Inductively Coupled Plasma Mass Spectrometry Research Articles

Inductively Coupled Plasma-Mass Spectrometry (ICP-MS): An Emerging Tool in Radiopharmaceutical Science.

Although radioactive experiments are necessary in radiopharmaceutical drug discovery and theranostic cancer research, they are expensive, require special facilities, and face certain restrictions. Thus, finding techniques not involving radioactivity is highly beneficial for minimizing these disadvantages in such research. In this regard, methods using inductively coupled plasma-mass spectrometry (ICP-MS) have emerged as viable alternatives to traditional radioactive approaches. Despite its potential, practical applications of ICP-MS in radiopharmaceutical cancer research have only emerged in recent years. This Perspective focuses on the development and implementation of nonradioactive ICP-MS-based assays in radiopharmaceutical research and aims to inspire future research efforts in this area.

Green and Mild Fabrication of Magnetic Poly(trithiocyanuric acid) Polymers for Rapid and Selective Separation of Mercury(II) Ions in Aqueous Samples.

The removal and detection of highly toxic mercury(II) ions (Hg2+) in water used daily is essential for human health and monitoring environmental pollution. Efficient porous organic polymers (POPs) can provide a strong adsorption capacity toward heavy metal ions, although the complex synthetic process and inconvenient phase separation steps limit their application. Hence, a combination of POPs and magnetic nanomaterials was proposed and a new magnetic porous organic polymer adsorbent was fabricated by a green and mild redox reaction in the aqueous phase with trithiocyanuric acid (TA) and its sodium salts acting as reductive monomers and iodine acting as an oxidant. In the preparation steps, no additional harmful organic solvent is required and the byproducts of sodium iodine are generally considered to be non-toxic. The resulting magnetic poly(trithiocyanuric acid) polymers (MPTAPs) are highly porous, have large surface areas, are rich in sulfhydryl groups and show easy magnetic separation ability. The experimental results show that MPTAPs exhibit good adsorption affinity toward Hg2+ with high selectivity, rapid adsorption kinetics (10 min), a large adsorption capacity (211 mg g-1) and wide adsorption applicability under various pH environments (pH 2~8). Additionally, MPTAPs can be reused for up to 10 cycles, and the magnetic separation step of MPTAPs is fast and convenient, reducing energy consumption compared to centrifugation and filtration steps required for non-magnetic adsorbents. These results demonstrate the promising capability of MPTAPs as superior adsorbents for effective adsorption and separation of Hg2+. Based on this, the prepared MPTAPs were adopted as magnetic solid-phase extraction (MSPE) materials for isolation of trace Hg2+ from aqueous samples. Under optimized conditions, the extraction and quantification of trace Hg2+ in water samples were accomplished using inductively coupled plasma mass spectrometry (ICP-MS) detection after MSPE procedures. The proposed MPTAPs-based MSPE-ICP-MS method is efficient, rapid, sensitive and selective for the determination of trace Hg2+, and was successfully employed for the accurate analysis of trace Hg2+ in tap water, wastewater, lake water and river water samples.

Application of Human Plasma Targeted Lipidomics and Analysis of Toxic Elements to Capture the Metabolic Complexities of Hypothyroidism.

Hypothyroidism (HT) affects millions worldwide and can lead to various lipid disorders. The metabolic complexity and the influence of toxic elements in autoimmune and non-autoimmune HT subtypes are not fully understood. This study aimed to investigate the relationships between plasma lipidome, toxic elements, and clinical classifications of HT in unexposed individuals. Samples were collected from 120 adults assigned to a study group with Hashimoto's disease and non-autoimmune HT, and a healthy control group. Quantification of 145 pre-defined lipids was performed by using triple quadrupole tandem mass spectrometry (TQ MS/MS) in multiple reactions monitoring (MRM) mode via positive electrospray ionization (ESI). Levels of toxic elements were determined using inductively coupled plasma mass spectrometry (ICP-MS). Significant associations between altered levels of several components of the plasma lipidome and Al, Cd, Ni, As, and Pb with HT were found. We show metabolic differences in lysophosphatidylcholines (LPC) and phosphatidylcholines (PC) between HT and controls, with distinct predicted activation patterns for lysolecithin acyltransferase and phospholipase A2. There are significant changes in the lipidome profiles of healthy subjects compared to euthyroid HT patients treated with L-thyroxine, which are related to the type of hypothyroidism and non-occupational exposure to toxic elements.

