Inorganic Arsenic Compounds Research Articles

Mo-doped Co LDHs as Raman enhanced substrate for detection of roxarsine

BackgroundRoxarsone (ROX) is widely used as a feed additive, which is indigestible after ingestion by poultry, and most of it can only be excreted into the natural environment and degraded into highly toxic and carcinogenic inorganic arsenic compounds, which pose a hazard to the ecosystem and human health. However, for roxarsone, traditional detection methods require complex and time-consuming procedures, so it is urgent to find a new fast detection method for detection of ROX. ResultsIn this work, we developed a novel Raman enhancement material and utilized the Surface-enhanced Raman scattering (SERS) technique to achieve rapid and sensitive detection of roxarsone. Specifically, Mo-doped cobalt layered double hydroxides (Co-LDHs) semiconductor material (abbreviated as CMM-100) was prepared by a simple method of using ion-assisted MOF etching. Under laser excitation at a wavelength of 532 nm, the CMM-100 showed excellent SERS property to various organic dye molecules such as methylene blue (MB), Toluidine Blue(TB), and Crystal Violet (CV). Especially, an enhancement factor (EF) of 1.4 × 106 was achieved for MB. Compared with the traditional method, this work utilized the fast and non-destructive SERS technology, which achieved a rapid detection of ROX. The detection limit was as low as 9.73 × 10−10 M, and the detection range was from 10−9 M to 10−3 M. SignificanceIn this work, SERS technology was adopted for the rapid and sensitive detection of ROX. This study provides a Raman-enhanced substrate named CMMs for detection of food additives, pesticides, biomolecules, etc., which also broadens the application areas of SERS materials.

Design and Synthesis of Thiourea-Conjugating Organic Arsenic D-Glucose with Anticancer Activities.

Organic arsenic compounds such as p-aminophenylarsine oxide (p-APAO) are easier for structural optimization to improve drug-like properties such as pharmacokinetic properties, therapeutic efficacy, and target selectivity. In order to strengthen the selectivity of 4-(1,3,2-dithiarsinan-2-yl) aniline 7 to tumor cell, a thiourea moiety was used to strengthen the anticancer activity. To avoid forming a mixture of α/β anomers, the strategy of 2-acetyl's neighboring group participation was used to lock the configuration of 2,3,4,6-tetra-O-acetyl-β-d-glucopyranosyl isothiocyanate from 2,3,4,6-tetra-O-acetyl-α-d-glucopyranosyl bromide. 1-(4-(1,3,2-dithiarsinan-2-yl) aniline)-2-N-(2,3,4,6-tetra-O-acetyl-β-d-glucopyranos-1-yl)-thiourea 2 can increase the selectivity of human colon cancer cells HCT-116 (0.82 ± 0.06 μM vs. 1.82 ± 0.07 μM) to human embryonic kidney 293T cells (1.38 ± 0.01 μM vs. 1.22 ± 0.06 μM) from 0.67 to 1.68, suggesting a feasible approach to improve the therapeutic index of arsenic-containing compounds as chemotherapeutic agents.

Iron scrap derived nano zero-valent iron/biochar activated persulfate for p-arsanilic acid decontamination with coexisting microplastics

P-arsanilic acid (AA) has received widespread attention because of its conversion to more toxic inorganic arsenic compounds (arsenate and arsenite) in the natural ecosystems. Its removal process and mechanisms with co-existence of microplastics remain unkown. In this study, biochar loaded with nano zero-valent iron (nZVI) particles (ISBC) was prepared by using iron scrap obtained from a steel works and wood chips collected from a wood processing plant. The advanced oxidation system of sodium persulfate (PDS) activated by ISBC was applied for AA degradation and inorganic arsenic control in aqueous media. More than 99% of the AA was completely degraded by the ISBC/PDS system, and the As(III) on AA was almost completely oxidized to As(V) and finally removed by ISBC. HCO3− inhibited the removal of AA by the ISBC/PDS system, while Cl− had a dual effect that showing inhibition at low concentrations yet promotion at high concentrations. The effect of microplastics on the degradation of AA by the ISBC/PDS system was further investigated due to the potential for combined microplastic and organic arsenic contamination in rural/remote areas. Microplastics were found to have little effect on AA degradation in the ISBC/PDS system, while affect the transport of inorganic arsenic generated from AA degradation. Overall, this study provides new insights and methods for efficient removal of p-arsanilic acid from water with coexisting microplastics.

