structure, promoting Cu(II) binding at multiple sites and scavenging ability, and inhibiting ion redox reactions. Low concentrations of Cu(II), through modifications of oligomeric interfaces, induce regulation of surface charge and hydrophobicity, resulting in an increase in chaperone activity. Subunit dynamics were regulated, maintaining stable interfaces, thereby inhibiting further aggregation and allowing the functional reversion to oligomers after stress. High Cu(II) disrupted charge/hydrophobicity balance, sewing sizable oligomers together through subunit-subunit interactions, suppressing oligomer dissociation, and reducing chaperone efficiency. This study offers insights into how Cu(II) and potassium ions influence αB-Cry, advancing our understanding of Cu(II)-related diseases.

Highly Robust Alginate-based Magnetic Nanosorbents of Pd Catalysts for the 4-Nitrophenol Reduction

This work presents the synthesis of alginate-coated magnetite nanoparticle (MNP) containing amino-enriched moieties for the immobilization of palladium (Pd), and its use as a recyclable catalyst for the reduction of 4-nitrophenol (4NP) in water. The alginate grafted onto the surface of MNP contained carboxylate anions that served as coordination sites for Pd. Additionally, the incorporation of amino-enriched components, such as poly(vinyl amine) (PVAm) and 2-(dimethyl amino)ethyl methacrylate (DMAEMA), onto the alginate-coated MNPs resulted in additional interactions, including the formation of carboxylate-ammonium salts. In this study, the influence of these amino groups on the efficiency of Pd immobilization, catalytic activity and reusability of nanosorbents for 4NP reduction was investigated. The existence of Pd in the nanosorbents was detected by inductively coupled plasma atomic emission spectroscopy, transmission electron microscopy, and energy-dispersive X-ray techniques. The average size of MNPs was approximately 12.3 ± 2.9 nm, and for Pd, it was about 3.9 ± 0.8 nm. It was found that the incorporation of these amino-enriched moieties into the particles significantly enhanced the catalytic activity of the nanosorbents. Notably, MNP containing extended DMAEMA units exhibited excellent tolerance to 4NP reduction, with an insignificant loss of catalytic performance even after 20 consecutive reuses, maintaining a conversion of over 98 %. HIGHLIGHTS Synthesis of alginate-based magnetite nanoparticle for the immobilization of Pd and its use as a catalyst for the reduction of 4-nitrophenol in water were presented The carboxylate groups in alginate provided the coordinating sites for Pd immobilization and improved the particle dispersibility in water The incorporation of amino-enriched components to the particle reduced the degree of Pd aggregation on the particle surface The catalysts had high catalytic performance for the reduction of 4-nitrophenol in water and exhibited highly robust properties with excellent reusability for up to 20 cycles with insignificant changes in their performance GRAPHICAL ABSTRACT

“Mining” the herbarium for hyperaccumulators: Discoveries of nickel and zinc (hyper)accumulation in the genus Noccaea (Brassicaceae) through X‐ray fluorescence herbarium scanning

AbstractX‐ray fluorescence spectroscopy (XRF) is a relatively new method for non‐destructive elemental analysis of herbarium material that meets the scientific interest in being capable of discovering new hyperaccumulator plant species. Since the genus Noccaea (Brassicaceae family) is known to be one of the most numerous in term of the hyperaccumulator plant species it contains, especially those that hyperaccumulate Ni, the herbarium material available worldwide represents a great resource for expanding our knowledge of their elemental profiles. In this first systematic XRF scanning of herbarium specimens of the genus Noccaea, a total of 794 specimens from the collection of the National Museum of Natural History in Paris (MNHN) were analyzed, and the raw values obtained were corrected using regression formulas against inductively coupled plasma atomic emission spectroscopy data. Hyperaccumulation of Ni was detected in 90 specimens covering 21 taxa, with Ni concentrations reaching up to 48,700 mg kg−1 in Noccaea cappadocica, an ultramaficophyte from Syria. Zinc concentrations above the hyperaccumulation threshold were found in 210 specimens covering 23 taxa, most of which belonged to different subspecies of Noccaea caerulescens, with the highest concentration reaching up to 56,200 mg kg−1 in N. caerulescens subsp. caerulescens. Although the accumulation of Ni and Zn is contrasting in most of the specimens studied, in 10 specimens, predominantly belonging to N. caerulescens, simultaneous hyperaccumulation of Ni and Zn was found. This study also revealed previously unknown hyperaccumulation of Ni in several Noccaea taxa, as well as a simultaneous hyperaccumulation of Ni and Zn that needs to be confirmed by further experimental and field studies.

