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Rice consumption is a pathway for human exposure to toxic elements. Although rice is a major staple in the Kingdom of Saudi Arabia (KSA) there is limited published data about its toxic element composition. Both imported and locally grown Hassawi rice in Saudi Arabia were collected, digested then analysed by HPLC-ICP-MS for inorganic arsenic (i-As) and by ICP-MS for As, Cd, Pb and Hg. Of these toxic elements, i-As was present at concentrations that might give rise to material concerns about human exposure and public health. Hassawi rice (mean 43 ± 5 µg/kg) was found to have significantly lower concentrations of i-As than imported rice (mean 73 ± 8 µg/kg). The estimated exposure of adults consuming imported rice in one KSA city reached 0.3 µg/kg-bw/day, within the margin of safety of the recently withdrawn WHO PTWI for i-As of 2.1 µg/kg-bw/day and higher than EFSA’s 0.06 µg/kg-bw/day skin cancer BMDL05. [ABSTRACT FROM AUTHOR]

Monosodium methanearsonate (MSMA), a sodium salt of monomethylarsonic acid (MMA), is a selective contact herbicide used for the control of a broad spectrum of weeds. In water, MSMA dissociates to ions of sodium (Na+) and monomethylarsonate (MMA−) that is stable and does not transform abiotically. In soils characteristic of MSMA use, several simultaneous processes can occur: (1) microbial methylation of MMA to dimethylarsinic acid (DMA), (2) microbial demethylation of MMA to inorganic arsenic (iAs), (3) methylation of iAs to MMA, and (4) sorption and sequestration of MMA and its metabolites to soil minerals. Sequestered residues are residues that cannot be desorbed from soil in environmental conditions. Sequestration is rapid in the initial several days after MSMA application and continues at a progressively slower rate over time. Once sequestered, MMA and its metabolites are inaccessible to soil microorganisms and cannot be transformed. The rate and extent of the sorption and sequestration as well as the mobility of MMA and its metabolites depend on the local edaphic conditions. In typical MSMA use areas, the variability of the edaphic conditions is constrained. The goal of this research was to estimate the amount of iAs potentially added to drinking water as a result of the use of MSMA, with models and scenarios developed by the US Environmental Protection Agency for pesticide risk assessment. In this project, the estimated drinking water concentrations (EDWCs) for iAs were assessed as the average concentration in the reservoir over a 30‐year simulation with annual applications of MSMA at maximum label rates. When the total area of suitable land was assumed to be treated, EDWCs ranged from <0.001 to 0.12 µg/L. When high estimates of actually treated acreage are considered, the EDWCs are below 0.06 µg/L across all scenarios. Integr Environ Assess Manag 2024;20:2076–2087. © 2024 The Author(s). Integrated Environmental Assessment and Management published by Wiley Periodicals LLC on behalf of Society of Environmental Toxicology & Chemistry (SETAC). Key Points: Inorganic arsenic (iAs) potentially added to drinking water from the use of monosodium methanearsonate (MSMA) was estimated with models (Pesticide Root Zone Model, version 5 [PRZM5], Variable Volume Water Model [VVWM], and aerial spray prediction model [AgDRIFT]) and based on scenarios developed by the USEPA for pesticide risk assessment.Sequestered residues (residues that could not be extracted by water or weak acids) were considered as losses to the modeled systems in PRZM5 and VVWM.Rate constants used for modeling sequestration and transformation were derived from empirical data representative of MSMA use environments.The modeled estimated drinking water concentration for iAs ranged from <0.001 to 0.12 µg/L when 100% of the suitable area of a watershed is treated with MSMA and below 0.06 µg/L across all scenarios when the actual area treated with MSMA is considered. [ABSTRACT FROM AUTHOR]

Monosodium methanearsonate (MSMA), the sodium salt of monomethylarsonic acid (MMA), is used as a selective, broad‐spectrum contact herbicide to control weeds in cotton and a variety of turf. In water, MSMA dissociates into ions of sodium (Na+) and of MMA−, which is the herbicide's active component. Certain soil microorganisms can methylate MMA to dimethylarsinic acid (DMA) other microorganisms can demethylate MMA to inorganic arsenic (iAs). To predict the groundwater concentration of iAs that may result from MSMA application, the processes affecting the environmental behavior of MSMA must be quantified and modeled. There is an extensive body of literature regarding the environmental behavior of MSMA. There is a consensus among scientists that the fate of MMA in soil is controlled by microbial activity and sorption to solid surfaces and that iAs sorption is even more extensive than that of MMA. The sorption and transformation of MMA and its metabolites are affected by several factors including aeration condition, temperature, pH, and the availability of nutrients. The precise nature and extent of each of these processes vary depending on site‐specific conditions; however, such variability is constrained in typical MSMA use areas that are highly managed. Monomethylarsonic acid is strongly sorbed on mineral surfaces and becomes sequestered into the soil matrix. Over time, a greater portion of MMA and iAs becomes immobile and unavailable to soil microorganisms and to leaching. This review synthesizes the results of studies that are relevant for the behavior of MSMA used as a herbicide to reliably predict the fate of MSMA in its use conditions. Integr Environ Assess Manag 2024;20:1859–1875. © 2024 The Author(s). Integrated Environmental Assessment and Management published by Wiley Periodicals LLC on behalf of Society of Environmental Toxicology & Chemistry (SETAC). Key Points: The environmental fate of monosodium methanearsonate (MSMA) used as a herbicide should be evaluated based on studies conducted with experimental conditions and setup that are relevant to MSMA use.The environmental fate of MSMA in soil is controlled by sorption and sequestration to soil minerals and by microbial activity.The rate and extent of sorption and sequestration of MSMA vary depending on site‐specific conditions; however, such variability is constrained in typical MSMA use areas.With time, the majority of MSMA and its metabolites become immobile and unavailable to soil microorganisms and transport in the environment. [ABSTRACT FROM AUTHOR]