Speciation analysis and toxicity evaluation of arsenolipids-an overview focusing on sea food.

Arsenic, which can be divided into inorganic and organic arsenic, is a toxic metalloid that has been identified as a human carcinogen. A common source of arsenic exposure in seafood is arsenolipid, which is a complex structure of lipid-soluble organic arsenic compounds. At present, the known arsenolipid species mainly include arsenic-containing fatty acids (AsFAs), arsenic-containing hydrocarbons (AsHCs), arsenic glycophospholipids (AsPLs), and cationic trimethyl fatty alcohols (TMAsFOHs). Furthermore, the toxicity between different species is unique. However, the mechanism underlying arsenolipid toxicity and anabolism remain unclear, as arsenolipids exhibit a complex structure, are present at low quantities, and are difficult to extract and detect. Therefore, the objective of this overview is to summarize the latest research progress on methods to evaluate the toxicity and analyze the main speciation of arsenolipids in seafood. In addition, novel insights are provided to further elucidate the speciation, toxicity, and anabolism of arsenolipids and assess the risks on human health.

Maternal Exposure to Arsenic and Its Impact on Maternal and Fetal Health: A Review.

Arsenic exposure is a significant public health issue, with harmful effects caused by its use in commercial products such as car batteries, pesticides, and herbicides. Arsenic has three main compounds: inorganic, organic, and arsine gas. Inorganic arsenic compounds in water are highly toxic. The daily intake of arsenic from food and beverages is between 20 and 300 mcg/day. Arsenic is known for its carcinogenic properties and is classified as a human carcinogen by different institutions. Exposure can lead to oxidative stress, DNA damage, and epigenetic deregulation, which can cause endocrine disorders, altered signal transduction pathways, and cell proliferation. In addition, arsenic can easily cross the placenta, making it a critical concern for maternal and fetal health. Exposure can lead to complications such as gestational diabetes, anemia, low birth weight, miscarriage, and congenital anomalies. Female babies are particularly vulnerable to the negative impact of arsenic exposure, with a higher risk of low weight for gestational age and congenital cardiac anomalies. Therefore, it is crucial to monitor and regulate the levels of arsenic in drinking water and food sources to prevent these adverse health outcomes. Further research is necessary to fully understand the impact of arsenic exposure on human health, especially during pregnancy and infancy, by implementing preventative measures and monitoring the levels of arsenic in the environment.

Interaction between roxarsone, an organic arsenic compound, with humic substances in the soil simulating environmental conditions

In environmental systems, the soil is a principal route of contamination by various potentially toxic species. Roxarsone (RX) is an arsenic (V) organic compound used to treat parasitic diseases and as an additive for animal fattening. When the animal excretes RX, the residues may lead to environmental contamination. Due to their physicochemical properties, the soil's humic substances (HS) are important in species distribution in the environment and are involved in various specific interaction/adsorption processes. Since RX, an arsenic (V) compound, is considered an emerging contaminant, its interaction with HS was evaluated in simulated environmental conditions. The HS-RX interaction was analyzed by monitoring intrinsic HS fluorescence intensity variations caused by complexation with RX, forming non-fluorescent supramolecular complexes that yielded a binding constant Kb (on the order of 103). The HS-RX interaction occurred through static quenching due to complex formation in the ground state, which was confirmed by spectrophotometry. The process was spontaneous (ΔG < 0), and the predominant interaction forces were van der Waals and hydrogen bonding (ΔH < 0 and ΔS < 0), with an electrostatic component evidenced by the influence of ionic strength in the interaction process. Structural changes in the HS were verified by synchronized and 3D fluorescence, with higher variation in the region referring to the protein-like fraction. In addition, metal ions (except ions Cu(II)) favored HS-RX interaction. When interacting with HS, the RX epitope was suggested by 1H NMR, which indicated that the entire molecule interacts with the superstructure. An enzyme inhibition assay verified the ability to reduce the alkaline phosphatase activity of free and complexed RX (RX-HS). Finally, this work revealed the main parameters associated with HS and RX interaction in simulated environmental conditions, thus, providing data that may help our understanding of the dynamics of organic arsenic-influenced soils.