Prospecting for rare earth element (hyper)accumulators in the Paris Herbarium using X-ray fluorescence spectroscopy reveals new distributional and taxon discoveries.

Rare earth elements (REEs) are increasingly crucial for modern technologies. Plants could be used as a biogeochemical pathfinder and a tool to extract REEs from deposits. However, a paucity of information on suitable plants for these tasks exists. We aimed to discover new REE-(hyper)accumulating plant species by performing an X-ray fluorescence (XRF) survey at the Herbarium of the Muséum national d'Histoire naturelle (MNHN, Paris, France). We selected specific families based on the likelihood of containing REE-hyperaccumulating species, using known taxa that accumulate REEs. A total of 4425 specimens, taken in the two main evolutionary lineages of extant vascular plants, were analysed, including the two fern families Blechnaceae (n = 561) and Gleicheniaceae (n = 1310), and the two flowering plant families Phytolaccaceae (n = 1137) and Juglandaceae (n = 1417). Yttrium (Y) was used as a proxy for REEs for methodological reasons, and a total of 268 specimens belonging to the genera Blechnopsis (n = 149), Dicranopteris (n = 75), Gleichenella (n = 32), Phytolacca (n = 6), Carya (n = 4), Juglans (n = 1) and Sticherus (n = 1) were identified with Y concentrations ranging from the limit of detection (LOD) >49 µg g-1 up to 1424 µg g-1. Subsequently, analysis of fragments of selected specimens by inductively coupled plasma atomic emission spectroscopy (ICP-AES) revealed that this translated to up to 6423 µg total REEs g-1 in Dicranopteris linearis and up to 4278 µg total REEs g-1 in Blechnopsis orientalis which are among the highest values ever recorded for REE hyperaccumulation in plants. It also proved the validity of Y as an indicator for REEs in XRF analysis of herbarium specimens. The presence of manganese (Mn) and zinc (Zn) was also studied by XRF in the selected specimens. Mn was detected in 1440 specimens ranging from the detection limit at 116 µg g-1 up to 3807 µg g-1 whilst Zn was detected in 345 specimens ranging from the detection limit at 77 µg g-1 up to 938 µg g-1. This study led to the discovery of REE accumulation in a range of plant species, substantially higher concentrations in species known to be REE hyperaccumulators, and records of REE hyperaccumulators outside of the well-studied populations in China.

Contribution of Mine-Derived Airborne Particulate Matter to Ca, Fe, Mn and S Content and Distribution in the Lichen Punctelia hypoleucites Transplanted to Bajo de la Alumbrera Mine, Catamarca (Argentina).

The aim of this work was to relate the contribution of mine-derived airborne particulate matter to Ca, Fe, Mn and S content and distribution in Punctelia hypoleucites transplanted to Bajo de la Alumbrera, an important open-pit mine in Catamarca, Argentina. Lichen samples were transplanted to four monitoring sites: two sites inside the mine perimeter and two sites outside the mine. After three months, elemental distribution in samples was analyzed by microparticle-induced X-ray emission (microPIXE), and elemental concentration was determined by specific techniques: Ca and Fe by instrumental neutron activation analysis, Mn by inductively coupled plasma atomic emission spectrometry and S by a turbidimetric method. A differential distribution of S and Ca in thalli transplanted in-mine sites was detected compared to that of samples transplanted outside-mine sites. An overlap of Fe and S in the upper cortex of the apothecium section was observed, leading to infer a mineral association of both elements. Similar association was observed for Ca and S. In addition to these results, the significantly higher concentration detected for S and Mn in in-mine site samples suggests a contribution of Fe, S, Ca and Mn of mining origin to the content and distribution of these elements in P. hypoleucites. MicroPIXE complemented with Mössbauer spectroscopy analysis determined the presence of pyrite particles together with other iron-bearing minerals displaying different degrees of oxidation. These results point to a mining origin of the airborne particulate matter trapped by the lichen thalli transplanted to Bajo de la Alumbrera. These findings indicate that P. Hypoleucites acts as an excellent air quality biomonitor in the Bajo de la Alumbrera mine area.