Inorganic arsenic (iAs), which predominantly occurs as arsenite (As3+) and arsenate (As5+) in natural water, is primarily accumulated by seaweed in marine environments. However, the detailed mechanisms through which As3+ and As5+ affect the physiological processes of these organisms remain largely unknown. This study focused on evaluating the toxicological effects of As3+ and As5+ on the seaweed Sarcodia suae. Exposure to As3+ and As5+ resulted in IC50 values of 401.5 ± 9.4 μg L−1 and 975.8 ± 13 μg L−1, respectively. Morphological alterations and a reduction in phycoerythrin content were observed, particularly under As3+ exposure, with increased lipid peroxidation as evidenced by higher malondialdehyde levels. Exposure to As3+ also elevated the production of superoxide radicals, while decreasing hydrogen peroxide levels specifically in the presence of As3+. The induction of antioxidative enzyme activities, namely superoxide dismutase, catalase, glutathione reductase, and ascorbate peroxidase was observed, signaling an adaptive response to iAs-induced oxidative stress. Moreover, levels of the antioxidants ascorbate and glutathione were elevated post-exposure, especially in response to As3+. Additionally, bioaccumulation of arsenic was significantly higher in the As3+ compared to As5+. Collectively, the data suggest that As3+ imposes greater adverse effects and oxidative stress to S. suae, which responds by adjusting its antioxidative defense mechanisms to mitigate oxidative stress. [ABSTRACT FROM AUTHOR]

• A MAE-IC-ICP-MS method was set up to determine Se species in rice plants. • The accumulated Se by rice plants in Se(VI)-added soil was higher than that in Se(IV)-added soil. • Arsenite and As(V) facilitated the conversion of Se(IV) into Se-Cys and Se-Me. • Arsenite and As(V) had higher antagonism on Se species in Se(VI)-added soil than that in Se(IV)-added soil. • Arsenite had higher inhibiting effect on the Se species than As(V) in Se(VI)-added soil. Selenium (Se) in paddy rice is one of the significant sources of human Se nutrition. However, the effect of arsenic (As) pollution in soil on the translocation of Se species in rice plants is unclear. In this research, a pot experiment was designed to examine the effect of the addition of 50 mg As/kg soil as arsenite or arsenate on the migration of Se species from soil to indica Minghui 63 and Luyoumingzhan. The results showed that the antagonism between inorganic As and Se was closely related to the rice cultivar and Se oxidation state in soil. Relative to the standalone selenate treatment, arsenite significantly (p < 0.05) decreased the accumulation of selenocystine, selenomethionine and selenate in the roots, stems, sheaths, leaves, brans and kernels of both cultivars by 21.4%-100.0%, 40.0%-100.0%, 41.0%-100%, 5.4%-96.3%, 11.3%-100.0% and 26.2%-39.7% respectively, except for selenocystine in the kernels of indica Minghui 63 and selenomethionine in the leaves of indica Minghui 63 and the stems of indica Luyoumingzhan. Arsenate also decreased (p < 0.05) the accumulation of selenocystine, selenomethionine and selenate in the roots, stems, brans and kernels of both cultivars by 34.9%-100.0%, 30.2%-100.0%, 11.3%-100.0% and 5.6%-39.6% respectively, except for selenate in the stems of indica Minghui 63. However, relative to the standalone selenite treatment, arsenite and arsenate decreased (p < 0.05) the accumulation of selenocystine, selenomethionine and selenite only in the roots of indica Minghui 63 by 45.5%-100.0%. Our results suggested that arsenite and arsenate had better antagonism toward Se species in selenate-added soil than that in selenite-added soil; moreover, arsenite had a higher inhibiting effect on the accumulation of Se species than arsenate. [Display omitted] [ABSTRACT FROM AUTHOR]

The valorization of massive strandings of holopelagic Sargassum spp. is strongly limited by high levels of inorganic arsenic (Asi) that are potentially above the limit of current regulations. Monitoring Asi in algal biomass is currently achieved using standard chromatographic separation followed by spectroscopic detection. Here, we propose an alternative simpler procedure based on the extraction of Asi from the freeze-dried algal powder in deionized water and the electroanalytical detection of the diluted extract at a gold-microwire electrode. The protocol was optimized both in terms of extraction (powder/water ratio, extraction time, temperature) and electrolyte used for the voltammetric detection. Two electrolytes were tested: one composed of citric acid, sulfamic acid and KCl (pH 2.0) and another composed of an acetate buffer (pH 4.7) and NaCl. We demonstrate here that Asi determination is possible with the first electrolyte but it is necessary to deal with a relative unstable signal. Measurement of Asi was best achieved with the second electrolyte (acetate buffer and NaCl) with the following optimized electrochemical conditions: deposition potential of −1.2 V, deposition time of 30 seconds and linear scan voltammetry. Voltammetric results were then compared to a reference method (HPLC-ICP-MS) using different morphotypes of holopelagic Sargassum spp. (S. natans VIII, S. natans I and S. fluitans III), using commercial extracts of brown seaweeds and using a Hijiki certified reference material. Very good agreement was obtained between our novel method and HPLC-ICP-MS. Both methods show that inorganic arsenic is almost entirely present as As(V) in Sargassum spp. extracts. [ABSTRACT FROM AUTHOR]

