Hydride Generation Atomic Absorption Research Articles

Arsenic accumulation pattern in water-soil-rice systems: A study of tolerance mechanisms and associated health risks

Regardless of the daunting challenge of arsenic (As) contamination in Pakistan, literature on tolerance and responsible factors in paddy fields remain elusive. In this regard, we aimed to explore physiochemical factors responsible for As availability in water-soil-rice systems. The study highlighted rice defense mechanisms to mitigate As toxicity on growth and yield. In the present study, basmati rice samples were collected along with irrigation and soil samples from control (<10 μg/L), low (11–25 μg/L), medium (26–100 μg/L), and high (>100 μg/L) contaminated regions. Oxidative stress markers (MDA and H2O2) and antioxidant enzymatic assays (SOD, CAT, POD, APX) were measured by spectrophotometer. The Durov diagram was constructed by using Grapher software to identify prevalent water types in irrigation wells. Total As was measured in water, soil, and rice tissues by hydride generation-atomic absorption spectroscopy (HG-AAS). The Durov diagram showed that the majority of irrigation water was Ca-Mg-Cl type. Furthermore, the FTIR analysis identified different organic compounds, i.e., OH, CC, CI, and CBr, particularly in soil from high regions. The results indicated higher accumulation and translocation of As in the water-soil-rice system from a high region compared to control and other regions. Phenotypic traits, i.e., grain yield, biological yield, chlorophyll, and root parameters were significantly impacted under high As-contaminated region. A concentration-dependent increase was indicated in oxidative stress and antioxidant activities except for APX. Risk assessment indicated a higher hazard quotient (1.09) and carcinogenic risk (5.0 × 10−03) due to grain consumption in high As-contaminated regions. The present study emphasized the need for strict regulations and policies to mitigate As calamity at the local level and protect human health.

Quantification of Arsenic in Soil Samples Collected in an Industrial Area of Brindisi (Apulia, Italy): Speciation Analysis and Availability

Arsenic (As) is a well-known toxic metalloid, but environmental risks due to excessive As content in soils or sediments depend on the chemical forms present and their relative mobility. Long-term exposure to arsenic may cause several diseases. In order to assess the possible risks in the heavily impacted Consorzio per lo Sviluppo Industriale e di Servizi Reali alle Imprese (Consortium for Industrial Development and Effective Services for Business, S.I.S.R.I.) industrial area of Brindisi (Apulia, southern Italy), 38 soil samples were collected in the area, from 18 sampling points previously determined as outliers. Total As determination, speciation analysis, and a cession test with acetic acid were performed. Speciation analysis was performed by HPLC coupled to hydride generation-atomic absorption spectroscopy (HG-AAS). Total As determination obtained by mineralization showed a concentration range between 51.8 and 169.6 mg kg−1, which is higher than the limit of 50 mg kg−1 established by D.M. (Ministerial Decree) 471/99 for industrial areas. The highest concentrations of extracted As were obtained in the top-soil layers. As(III) and As(V) were detected in all the samples, while the concentrations of the organic species monomethyl arsonic acid (MMAA) and dimethyl arsenic acid (DMAA) were always under the detection limit. The samples releasing the highest As quantities in the acetic acid cession test were in every circumstance collected from the superficial soil levels. The different amounts of As determined in the sampling sites could depend on the distance from the specific sources of pollution, even if it is very difficult to identify them in a very complex industrial zone such as the S.I.S.R.I. area of Brindisi. In this study, As occurs mainly as relatively immobile or slowly exchangeable forms: for this reason, it is more abundant in the top-soil and is little affected by the action of rainwater, which transports only reduced quantities of As into the deeper layers.

