Determination Of Trace Elements Research Articles

PHYTOCHEMICALS SCREENING, ANTIOXIDANT AND ANTIMICROBIAL ACTIVITY OF CARICA PAPAYA LEAF EXTRACTS

Objective: The objective of the present study aimed at investigating the phytochemical antioxidant and anti-microbial properties of Carica papaya leaf extracts. Methods: As phytochemicals are biologically active compounds and a powerful group of plant chemicals believed to stimulate the immune system along with antioxidants, the molecules which hinder oxidation of other molecules by the process of inhibiting or by generating the oxidizing chain reactions and preventing diseases. The anti-microbial activity on various gram-positive and gram-negative bacteria were determined using zone of inhibition and antioxidant by the 2,2,1-diphenyl-1-picrylhydrazyl method. Results: Phytochemical screening, antioxidant and antibacterial potential were determined using different aqueous and organic solvents in addition to the determination of trace element in leaves of C. papaya. Antioxidant activity using DPPH free radical scavenging assay indicated leaves extracts leaves showed inhibition of per oxidation. The result showed that the ethanolic extract of C. papaya possessed a significant antioxidant activity as compared to methanol and aqueous extract. The antibacterial study showed leaves extract is the best to cope infectious action of bacteria. Conclusion: This study was conducted to test the medicinal profile of C. papaya by extracting secondary metabolites with organic and aqueous solvents. Ethanol was found to be the best solvents of choice to extract natural products to get maximum medicinal benefits and could be used to medicinal formulation against different infectious diseases.

Supramolecular deep eutectic solvent: a powerful tool for pre-concentration of trace metals in edible oil.

The utilization of supramolecular deep eutectic solvent eddy-assisted liquid-liquid microextraction utilizing 2-hydroxypropyl β-cyclodextrin (SUPRADES) has been identified as a successful method for pre-enriching Cu, Zn, and Mn in vegetable oil samples. Determination of each element was conducted by inductively coupled plasma optical emission spectrometry (ICP-OES) after digestion of metal-enriched phases. Various parameters were examined, including the composition of SUPRADES species [2HP-β-CD: DL-lactic acid], a cyclodextrin mass ratio of 20wt%, a water bath temperature of 75 °C, an extractor volume of 800 μL, a dispersant volume of 50μL, and an eddy current time of 5min. Optimal conditions resulted in extraction rates of 99.6% for Cu, 105.2% for Zn, and 101.5% for Mn. The method exhibits a broad linear range spanning from 10 to 20,000μg L-1, with determination coefficients exceeding 0.99 for all analytes. Enrichment coefficients of 24, 21, and 35 were observed. Limits of detection ranged from 0.89 to 1.30μg L-1, while limits of quantification ranged from 3.23 to 4.29 μg L-1. The unique structural characteristics of the method enablethe successful determination of trace elements in a variety of edible vegetable oils.

The Determination and evaluation of trace elements in the blood of radiography workers using graphite furnace atomic absorption spectrometry

This study aimed to evaluate the potentially toxic effects of trace elements in the blood of Iraqi medical radiography workers by analyzing them through GF-AAS. The study involved 50 male blood radiography workers from the medical imaging field at Al-Shatrah General Hospital in Thi-Qar City, Iraq. All workers were aged between 35-50 years and had worked for less than 10 years. The study compared these workers with 50 healthy men. The study found a significant increase in the levels of Cu, Pb, Cd, and Ca among radiography workers compared to the healthy control group, while Zn and Se levels decreased significantly. Moreover, Specificity and confidence interval (95%) were estimated via the receiver operating characteristic curve (ROC). The study provided conclusive evidence of disturbances in the levels of trace elements in the blood of radiographer workers, which makes them more susceptible to many diseases because of their radiation exposure. which portends the more preventive measures of radiation. The linear range of Cd, Cu, Zn, Se and Pb in human serum were obtained 0.2-6.0 µg dL-1, 6.0-200 µg dL-1, 8.0-200 µg dL-1, 10-250 µg dL-1, 4-120 µg dL-1 by GF-AAS after dilution samples with DW up to 20 (n=10, RSD< 5%).

Determination of copper and other trace elements in serum samples from patients with biliary tract cancers: prospective noninterventional nonrandomized clinical study protocol.

