Graphite Furnace Atomic Absorption Spectrometry Research Articles

Physicochemical, Pharmacognostical, Phytochemical, Heavy Metal and Pesticidal Residue Analysis of Angelica glauca Edgew roots: An Approach to Establish Quality Standards Using Advanced Analytical Techniques

Background: Angelica glauca (AG) (family Apiaceae) is used by tribes as a spice and to treat various diseases. Before consumption, effective measures must be used for quality control tests. This study establishes quality standards for A. glauca. The study analyses A. glauca roots for physico-chemical, pharmacognostic, phytochemical, heavy metals, pesticidal residue, microbial load, and aflatoxin Methods: The standard procedure was used for powder microscopy and physiochemical parameters. Multiple culture media were used to measure microbial load. Aflatoxins were estimated using HPLC. Mercury, arsenic, lead, cadmium, chromium, and nickel were estimated using graphite furnace atomic absorption spectrometry. To identify 87 pesticide residues in A. glauca roots, LC-MS was used Results: On root powder microscopy, parenchymatous cells packed with yellow material, capillaries with reticulate thickenings, and simple oval to circular starch grains were found. Foreign matter, LOD, total ash, and extractive values were all within range. Salmonela, Pseudomnas, and Coliform (E. coli) were absent. The total viable aerobic bacterial count was 1.14 x 103 cfu/ml, compared to 1.0 x 105 permitted. Aflatoxins were absent in all samples. Heavy metal levels met the FSSR 2011 maximum residue standard for foods not specified. All 87 pesticides in the crude sample were below detection limits, indicating the safety and quality of the A. glauca root sample. Conclusion: The current findings can be utilized in quality control procedures and to assess the quality of A. glauca samples before incorporating them into formulations. Phytochemical tests, heavy metal analysis, and pesticide residue contents can be used to assess quality before using A. glauca raw materials.

Ultra-trace elemental determination of Si by means of graphite furnace-atomic absorption spectrometry

We present a validated GF-AAS method for ultra-trace Si determination in food simulants, achieving quantification limits of 0.2 μg L− 1 in ethanol and 0.4 μg L−1 in acetic acid, supporting safety standards for dietary supplements and food products.

The Impact of Fireworks on Selected Ambient Particulate Metal Concentrations Associated with the Independence Day Holiday

Fireworks are often used in celebrations and are a known transient source of extreme particulate air pollution, and the particles produced by fireworks are known to contain potentially harmful heavy metals. This study investigated ambient particulate metal concentrations associated with heavy firework use during the United States Independence Day holiday in July 2020 and July 2021 in Fullerton, California, located within the greater Los Angeles metropolitan area. For this study, barium (Ba), chromium (Cr), copper (Cu), lead (Pb), and strontium (Sr) were quantified, with Ba, Cu, and Sr being known tracers for fireworks and Cr and Pb being potentially harmful. Total suspended particulates (TSP) were collected with filters and then extracted and analyzed by graphite furnace atomic absorption spectroscopy. Hourly ambient particulate concentrations at a nearby monitoring station exceeded 500 μg m−3 and 300 μg m−3 in 2020 and 2021, respectively. Greater concentrations of overall particulate matter and ambient metal concentrations were observed during 2020 when compared to 2021, consistent with studies in the literature that have shown increased firework use in the area, likely due to the COVID-19 restrictions in place in 2020. In 2021, the Ba, Cu, and Sr concentrations peaked overnight on 4–5 July as expected, but the Cr and Pb concentrations peaked in the afternoon on July 5. In 2020, the peak concentrations of Cr and Pb were 510 ± 40 ng m−3 and 710 ± 30 ng m−3, respectively, while 4900 ± 200 ng m−3, 3860 ± 40 ng m−3, and 1810 ± 30 ng m−3 were observed for Ba, Cu, and Sr, respectively, among the highest ever observed to our knowledge.

Analysis of Trace Heavy Metal in Solution Using Liquid Cathode Glow Discharge Spectroscopy.