Microwave-associated ZnCl2 pretreatment followed by enzymatic hydrolysis for high-efficiency production of nanocellulose from Eucalyptus dissolving pulp

Herein, we developed a novel microwave-associated ZnCl2 pretreatment followed by enzymatic hydrolysis for high-efficiency and environmentally friendly production of nanocellulose. With a short pretreatment time (60 s), nanocellulose was yielded with a high overall yield of 87.99 % from Eucalyptus Dissolving Pulp (EDP). Characterization analysis revealed that microwave-associated ZnCl2 pretreatment can efficiently swollen the structure of EDP, and after enzymatic hydrolysis, the nanocellulose in spherical shape was formed with abundant functional groups, low crystalline index, and poor thermal stability. By Energy Dispersive X-Ray Spectroscopy (EDS) and inductively coupled plasma mass spectrometry (ICP-MS) analysis, approximately 20 wt% of zinc distributed on the surface and in the interior of cellulose, that may lead to the low Zeta potential of the nanocellulose and the formation of nanospheres. Furthermore, through optimization of the pretreatment process, it was feasible to increase the solid concentration of EDP to 3 wt% while concurrently reducing the ZnCl2 concentration to 0.1 mol (ZnCl2·9H2O). Under this condition, ultrafine cellulose nanocrystals (CNC) and cellulose nanofiber (CNF)/CNC blend were produced with an outstanding yield of 93.3 %. Moreover, the recyclability of ZnCl2 post-pretreatment was demonstrated, as ZnCl2 could be efficiently reused for subsequent pretreatment cycles. Notably, even after five cycles of recycling, the nanocellulose yield remained consistently above 90 %. Overall, this study highlights the viability and sustainability of microwave-assisted ZnCl2 pretreatment for efficient nanocellulose production, offering a sustainable and cost-effective route for industrial-scale applications.

Geochemical Dynamics and Evolutionary Implications of Sediments at the Xingu–Amazon Rivers’ Confluence: Proxies for Mixing, Mobility and Weathering

This study investigates the geochemical characteristics and evolutionary implications of sediments at the confluence of the Xingu and Amazon Rivers. The main objective is to understand sediment mixing, mobility, and weathering processes through geochemical proxies. Samples were collected from various sections of the lower Xingu River, focusing on its interaction with the Amazon River. Analytical techniques such as X-ray diffraction (XRD), X-ray fluorescence (XRF), and inductively coupled plasma mass spectrometry (ICP-MS) were employed to analyze major and trace elements. The results reveal significant spatial variations in mineralogical and textural patterns, with sediments forming distinct groupings based on their location. The data suggest that the lower Xingu River is strongly influenced by sediment inputs from the Amazon River, particularly affecting sediment composition and chemical weathering processes. This research highlights the critical interactions between river systems and their implications for the evolution of the Amazon basin, especially regarding sediment contributions from various geological sources. Even though the Xingu River drains cratonic regions at higher elevations, the geochemistry of the bottom sediments confirms that the bedload is derived from heterogeneous sources with primarily intermediate igneous compositions and has undergone substantial recycling during river transport.