Ecological Risk Assessment of Inorganic Arsenic and Mercuric Fungicides Through Biological Tools

This review discusses the use, mode of action, biomarkers, and bioindicators of inorganic arsenic and mercuric fungicides, as well as their effects on the environment and human health. The most prevalent indicator of exposure to arsenic is the measurement of total arsenic in urine. Biomarkers of exposure for arsenic and inorganic fungicides incudes the analysis of hair, urine, blooda and nails. Bio indicators are species or group of species that are used to indicate adverse effect of contamination. Freshwater fish species act as a very good bio indicator for inorganic arsenic. Tree bark, rice fields and sea birds could be a valuable indicator of inorganic arsenic contamination. Black Piranha, fish and earthworms are an ideal bio indicator of inorganic mercury. Inorganic arsenic compounds are known to be highly carcinogenic and toxic compounds. Mercuric fungicide is very toxic when inhaled by humans or animals it causes severe health issues and when absorbed by plants it retards their growth. To estimate the daily dose of arsenic exposure to humans through absorption, ingestion and other pathways, Average daily dose is implemented by using two equations from the US EPA. To determine the ecological risk assessment a simplified equation was proposed by FDA i.e. HQ = E/RfD. Overall, the review emphasizes the need for heightened awareness, regulation, and alternative approaches to fungicide use, with a focus on minimizing the use of inorganic arsenic and mercuric fungicides to safeguard the environment and promote sustainable agricultural practices.

Selective Quantification of Organic and Inorganic Arsenic in Kelp Thalli and Kelp-Based Products

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.

Adsorption mechanism of AsH3 pollutant on metal-functionalized coronene C24H12-X (X = Mg, Al, K) quantum dots

Inorganic arsenic compounds are frequently found to occur naturally or as a result of mining in soils, sediments, and groundwater. Organic arsenic exists mainly in fish, shellfish, and other aquatic life and as a result of this, it may be contaminated in edible consumables such as rice and poorly purified drinking water. Exposure to this toxic gas can cause severe lung and skin cancer as well as other related cancer cases. Therefore, the need to develop more efficient sensing/monitoring devices to signal or detect the presence of excessive accumulation of this gas in our atmosphere is highly demanding. This study has effectively employed quantum mechanical approach, utilizing density functional theory (DFT) to investigate the nanosensing efficacy of metal-decorated coronene quantum dot (QD); (CadecQD, AldecQD, KdecQD, and MgdecQD) surface towards the efficient trapping of AsH3 gas molecule in an attempt to effectively detect the presence of the gas molecule which would help in reducing the health risk imposed by the AsH3. The result obtained from the electronic studies reveals that the engineered molecules interacted more favorably at the gas and water phase than other solvents, owing to their varying calculated adsorption energies (Eads). It was observed that the decoration of potassium and aluminum into the QD surface enhanced the adsorption process of AsH3 gas onto KdecQD and AldecQD surfaces with a comparably moderate level of stability exhibited by the said systems, which is evidently shown by the excellent energy gap (Eg) of 6.9599 eV and 7.3313 eV respectively for the aforementioned surfaces.

Toward surface-enhanced Raman scattering using electroless substrate for trace arsenic detection and speciation

Arsenic is one of the most toxic elements present in the environment, especially in water. The World Health Organization (WHO) recommends a maximum concentration of arsenic in drinkable water of 10 μg/l (10 ppb). Sensors implementing Surface Enhanced Raman Scattering (SERS) can detect chemical species at low concentrations. The aim of this study is to compare two kinds of silver-coated SERS substrates for detection and speciation of trace, trivalent and pentavalent, inorganic arsenic compounds. One type of substrate was prepared by a classical thermal evaporation technique, and the second type by an electroless process. The thermally evaporated substrates allowed the detection of As(III) only, at a limit of detection (LOD) of approximately 50 mg/l, whereas As(V) could not be detected at any analyte concentration. The electroless substrates allow one to differentiate As(III) and As(V) with a LOD 1 μg/l (1 ppb) equal for each valency, below the WHO recommendation. The electroless substrates show a very large sensitivity across up to five orders of magnitude in terms of analyte concentration. Although the SERS intensity shows a nonlinear behavior over this range of concentrations, these preliminary results are encouraging in the framework of the demonstration of trace As SERS sensors in drinkable water.

Characterization and Quantification of Arsenic Species in Foodstuffs of Plant Origin by HPLC/ICP-MS.