Arsenic contamination in environmental waters poses global health and environmental risks. This study addresses the urgent need for rapid, selective, and sensitive detection of inorganic arsenic (iAsIII) in environmental samples. Leveraging the unique properties of gold nanoparticles (AuNPs) and the selective binding affinity of homocysteine (Hcy), we developed a novel colorimetric sensor for iAsIII detection. Our investigation elucidates the mechanism by which Hcy modifies AuNPs, enabling the selective detection of iAsIII ions through chelation between amine and carboxyl groups, primarily with the predominant species H2AsO3− at pH 12.0. Our sensor achieves high selectivity (>10‐fold) for iAsIII amid various interfering ions commonly found in environmental samples. Furthermore, we demonstrate exceptional sensitivity in detecting iAsIII, with a low limit of detection (LOD) of 67 nM, aligning with regulatory standards for arsenic concentration in drinking water. The selectivity and sensitivity of our sensor were validated through experiments with various metal ions and real water samples. In conclusion, our study presents a comprehensive understanding of the mechanism, selectivity, and sensitivity of Hcy‐modified AuNPs in detecting iAsIII, offering a versatile nanosensor platform with significant implications for environmental monitoring and public health. [ABSTRACT FROM AUTHOR]

The present study is the first assessment of inorganic arsenic exposure from various fishery products to the Indonesian population based on a national total diet study (TDS). Based on the TDS report on food chemical contaminants, fish and processed fishery products are among the foodstuffs significantly contributing to total arsenic (t-As) exposure in Indonesia. However, there is no assessment yet for the Indonesian population to inorganic arsenic (i-As), which is known as the most harmful of arsenic compounds as it potentially promotes acute and chronic poisoning. The present assessment is aimed to estimate the exposure to i-As from fish and processed fishery products as well as the level of health risks in different age groups in Indonesia, based on the available t-As concentration data. The results showed that the mean exposure to t-As and i-As from fish and processed fishery products in various age groups were 1.19–2.67 μg/kg bw/day and 0.04–0.08 μg/kg bw/day, respectively. Exposure in various age groups revealed that the highest arsenic exposure was in toddlers (0–4 years) and the lowest in the age group of 19–55 years. Wet seasonings and marine fish consumption led to the most contributors to i-As exposure. The carcinogenic risk of i-As exposure based on the margin of exposure (MOE) demonstrated a low to moderate risk. However, a particular concern to the toddler group is required as the cancer risk (CR) value is higher than the acceptable threshold (>10−4). Additionally, the hazard quotient (HQ) of i-As exposure was determined as a low possibility of chronic risk.

Myanmar is a major rice exporter. Rice is an important source of nourishment for its population. However, rice can be contaminated with toxic elements, including arsenic, long-term exposure to which has been linked to several illnesses, including cancer. There is a paucity of published data on arsenic in Myanmar rice. This study analysed rice (n = 50) from southern, middle and northern Myanmar for both total arsenic (T-As) (by ICP-MS) and inorganic arsenic (i-As) (by species–specific hydride generation ICP-MS or HPLC-ICP-MS). The mean concentration of T-As was 110 μg kg−1(IQR 75–142 μg kg−1), of which 86 μg kg−1 (IQR 58–113 μg kg−1) was high toxicity i-As. The calculated mean i-As intake arising from typical consumption of this rice normalised to typical body weights in Myanmar was approximately 1 μg.kg-bw−1.day−1, close to the recently withdrawn WHO, PTWI of 2.1 μg.kg-bw−1.day−1and higher than the EFSA reported BMDL05 for skin cancers of 0.06 μg.kg-bw−1.day−1.

A rapid, simple, and accurate voltammetric method for quantifying total inorganic arsenic in rice was described in this work. The simplified sample pretreatment involved the addition of a mixed solution of nitric acid and L-cysteine, which facilitated the simultaneous extraction and speciation of arsenic (As(III)). To eliminate interference from complex rice matrices, magnetic composites were employed to absorb copper and other potential interference. Furthermore, As(III) was detected using linear stripping voltammetry with screen-printed electrodes modified in-situ with gold nanoparticles and L-cysteine, enhancing both sensitivity and selectivity. With this strategy, the methodology demonstrated good resistance to interference and high sensitivity, with a detection limit of 0.018 mg/kg. A comparative analysis between this method and liquid chromatography coupled with inductively coupled plasma mass spectrometry (ICP-MS) showed a good correlation with an R2 of 0.995. Additionally, the method was successfully applied to determine total inorganic arsenic in commercial rice samples, yielding satisfactory results.

This study estimated the incremental lifetime cancer risk (ILCR) of inorganic arsenic (iAs) from white rice ingestion in eight countries (China, Korea, Pakistan, Saudi Arabia, Thailand, Vietnam, Bangladesh, and Cambodia) in Asia by using data collected from published literature (n = 4857). ILCR of iAs exposure from white rice ingestion substantially varied with region, ranging from 0.37 to 13.46 per 10000 people, with an average of 6.12 per 10000 people. Bangladesh had the highest ILCR, followed by Cambodia, Vietnam, Thailand, China, Korea, Saudi Arabia, and Pakistan. Carcinogenic risks of iAs exposure from white rice ingestion in China, Korea, Thailand, Vietnam, Bangladesh, and Cambodia are at an unacceptable level (more than 1 per 10000 people). Linear regression analysis indicated that ingestion rate and inorganic arsenic content were the critical factors determining regional differences in carcinogenic risk of iAs exposure from white rice ingestion in Asia.