Bioaccumulation Patterns of Trace Elements in Jellyfish (Crambionella orsini and Cassiopea andromeda) from Northwestern Coastal Waters of the Persian Gulf

Trace element pollution in the Persian Gulf originates from industrial activities, urbanization, shipping, and oil extraction, leading to accumulation in sediments, water, and marine life such as jellyfish. This study investigated trace element bioaccumulation in two jellyfish species, Crambionella orsini and Cassiopea andromeda, across different locations. Jellyfish samples were collected from the Mahshahr and Dilam ports, and their trace element concentrations were analyzed using inductively coupled plasma mass spectrometry (ICP-MS). The study revealed no significant differences in trace element concentrations between C. orsini and C. andromeda. However, levels of copper, iron, manganese, and nickel were significantly higher in specimens from Mahshahr compared to those from Dilam. No significant differences were observed for cadmium, mercury, vanadium, tin, magnesium, and selenium across sites. Lower concentrations of lead, arsenic, zinc, and cobalt were found in C. orsini from Dilam compared to Mahshahr. Additionally, the study found no significant correlation between trace element concentrations in the water and their accumulation in jellyfish bodies. These findings offer valuable insights into the distribution and bioaccumulation of trace elements in jellyfish populations across different marine environments in the Persian Gulf.

The influence of weathering and pedogenesis on the geochemical record of Miocene marls and Plio-Quaternary sediments, Medvednica Mt., Croatia

The geochemical signature of weathering and pedogenesis in a temperate humid climate on two parent material types in the foothills of Medvednica Mt. was studied. Five soil profiles on Miocene marls and three sections of Plio-Quaternary (PlQ) proluvial sediments with overlying soil and weathered material were analyzed. The (clay) mineralogy of all profiles and sections had been determined in previous studies. The chemical composition of the samples was determined by inductively coupled plasma emission spectroscopy (ICP-OES) and inductively coupled plasma mass spectroscopy (ICP-MS). Poorly ordered Fe and Mn oxides were determined in the PlQ sediment and overlying soil samples by atomic absorption spectroscopy (AAS), after oxalate dissolution in the dark. The concentrations and element ratios were used to determine element enrichment/mobility and intensity of chemical weathering, material provenance, and to compare the geochemical signatures with previously obtained clay mineralogy results. Trace elements in the Miocene marls, including rare earth elements (REE), indicate the continental origin of the marl siliciclastic component, while more scattered geochemical data of the PlQ sediments reflect their proluvial/torrential nature. The mass transfer coefficient (τ) for major elements and element ratios of the Miocene marl profiles indicate chemical weathering and pedogenesis of lower intensity. The geochemistry of these samples shows homogeneity within the profiles. In the geochemical signature of the PlQ sections, a chaotic proluvial deposition of the material is visible, as well as the heterogeneity with the overlying soil and weathered material. Overall, the geochemistry results largely support the clay mineralogy of the samples and demonstrate how a multiproxy approach can help test hypotheses about past environments and provide valuable additional information for complex paleoenvironmental studies.

Assessment of heavy metal contamination in groundwater of rural areas of Kurdistan Province Iran: A comprehensive study

This study focuses on the contamination of groundwater by heavy metals (HMs) in the Kurdistan Province of Iran, an area heavily reliant on these water resources, especially in rural regions. This research aimed to quantify the concentrations of 20 HMs in groundwater sources and assess the associated health risks, including both carcinogenic and non-carcinogenic effects, for different age groups. The study was conducted in 2024. We collected 155 groundwater samples from water resources of the villages in Kurdistan Province, west of Iran. The study encompassed comprehensive sampling of groundwater from various wells and springs throughout the province, which was subsequently subjected to thorough laboratory analysis utilizing Inductively Coupled Plasma Mass Spectroscopy (ICP-MS) for the quantification of heavy metal (HM) concentrations. The highest concentrations of As, Co, Cu, and Mo were 7.90, 0.22, 2.48, and 1.68 μg/l, respectively. It was related to the cities of Qorveh, Sanandaj, Baneh, and Qorveh respectively. A Health Risk Assessment (HRA) was performed, indicating that, while the concentrations of most HMs were within the thresholds established by national and international standards, certain metals, such as arsenic and lithium, presented notable non-carcinogenic risks, especially to children. These metals were responsible for over 48 % of the cumulative hazard index (HI) across all ten cities evaluated. Furthermore, the HI for the adult demographic exceeded 1.0 (specifically 1.23) exclusively in Qorwe city. The study also identified a high carcinogenic risk associated with lead across the province, which has a carcinogenic risk of 7.3 × 10−03 in 10 studied cities, which is more than the guideline value of 10−04. The findings underscore the urgent need for continuous monitoring and the implementation of preventive measures to safeguard public health. The results provide crucial insights for policymakers and health authorities, facilitating informed decisions to mitigate the health risks posed by HM contamination in the region's groundwater.