Heavy metal pollution, particularly from cadmium (Cd) and copper (Cu), poses significant environmental and health risks. To address the need for efficient, portable, and sensitive detection methods, this study introduces an improved atmospheric pressure glow discharge atomic emission spectrometry (APGD-AES) technique for quantifying Cd and Cu in water samples. The APGD-AES method offers key advantages, including low energy consumption (<33 W), high excitation energy, and compact design. The system was optimized for a discharge voltage of 550 V (Cd) and 570 V (Cu), a flow rate of 3.6 mL/min, and a solution pH of 1.0. Under these conditions, detection limits reached 16 µg/L for Cd and 1.3 µg/L for Cu. APGD-AES was tested on real water samples, including sewage and tap water, demonstrating compliance with national safety standards and comparable performance to graphite furnace atomic absorption spectrometry (GFAAS). This technique shows promise for real-time, on-site monitoring of trace heavy metals due to its portability, precision, and cost-efficiency.

Association between exposure to arsenic, cadmium, and lead and chronic kidney disease: evidence from four practical statistical models.

Environmental exposure to arsenic (As), lead (Pb) and cadmium (Cd) may cause chronic kidney disease (CKD), with varying independent effects and unclear combined impact. This study aimed to evaluate these effects on CKD. 1,398 individuals were included. Urine arsenic (UAs) was determined by atomic fluorescence method. Urinary cadmium (UCd) and blood lead (BPb) levels were determined by graphite-furnace atomic absorption spectrometry. CKD was defined as an estimated glomerular filtration rate (eGFR) < 60mL/min/1.73m2or proteinuria. Generalized linear models (GLM), restricted cubic spline (RCS) models, weighted quantile sum (WQS) regression, and Bayesian kernel machine regression (BKMR) models were employed to study the independent and combined effects of exposure to As, Pb and Cd on CKD risk. Compared with non-CKD subjects, UAs, UCd, BPb, and creatinine adjusted urinary cadmium (UCdCr) were all significantly higher in CKD subjects. Compared with the lowest quartiles, the ORs (95%CIs) of CKD risk in the highest quartiles were 2.09 (1.16-3.74) for UAs, 2.84(1.56-5.18) for UCd, and 1.79 (1.05-3.06) for UCdCr, respectively. UAs, UCd, and UCdCr were all significantly positively associated with CKD risk in p-trend tests. RCS models revealed non-linear links between UAs, UCd, UCdCr and CKD risk, while a linear dose-response existed for BPb and CKD risk. The OR (95%CI) in WQS models were 1.72 (1.25-2.36) with UAs being the highest weighing metal(loid). BKMR models showed co-exposure mixture linked to higher CKD risk when the ln-transformed metal(loid)s above their 55th percentile. The ln-transformed UAs and UCdCr was significantly positively associated with CKD risk when the other two ln-transformed metals levels were all fixed at their different percentile levels. Synergism between Cd and Pb was also apparent. Single As, and Cd exposure were positively associated with an increased CKD risk. Co-exposure to As, Pb and Cd was positively associated with CKD risk, with As playing a dominant role.

Comparative Seasonal Trends and Potential Health Impacts of Arsenic and Chromium in Surface Water after Adsorption Using Highly Dispersed Fe3O4 Nanoparticles.

Surface water from springs, rivers, and dams is often used as an unconventional drinking water source in rural areas where potable water is often unavailable. However, this practice carries significant health risks due to potential contaminants. In this study, the concentrations of arsenic (As) and chromium (Cr) were assessed seasonally using graphite furnace atomic absorption spectrometry (GFAAS). Highly dispersed Fe3O4 nanoparticles were synthesized, characterized, and utilized as adsorbents to remove As and Cr ions from various water matrices. The removal process was optimized by adjusting the mass of the nanoparticles, pH levels, and sonication time. To further understand the adsorption process, adsorption isotherms and kinetics were conducted. Physicochemical properties such as pH, electrical conductivity, and total dissolved solids were seasonally evaluated. The average As concentrations were in the range of 13.3-46.8µg/L, while Cr was in the range of 1.02-5.04µg/L. Expectedly, higher concentrations of As and Cr were observed in summer when there was intense precipitation, and the lowest concentrations were observed in winter, with little to no precipitation. The calibrated GFAAS displayed an excellent limit of detection, limit of quantification, and linearity of 0.092-0.13, 0.27-0.34, and 0.27-70µg/L for As, while 0.031-0.07, 0.16-0.21, and 0.16-70µg/L were attained for Cr, respectively. Arsenic levels exceeded 10µg/L in all seasons, indicating that these concentrations were above the maximum permitted levels set by the World Health Organization and the South African National Standards. According to the health risk assessment, high As concentrations were alarming, as they were seasonally increasing, with the chronic daily intake exceeding the oral reference dose, whilst the incremental lifetime cancer risk was significantly high.