Development of the Purification Process of Gallium-68 Eluted from Germanium-68/Gallium-68 Generator

Objective: 68Ga has a half-life of 68 minutes, with 89% of its decay is through positron emission. It is available from generator systems and possesses suitable property for labeling radioligands. These aspects make 68Ga a promising tracer for positron emission tomography (PET) imaging. This study aims to develop the purification process of the 68Ga eluates from 68Ge/68Ga generator after its recommended shelf-life and ensuring the quality through the radiolabeling process. Materials and Methods: In this study, we explored the development of a purification method for 68Ga eluted from a68Ge/68Ga generator before radiolabeling was investigated. Cation and anion exchange chromatography techniques were combined to remove trace amounts of competing metal ion impurities. Post-purification, the eluate’s metal contents were analyzed using inductively coupled plasma atomic emission spectroscopy (ICP-AES). Breakthrough of 68Ge was measured using a multi-channel analyzer (MCA) spectrometer with high-purity germanium (HPGe) radiation detectors. Additionally, the radiochemical purity of 68Ga-NOTA-RGD was analyzed by high-performance liquid chromatography (HPLC). Results: Metal impurities including Fe(II), Zn(II) and Al(III) were reduced by 61%, 38% and 44% respectively. The 68Ge breakthrough was approximately ~10–3%. The labeling efficiency with NOTA-RGD, a tracer for angiogenesis imaging, resulted in an average yield of 68Ga-NOTA-RGD (not corrected for decay) of around 50%, with aradiochemical purity by HPLC of approximately 98%–99%. Conclusion: Cation exchange in combination with anion exchange chromatography was thus proven to be an efficient method for purification of the 68Ga eluate from a 68Ge/68Ga generator prior to labeling the 68Ga PET radiotracer.

DEVELOPMENT OF APPROACHES TO THE ANALYSIS OF ELEMENTAL IMPURITIES IN TITANIUM DIOXIDE (BARIUM AND LEAD DEFINITION)

Relevance. Titanium dioxide (TiO2) is widely used in the pharmaceutical industry as a drug excipient (DE). Therefore, control of its content of ele-mental impurities (EI) plays an important role in ensuring the stability of quality and safety of drugs. The lack of harmonized pharmacopoeial require-ments for the content of EIs in TiO2, as well as the need for specialized validated methods of their analysis determine the actual task in the field of quality control of this substance. Research objective. This work is devoted to the development and validation of a method for the determination of barium and lead in TiO2 sub-stance. Material and Methods. The inductively coupled plasma atomic emission spectrometry (ICP-AES) method was used to determine the barium and lead content in the TiO2 substance. Acid extraction was used in the sample preparation process. All used reagents and materials were in accordance with pharmacopoeial requirements. A sample of TiO2 substance, manufactured by Venator Germany GmbH, Germany, was used as an object of study. Validation of the method was carried out in accordance with the requirements of GF RF for the following characteristics: specificity, linearity, LOQ, correctness, repeatability, intra-laboratory precision and range of the technique. Results. The method of barium and lead determination in TiO2 substance using ICP-AES demonstrates high accuracy and sensitivity. The results ob-tained during validation meet the acceptance criteria, which confirms the applicability of the technique for control of barium and lead content in TiO2 substance. Conclusions. A method for the determination of barium and lead impurities in TiO2 substance using the ICP-AES method and acid extraction during sample preparation has been developed. This approach enables the determination of barium and lead at the specification level (20 ppm and 5 ppm, re-spectively). The validation results meet the acceptance criteria for all characteristics investigated, confirming the ability to quantify barium and lead in the range of 50% to 150% of the specification level.