Prenatal exposure to dietary toxicants is linked to neurocognitive issues, but its effect on early emotional and behavioral development in children is less clear. To explore the relationship between prenatal intake of As, iAs, Cd, MeHg, Pb, PCDD/Fs, DL-PCBs, and NDL-PCBs and emotional and behavioral issues in four-year-old children. This study included 192 mother–child pairs from the ECLIPSES study, assessing prenatal dietary toxicant exposure through a food-frequency questionnaire and Catalan Food Safety Agency data. Children's emotional and behavioral scores were evaluated using the Child Behavior Checklist for ages 1.5–5 years. Multivariable regression and logistic models were used, focusing on iAs after finding significant preliminary associations. Increased prenatal dietary intake of iAs was associated with internalizing, externalizing, and attention-deficit/hyperactivity problems. Higher iAs levels (>4.16 μg/day) significantly increased the risk of total problems (OR = 2.94) and specific issues like anxious/depressed (OR = 4.88), anxiety (OR = 3.27), and oppositional defiant problems (OR = 4.30). High iAs consumption correlated with the intake of meat, eggs, cereals, tubers, fruits, and pulses Prenatal dietary iAs exposure is associated with various emotional and behavioral problems in children. Monitoring and reducing iAs levels in food are crucial for public health. [ABSTRACT FROM AUTHOR]

Environmental context: Seaweeds are known to accumulate high levels of arsenic, and cellular concentrations may reach several orders of magnitude higher than that of the surrounding environment. Arsenic may be methylated by seaweed cells and further metabolised to water-soluble arsenic-containing sugars through unknown pathways. Whether these compounds are the result of a detoxification process or are produced with a biological purpose remains to be seen. Rationale: Seaweeds are known to accumulate high levels of arsenic, which may be subsequently metabolised to small, methylated compounds or become incorporated into large biological molecules such as arsenosugars. The mechanism of arsenosugars production in macroalgae is still largely unknown. Method: This study reports the arsenic speciation of 13 brown, red and green macroalgae collected in May 2021 and February 2022. Water-soluble arsenic speciation was measured using high-performance liquid chromatography–inductively coupled plasma–mass spectrometry (HPLC-ICP-MS) after extraction with a 3% (v/v) hydrogen peroxide solution. Results: Arsenosugars were found to account for the majority of the extracted arsenic in all seaweed samples (>50%), with only small amounts of dimethylarsinate and monomethylarsonate present. Levels of toxic iAs were also low (−1). Sulfur-containing arsenosugars were the dominant arsenicals in brown macroalgae, whereas the phosphate ribose was most abundant in red and green. Discussion: The majority of seaweed species appear to have the ability to synthesise all four arsenosugar derivatives; however, it is unclear why some are produced in higher abundances. The production of arsenosugars may be an efficient way of excluding arsenic from the cytosol, or may serve as useful components in the cell wall matrix, as extremely high levels can be tolerated by the seaweed with no ill effects. AsSug-gly and AsSug-PO4 were detected in every sample analysed, which might suggest that AsSug-gly is the starting point for AsSug-PO4, which could be formed by AsSug-gly binding to phosphate-containing lipids in the cell membrane. Further studies should use both imaging and speciation techniques to investigate the formation of arsenosugars. Environmental context. Seaweeds are known to accumulate high levels of arsenic, and cellular concentrations may reach several orders of magnitude higher than that of the surrounding environment. Arsenic may be methylated by seaweed cells and further metabolised to water-soluble arsenic-containing sugars through unknown pathways. Whether these compounds are the result of a detoxification process or are produced with a biological purpose remains to be seen. (Image credit: Rebecca Sim.) [ABSTRACT FROM AUTHOR]

Seaweed is becoming increasingly popular in the Western diet as consumers opt for more sustainable food sources. However, seaweed is known to accumulate high levels of arsenic—which may be in the form of carcinogenic inorganic arsenic (iAs). Here we propose a fast method for the routine measurement of iAs in seaweed using HPLC-ICP-MS without coelution of arsenosugars that may complicate quantification. The developed method was optimised using design of experiments (DOE) and tested on a range of reference materials including TORT-3 (0.36 ± 0.03 mg kg−1), DORM-5 (0.02 ± 0.003 mg kg−1), and DOLT-5 (0.07 ± 0.007 mg kg−1). The use of nitric acid in the extraction solution allowed for the successful removal of interferences from arsenosugars by causing degradation to an unretained arsenosugar species, and a recovery of 99 ± 9% was obtained for iAs in Hijiki 7405-b when compared with the certified value. The method was found to be suitable for high-throughput analysis of iAs in a range of food and feed matrices including Asparagopsis taxiformis seaweed, grass silage, and insect proteins, and offers a cost-effective, fast, and robust option for routine analysis that requires minimal sample preparation. The method may be limited with regards to the quantification of dimethylarsenate (DMA) in seaweed, as the acidic extraction may lead to overestimation of this analyte by causing degradation of lipid species that are typically more abundant in seaweed than other marine matrices (i.e. arsenophospholipids). However, the concentrations of DMA quantified using this method may provide a better estimation with regard to exposure after ingestion and subsequent digestion of seaweed. [ABSTRACT FROM AUTHOR]

Rice is a staple food and known to accumulate inorganic arsenic (iAs), which is a class 1 carcinogen to humans. Arsenic field-deployable method kits, designed for water testing, are able to screen iAs in rice, to assure food safety and quick decision-making without the need for laboratory analysis. For the arsenic extraction within the field method, nitric acid is used. To make the field method on-site safer, cost-effective and easier to handle, the method was adapted using a Cola in the extraction process. The adapted field-deployable method was tested by screening a total of 30 rice and rice products from the Austrian market. To verify the results obtained by the Cola extraction field-deployable method, the obtained iAs concentration was compared to HPLC-ICP-MS results. The Cola extraction field method obtained an LOD of 39 µg iAs kg−1 rice, and with an average reproducibility of 14% RSD, the method was capable of recording no false-negative but 7% false-positive values at the 2023 updated European Commission (EC) limits for rice. All, but one, screened rice samples were within the EU limits for iAs in rice and rice products. [ABSTRACT FROM AUTHOR]