Heavy Metal Contamination Suspected Cause of Mass Deaths in Seaweed Cultivation in Waters Affected by Mine Waste

Since 2012 until this year, there has been a decrease and a mass death of seaweed, especially in centers where mining exploitation is located. The need for technology on seaweed that is almost extinct is eroded due to environmental damage caused by mining industry waste. One technology that can be used in genome editing is mapping and selecting potential superior genes in several seaweeds cultivated in Morowali waters. This research uses experimental research methods. The data collection technique in this study is observation—water measurement and sampling at 16 stations. The collected data were then analyzed by the International Modification Association of Official Analytical Chemists (AOAC) method 2005: 999.10, using Flame Atomic Absorption Spectrophotometer (FAAS) and Graphite Furnace Atomic Absorption Spectroscopy (GFAAS). The results showed that the heavy metal content in mercury/mercury, arsenic, nickel, and lead exceeded the aquatic biota threshold. In addition, the highest heavy metal content in Fatufia and Lalampu waters is accompanied by reddish and muddy watercolor.

Study on the Thermal Control Performance of Mg-Li Alloy Micro-Arc Oxidation Coating in High-Temperature Environments

This paper reports on the successful preparation of a low absorption–emission thermal control coating on the surface of LAZ933 magnesium–lithium alloy using the micro-arc oxidation method. This study analyzed the microstructure, phase composition, and thermal control properties of the coating using Scanning Electron Microscopy (SEM), X-ray diffraction (XRD), UV–visible near-infrared spectroscopy (UV-VIS-NIR) and infrared emissivity measurements. The results indicate that the hemispherical emissivity of the coating remains unaffected with an increase in temperature and holding time, while the solar absorption ratio gradually increases. The thermal control performance of the coating after a high-temperature experiment was found to be related to the diffusion of the Li metal element in the magnesium lithium alloy matrix, as determined by X-ray photoelectron spectroscopy (XPS), flame graphite furnace atomic absorption spectrometry (GFAAS) and Glow Discharge Optical Emission Spectroscopy (GD-OES). As the holding time is extended, the coating structure gradually loosens under thermal stress. The Li metal element in the substrate diffuses outward and reacts with O2, H2O and CO2 in the air, forming LiO2, LiOH, Li2CO3 and other products. This reaction affects the coating’s solar absorption ratio in the end.

Metallomic Approach to Mercury and Selenium in the Liver Tissue of Psectrogaster amazonica and Raphiodon vulpinus from the Brazilian Amazon.

This paper reports the results of a mercury (Hg) and selenium (Se) metallomic study in the liver tissues of Psectrogaster amazonica and Raphiodon vulpinus from the Brazilian Amazon. Two-dimensional electrophoresis, graphite furnace atomic absorption spectrometry, and liquid chromatography-tandem mass spectrometry were performed. Hg and Se determinations allowed the calculation of Hg:Se and Se:Hg molar ratio and Se values for health benefits (Se HBVs). The Se:Hg values were >1 for both fish species, whereas the Se HBVs were >5 for P. amazonica and >10 for R. vulpinus, indicating that both possess Se reserves to control Hg toxicity. The metallomic data allowed the identification of 11 Hg/Se-associated protein spots in the two fish species, with concentrations in the range of 9.70 ± 0.14 and 28.44 ± 0.31 mg kg-1 of Hg and 16.15 ± 0.21 and 43.12 ± 0.51 mg kg-1 of Se. Five metal binding proteins (MBP) in the Hg/Se-associated protein spots in the liver proteome of P. amazonica and eight in R. vulpinus were identified, indicating the possible formation of Hg/Se complexes on the MBP structures. The activities analysis of catalase, superoxide dismutase, GPx enzymes, and lipoperoxide concentrations demonstrated that Hg-induced oxidative stress did not occur, possibly because both fish species possess Se reserves necessary to inhibit the Hg's deleterious effects.