Changes in heavy metal levels in the oral fluid of young patients with and without plaque-induced gingivitis undergoing treatment with braces

Relevance. Research into the effects of nickel-titanium alloys and heavy metal ions on the development of inflammatory oral diseases is becoming increasingly significant in orthodontics. The relationship between toxic elements and inflammatory responses remains under-researched and controversial. Data on the connection between heavy metals and inflammatory reactions could influence the choice of orthodontic appliance materials and guide the subsequent management and monitoring of patients with braces. The question of the safe use of nickel-titanium alloy braces continues to be a relevant concern.Purpose. To assess the levels of heavy metals in the oral fluid of young patients with braces, both in those who developed plaque-induced gingivitis and those who did not.Materials and Methods. The study involved 50 clinically healthy patients (Groups I and II health categories) with intact teeth, including patients with compensated dental caries (isolated carious lesions – Grade I) and no periodontal diseases (PMA index <20), presenting with dental crowding and malocclusion (K07.2, K07.3). The average age of the patients was 22.1 ± 2.7 years, all of whom were undergoing treatment with metal braces. Oral fluid samples were analyzed for 12 heavy metal elements using inductively coupled plasma mass spectrometry (ICP-MS) in a laboratory setting. Additionally, lysozyme activity and oral fluid pH were measured before appliance placement and six months into orthodontic treatment.Results. Adaptation to braces in young patients is frequently complicated by the development of gingivitis and periodontitis due to impaired oral hygiene and the mechanical pressure exerted on teeth and gums, leading to elemental imbalances. Patients with gingivitis during orthodontic treatment are particularly at risk of developing such imbalances and therefore require timely correction of their mineral metabolism.

Reference values for plasma and urine trace elements in a Swiss population-based cohort.

Trace elements (TEs) are ubiquitous. TE concentrations vary among individuals and countries, depending on factors such as living area, workplaces and diet. Deficit or excessive TEs concentrations have consequences on the proper functioning of human organism so their biomonitoring is important. The aim of this project was to provide reference values for TEs concentrations in the Swiss population. The 1,078 participants to the SKiPOGH cohort included in this study were aged 18-90 years. Their 24-h urine and/or plasma samples were analyzed by inductively coupled plasma mass spectrometry (ICP-MS) to determine 24 TEs concentrations: Ag, Al, As, Be, Bi, Cd, Co, Cr, Cu, Hg, I, Li, Mn, Mo, Ni, Pb, Pd, Pt, Sb, Se, Sn, Tl, V and Zn. Statistical tests were performed to evaluate the influence of covariates (sex, age, BMI, smoking) on these results. Reference intervals for the Swiss adult population were also defined. TEs concentrations were obtained for respectively 994 and 903 persons in plasma and urine matrices. It was possible to define percentiles of interest (P50 and P95) for almost all the TEs. Differences in TEs distribution between men and women were noticed in both matrices; age was also a cofactor. This first Swiss biomonitoring of a large TEs-panel offers reference values in plasma and in urine for the Swiss population. The results obtained in this study were generally in line with clinical recommendations and comparable to levels reported in other population-based surveys.

Authenticating the Geographical Origin of Jingbai Pear in Northern China by Multiple Stable Isotope and Elemental Analysis.