An analytical method for determination of inorganic arsenic species in retorted oil shale slurry by atomic absorption spectrometry coupled to hydride technique with ultrasound assisted acidic extraction is reported. Trivalent arsenic measurement employed sample stabilization with a pH 4.5 prior to reaction with the reducing agent and analysis. In contrast, total inorganic As depended upon the pre-reduction of As(V) to As(III) with KI and ascorbic acid in 6.0 M HCl and of As(V) was estimated by the difference of the total inorganic As and As(III) concentrations. The limit of quantification was 3.7 mg kg−1 for As(III) and 1.3 mg kg−1 for itAs. [ABSTRACT FROM AUTHOR]

This study evaluated the effectiveness of coke and lemonade extraction methods compared to the standard 1 % v/v HNO3 method for determining inorganic arsenic (iAs) concentrations in rice bran samples using a field-deployable method (Arsenator field kit). The limit of detection (LOD) for the methods was 45 μg kg−1, comparable to existing literature. The extraction efficiencies were assessed by comparing iAs recovery rates, with coke extraction yielding the highest recovery of 127.4 %, followed by lemonade at 116.2 %, and HNO3 at 100 %. Statistical analysis indicated strong correlations between the extraction methods, particularly between HNO3 and coke (Pearson correlation coefficient, 0.990), suggesting that coke extraction is a reliable alternative to the traditional HNO3 method. However, lemonade extraction showed a lower correlation (0.940) and higher false negative rates, indicating potential limitations for regulatory compliance. Notably, at the maximum contaminant limit (MCL) of 0.100 mg kg−1, coke extraction produced an 8 % false positive rate with no false negatives, while lemonade extraction had an 8 % false positive rate and a 17 % false negative rate. This study underscores the potential of coke extraction as a cost-effective and efficient alternative for assessing iAs levels in rice products, especially in resource-limited settings. Recommendations include the standardization of coke extraction protocols and the development of robust monitoring programs to ensure food safety and public health protection against arsenic contamination. Overall, the findings contribute valuable insights for improving arsenic detection methods and regulatory compliance in food safety practices.

Chromium (Cr), total arsenic (As), inorganic arsenic (iAs), cadmium (Cd), mercury (Hg), methylmercury (MeHg), and lead (Pb) were analyzed in in Agaricus blazei, Tricholoma matsutake, Pholiota nameko, agrocybe aegirit, Boletus edulis, Auricularia auricula, and Lentinus edodes collected from online supermarket in China from 2015 to 2017. The order of mean concentrations for the five heavy metals in edible mushrooms was As > Cd > Cr > Pb > Hg. No positive correlation was found between total As and iAs, nor between total Hg and MeHg. The contents of iAs were at a low level except for A. blazei samples. The contents of MeHg were at a low level in all test mushroom samples. And Cr, Cd, and Pb pollution were common problems in the test mushroom samples. The comprehensive factor pollution index was between 0.569 (A. auricula) and 3.056 (B. edulis). The THQ values for the five heavy metals from P. nameko, A. auricula, A. aegirit, and L. edodes samples were less than 1. The hazard index (HI) values of A. blazei, T. matsutake, and B. edulis samples for adults and children were greater than 1, indicating significant health hazard to the adults and children consumers. The cancer risk (CR) values for iAs ranged from 3.82 × 10− 6 (T. matsutake) to 8.61 × 10− 5 (A. blazei), indicating no potential carcinogenic risk to the consumers. The order for carcinogenic risk of each edible mushroom species was A. blazei > L. edodes > P. nameko > A. aegirit > A. auricula > B. edulis > T. matsutake. [ABSTRACT FROM AUTHOR]

Previous studies have shown that inorganic arsenic (iAs) exposure may be associated with genotoxic and cytotoxic effects. The aim of this study was to evaluate the relationship between several polymorphisms in AS3MT and APOE genes and urinary As and the relationship between these polymorphisms and pregnancy loss. We determined urinary As concentrations and performed genotyping analysis in 50 cases of spontaneous pregnancy loss and 50 controls, matched to cases on gestational age. The most frequently identified AS3MT polymorphisms in both cases and controls were in rs10748835 (80% cases and 68% controls), rs3740400 (78% cases and 64% controls), rs7085104 (74% cases and 48% controls), and rs1046778 (62% cases and 54% controls). We identified 30 different haplotypes in AS3MT SNPs, with four predominant haplotypes (>8%). Cases with Haplotype 1 had four-fold higher urinary DMA and two-fold higher MMA concentration than those without this haplotype, the MMA levels were lower in cases and controls with Haplotype 4 compared to Haplotype 1, and the DMA levels were significantly lower in cases with Haplotype 4 compared to Haplotype 3. Cases with Haplotype 1 had higher levels of all analyzed biomarkers, suggesting that Haplotype 1 may be associated with greater exposure to iAs and tobacco smoke. Our results suggest the importance of the AS3MT gene in iAs metabolism among pregnant women with low-level drinking water iAs exposure. [ABSTRACT FROM AUTHOR]