Biliary tract cancers (BTCs) are usually diagnosed at an advanced stage, when the disease is incurable. Currently used tumor biomarkers have limited diagnostic value for BTCs, so there is an urgent need for sensitive and specific biomarkers for their earlier diagnosis. Deregulation of the homeostasis of trace elements is involved in the carcinogenesis of different cancers, including BTCs. The objective of the study is to determine/compare the total concentrations of copper (Cu), zinc (Zn) and iron (Fe) and the proportions of free Cu and Cu bound to ceruloplasmin (Cp) and the isotopic ratio of 65Cu/63Cu in serum samples from healthy volunteers and cancer patients using inductively coupled plasma-mass spectrometry-based methods (ICP-MS). In this prospective, noninterventional, nonrandomized study 20 patients and 20 healthy volunteers will be enrolled to identify serum Cu, Zn and Fe levels, Cu isotopic fractionation as a predictive biomarker of response to systemic therapy of BTCs, which will be evaluated by computed tomography. Newly developed analytical methods based on ICP-MS will be applied to metal-based biomarker research in oncology. In the study the comparison of the total concentration of selected trace elements, the proportion of free Cu and Cu bound to Cp and the isotopic ratio of 65Cu/63Cu in serum samples from healthy volunteers and cancer patients will be conducted to provide the foundation for the development of a BTC cancer screening methodology and the data on their usability as a potential predictive biomarker for BTCs of response to systemic therapy.

The incidence of upper respiratory infections in children is related to the concentration of vanadium in indoor dust aggregates.

It has been reported that the disease-initiated and disease-mediated effects of aerosol pollutants can be related to concentration, site of deposition, duration of exposure, as well as the specific chemical composition of pollutants. To investigate the microelemental composition of dust aggregates in primary schools of Vilnius and determine trace elements related to acute upper respiratory infections among 6-to 11-year-old children. Microelemental analysis of aerosol pollution was performed using dust samples collected in the classrooms of 11 primary schools in Vilnius from 2016 to 2020. Sites included areas of its natural accumulation behind the radiator heaters and from the surface of high cupboards. The concentrations of heavy metals (Pb, W, Sb, Sn, Zr, Zn, Cu, Ni, Mn, Cr, V, and As) in dust samples were analyzed using a SPECTRO XEPOS spectrometer. The annual incidence rates of respiratory diseases in children of each school were calculated based on data from medical records. The mean annual incidence of physician-diagnosed acute upper respiratory infections (J00-J06 according to ICD-10A) among younger school-age children was between 25.1 and 71.3% per school. A significant correlation was found between vanadium concentration and the number of episodes of acute upper respiratory infections during each study year from 2016 to 2020. The lowest was r = 0.67 (p = 0.024), and the highest was r = 0.82 (p = 0.002). The concentration of vanadium in the samples of dust aggregates varied from 12.7 to 52.1 parts per million (ppm). No significant correlations between the other trace elements and the incidence of upper respiratory infections were found, which could be caused by a small number of study schools and relatively low concentrations of other heavy metals found in the samples of indoor dust aggregates. A significant and replicable correlation was found between the concentration of vanadium in the samples of natural dust aggregates collected in primary schools and the incidence of acute upper respiratory infections in children. Monitoring the concentration of heavy metals in the indoor environment can be an important instrument for the prevention and control of respiratory morbidity in children.

WITHDRAWN: Trace metals translocation from soil to plants: Health risk assessment via consumption of vegetables in the urban sprawl of a developing country

The study was conducted at 15 locations around the thermal power plant of Patuakhali district at the coastal area of Bangladesh to determine trace elements in vegetable and assess risk of toxicity. Eight vegetables, namely, tomato (Solanum lycopersicum L.), radish (Raphanus raphanistrum L.), bean (Phaseolus vulgaris L.), brinjal (Solanum melongena L.), bottle gourd (Lagenaria siceraria L.), red amaranth (Amaranthus cruentus L.), arum (Arum maculatum L.) and lady's finger (Abelmoschus esculentus L.) were analyzed for nine trace metals (Cr, Ni, Cu, As, Cd, Pb, Fe, Mn and Zn) to assess contamination load of trace elements in agricultural soil, and health risks posed from vegetable consumption. The mean concentrations of Cr, Cr, Ni, Cu, As, Cd, Pb, Fe, Mn, and Zn in soil were 16.6, 14.8, 5.8, 1.3, 0.72, 9.7, 55261, 456.1, and 105.8 mg/kg, respectively. Average concentrations of As, Cd, and Pb in vegetable species were higher than the maximum allowable concentration (MAC), indicating vegetables species were contaminated by these elements and may pose potential risk to human. Fe, Mn, Zn, Cr, Cu, Pb, and As in soil and vegetables of the study area may arise from anthropogenic activities. The present study suggests that surface soil used for vegetables production should be continuously monitored to check the transfer of toxic metals into the vegetables to minimize the adverse health impacts on consumers and potential threats to food safety.