The Jingbai pear is one of the best pear species in China with high quality and nutrition values which are closely linked to its geographical origin. With the purpose of discriminating the PGI Mentougou Jingbai pear from three other producing regions, the stable isotope ratios and elemental profiles of the pears (n = 52) and the corresponding soils and groundwater were determined using isotope ratio mass spectrometry (IRMS) and inductively coupled plasma mass spectrometry (ICP-MS), respectively. The results revealed that δ15N, δ18OJ, and Li were significantly different (p < 0.05) in samples from different regions, which indicated their potential to be used in the geographical origin classification of the Jingbai pear. The nitrogen isotopic values of the pear pulp were positively correlated with the δ15N value and nitrogen content of the corresponding soils, whilst the B, Na, K, Cr, and Cd contents of the pear pulps were positively correlated with their corresponding soils. Orthogonal partial least squares discriminant analysis (OPLS-DA) was performed in combination with analysis of the stable isotopes and elemental profiles, making it possible to distinguish the cultivation regions from each other with a high prediction accuracy (a correct classification rate of 92.3%). The results of this study highlight the potential of stable isotope ratios and elemental profiles to trace the geographical origin of pears at a small spatial scale.

Monazite Beats Zircon Regarding Dating of Young Metamorphic Events—An Example From Polycyclic Granitic Gneiss of the Pohorje Mountains, Slovenia

ABSTRACTThe result of dating U–(Th)–Pb bearing minerals in metamorphic rocks frequently suffers from the interpretative relation of their growth to a specific metamorphic event. This problem occurs in the southern Pohorje Mountains. Therefore, granitic gneiss from this area was studied. Rims of zircon in these rocks gave U–Pb ages around 90 Ma interpreted as an indicator of Late Cretaceous metamorphism. However, in situ dating of monazite with LA–ICP–MS yielded Early Miocene U–Th–Pb ages consistent with contact metamorphism by magmas forming the Pohorje pluton. This is supported by geothermobarometry using compositions of garnet and muscovite in granitic gneiss. This method led to pressure–temperature conditions of 6.5 kbar and 625°C, in line with intrusion depths estimated for the southeastern part of the Pohorje pluton. Consequently, zircon was not suitable for dating the latest metamorphic event but monazite was. Furthermore, monazite dating suggests two main intrusion pulses of magmas differing by 2–3 Ma.

Association between the levels of toxic heavy metals and schizophrenia in the population of Guangxi, China: A case-control study

The relationship between body levels of heavy metals and the risk of schizophrenia remains unclear. This study investigates the relationship between plasma levels of toxic heavy metals and the risk of schizophrenia among adults in Guangxi, China. Plasma concentrations of lead (Pb), cadmium (Cd), arsenic (As), and chromium (Cr) were measured using inductively coupled plasma mass spectrometry (ICP-MS). To evaluate both the single and combined effects of metal exposure on the risk of schizophrenia, we employed multivariate logistic regression, Bayesian Kernel Machine Regression (BKMR), and generalized Weighted Quantile Sum (gWQS) models. Additionally, we employed the Comparative Toxicogenomics Database (CTD) to analyze the mechanistic pathways through which metal mixtures may induce schizophrenia. Relative mRNA expression levels were measured using Real-Time Quantitative Reverse Transcription Polymerase Chain Reaction (RT-qPCR). Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were conducted to predict potential biological functions. In logistic regression models, compared to the lowest exposure group (Q1), the odds ratios (ORs) for Pb in groups Q2, Q3, and Q4 were 2.18 (95% CI: 1.20–3.94), 4.74 (95% CI: 2.52–8.95), and 3.62 (95% CI: 1.80–7.28), respectively. Both BKMR and gWQS models indicated a positive correlation between the combined effects of toxic heavy metal mixtures and the risk of schizophrenia, with Pb demonstrating the most substantial impact, particularly in older adults and females. Elevated levels of tumor necrosis factor (TNF) and interleukin-1 beta (IL-1β) were observed in patients with schizophrenia, while the expression of tumor protein p53 (TP53) was significantly reduced. These findings underscore the critical need to avoid exposure to toxic heavy metals to prevent schizophrenia, highlighting significant public health implications.