Contents of twelve chemical elements in normal human breast determined using inductively coupled plasma atomic emission spectrometry

Inductively coupled plasma atomic emission spectrometry (ICP-AES) has been shown to be an effective method for determining the content of Al, Ca, Cu, Fe, K, Mg, Na, P, S, Si, Sr and Zn in small mass samples of breast tissue. The method is relatively simple and applicable directly in the clinic for express diagnostics. The autopsy material of 38 practically healthy women aged 16–60 years who died suddenly was studied using the developed method of ICP-AES. Mean values (M ± SD) of mass fractions (mg kg-1 of dry tissue) of chemical elements in normal breast tissue of women were: Al 3.62 ± 2.44, Ca 77.7 ± 61.8, Cu 1.03 ± 1.01, Fe 13.8 ± 12.3, K 194 ± 114, Mg 18.5 ± 9.0, Na 686 ± 516, P 201 ± 74, S 385 ± 224, Si 8.75 ± 6.22b, Sr 0.50 ± 0.24, and Zn 3.29 ± 1.65. The ability of breast tissue to absorb Al, Fe and Sr from the interstitial fluid was revealed. The selective accumulation of Al, Fe, and Sr should be taken into account in further studies of the role of chemical elements in the etiology of breast pathologies, as well as in the development of methods for the differential diagnosis of diseases, for example, benign and malignant tumors of the mammary gland.

Doping zinc oxide and titanium dioxide nanoparticles with gold induces additional oxidative stress, membrane damage, and neurotoxicity in Mytilus galloprovincialis: Results from a laboratory bioassay

BackgroundWhile previous studies have provided insights into the effects of zinc oxide (ZnO) and titanium dioxide (TiO2) nanoparticles (NPs) on aquatic organisms, there is still a substantial amount of information lacking about the possible effects of their doped counterparts. The goal of the current work was to address this gap by examining Mytilus galloprovincialis reaction to exposure to doped and undoped nanoparticles. MethodsTwo concentrations (50 or 100 µg/L) of undoped ZnO and TiO2 NPs, as well as their gold (Au) doped counterparts, were applied on mussels for 14 days, and the effects on biomarkers activities in digestive glands and gills were assessed by spectrophotometry. ResultsThe NPs were quasi-spherical in shape (below 100 nm), stable in seawater, and with no aggregation for both doped and undoped forms. Analytical results using inductively coupled plasma atomic emission spectroscopy indicated the uptake of NPs in mussels. Furthermore, it was found that biometal dyshomeostasis could occur following NP treatment and that doping the NPs aggravated this response. At the biochemical level, exposure to undoped NPs caused membrane damage, neurotoxic effect, and changes in the activities in the gills and digestive glands of superoxide dismutase, catalase, and glutathione-S-transferase, in a concentration and organ-dependent manner. ConclusionDoping ZnO NPs and TiO2NPs with Au induced additional oxidative stress, membrane damage, and neurotoxicity in mussels.

Visible Light Activation of Gold Nanoparticles Embedded into Titanium Dioxide Surface in Electrospun Polymeric Coatings

This work reports the development of a functional photocatalytic coating based on a combination of polymeric electrospun fibres and nanoparticles that is intended to be activated in the visible light range. In this sense, the resulting fibres can act as an effective matrix for the incorporation of titanium dioxide (TiO2) particles, which are covered by gold nanoparticles (AuNPs), in the outer surface of the metal oxide precursor. In the first step of the process, the optical properties of the nanoparticles were determined by UV-Vis spectroscopy. The extension of the visible absorption can be associated to the localized surface plasmon resonance (LSPR) of the metallic AuNPs. In addition, the resultant particle size distribution and average particle diameter was evaluated by dynamic light scattering (DLS) measurements. Furthermore, the phase composition and porosity of the functional particle powder were analysed by an XRD and N2 adsorption test. In the second step, these synthesized particles have been successfully immobilized into a PAA + β-CD electrospun fibre matrix by using the two different deposition methods of dip-coating and solution-casting, respectively. The morphological characterization of the samples was implemented by means of scanning electron microscopy (SEM), showing uniform and homogeneous, free-beaded fibres with a random distribution of the synthesized particles deposited onto the electrospun fibres. Then, the functional coatings were removed from the substrate, and a thermogravimetric (TGA) analysis was carried out for each sample in order to obtain the precursor mass immobilized in the coating. Once the overall mass of precursor was obtained, the percentage of TiO2 particles and AuNPs in the precursor was calculated by using inductively coupled plasma atomic emission spectrometry (ICP-AES). Finally, the photocatalytic activity of both functional solution and electrospun coatings were evaluated in terms of a gradual degradation of rhodamine B (RhB) dye after continuous exposition to a visible-light lamp.