Arsenic is a well-known carcinogenic, mutagenic and toxic element and occurs in the environment both as inorganic arsenic (iAs) and organoarsenical compounds (oAsCs). Since the toxicity of arsenic compounds depends on their chemical form, the identification and determination of arsenic species are essential. Recently, the European Food Safety Authority, following the European Commission request, published a report on chronic dietary exposure to iAs and recommended the development and validation of analytical methods with adequate sensitivity and refined extraction procedures for this determination. Moreover, the authority called upon new arsenic speciation data for complex food matrices such as seaweeds, grains and grain-based products. Looking at this context, an optimized, sensitive and fast analytical method using high performance liquid chromatography followed by inductively coupled plasma-mass spectrometry (HPLC/ICP-MS) was developed for the determination of iAs (sum of arsenite-AsIII and arsenate-AsV) and the most relevant oAsCs, arsenobetaine, dimethylarsinic acid and monomethylarsonic acid. The method was validated with satisfactory results in terms of linearity, sensitivity, selectivity, precision, recovery, uncertainty, ruggedness and matrix effect, and then successfully applied for the analysis of several matrices, i.e., processed and unprocessed cereal and cereal products, fruits, vegetables, legumes, seaweeds, nuts and seeds. The results obtained indicate that not only seaweed and rice matrices but also many cereals, legumes and plant-based foods for infants and young children contain significant concentrations of iAs and oAsCs. These findings contribute to the data collection necessary to assess the role of these matrices in the total arsenic exposure and if specific maximum limits have to be established.

Induction of filamin-C and its involvement in the regulation of cellular senescence and apoptosis in Huh-7 hepatoma cells during arsenic trioxide exposure

Arsenic trioxide (ATO) is one of the most toxic inorganic arsenic compounds. In this study, we examined the effects of long-term (7 days) exposure to low dose (5 μM) ATO on a human hepatocellular carcinoma cell line, Huh-7. Along with apoptosis accompanied by secondary necrosis though GSDME cleavage, we observed enlarged and flattened cells adhering to the culture dish and surviving even after exposure to ATO. An increase in cyclin-dependent kinase inhibitor p21 levels as well as positive staining for senescence-associated β-galactosidase activity were observed in ATO-treated cells, indicating cellular senescence. Screening for both ATO-inducible proteins by MALDI-TOF-MS analysis and ATO-inducible genes by DNA microarray analysis showed a marked increase in filamin-C (FLNC), an actin cross-linking protein. Interestingly, the increase in FLNC was observed in both dead and surviving cells, suggesting that the upregulation of FLNC by ATO occurs in both apoptotic and senescent cells. Small interference RNA-mediated knock down of FLNC resulted in not only a reduction of senescence-associated enlarged morphology of the cells, but also an exacerbation of cell death. Taken together, these results suggest a regulatory role of FLNC in the execution of senescence as well as apoptosis during ATO exposure.

Magnetic Fe3O4/MIL-101 composite as a robust adsorbent for removal of p-arsanilic acid and roxarsenic in the aqueous solution

The p-arsanilic acid (p-ASA) and roxarsenic (ROX) are typical organic arsenic compounds (OACs), which can be evolved into highly poisonous inorganic arsenic species in the aqueous solution. Herein, a magnetic MOFs-based composite of Fe3O4/MIL-101 was successfully obtained by a stepwise solvothermal method and further used in the adsorption of p-ASA and ROX. The structural and physicochemical characteristics of Fe3O4/MIL-101 were firstly investigated in detail. It was found that Fe3O4 microspheres were evenly embedded on the polyhedral MIL-101 surface after the solvothermal process and exhibited a strong superparamagnetic property. After adsorption, a simple external magnetic field can be used to quickly separate the composite from the aqueous solution. The adsorption experiments indicated that the composite is an excellent adsorbent with maximum adsorption capacities of 683.44 and 946.57 mg·g−1 for p-ASA and ROX, respectively. In addition, the effects of composite dosage, initial pH and co-existing anions on the adsorption efficiency were investigated. The main adsorption mechanism consists of the existence of hydrogen bonding, π-π stacking and As-O-Fe coordination between Fe3O4/MIL-101 composite and OACs. We believe that this study would be very meaningful to promote the application of magnetic MOFs based composites for effective adsorption for OACs in the environmental remediation.