Rapid Determination of Calcium, Iron, and Zinc in Gluconate Oral Solutions by Solution Cathode Glow Discharge – Atomic Emission Spectroscopy (SCGD-AES)

A novel solution cathode glow discharge atomic emission spectroscopy (SCGD-AES) system coupled with simplified sample preparation was developed for determining Ca, Fe, and Zn in gluconate oral solution. The preparation of the oral solution only involves diluting 1 g of the sample 100-fold and acidification with HNO3 to a concentration of 0.1 mol L−1. The preparation of each solution requires less than 5 min. Five oral solutions containing Ca, Fe, and Zn were analyzed. The results indicate that the optimal parameters are HNO3 of pH 1.0 as the electrolyte, a sample flow rate of 2.05 mL min−1, and a discharge current of 65 mA. The detection limits (DLs) of Ca, Fe, and Zn were 58.64, 64.29, and 15.92 µg L−1. The analyses by SCGD-AES for Ca, Fe, and Zn using direct dilution are in agreement with the values by ICP-OES and SCGD-AES with digestion. A t-test was conducted on the oral liquid samples, revealing that the majority of the obtained p-values exceeded .05. In addition, SCGD-AES reduces the time, energy, and quantity of concentrated HNO3 compared with previous studies, and the measurement time of each oral liquid sample was less than 2 min. These findings demonstrate the use of SCGD-AES as an expedited and dependable method for the determination of trace elements in health food products.

Study of photon interaction parameters in malignant and healthy breast tissues using experimentally determined trace elements

Study of photon interaction parameters in malignant and healthy breast tissues using experimentally determined trace elements

Determination of trace elements in titanium oxides by wavelength dispersive x‐ray fluorescence spectrometry (WD‐XRF)

AbstractTiO2 is used in a great variety of industries (foods, medicines, cosmetics, etc.). In food industry, although the use of TiO2 as additive was banned by EU in 2022, it is still authorized in medicinal products, and is allowed as food ingredient in US and Canada. Focusing on cosmetics, regulations state some forbidden elements (As, Cd, Ni, Hg, Sb, and Pb), and others allowed with a specific limit (Co, Cr, and Se). Most researches about TiO2 characterization are focused on the purity determination and no studies analyzing trace metals in this material have been found. Due to the potential impact of those trace elements on health and safety, a robust method for determining them in TiO2 is required. A methodology for the determination of As, Cd, Co, Cr, Hg, Ni, Pb, Sb, and Se at trace level in TiO2 by WD‐XRF has been developed. Sample was prepared as pressed pellets to achieve low limits required by regulations, and the best conditions were established using n‐butyl methacrylate as binder and plastic spatula to avoid Cr contamination coming from the stainless‐steel one. An in‐depth inquiry conducted to get calibration and validation standards revealed a lack of reference materials; therefore, additions of pure oxides of each element were made to high‐purity TiO2. Validation was performed by two means: analyzing synthetic standards prepared as stated and analyzing two commercial TiO2 by an independent method (ICP‐OES). The developed methodology was suitable to be used as control method to assess whether the materials meet the regulations, since time required to undertake the analysis is much less than other methods.

An overview of preconcentration techniques combined with inductively coupled plasma mass spectrometry for trace element determination in biological studies.

In the last decades, the determination of trace elements in biological materials has emerged as an important area of study because of its relevance to human health and the environment. Inductively coupled plasma mass spectrometry (ICP-MS) has proven to be a powerful tool for trace element analysis, owing to its high sensitivity and ability to determine several elements in a single measurement. However, given the complex nature of biological matrices and the presence of elements, most of them at ultratrace levels, it becomes crucial to complement ICP-MS with preconcentration techniques to increase the sensitivity and selectivity of analytical methods. This article presents an exhaustive overview of liquid- and solid-phase preconcentration techniques used in combination with ICP-MS for trace element determination in different biological samples from 2000 to the present. An in-depth discussion of the advances on the application of state-of-the-art solvents and materials in trace element extraction and preconcentration is presented. Special attention is given to different strategies for elemental speciation analysis, employing both chromatographic and non-chromatographic techniques. The role of automation in these methodologies is also described. Finally, future trends and challenges related to this topic are discussed.