Influence of Ultrahigh Dilution Treatment of the Charge on the Growth and Spectroscopic Properties of Nd:MgMoO4 Potential Laser Crystal

The influence of the charge treatment by ultrahigh dilution (UHD) technology on oxide single crystals grown by the Czochralski technique was studied for monoclinic MgMoO4 crystals doped by 1 at. % of Nd3+ ions. The series of 10 Nd:MgMoO4 crystals was grown from the charges that were subjected to UHD treatment, as well as from the charges treated with two types of control or with no special treatment at all. The grown crystals were studied by X-ray powder diffraction analysis, inductively coupled plasma atomic emission spectroscopy, mass-spectrometry, optical absorption, emission spectroscopy and luminescence kinetic analysis. We found that: (i) wetting of MgO + MoO3 mixture by a water-ethanol solution before calcining leads to some enrichment of the mixture with MoO3, whereas the wetting of the charge after the calcining leads to some enrichment of it with MgO; (ii) congruent melting composition of MgMoO4 crystal is in the field of some MoO3 excess; (iii) the solid-phase solubility of the excess MoO3 in MgMoO4 probably does not depend on temperature, whereas the solid-phase solubility of the excess MgO in MgMoO4 crystal depends on temperature. We suggest that the corresponding solidus line passes through the range of retrograde solubility; (iv) the crystals grown within this range are characterized by the enhanced Nd3+ segregation coefficient between the crystal and the melt (approximately 0.006 versus 0.004); (v) unit cell parameters of MgMoO4 crystal with the excess of MoO3 are larger than those of the crystal of the stoichiometric composition and of the crystal with the excess of MgO; (vi) the shapes of the optical absorption and luminescence spectra of Nd:MgMoO4 crystal do not depend on the charge treatment; (vii) luminescence decay kinetics are single-exponential for all the studied crystals, the luminescence decay time being different for the crystals grown from the charges that underwent different types of treatment; (viii) the luminescence intensity of Nd:MgMoO4 crystal grown from the charge that underwent UHD treatment before calcining (solid-phase synthesis) is reduced by an order of magnitude in comparison with the other studied crystals.

Coordination polymer gel mediated spectrophotometric, ICP-AES and spectrofluorimetric methods for trace As(III) determination in water and food samples

Herein, a coordination polymer gel is proposed for the determination of As(III) in real samples through multispectroscopic techniques viz. spectrophotometry, spectrofluorimetry, and inductively coupled plasma atomic emission spectroscopy (ICP-AES). Taguchi L32 (46 21) design and adaptive neuro fuzzy inference system (ANFIS) optimized the controllable factors affecting the extraction yielding an experimental S/N ratio of 39.94 dB. The fluorescence quenching (KSV = 2.63 × 106 L mol−1) was static with photoelectron transfer being the main mechanism confirmed by the density functional theory calculations. The limits of detection (LODs), limits of quantification (LOQs) and linear ranges were 0.038 μg L−1, 0.13 μg L−1 and 1.67–116.67 μg L−1, 0.40 μg L−1, 1.21 μg L−1 and 1.67–33.33 μg L−1, 1.07 μg L−1, 3.24 μg L−1 and 3.32–35.37 μg L−1 for the developed enrichment coupled ICP-AES, spectrophotometry and fluorescence sensing methods. Among these methods, the enrichment - ICP-AES method has the lowest LOD, LOQ and the widest linear range followed by the enrichment - spectrophotometry and fluorescene sensing methods. Spectrofluorimetry offers high sensitivity, selectivity, and possible real time monitoring, spectrophotometry provides a cost-effective and versatile option, while ICP-AES manifests multi-element analysis with high sensitivity and low interference. The developed methods were validated and employed for the successful determination of trace As(III) in real samples. The employment of these methods enhances the overall analytical capability for a wide range of sample types and concentrations.