Optimization of sample preparation conditions in the determination of total arsenic in fish and seafoods by atomic absorption spectrometry with electrothermal atomization

The conditions for sample preparation and determination of total arsenic in fish and seafoods by atomic absorption spectroscopy with electrothermal atomization have been optimized. When using a standard sample preparation procedure (GOST R 53100), a complete decomposition of the organic arsenic compound, arsenobetaine, appeared impossible which leads to underestimated results. A novel sample preparation procedure for the determination of total arsenic, including the addition of concentrated sulfuric acid for complete decomposition of the organic forms of arsenic to inorganic ones is proposed. During the atomization of the sample, an additional stage of drying was introduced with smooth heating from 200 to 250°C, which contributed to a complete removal of sulfuric acid residues from the injected sample volume. The correctness of the proposed methodology was verified using the ICP-MS method and in the analysis of reference samples of fish and seafoods.

Effective roxarsone (ROX) and arsenate (As(V)) sequestration from water with magnetic hollow Fe3O4-based Mg/Al layered double hydroxide: Performance and mechanism

Magnetic hollow Fe3O4-based Mg/Al layered double hydroxide (Fe3O4@SiO2@LDH) was successfully synthesized and subsequently the laboratory scale tests were conducted to systematically investigate the sequestration of roxarsone (ROX) and arsenate (As(V)). Owing to its abundant surface metal hydroxyl (M-OH) groups and exchangeable CO32− groups in the interlayer of MgAl-LDH nanosheets, the obtained Fe3O4@SiO2@LDH exhibited remarkable behavior for As(V) and ROX removal. Both As(V) and ROX could be effectively immobilized at a relatively wide pH range (3–8), and the maximum adsorption capacities of As(V) and ROX were 96.47 and 71.67 mg/g, respectively. Meanwhile, the negligible mutual effect demonstrated the Fe3O4@SiO2@LDH can simultaneously remove inorganic and organic arsenic compounds. The competitive cations/anions (except for PO43− ions) and ionic strength were negligible on As(V) and ROX removal, whereas the inhibitory effect stem from humic acid (HA) seemed to be more seriously for As(V) than that of ROX. Adsorption mechanism of As(V)/ROX were attributed to electrostatic attraction and ion/ligand exchange process, whereas hydrogen bonding and π-π interaction may also involve in the ROX removal. Furthermore, the excellent performance in fix-bed column tests and prominent reusability indicated this magnetic Fe3O4@SiO2@LDH was a promising candidate adsorbent and of great potential application in organic/inorganic As-contamination wastewater treatment.

Study on Arsenic Methyltransferase of &lt;i&gt;Cellulomonas&lt;/i&gt; sp. K31 Expressed in Recombinant &lt;i&gt;E. coli&lt;/i&gt;

This study aimed to facilitate efficient arsenic detoxification by inducing the microbial methylation of inorganic arsenic. Recombinant Escherichia coli strains K31 was transformed to overexpress arsenic methyltransferase, and the methylation of inorganic arsenic was evaluated using the enzyme extracted from the strain. To ensure continuous reactions by maintaining enzymatic activity, the extracted enzyme was immobilized in microcapsules (MC) to catalyze the methylation of inorganic arsenic. The total yield of methylated organic arsenic compounds in strain K31 was 57.0% (after 2 h of incubation at pH 6.5 and 40°C), of which trimethyl arsenic compounds (TMAC) accounted for 17.9%. When arsenic was methylated using MC prepared with the crude enzyme solution, the total yield of methylated organic arsenic compounds was 15.6%. The residual enzymatic activity was calculated to be 55.8%. Future studies should aim to increase the efficiency of conversion to TMAC, thus elevating the yield of organic arsenic compounds, by optimizing the conditions for enzyme immobilization in MC.

Identification and Priority Setting for Occupational Carcinogens (OCs) in Industries in Thailand

Several chemicals, including occupational carcinogens (OCs), have been used in Thailand. Apart from asbestos and silica, other OCs need to be identified for further monitoring and management. The study aimed to identify and conduct priority setting of these carcinogens in Thailand. The methods of the study were applied from Hanlon’s method for priority setting. The first step was to identify OCs from the lists of the National Hazardous Substance Registry by using the criteria as follows: 1) being classified as OCs by Loomis et al., and 2) having high amount of import/export in the country during 2018–2020. After that, the identified agents were ranked according to three criteria: 1) size of the problem, 2) severity of the problem, and 3) feasibility of interventions. The results found that 18 occupational carcinogens were identified and 12 of them were still allowed to be used in the country. According to available information, seven agents were matched for priority setting, and the top three scored OCs included 1) arsenic and inorganic arsenic compounds, 2) trichloroethylene, and 3) formaldehyde. Further action plan includes health risk assessment, setting up of health surveillance, and implementation of preventive and control measures in the target workplaces.