Determination of major and trace elements in silicate rock fused with lithium metaborate using laser ablation-inductively coupled plasma-mass spectrometry

A novel lithium metaborate fusion technique using a homemade fusion furnace and graphite crucibles was developed for the determination of major and trace elements in silicate rocks using LA-ICP-MS.

Comparison between Microwave Digestion and Conventional Open Digestion Method for Heavy Metals determination

In the present study a comparison between microwave assisted digestion and conventional wet acid open digestion system for dissolution of bivalve tissue samples was carried out. Sample matrix decomposition was done by using a mixture of concentrated nitric acid and hydrogen peroxide. The determination of trace elements (Zn, Co, Cu, Cd and Pb) in commercially popular bivalve species from two important fish landing centers in Mumbai was used for this purpose. The recovery of heavy metals after analysis was done using certified reference material TORT 2- Lobster hepatopancreas for both the digestion methods. The results of the present study indicate that microwave digestion system for heavy metal analysis is the preferred method for rapid and good quality results. It provides better recovery and precision for heavy metal analysis. The sample preparation step is much easier by microwave digestion system compared to conventional open digestion methods for heavy metal analysis. It is particularly ideal for trace metals like lead and cadmium as they are generally present in very small concentration in biological samples. In the current study microwave digestion proved to be better method than conventional open digestion method with rapid sample digestion process and least sample contamination problem.

Determination of Trace Elements in Some Beverages

Determination of Trace Elements in Some Beverages

Trace elements and the inflammatory process development: predictive possibilities

Introduction. Late diagnosis of inflammatory pathologies leads to increased risks of chronicization of the process, generalization, development of complications, and reduced effectiveness of therapy. Routine methods of clinical laboratory diagnostics often have diagnostic value at the stage of already developed disease with pronounced clinical manifestations. Determination of blood serum trace elements may have prognostic value in the diagnosis of inflammatory diseases. The trace elements most extensively studied in the context of inflammation and immune defense are copper and zinc. The aim of the study. The aim of the study was to investigate the prognostic significance of determining copper and zinc concentrations in serum in the diagnosis of inflammation. Material and methods. Concentrations of CRP, ferritin, ceruloplasmin, leukocytes, neutrophils, fibrinogen, copper, and zinc were determined in 1153 examined people aged 18 to 86 years. Serum trace elements were determined by ICP-MS method, the rest of the parameters were measured by standard methods. ROC analysis was used to evaluate the prognostic significance of serum copper and zinc measurements. Positive predictive value and negative predictive value were also calculated for the laboratory tests. Results. It was shown that serum copper concentration in both men and women can be used as a predictor of abnormalities of CRP, ceruloplasmin, and fibrinogen. By abnormalities in serum copper concentration, it is possible to predict increased leukocytes in men and women; decreased leukocytes in men; and increased neutrophil levels in men and women. The prognostic significance of the laboratory test for serum zinc was found in relation to the detection of ferritin deficiency in women and ceruloplasmin deficiency in men and women. Conclusion. The results obtained in the study suggest the possible use of serum copper and zinc laboratory tests for prognostic purposes.

Final report for SIM.QM-S12: supplementary comparison for trace elements in natural water

Main textThe SIM Supplementary Comparison SIM.QM-S12 for Trace Elements in Natural Water was undertaken to assess and demonstrate the analytical capabilities of national metrology institutes (NMIs) and designated institutes (DIs) of SIM members (or other regions) for the accurate determination of trace elements in natural water at µg/kg levels.Evidence of successful participation in formal, relevant international comparisons is needed to document calibration and measurement capability claims (CMCs) made by NMIs and DIs.Seventeen NMIs and DIs participated. Participants were requested to evaluate the mass fractions, expressed in µg/kg, of arsenic, cadmium, lead and antimony in a natural mineral groundwater that was spiked with the respective elements. A variety of instrumental techniques including inductively coupled plasma mass spectrometry (ICP-MS), isotope dilution ICP-MS (ID-ICP-MS), inductively coupled plasma optical emission spectrometry (ICP-OES), electrothermal atomic absorption spectrometry (ETAAS) and hydride generation flame atomic absorption spectrometry (HG-FAAS) were used by the participants for the determination.The NIST decision tree was used to assign the SCRV estimate for the proposed measurands and to calculate the degrees of equivalence of each national measurement standard following the IAWG Guidance on Using NIST Decision Tree for Comparison Reporting from 30 June 2023.Successful participation in SIM.QM-S12 demonstrates measurement for determination of elements in water matrices. Considering the IAWG Core Capability Matrix, this material falls into the matrix challenge called "Water/aqueous", which corresponds to the CCQM amount-of-substance category fresh water, and so will support CMCs for the metalloids and semi-metals at mass fraction levels below 50 µg/kg (As and Sb measurements) and transition elements at mass fraction levels below 50 µg/kg (except Hg) (for Cd and Pb measurements).To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database https://www.bipm.org/kcdb/.The final report has been peer-reviewed and approved for publication by the CCQM, according to the provisions of the CIPM Mutual Recognition Arrangement (CIPM MRA).