Assessment of trace metal levels in water, sediment and fish tissue from Lake Small Abaya, Ethiopia

The environmental impact of trace metal contamination is a concern for Lake Small Abaya, Ethiopia, because of nearby agricultural and industrial activities. This study assessed the levels of trace metals (Pb, Zn, Cd, Cu, Fe, Mn, and Cr) in water, sediment, and fish samples, as well as the physicochemical parameters of the water. Samples were collected from five sites and analyzed via graphite furnace atomic absorption spectrometry (GFAAS). The mean concentrations in the water were Zn: 0.6971 mg/l, Fe: 0.5628 mg/l, Cu: 0.1168 mg/l, Mn: 0.2129 mg/l, Pb: 0.0057 mg/l, Cr: 0.0021 mg/l, and Cd: 0.0014 mg/l. In the sediments, the mean concentrations were as follows: Fe, 33.066 mg/kg; Zn, 18.263 mg/kg; Mn, 22.777 mg/kg; Cu, 7.5663 mg/kg; Pb, 0.0751 mg/kg; Cr, 0.0233 mg/kg; and Cd, 0.0183 mg/kg. The fish samples presented mean concentrations of Fe: 21.855 mg/kg, Zn: 12.686 mg/kg, Cu: 0.3185 mg/kg, Mn: 0.9181 mg/kg, Pb: 0.0089 mg/kg, Cd: 0.0075 mg/kg, and Cr: 0.0015 mg/kg. All the metal concentrations were generally below the World Health Organization (WHO) regulatory limits. The physicochemical parameters indicated slightly alkaline to neutral conditions, with electrical conductivity and total dissolved solids within acceptable ranges. These findings suggest that current agricultural and industrial activities do not significantly contribute to trace metal pollution. However, continued monitoring and pollution control measures are recommended to ensure the long-term health and sustainability of the lake. This study highlights the importance of effective environmental management strategies to safeguard this crucial aquatic resource.

Copper supplementation alleviates hypoxia‑induced ferroptosis and oxidative stress in neuronal cells.

Hypoxic ischemia is the primary cause of brain damage in newborns. Notably, copper supplementation has potential benefits in ischemic brain damage; however, the precise mechanisms underlying this protective effect remain unclear. In the present study, a hypoxic HT22 cell model was developed to examine the mechanism by which copper mitigates hypoxia‑induced oxidative stress. Cell viability was assessed using the Cell Counting Kit‑8 assay, mitochondrial structure was examined with a transmission electron microscope, intracellular ferrous ions and lipid reactive oxygen species levels in HT22 cells were measured using FerroOrange and BODIPY 581/591 C11 staining, copper content was determined using graphite furnace atomic absorption spectroscopy, and gene and protein expression were analyzed by reverse transcription‑quantitative PCR and western blotting. The present findings indicated that hypoxic exposure may lead to reduced cell viability, along with the upregulation of various markers associated with ferroptosis. Furthermore, hypoxia elevated the levels of reactive oxygen species, hydrogen peroxide and malondialdehyde, and decreased the activity of superoxide dismutase 1 (SOD1) in HT22 cells. In addition, the intracellular copper concentration exhibited a notable decrease, while supplementation with an appropriate dose of copper effectively shielded neurons from hypoxia‑induced oxidative stress and ferroptosis, and elevated cell viability in hypoxia‑exposed HT22 cells through the copper chaperone for superoxide dismutase/SOD1/glutathione peroxidase 4 axis. In conclusion, the present study identified a novel function of copper in protecting neurons from oxidative stress and ferroptosis under hypoxic conditions, providing fresh insights into the therapeutic potential of copper in mitigating hypoxia‑induced neuronal injury.