The data gap in food safety regulations have created misinformation leading to the rejection of commodities for trade. The evidence presented is the local regulation of arsenic in sea produce which is based on total arsenic, tAs, instead of toxic inorganic arsenic, iAs. Furthermore, tAs data in animal origin seafood has been widely proven to be dominated by the non-toxic Arsenobetaine, AsB. Therefore, if arsenic regulatory limit was set based only on tAs without reference to iAs data, seafood products might be wrongfully rejected for trade because of non-compliance to tAs limit. We provided analysis of tAs and iAs of 14 local prawn and shrimp commodities from three shrimp/prawn sector namely aquaculture (n = 3), capture (n = 5) and processed (n = 6) using effective extraction, as well as, a fit-for-purpose analytical method for iAs. A HVG-AAS method was developed and validated for iAs with LoQ of 1.6 ppb, analytical range of 0–6 ppb, repeatability RSDr of 0.5–3.1 %, coefficient of determination R2 of 0.9975, and percentage recovery of 90.9 %, while an existing method using ICP-MS was used to verify the tAs. Based on the AOAC Official Method 999.10 2005 with minor adjustments, seafood samples were digested with concentrated nitric acid and hydrogen peroxide under pressure in a closed vessel heated by a microwave digester. An additional step for iAs determination was necessary to ensure compatibility in HVG-AAS analysis. Further subdivision of the aquaculture and capture samples was done by dividing them into 3 fractions, namely head, flesh and peel. Comparison of tAs in all the three fractions indicated that for aquaculture sector, the highest tAs were found in the flesh (2nd highest in % weight) whereas for the capture sector, the highest amount of tAs correlated with the highest % weight of the fraction. On regulatory aspects, speciation analysis on the iAs indicated samples with quantifiable iAs value were in-compliance despite tAs were initially found to be higher than the national limits. Risk assessment of iAs indicated there were no risk for human daily intake based on the BDML0.5 value of 3.0 μg/kg b.w per day for an average 70 kg man. All findings concluded the need for doing arsenic speciation analysis of iAs along with tAs for routine monitoring of prawn/shrimp samples and to revise the local limits from tAs to iAs particularly for seafood commodities.

ObjectiveTo understand the speciation of arsenic in seafood sold in Jiaxing City， the health risks of arsenic exposure due to seafood consumption were evaluated.MethodsTotal arsenic levels and arsenic speciation in 105 samples collected from five seafood categories were detected by high-performance liquid chromatography inductively coupled plasma mass spectrometry. The health risks of inorganic arsenic exposure caused by edible seafood were analyzed based on data for the consumption of aquatic products.ResultsAfter testing 105 samples， the average total arsenic content in the five major types of seafood ranged from 0.85 to 41.85 mg/kg. However， it was primarily in the form of nontoxic arsenobetaine or arsenosugars， with organic arsenic accounting for more than 90% of the total arsenic content. The detection rate of inorganic arsenic was 45.7%， with concentrations ranging from 0.008 to 1.169 mg/kg， and a median value of 0.011 mg/kg. Seafood products with the highest levels of arsenic were mainly seaweed and crustaceans， and one sample exceeded the maximum limit set by the National Food Safety standard GB 2762—2017 for water products by 0.95%. The results of the margin of exposure health risk analysis indicated that the health risks associated with consuming seafood for residents of Jiaxing City were relatively low （margin of exposure values significantly higher than 1）. The risk level was slightly higher for urban residents than for rural residents and slightly higher for females than for males. Increased seafood consumption increased the risk level. Considering factors， such as overall dietary exposure， cooking methods， and transformation during consumption， the risk level would further increase.ConclusionThe health risk caused by inorganic arsenic exposure in seafood is relatively low， but long-term intake of seafood （seaweed and chitin） with high inorganic arsenic content should be avoided.

Nutrients involved in the metabolism of inorganic arsenic (iAs) may play a crucial role in mitigating the adverse health effects associated with such exposure. Consequently, the objective of this study was to analyze the association between the intake levels of nutrients involved in iAs metabolism and alterations in the metabolic profile during arsenic exposure. The study cohort comprised environmentally exposed women: WL (lower total urinary arsenic (As), n = 73) and WH (higher As, n = 73). The analysis included urinary untargeted metabolomics (conducted via liquid chromatography–mass spectrometry) and the assessment of nutrient intake involved in iAs metabolism, specifically methionine, vitamins B2, B6, and B12, folate, and zinc (based on 3-day dietary records of food and beverages). In the WL group, the intake of all analyzed nutrients exhibited a negative correlation with 5 metabolites (argininosuccinic acid, 5-hydroxy-L-tryptophan, 11-trans-LTE4, mevalonic acid, aminoadipic acid), while in the WH group, it correlated with 10 metabolites (5-hydroxy-L-tryptophan, dihyroxy-1H-indole glucuronide I, 11-trans-LTE4, isovalerylglucuronide, 18-oxocortisol, 3-hydroxydecanedioic acid, S-3-oxodecanoyl cysteamine, L-arginine, p-cresol glucuronide, thromboxane B2). Furthermore, nutrient intake demonstrated a positive association with 3 metabolites in the WL group (inosine, deoxyuridine, glutamine) and the WH group (inosine, N-acetyl-L-aspartic acid, tetrahydrodeoxycorticosterone). Altering the intake of nutrients involved in iAs metabolism could be a pivotal factor in reducing the negative impact of arsenic exposure on the human body. This study underscores the significance of maintaining adequate nutrient intake, particularly in populations exposed to arsenic. [ABSTRACT FROM AUTHOR]

The issue of heavy metals contamination of environmental segments is becoming serious day by day with industrial and electronic developments. Economic growth and environmental issue are parallel in many aspects. For instance, increased number of vehicles and rapid industrialisation are indicators of economic growth. Economic run is important and shall continue because it is associated with global needs while environmental pollution is otherwise. Necessary steps are required to be taken to control the release of unwanted chemicals including heavy metals and arsenic to the environment. Arsenic is present in water both in its organic and inorganic form. Among these forms inorganic arsenic (As(III) and As(V)) are very toxic. WHO has recommended a threshold limit for As(III) in drinking water i.e. 10 ppb (equivalent to 10 μg L−1 or 133 nM). Sensing of arsenic has been made possible due to several techniques with a wide range of detection limit. Herein very recent As(III) sensors with detection limit below 10 ppb, mechanism of detection at certain instances, interferants during measurements and future goals have been discussed. Further, the review article covers literature mostly from 2015 to 2021. [ABSTRACT FROM AUTHOR]