Analysis of the Concentration of Heavy Metals in Khat Grown in Meru County and the Assessment of Their Associated Health Risks

Contamination of farm produce by toxic heavy metals has become a serious global health concern. These metals can bioaccumulate in plant tissues and are precursors for major public health problems such as cancer and neural impairment. Khat (Catha edulis) also referred to as miraa has the potential to sequester and accumulate both micronutrients and potentially toxic heavy metals in its consumable parts—tender leaves and soft barks of young shoots which are known to possess psychoactive properties when consumed. Therefore, the motivation behind this contribution is to determine the levels of six heavy metals, namely, cadmium (Cd), copper (Cu), chromium (Cr), lead (Pb), iron (Fe), and nickel (Ni) in consumable Meru khat samples, compare these levels with the permissible limits of World Health Organization (WHO) in order to predict associated health risks, and to estimate the noncarcinogenic risks of these metals by total health quotient (THQ) and health index (HI) on khat consumers. 1.0 g of dry ground khat samples was digested in 0.05 M HCl and allowed to stand for 5 hours before being analyzed for heavy metals using inductively coupled plasma atomic emission spectroscopy (ICP-AES). The mean heavy metal concentrations (mg/kg) in dry khat samples of six toxic heavy metals were Cd (7.81 ± 1.56), Cr (15.98 ± 2.22), Cu (15.81 ± 2.84), Fe (97.35 ± 32.67), Ni (0.37 ± 0.02), and Pb (32.36 ± 9.95). Based on the results, the mean levels of Pb, Cd, and Cr exceeded WHO permissible limits. In addition, the Pb and Cd THQ values and the HI of the six heavy metals investigated in the khat samples exceeded the threshold value of 1.0. Furthermore, the THQ and HI values showed that Pb and Cd were potentially the major contributors to noncarcinogenic risks on regular khat consumers. This is a matter of concern on the excessive consumption of Meru khat-based products, which over time may cause a toxicological response. Based on the findings of this study, the use of agrochemicals should significantly be minimized in khat farming. Accordingly, the Meru khat farmers should be sensitized on alternative farming practices that do not potentially cause heavy metal contamination in khat.

Cadmium in Selected Organs of Game Animals from Areas with Different Degrees of Industrialisation and Its Intake by Human Consumers.

The aim of this study was to determine the concentration of cadmium (Cd) in the organs of game animals from areas with different degrees of industrialisation and to assess its intake following the consumption of the livers of these animals. The material for this study consisted of liver and kidney samples taken from roe deer (Capreolus capreolus), red deer (Cervus elaphus), and wild boar (Sus scrofa) from five regions differing in land use and industrialisation. Compared to the kidneys, the liver was an indicator of the current state of the environment and Cd intake, while the kidney was used to assess the long-term accumulation of Cd in the body. The cadmium concentration in the samples was determined by inductively coupled plasma atomic emission spectrometry. The cadmium concentrations of the organs were found to vary according to geographical location, with the highest levels being observed in Southern Poland, i.e., areas characterised by the highest degree of industrialisation and the presence of heavy industry. However, high Cd concentrations were also reported in the northeastern region. Examples of excessive cadmium levels in the kidneys were noted in all tested regions. Cd intake by humans was evaluated by calculating the estimated daily cadmium intake, and this was compared with the tolerable weekly intake (TWI). The TWI was only exceeded by children frequently consuming wild boar liver from the southwest region.