Contaminants in the Soil and Typical Crops of the Pannonian Region of Slovenia

Soil contamination and the uptake of pollutants by food crops are widespread issues that vary greatly by region and are influenced by the mineral composition of the soil and local human activities. The Pannonian region, where agriculture has played a key role since Roman times, has been particularly impacted by the long-standing agricultural and industrial practices. While soil contamination with heavy metals is monitored by the Slovenian government, microplastic contamination and the uptake of pollutants into food crops have yet to become a regular component of monitoring efforts. In this study, we conducted a preliminary investigation into soil and crop contamination across the Pannonian region, focusing on identifying harmful contaminants and their potential uptake into food crops. Both soil and crop samples were analyzed for the presence of heavy metals with proven methods such as atomic absorption spectrometry (FASS), graphite furnace atomic absorption spectrometry (GF-AAS), atomic fluorescence spectrometry (AFS), and inductively coupled plasma–mass spectrometry (ICP-MS). Energy-dispersive X-ray spectroscopy (EDS) was found to be a potentially faster method of obtaining data on soil composition. Special attention was also given to the potential presence of microplastics in the region’s soils.

Development of a novel method based on extraction mediated by a semipermeable membrane to determine Cd and Cr in sugar by graphite furnace atomic absorption spectrometry

This work proposes a novel method to determine the Cd(II) and Cr(III) content in commercial sugar samples. It is based on the extraction of the analytes (as ammonium pyrrolidine dithiocarbamate complexes) into a semipermeable membrane device (SPMD) filled with CHCl3. After extraction, the SPMD was deployed and opened, and the analytes were recovered from the organic phase by back extraction with a 4.2 mol L−1 HNO3 solution. The analytes present in the acid extract were measured with graphite furnace atomic absorption spectrometry. Under optimized conditions, the limit of quantification of the method was 1.2 and 3.1 ng g−1 for Cd(II) and Cr(III), respectively. Twelve samples of different types of sugar were analyzed. In addition, a recovery test was performed to evaluate the accuracy of the method. The recovery percentage was 90 %–102 % for Cd(II) and 85.2 %–103 % for Cr(III).

Development of CadR-based cadmium whole cell biosensor for visual detection of environmental Cd2+

BackgroundAs a threat to human health and public health, cadmium (Cd) pollution has received widespread social concern. Our previously constructed CadR-based bacterial whole cell biosensor (WCB) epCadR5 showed high sensitivity and specificity in cadmium detection. However, the application of the sensor is still hindered by the need for laboratory equipment to read the fluorescence signal output. In this study, we aimed to optimizing the sensor to make it available for visual detection of environmental cadmium and simplify the detection process to advance practical application of the sensor. ResultsBy replacing the constitutive promoter with J110, the fluorescence signal output of the sensor was significantly increased and the fluorescence leakage was decreased. In addition, the fluorescence signal output of green fluorescence protein (GFP) was enhanced by the addition of a 5′ untranslated region (5′-UTR) mlcR10. The fluorescence signal output of the WCB is sufficiently robust to be visible and distinguishable to the naked eye, which is of paramount importance for visual detection. The sensor readout can be conveniently recorded by mobile phone camera and quantified. For ease of on-site application, the WCB's visual detection procedures and conditions were further optimized and simplified. The WCB demonstrated good linearity and detection limit (1.81 μg/L) for visual detection of Cd2+ without the assistance of bulky laboratory equipment. For the detection of real environmental samples, the WCB visual detection results were close to those of WCB-flow cytometry (FACS) and graphite furnace atomic absorption spectroscopy (GFAAS). SignificanceIn this work, we developed an easy-to-use, on-site and visual detection biosensor for monitoring environmental Cd2+. It will advance the utilization of cadmium WCBs in practical settings. The optimization and simplification strategy in the study also provide new insights into the visualization of other bacterial biosensors, and will advance the practical application of WCBs.