A mixture risk assessment (MRA) for four metals relevant to chronic kidney disease (CKD) was performed. Dietary exposure to cadmium or lead alone exceeded the respective reference values in the majority of the 10 European countries included in our study. When the dietary exposure to those metals and inorganic mercury and inorganic arsenic was combined following a classical or personalised modified reference point index (mRPI) approach, not only high exposure (95th percentile) estimates but also the mean exceeded the tolerable intake of the mixture in all countries studied. Cadmium and lead contributed most to the combined exposure, followed by inorganic arsenic and inorganic mercury. The use of conversion factors for inorganic arsenic and inorganic mercury from total arsenic and total mercury concentration data was a source of uncertainty. Other uncertainties were related to the use of different principles to derive reference points. Yet, MRA at the target organ level, as performed in our study, could be used as a way to efficiently prioritise assessment groups for higher-tier MRA. Since the combined exposure to the four metals exceeded the tolerable intake, we recommend a refined MRA based on a common, specific nephrotoxic effect and relative potency factors (RPFs) based on a similar effect size. [ABSTRACT FROM AUTHOR]

Based on ultrasound-assisted extraction, a method for determination of inorganic arsenic in various supplementary food for infants and young children was established. The samples were successively subjected to ultrasonic extraction, n-hexane purification, membrane filtration, and anion column (PRP-X 100, 10 μm, 4.1 mm×250 mm) separation. Then, 15 mmol/L diammonium hydrogen phosphate solution (pH=6.0) was used as the mobile phase. After isocratic elution, it was detected by atomic fluorescence spectrometer. The results showed that the linear relationship of arsenic forms was good in the concentration range of 5~100 ng/mL, with correlation coefficient of each component of above 0.999. The detection limit of the method was 0.010 mg/kg. The recoveries of inorganic arsenic at three spiked concentration levels ranged from 88.7% to 96.3%, and the relative standard deviation (RSD) was 1.8% to 4.9%. The method had the advantages of simple pretreatment, high extraction efficiency, fast analysis speed, high accuracy and good repeatability. Therefore, it could meet the detection requirements of different forms of inorganic arsenic in various supplementary food for infants and young children.

Kelp can accumulate large quantities of arsenic compounds even in the absence of considerable environmental pollution. A substantial difference in toxicity between organic and inorganic arsenic compounds makes the form of arsenic relevant for the risk assessment of consuming kelp thalli and kelp-based products.The aim of the study was to develop an analytical procedure for the selective quantification of organic and inorganic arsenic in kelp thalli by inductively coupled plasma mass spectrometry and solid-phase extraction without scheduled precursors.Materials and methods. The authors studied samples of Laminaria saccharina and Laminaria japonica, spiking mixtures of chemical compounds containing arsenic in different oxidation states, and bioactive dietary supplements based on kelp thalli. Solid-phase extraction was performed using Maxi-Clean SAX cartridges. The arsenic content was determined using an Agilent 7900 inductively coupled plasma mass spectrometer.Results. Microwave-assisted extraction with deionised water ensures 91% recovery of arsenic-containing compounds from kelp thalli, and the addition of hydrogen peroxide to the extractant provides complete extraction. Solid-phase extraction with an eluent based on 3% H2O2 can extract the organic fraction from a mixture of organic and inorganic arsenic compounds without washing the inorganic fraction off the cartridge.Conclusions. The authors offer an effective analytical procedure for the selective quantification of organic and inorganic arsenic in kelp thalli and kelp-based products. This procedure allows for the isolation of arsenic-containing compounds from the organic matrix of kelp with 3% hydrogen peroxide. Solid-phase extraction with this extractant can effectively separate organic and inorganic fractions without prior neutralisation of the test solution.

Prenatal exposure to dietary toxicants is linked to neurocognitive issues, but its effect on early emotional and behavioral development in children is less clear. To explore the relationship between prenatal intake of As, iAs, Cd, MeHg, Pb, PCDD/Fs, DL-PCBs, and NDL-PCBs and emotional and behavioral issues in four-year-old children. This study included 192 mother–child pairs from the ECLIPSES study, assessing prenatal dietary toxicant exposure through a food-frequency questionnaire and Catalan Food Safety Agency data. Children’s emotional and behavioral scores were evaluated using the Child Behavior Checklist for ages 1.5–5 years. Multivariable regression and logistic models were used, focusing on iAs after finding significant preliminary associations. Increased prenatal dietary intake of iAs was associated with internalizing, externalizing, and attention-deficit/hyperactivity problems. Higher iAs levels (>4.16 μg/day) significantly increased the risk of total problems (OR = 2.94) and specific issues like anxious/depressed (OR = 4.88), anxiety (OR = 3.27), and oppositional defiant problems (OR = 4.30). High iAs consumption correlated with the intake of meat, eggs, cereals, tubers, fruits, and pulses Prenatal dietary iAs exposure is associated with various emotional and behavioral problems in children. Monitoring and reducing iAs levels in food are crucial for public health.