Assessment of Atmospheric Deposition of Potentially Toxic Elements in Macedonia Using a Moss Biomonitoring Technique

This study aims to investigate the changes in atmospheric deposition trends in Macedonia, using a moss biomonitoring technique. This technique has been used to assess the content of potentially toxic elements in Macedonia in 2002, 2005, 2010, and 2015, within the framework of the International Cooperative Program on Effects of Air Pollution on Natural Vegetation and Crops. The content of 42 elements was analyzed using instrumental neutron activation analysis (INAA), inductively coupled plasma–atomic emission spectrometry (ICP–AES), and atomic absorption spectrometry (AAS), on 72 moss samples collected in the summer of 2015. The median values of the elements studied were compared with data from previous years and with median values obtained from comparable studies in Norway and the neighboring countries. Through factor and cluster analysis, three geogenic factors were identified: Factor 1, which includes the elements Al, Ce, Fe, Hf, La, Li, Na, Sc, Sm, Tb, Ti, Th, V, and U; Factor 4, which includes As, Cl, and I; and Factor 5, which includes the elements Ba and Sr. In addition, one geogenic-anthropogenic factor containing Co, Cr, and Ni (Factor 2), was identified, and one anthropogenic factor containing Cd, Pb, Sb, and Zn (Factor 3). The lead and zinc mines near the towns of Kriva Palanka, Probištip, and Makedonska Kamenica in the eastern region of the country, the former lead and zinc smelter in the town of Veles, and the ferronickel smelter near Kavadarci, have continuously had the greatest anthropogenic impact on the atmospheric deposition of potentially toxic elements during the time period of the study. In addition to the human influences, the lithology and the composition of the soil continue to play a significant role in the distribution of the elements.

Synthesis of Zinc Nanoparticles by the Gas Condensation Method in a Non-Contact Crucible and Their Physical-Chemical Characterization.

This work explored the zinc nanoparticles obtained by the one-stage induction flow levitation method. A 10 kW tube generator with an operating frequency of 440 kHz was used. The process used 8 mm diameter zinc granules (2 g weight) with a purity of 99.9%. Zinc wire was fed to replace the evaporated metal from the granule surface. This method productivity was 30 g/h of nanoparticles. In addition, various methods were used to characterize the resulting nanoparticles: scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-Ray fluorescence analysis (XRF), dynamic light scattering (DLS), porosimetry and inductively coupled plasma atomic emission spectroscopy (ICP-MS). The resulting nanoparticle size, determined by SEM and porosimetry, was 350 nm, while the size of the primary crystallites was 21 nm. The amount of impurities in the resulting nanoparticles did not exceed 1000 ppm.

A novel method for simultaneously measuring boronophenylalanine uptake in brain tumor cells and number of cells using inductively coupled plasma atomic emission spectroscopy

Boron neutron capture therapy (BNCT) combines neutron irradiation with boron compounds that are selectively uptaken by tumor cells. Boronophenylalanine (BPA) is a boron compound used to treat malignant brain tumors. The determination of boron concentration in cells is of great relevance to the field of BNCT. This study was designed to develop a novel method for simultaneously measuring the uptake of BPA by U87 and U251 cells (two brain tumor cell lines) and number of cells using inductively coupled plasma atomic emission spectroscopy (ICP-AES). The results revealed a linear correlation between phosphorus intensity and the numbers of U87 and U251 cells, with correlation coefficients (R2) of 0.9995 and 0.9994, respectively. High accuracy and reliability of phosphorus concentration standard curve were also found. Using this new method, we found that BPA had no significant effect on phosphorus concentration in either U87 or U251 cells. However, BPA increased the boron concentration in U87 and U251 cells in a concentration-dependent manner, with the boron concentration in U87 cells being higher than that in U251 cells. In both U87 and U251 cells, boron was mainly distributed in the cytoplasm and nucleus, accounting for 85% and 13% of the total boron uptake by U87 cells and 86% and 11% of the total boron uptake by U251 cells, respectively. In the U87 and U251 cell-derived xenograft (CDX) animal model, tumor exhibited higher boron concentration values than blood, heart, liver, lung, and brain, with a tumor/blood ratio of 2.87 for U87 cells and 3.11 for U251 cells, respectively. These results suggest that the phosphorus concentration in U87 and U251 cells can represent the number of cells and BPA is easily uptaken by tumor cells as well as in tumor tissue.