Validation of GF-AAS Method for the Determination of Aluminium Content in Human Albumin Finished Product

Background: Purified human albumin fractionated from plasma has a complex matrix that imposes a lot of interference in quality control testing, particularly for impurities at trace level. In this study, a simple approach has been studied and validated for the quantification of aluminium content using Graphite Furnace Atomic Absorption Spectrometry (GF-AAS). As per international guidelines, the linearity, accuracy, precision, specificity, limit of detection, and quantification have been assessed. Results: The linearity of the analyte response was evaluated over the range of concentrations from 5μg/L to 45 μg/L, and the correlation coefficient obtained was greater than 0.99. The mean recovery obtained for the accuracy ranged from 102.29% to 106.81% at three concentration levels. The specificity/selectivity evaluated for possible interference from other metal ions and relative standard deviation for the high and low content was 10.24% and 6.50%, respectively, which was statistically verified and not significant. Method precision was evaluated for repeatability and intermediate precision, and the relative standard deviation obtained was 1.83% and 4.61%, respectively. The limit of detection and quantification obtained was 1.30 μg/L and 4.10 μg/L, respectively. Conclusion: Results obtained for the method performance show the suitability of the method for aluminium estimation in human albumin samples and should be used to control the limit of aluminium in human albumin blood products.

Determination of Trace Cobalt in Water Samples by Ionic Liquid-Dispersive Liquid–Liquid Microextraction and Graphite Furnace Atomic Absorption Spectrometry

Determination of Trace Cobalt in Water Samples by Ionic Liquid-Dispersive Liquid–Liquid Microextraction and Graphite Furnace Atomic Absorption Spectrometry

Identification of Major Interfering Substances for Heavy Metal Determination in Northern Sea Areas of Sri Lanka

This study investigated the physicochemical characteristics of seawater from five locations along the northern Sri Lankan coast, encompassing areas with varying degrees of anthropogenic activity. The analysis revealed significant variations in several parameters, potentially influenced by human influences. The results reveal significant variations in several parameters. For instance, turbidity levels varied from 1.88 NTU in Thalaiyadi to 13.3 NTU in Pannai, with Pannai, Myliddy, and Kakkaithivu exceeding the recommended limit of 5 NTU. Total suspended solids (TSS) ranged from 3 mg/L in Thalaiyadi to 83 mg/L in Pannai, surpassing the recommended limit of 30 mg/L. Electrical conductivity (EC) ranged from 45,700 µS/cm in Nainathivu to 49,500 µS/cm in Pannai, exceeding the typical seawater range. Nitrate levels ranged from 10.4 mg/L in Thalaiyadi to 19.1 mg/L in Myliddy. Major cations such as calcium (361 mg/L to 417 mg/L), magnesium (1,222 mg/L to 1,327 mg/L), and sodium (10,140 mg/L to 10,530 mg/L) also showed significant differences across locations. These findings highlight the need for continuous monitoring and effective management strategies to mitigate the negative impacts of anthropogenic activities on these coastal ecosystems. Furthermore, the complex seawater matrix presents challenges for heavy metal determination using Graphite Furnace Atomic Absorption Spectroscopy (GFAAS) due to spectral interferences from major cations, non-specific matrix effects, and interferences from organic matter, turbidity, and suspended solids. Careful consideration of these factors through background correction techniques, matrix modifiers, sample pre-treatment, and optimization of analysis parameters is crucial for accurate heavy metal determination in these environments. This study contributes to a better understanding of the environmental conditions and emphasizes the need for further research on heavy metal contamination and the development of robust analytical methods tailored to address the challenges posed by the complex seawater matrix in northern Sri Lanka.