Arsenic (As) is a notorious toxic contamination in marine environments, while the toxicity and health risk of As is highly dependent on As species in seafoods. In this study, we hypothesized that the species-specific As bioaccumulation and species resulted in species-specific healthy risk of As in seaweeds. To test the hypothesis, we collected 10 common edible seaweeds from the coast of Hainan Island in South China Sea. Then we comparatively quantified concentration of total As and 5 major As species [AsB, DMA, MMA, As(III), and As(V)] in seaweeds. The results revealed that the concentrations of total As varied significantly among 10 seaweed species. Specially, the highest total As concentration were found in brown seaweeds, followed by red seaweeds, and green seaweeds. Furthermore, the percentage of 5 As species to total As differed significantly among 10 seaweeds. The percentage of AsB was highest in Caulerpa lentillifera (53%) and lowest in Sargassum oligocystum (13%), while that of As(V) was lowest in Caulerpa lentillifera (21%) and highest in Sargassum oligocystum (81%). The iAs [As(III) + As(V)] exhibited highest value in brown seaweeds and least value in green seaweeds. The potential human health risk assessment indicated that the consumption of brown seaweeds of Sargassum oligocystum and Sargassum polycystum could cause a considerable carcinogenic risk and non-carcinogenic risk to residents. Overall, our findings here largely validated our hypothesis that the species-specific As bioaccumulation and As species had great significance to healthy risk of As in seaweeds.

Water management and soil conditions affect the bioavailability of cadmium (Cd) and inorganic arsenic (As) in the soil, and hence, their accumulation in rice grains. A field experiment was conducted to investigate the effects of two water management regimes (flooding and dry–wet alternation) on Cd and inorganic As uptake and transport in rice under different soil conditions (paddy soil developed from gray-brown alluvium, K1; paddy soil developed from weathered shale and slate, K2) in the Sichuan Basin, Western China. The results indicated that compared to the wet–dry rotation, long-term flooding led to a substantial decrease of 49.3~55.8% in soil-available Cd content (p < 0.05), accompanied by a significant increase of 16.0~74.2% in As(Ⅲ) content (p < 0.05), causing no significant difference in As(V) content at the K1 site (p > 0.05). However, differences in soil-available Cd and inorganic As content under different water management treatments were both insignificant at the K2 site (p > 0.05). Long-term flooding treatment at the K1 site resulted in a remarkable reduction of 90.2% in Cd content in rice husks and 92.2% in brown rice (p < 0.05), along with a significant increase of 263.6% and 153.3%, respectively, in As(Ⅲ) content; no significant differences in As(V) content were observed at the K2 site (p > 0.05). In conclusion, the effect of water management on rice Cd and inorganic As varied under different soil conditions, with the change in rice Cd and inorganic As in paddy soil developed from gray-brown alluvium being significantly greater than that in paddy soil developed from weathered shale and slate. [ABSTRACT FROM AUTHOR]

In the present work, the adsorption of arsenic (V) on a new porous material (named BENFEP), was studied for the first time. The parameters pH, adsorbent dosage, initial concentration and contact time were evaluated on the adsorption performance in a batch system. The results show that maximum arsenic removal is achieved at pH 7.0–7.5 with 1.5 g/L adsorbent. The observed data were found to follow the Langmuir adsorption isotherm between pH values of 5 and 9, indicating that the adsorbent had mainly homogeneous sites on its surface. The experimental data obtained from the thermodynamic study showed that the reaction was viable, spontaneous and exothermic. No significant deterioration in water quality was observed after the adsorption process, a characteristic that is fundamental for its application in small-scale water treatment systems, particularly in isolated rural areas. [ABSTRACT FROM AUTHOR]

Inorganic arsenic (iAs) has been a human health concern and is associated with intestinal malignancies. However, the molecular mechanisms of the iAs‐induced oncogenic process in intestine epithelial cells remain elusive, partly because of the known hormesis effect of arsenic. Here, we established that six‐month exposure to iAs at a concentration similar to those found in contaminated drinking water could promote malignant characteristics, including enhanced proliferation and migration, resistance to apoptosis, and mesenchymal‐like transition in Caco‐2 cells. Transcriptome analysis and mechanism study revealed that key genes and pathways involved in cell adhesion, inflammation and oncogenic regulation were altered during chronic iAs exposure. Specifically, we uncovered that down‐regulation of HTRA1 was essential for the iAs‐induced acquisition of the cancer hallmarks. Further, we evidenced that the loss of HTRA1 during iAs‐exposure could be restored by HDAC6 inhibition. Caco‐2 cells with chronic exposure to iAs exhibited enhanced sensitivity to WT‐161, a specific inhibitor of HDAC6, when used alone than in combination with a chemotherapeutic agent. These findings provide valuable information for understanding the mechanisms of arsenic‐induced carcinogenesis and facilitating the health management of populations in arsenic‐polluted areas. This study explored the molecular mechanism associated with long‐term inorganic arsenic exposure in the colon epithelial Caco‐2 cell model. Our findings revealed that the down‐regulation of HTRA1 was essential for the malignant progression induced by chronic arsenic exposure, which could be restored by HDAC6 inhibition. These findings provide valuable information for understanding the key regulators of arsenic‐induced carcinogenesis. [ABSTRACT FROM AUTHOR]

Objective: Establishing a simple and convenient method for the analysis of inorganic arsenic in mineral water and tea beverages. Methods: Amino-functioned polyacrylonitrile nanofibers (NH2-PAN nanofibers) was fabricated and used as adsorbent for pipette-tip solid-phase extraction (PT-SPE) of inorganic arsenic in mineral water and tea beverages followed by hydride generation-atomic fluorescence spectrometry (HG-AFS) analysis. Results: The optimal extraction conditions of pipette-tip solid phase extraction were that the pH of the sample solution was 8, the adsorbent was 12 mg NH2-PAN nanofibers, and the elution solution was 5 mL HCl with a concentration of 0.01 mol/L. Under the optimum conditions, the established method showed good linearity in the range of 0.0235~60 μg/L with correlation coefficient greater than 0.994 and a precision of less than 6%. The spiked recoveries of inorganic arsenic were above 85% for both mineral water and tea beverages at two levels of spiked concentrations. Conclusion: The established NH2-PAN nanofibers based PT-SPE/HG-AFS method is simple, accurate and expected to provide a prospective solution for the detection of inorganic arsenic.