Exposure to low-dose arsenic caused teratogenicity and upregulation of proinflammatory cytokines in zebrafish embryos.

Arsenic is currently ranked as the most toxicant on the ATSDR 2015 substance priority list and is categorised as a Group 1 human carcinogen. Biota that are subjected to inorganic arsenicals through food, water, occupational or medical exposure pose a risk to the environment and to human health. The present study was carried out to investigate the toxicity caused by inorganic arsenic. After fertilisation, zebrafish embryos were exposed to sodium arsenite at several concentrations (100nM to 600nM) for 24 to 96 hpf. The indicators of teratogenicity (hatchability, morphological abnormalities, mortality), behavioural modifications (touch induced escape response (TIER), startle response (SR) and turning behaviour (TB)), biochemical testing (superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPX), and glutathione S transferase (GST)) and the expressions of tumor necrosis factor α (TNF-α), interleukin-1β (IL-1β), interleukin-6 (IL-6) and cyclooxygenase-2 (COX-2) were investigated. The aforementioned parameters were found to be altered in embryos exposed to sodium arsenite. According to the findings of the current study, even a low dose of inorganic arsenic compound caused teratogenicity, behavioural abnormalities, altered enzyme activities and the expression of proinflammatory cytokines in zebrafish embryos.

Arsenic exposure elevated ROS promotes energy metabolic reprogramming with enhanced AKT-dependent HK2 expression.

Exposure to inorganic or organic arsenic compounds continues to pose substantial public health concerns for hundreds of millions of people around the globe. Highly exposed individuals are susceptible to various illnesses, including impairments and cancers of the lung, liver, skin and bladder. Long-term exposure to low-dose arsenic has been identified to induce aerobic glycolysis, which contributes to cells aberrant proliferation. However, the mechanism underlying arsenic-induced aerobic glycolysis is still unclear. Here, mtDNA copy number is enhanced in arsenic-exposed populations and a positive correlation between serum HK2 and urinary total arsenic was observed in the individuals with high urine arsenic (≥ 0.032 mg/L). In a rat model of trivalent arsenic (iAs3+) exposure, the levels of HK2, NDUFA9 and NDUFB8 were increased in the rats treated with iAs3+ daily by gavage for 12 weeks than those in the control rats. Subsequently, in a low-dose arsenic exposure cell model we found that 0.2 μmol/L iAs3+ induced aerobic glycolysis to promote L-02 cells proliferation and inhibit apoptosis, in which HK2 played an important role. Further studies showed accumulated ROS determined the metabolic reprogramming via activating AKT and then increasing HK2 expression. On the one hand, activated AKT induced aerobic glycolysis by increasing HK2 to promote L-02 cells viability and DNA synthesis; on the other hand, phosphorylated AKT induced HK2 mitochondrial outer-membrane location with VDAC1 to inhibit apoptosis. Taken together, our results indicated that ROS induced by low-dose arsenic exposure determined energy metabolic reprogramming and acted a critical regulator for AKT-dependent HK2 expression and aerobic glycolysis.

Ultrasensitive detection of four organic arsenic compounds at the same time using a five-link cardboard-based assay

In order to effectively control the excessive use of organic arsenic reagents in livestock and poultry products, there is an urgent need to develop a method for rapid detection of multiple organic arsenic reagents. In this study, two haptens were designed and derivatized around the structural formula of roxarsone, and a highly-sensitive group-selective mAb 3F2 was prepared, which can simultaneously detect roxarsone, 4-aminophenylarsonic acid, 2-aminophenylarsonic acid and phenylarsonic acid. We further developed a colloidal gold immunochromatographic test strip (ICS) and prepared a five-link card that can simultaneously detect four organic arsenics in chicken and pork samples. Its quantitative detection limits (LOQ) for the four compounds in chicken and pork samples were 0.06 and 0.32 ng/mL, 0.11 and 0.29 ng/mL, 0.34 and 0.99 ng/mL, and 0.88 and 1.5 ng/mL, respectively. This multi-ICS detection provides a powerful tool for the on-site detection and rapid screening of organic arsenic reagents in actual samples.