A Catalyst Tube-Equipped Dual-Stage Tube Furnace System for Accurate Hg Isotopic Determination of Ore Samples Using Neptune Plus Multicollector Inductively Coupled Plasma Mass Spectrometry.

Mercury (Hg) isotopes, which display mass-dependent fractionation and mass-independent fractionation, provide a multidimensional tracer to decipher the source of metals in mineral deposits. However, mineral ore samples usually contain abundant interfering elements (e.g., Te) that can cause inaccurate Hg isotopic analysis. Available acid digestion and combustion methods failed to remove these interfering elements, hindering the application of Hg isotopes for metallogenetic tracing. Here, we developed a new dual-stage tube furnace system employing a Mn-containing catalyst tube to pretreat mineral ore samples. This method yielded good Hg recoveries (100.5 ± 3.8%, 1SD, n = 15) and low levels of interfering elements in sample solutions, allowing for accurate analysis of a series of ore standard reference materials (GBW-11108v: coal; GSO-3: Cu-Ag sulfide ore; GBW 07859: Au-Te sulfide ore). The new method was also successfully applied to measure the Hg isotopic composition of magmatic and hydrothermal ore deposits, which yielded a large range in Δ199Hg value (-0.19 to 0.22‰) for ore deposits formed in different geological settings, highlighting the future applications of this method for metallogenic tracing, especially tracing the source of metals in mineral ore deposits.

Evaluation of the Potential of High-Performance Liquid Chromatography-Inductively Coupled Plasma-Mass Spectrometry for the Determination of Chemical Warfare Agents and Their Toxic Degradation Products.

The determination of chemical warfare agents (CWAs) and their toxic degradation products (DPs) has become increasingly important for public and military safety in recent years. We focused on assessing the possibility of the HPLC-ICP-MS analytical technique to verify the provisions of the Chemical Weapons Convention. This technique enables the identification and determination of minimal concentrations (ppt range) of elements in various matrices. This fact is important for the determination of CWAs and other highly harmful compounds, even small amounts of which can have serious consequences for living organisms. We have critically analysed the results of scientific research on the identification and quantitative determination of extremely toxic organophosphorus, organosulfur and organoarsenic CWAs, their derivatives and their degradation products using high-performance liquid chromatography (HPLC) coupled with inductively coupled plasma-mass spectrometry (ICP-MS).

Mineralogical Characteristics and Their Usability as Gemstones of Jaspers in Altered Metavolcanics Belonging to the Topçam Formation, Tokat, Turkiye

The jaspers located in the Topçam Mountain, Tepeyurt region (Tokat, Turkey), were formed at green-colored metavolcanic levels within Permian–Triassic schists. The sizes of the jaspers generally vary from a few cm to 1.5 m, and their colors vary from grayish–reddish–brownish/blackish tones depending on the increase in the amount of Fe and Mn elements they contain. According to thin section and X-ray Diffraction (XRD) analysis examinations, it was determined that the composition of jaspers includes quartz, hematite, calcite, and pyrite. As stated by the Wavelength Dispersive X-ray Fluorescence (WDXRF) analysis results, it was observed that the amount of SiO2 in jaspers was 82.5%, and the amount of Fe2O3 was 15.5%. According to Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) analysis results, Fe and Mn impurities, which are thought to cause the color of jaspers, as well as the amount of Fe (6975.5 ppm–46,893.9 ppm–96,431.1 ppm) and the amount of Mn (935.9–3219.7–6040.4 ppm), caused a darkening in color tones (grayish–reddish–brownish/blackish). Cabochon cutting applications were made of jaspers taken from the study area. As a result of these applications, it has been determined that jaspers can be used as gemstones due to their properties, such as their workability, polish retention, and color and light reflection.