A comparison of calibration strategies for quantitative laser ablation ICP-mass spectrometry (LA-ICP-MS) analysis of fused catalyst samples

Alternative calibration approaches relying on either aqueous standard solutions or a single solid standard measured under different LA settings, were evaluated in the context of quantitative LA-ICP-MS bulk analysis of fused catalyst samples.

Empirical evaluation of the TXRF detector field of view – a coffee-ring case study

In TXRF the position-dependent signals were studied for concentric ring structures showing elemental separation between inner and outer rings. The specimens were obtained from picoliter printed micro preparation.

A convective heated digestion system with closed vessels: a new digestor for elemental inorganic analysis

A CHDS with closed vessels is now available as a simple, fast and safe alternative for sample preparation for trace element determination. The analytical performance in terms of residual carbon, accuracy, precision and LODs was demonstrated.

Metal-free sampling methods for dust, rainwater, surface water, plants, and sediments: A selection of unique tools from the SWAMP laboratory

Contamination control remains one of the greatest challenges for the reliable determination of many trace elements in environmental samples. Here we describe a series of metal-free sampling devices and tools designed and constructed specifically to minimize the risk of contamination by trace elements during sampling of dust, rainwater, surface water, plants, and sediments. Plastic components fabricated using 3-D printing include polylactic acid (PLA), polyethylene terephthalate (PET), polyethylene terephthalate glycol (PETG), polypropylene (PP), polycarbonate (PC) and PC with carbon fibre. When additional strength is needed (e.g. supporting structural components), carbon fibre, aluminum (Al), or 316 stainless steel (SS) is used. Other plastics employed include acrylic and vinyl. Epoxy glue or SS may be used for joining components, but do not come into contact with the samples. Ceramic (zirconium dioxide) cutting blades are used where needed. Each plastic material was evaluated for contaminant trace elements by leaching with high purity nitric acid in the metal-free, ultraclean SWAMP laboratory. The devices were tested in the field to evaluate their performance and durability. When combined with appropriate cleaning procedures, the equipment enables ultraclean collection for trace element analysis of environmental media.•Plastic sampling devices were designed and constructed using 3D printing of PLA, PET, PETG or PP.•Leaching characteristics of plastic components were evaluated using high purity nitric acid in a metal-free, ultraclean laboratory.•Each sampling device was successfully field-tested in industrial settings (near open pit bitumen mines and upgraders), and in remote locations of northern Alberta, Canada.

Hydrogeochemical characteristics and evaluation of groundwater resources of Jilin Province, China

As one of China's nine border provinces, Jilin Province is an important window for China's “Belt and Road” to open up to the north, and an important channel for China's foreign trade and foreign exchanges. Therefore, understanding hydrogeochemical characteristics is very important for effective water resources management in Jilin Province. A total of 64 groundwater samples were collected from 32 monitoring Wells in Jilin Province. Use of hydrogeochemical analysis techniques, WQI index and human health risk index methods to assess hydrogeochemical processes and groundwater quality, including the determination of hydrogeochemical parameters, conventional ions, trace elements and stable isotopes (δD and δ18O). The results show that the groundwater is slightly alkaline, the cations are mainly Na+, Ca2+, Mg2+, and K+, and the anions are mainly HCO3-, Cl−, and SO42-. Most of the groundwater samples belong to Ca-HCO3 and Na-HCO3 types, which are formed by the dissolution of calcite, dolomite, gypsum, silicates and carbonates. Stable isotope analysis shows that groundwater recharge in Jilin mainly comes from atmospheric precipitation at an altitude of 1,430~2,348 m. The strong correlation between trace elements indicates a common source. Most of the groundwater quality index (WQI) in the study area is Class I to Class III, and hazard quotient (HQ) and hazard index (HI) are both below 1. This indicates excellent water quality and minimal health risks associated with human consumption. It is worth noting that trace elements are enriched in the Tanlu fault zone. It provides scientific guidance for the utilization and allocation of groundwater resources in Jilin Province.