Effects of Processing on Nickel Content and its Relationship with Proximate Composition in dead fresh and canned tuna fish in Iran

Background: The presence of toxic metals in food can be a risk to food safety and public health. Methods: The Iranian canned tuna was analyzed for nickel level after wet digestion with acids using Graphite Furnace Atomic Absorption Spectrometry (GFAAS). Results: The average concentration of nickel in canned and dead fresh fish found 4.20 ppb and 1.64 ppb. A significant difference in nickel level was observed between canned and dead fresh fish samples in this study. Although the concentration of nickel per g in the fillet after processing was relatively low, but the total amount of nickel in the sample shown change (256.01%). The results in present study showed the protein content in the canned fish increased to 13.17%. The moisture content in the processed fish decreased to 8.80%. The fat content in the canned fish increased to 12.86%. Conclusion: Although the protein and moisture contents significantly increased and decreased respectively after processing, but none of these factors were related to the change in nickel concentration. It may be recommended to regularly monitor the concentration of nickel metal in aquatic food products, so that human health was not at risk.

Cadmium Exposure and Noncommunicable Diseases in Environmentally Exposed Brazilian Population: Cross-Sectional Study without Association of GSTP1 Polymorphism.

Cadmium (Cd) is a toxic metal which is harmful to humans and the environment. Cd levels and adverse effects may be associated with genetic polymorphisms in genes involved in its toxicokinetics. This study investigated Cd levels in 198 residents of a condominium in Rio de Janeiro, Brazil, built on industrial steel slag waste and the influence of glutathione S-transferase pi isoform 1 (GSTP1) rs1695 A>G polymorphism. Polymorphism was genotyped using a validated TaqMan assay; Cd levels were measured in blood (BCd) and urine (UCd) by graphite furnace atomic absorption spectrometry. Associations were evaluated by multiple logistic regression, odds ratios (ORs), and 95% confidence intervals (CIs). The mean Cd levels were 0.70 ± 0.20 µg L-1 (BCd), 0.58 ± 0.57 µg L-1 (UCd), and 0.61 ± 0.65 µg g-1 in urine corrected by creatinine (UcCd), and the Cd results were above tolerable levels (BCd > 0.5 µg L-1) in 87.4% of subjects. Higher blood Cd levels (>0.69 µg L-1) were associated with respiratory disease (OR = 2.4; 95%CI = 1.2-5.0), as almost 30% of people with respiratory diseases had higher Cd levels. The GSTP1 rs1695AA genotype frequency was 38.1%, and there were no significant differences between the SNP and Cd levels. High Cd levels and a high prevalence of diseases highlight the importance of implementing public policies and the continuous monitoring of this at-risk population.

Engineering Novel Amphiphilic Platinum(IV) Complexes to Co-Deliver Cisplatin and Doxorubicin.

In this study, we report a novel platinum-doxorubicin conjugate that demonstrates superior therapeutic indices to cisplatin, doxorubicin, or their combination, which are commonly used in cancer treatment. This new molecular structure (1) was formed by conjugating an amphiphilic Pt(IV) prodrug of cisplatin with doxorubicin. Due to its amphiphilic nature, the Pt(IV)-doxorubicin conjugate effectively penetrates cell membranes, delivering both cisplatin and doxorubicin payloads intracellularly. The intracellular accumulation of these payloads was assessed using graphite furnace atomic absorption spectrometry and fluorescence imaging. Since the therapeutic effects of cisplatin and doxorubicin stem from their ability to target nuclear DNA, we hypothesized that the amphiphilic Pt(IV)-doxorubicin conjugate (1) would effectively induce nuclear DNA damage toward killing cancer cells. To test this hypothesis, we used flow the cytometric analysis of phosphorylated H2AX (γH2AX), a biomarker of nuclear DNA damage. The Pt(IV)-doxorubicin conjugate (1) markedly induced γH2AX in treated MDA-MB-231 breast cancer cells, showing higher levels than cells treated with either cisplatin or doxorubicin alone. Furthermore, MTT cell viability assays revealed that the enhanced DNA-damaging capability of complex 1 resulted in superior cytotoxicity and selectivity against human cancer cells compared to cisplatin, doxorubicin, or their combination. Overall, the development of this amphiphilic Pt(IV)-doxorubicin conjugate represents a new form of combination therapy with improved therapeutic efficacy.