Portable X-ray fluorescence of zinc and selenium with nail clippings-Mother and Infant Nutrition Investigation (MINI).

Zinc and selenium are essential minerals for human nutrition. Reliable biomarkers of zinc status and selenium status in humans are therefore important. This work investigates a novel portable X-ray fluorescence (XRF) method with the ability to rapidly assess zinc and selenium in nail clippings. This approach used a mono-energetic X-ray beam to excite characteristic X-rays from the clippings. Nail clippings were obtained from the Mother and Infant Nutrition Investigation (MINI), a study designed to assess nutrition in a population of women and their breastfed children in New Zealand. Twenty mother-infant pairings were selected to provide nail clippings at two time points (visit 1 at 3 months postpartum; visit 2 at 6 months postpartum). Nail clippings from each mother-infant pairing were divided into three groupings of clippings prior to analysis: those obtained from a big toe of the mother, those from the other toes of the mother, and those from the toes and fingers of the infant. Clippings were prepared and mounted prior to XRF measurement, providing four distinct fragments from each clipping grouping. These fragments were assessed by XRF using a measurement time of either 300 s (visit 1) or 180 s (visit 2). XRF results were determined through both an automated system output and an analysis of the X-ray energy spectrum. Following this assessment of zinc and selenium with the non-destructive XRF method, clippings were measured for zinc and selenium concentration using a "gold standard" technique of inductively coupled plasma mass spectrometry (ICP-MS). Mean ICP-MS concentrations ranged from 122 μg/g to 127 μg/g for zinc, and from 0.646 μg/g to 0.659 μg/g for selenium. Precision, assessed by a relative standard deviation of measurement, was superior for ICP-MS relative to XRF. For both zinc and selenium, XRF results were compared with ICP-MS concentrations. Linear equations of best fit were determined for each comparison between XRF and ICP-MS results. Coefficients of determination (r2) were stronger for zinc (from 0.74 to 0.95) than selenium (from 0.53 to 0.70). A decrease in XRF measurement time from 300 s to 180 s did not appear to adversely affect the correlation between XRF and ICP-MS results. Using the mono-energetic portable XRF method, the correlation of XRF zinc results with ICP-MS zinc concentrations was improved over previous findings, and selenium measurement was reported for the first time. The method may prove useful for future applications to trace element analysis using nail clippings as a biomarker.

Eliminating the «memory effect» during mass spectrometric determination of mercury

When estimating mercury content by inductively coupled plasma mass spectrometry (ICP-MS), this element adsorbs on the surface of the sample introduction system of the instrument, which creates problems in the determination of trace amounts of mercury. Various methods of cleaning the instrument have been proposed in the literature. Objective: to experimentally compare the effectiveness of trace mercury removal methods proposed in the literature for elemental analysis by ICP-MS and to select the optimal cleaning agent. Methods: Mercury content in solution was determined by the Agilent Technologies 7900 inductively coupled plasma mass spectrometer using 202Hg isotope. Diluted solutions of nitric and hydrochloric acids, solutions of gold chloride, potassium dichromate, thiourea, L-cysteine, potassium bromide, potassium bromate of different concentrations in water and 1% nitric and hydrochloric acids, aqueous solution of ammonium pyrrolidinedithiocarbomate were used as washing agents. Results: The background level of mercury content is achieved by using solutions of copper chloride (5%), thiourea (0.01, 0.1, and 0.5%), L-cysteine (2%), potassium bromide and bromate (0.0005 M) in 1.0% hydrochloric acid solution. The background is lowered by using 3 and 5% HCl, potassium dichromate (60 mg/liter), potassium bromide and bromate (0.01 and 0.05 M) solutions in 1% hydrochloric acid. Application of aqueous solution of ammonium pyrrolidinedithiocarbamate causes sharp degradation of plastic tubes of the sample introduction system. Conclusion: The efficiency of washing agents based on hydrochloric acid is higher than that based on nitric acid and water. The most promising washing agents are bromide-containing solutions and potassium bichromate solution in hydrochloric acid. The optimal way to clean the device is its washing with 0.5 mM potassium bromide solution in 1.0% hydrochloric acid. Its use allows to reduce the background content of mercury and does not complicate the analysis of the content of other elements.

Accumulation of heavy metals (Cr, Cu, As, Cd, Pb, Zn, Fe, Ni, Co) in the water, soil, and plants collected from Edayar Region, Ernakulam, Kerala, India

The accumulation of heavy metals in the environment is a significant concern due to their potential toxicity and persistence. This study investigates the levels of heavy metal contamination in the water, soil, and plants of the Edayar region in Ernakulam, Kerala, India. The region has experienced industrialization and urbanization, leading to concerns about heavy metal pollution. The study aims to assess the concentrations of chromium (Cr), copper (Cu), arsenic (As), cadmium (Cd), lead (Pb), zinc (Zn), iron (Fe), nickel (Ni), and cobalt (Co) in water, soil, aquatic and terrestrial plants. Samples were collected from various locations within the Edayar region, and Inductively Coupled Plasma Mass Spectrometry (ICP-MS) was conducted to quantify heavy metal concentrations. The findings of this study will contribute to the assessment of heavy metal pollution in the Edayar region. Plants with a high diversity index were taken for analysis from both aquatic and terrestrial habitats. Scoparia dulcis L. seems to specialize in metal accumulation, possibly for protective purposes. Synedrella nodiflora Gaertn demonstrates adaptability to metal-rich environments through robust metal uptake and tolerance mechanisms. Alternanthera philoxeroides (Mart.) Griseb, on the other hand, appears to have developed mechanisms to manage heavy metal exposure. The results indicate significant levels of heavy metal contamination across all samples, with the highest concentrations detected in soil, followed by water and plants. Chromium and lead levels in soil exceeded the permissible limits set by international standards, posing potential risks to human health and the ecosystem. The accumulation patterns in plants varied, with higher bioaccumulation factors observed for zinc and copper, suggesting their preferential uptake. This study highlights the urgent need for remediation strategies and continuous monitoring to mitigate the impact of heavy metal pollution in the Edayar region. The results will help in understanding the environmental impact of human activities.

Biophysical contrast sources for magnetic susceptibility and R2* mapping: A combined 7 Tesla, mass spectrometry and electron paramagnetic resonance study

Iron is the most abundant trace metal in the human brain and consistently shown elevated in prevalent neurological disorders. Because of its paramagnetism, brain iron can be assessed in vivo by quantitative MRI techniques such as R2* mapping and Quantitative Susceptibility Mapping (QSM). While Inductively Coupled Plasma Mass Spectrometry (ICP-MS) has demonstrated good correlations of the total iron content to MRI parameters in gray matter, the relationship to ferritin levels as assessed by Electron Paramagnetic Resonance (EPR) has not been systematically analyzed. Therefore, we included 15 postmortem subjects (age: 26–91 years) which underwent quantitative in-situ MRI at 7 Tesla within a post-mortem interval of 24 h after death. ICP-MS and EPR were used to measure the total iron and ferritin content in 8 selected gray matter (GM) structures and the correlations to R2* and QSM were calculated. We found that R2* and QSM in the iron rich basal ganglia and the red nucleus were highly correlated with iron (R² > 0.7) and ferritin (R² > 0.6), whereas those correlations were lost in cortical regions and the hippocampus. The neuromelanin-rich substantia nigra showed a different behavior with a correlation with total iron only (R² > 0.5) but not with ferritin. Although qualitative results were similar for both qMRI techniques the observed correlation was always stronger for QSM than R2*. This study demonstrated the quantitative correlations between R2*, QSM, total iron and ferritin levels in an in-situ MRI setup and therefore aids to understand how molecular forms of iron are responsible for MRI contrast generation.