Evaluation of Different Extractants to Estimate Bioavailable Arsenic in Soil

ABSTRACT Owing to the similar chemistry of phosphorus (P) and arsenic (As), sodium bicarbonate (0.5 N NaHCO3) is commonly used to extract plant accessible As in soil. This extractant has neither been tested widely in relation to plant As, nor is this extractant compatible with inductively coupled plasma mass spectrometry (ICP-MS) due to the high concentration of dissolved solid. Subsequently, it is of utmost important to design a suitable chemical extraction method in order to estimate plant available As compatibility with ICP-MS. For this purpose, paired soil and plant samples were collected from paddy fields located in Nadia, West Bengal, India. Soil was extracted with 0.5 M NaHCO3, 0.1 N and 0.5 N phosphoric acid (H3PO4), 0.1 N and 0.5 N sulfuric acid (H2SO4), 0.1 N, 0.5 N, 1.0 N, 1.5 N HNO3 and 0.01 M calcium chloride (CaCl2) solution. Arsenic extracted with NaHCO3, H3PO4 and H2SO4 was determined in hydride generation-atomic absorption spectrophotometer (HG-AAS), while ICP-MS served to determine As extracted from soil with HNO3. Olsen-extractable As in soils ranged from 0.48 to 3.57 mg kg−1 with a mean value of 1.45 mg kg−1. The extractable As content in soil varied from 0.01 to 10.1 mg kg−1 across the extractants. In the case of grain As, 0.1 N H3PO4, 0.5 N NaHCO3 and 1.5 N HNO3 extractable As had distinctly higher correlation coefficients (r = 0.49**, r = 0.47**, r = 0.45**) when compared to other extractants. More or less similar relationships of extractable As were obtained with straw As content like that of rice grain. In view of rapidity of the soil test method for As, 1.5 N HNO3 can be recommended for assessing available As in soil.

Aqueous phase synthesis of ion-imprinted cryogel for paper-based colorimetric detection of As(V) with high selectivity.

A novel hydrophilic As(V) ion-imprinted cryogel (IIC) was green prepared by cryogelation in aqueous environment which was coincident with the adsorption condition and can improve the specific recognition performance. The methacrylamido propyl trimethyl ammonium chloride (MPTAC) was selected as the functional monomer and the saturated adsorption capacity of the prepared IIC and NIC were 55.0mg/g and 29.4mg/g, and with high imprinting factor of 1.87. Additionally, the prepared IIC showed admirable reusability and highselectivity, and the recovery was in the range 81.2-97.9% with RSD range of 1.9-4.3%, which was similar to the value obtained by hydride generationatomic absorption spectrometry. IIC can be used as solid material for colorimetric detection at the ultraviolet wavelength of 858nm without color interference of material matrix, in the range 5-200μg/L (R2 = 0.990)with a detection limit of 0.970 µg/L. Obviously, this synthetic strategy provides a simple, efficient, and green method for the preparation of water-compatible ion-imprinted polymers providingselectiveseparation and detection of trace As(V) in real complex samples.

Assessment of arsenic in water, rice and honey samples using new and green vortex-assisted liquid phase microextraction procedure based on deep eutectic solvent: Multivariate study

The aim of present study was to determine the arsenic in water, honey and rice samples using a new and green vortex-assisted liquid phase microextraction (VA-LPME), which is based on deep eutectic solvent (DES) by hydride generation-atomic absorption spectrometry. Ethylenediamine-N,N'-disuccinic acid (EDDS) was used as chelating reagent for As(III) ions. Four different DES was prepared by using different combination and molar ratios of hydrogen bond donor (HBD) as benzyltriphenylphosphonium chloride, tetra-n-butylammonium bromide, choline chloride and hydrogen bond acceptor (HBA) groups as ethylene glycol, glycerol and diethanolamine. Different parameters such as pH, chelating agent amount, DES types, molar ratio and its volume, emulsifier agents and its volume, vortex time and sample volume were optimized. The accuracy of the method was confirmed with certified reference materials. The DES-VA-LPME method was validated by using linearity r2 0.9985, working range 20–600 ng L−1, limit of detection 6.5 ng L−1, limit of quantitation 20 ng L−1 and enhancement factor 70. Intra and inter day relative standard deviation was found in the range of 3.6 and 4.1% and 4.2 and 4.9%, respectively. The developed procedure was successfully utilized for determination of arsenic in water, honey and rice samples. The factorial design was used to investigate the individual and combined effects of variables as well significant and insignificant effects.

Assessment of Toxic Arsenic in Water, Rice and Honey Samples Using New and Green Vortex-Assisted Liquid Phase Microextraction Procedure Based on Deep Eutectic Solvent Followed by Hydride Generation-Atomic Absorption Spectrometry: Multivariate Study

Assessment of Toxic Arsenic in Water, Rice and Honey Samples Using New and Green Vortex-Assisted Liquid Phase Microextraction Procedure Based on Deep Eutectic Solvent Followed by Hydride Generation-Atomic Absorption Spectrometry: Multivariate Study

Biochemical Investigation of Therapeutic Potential of Resveratrol Against Arsenic Intoxication.

Arsenic has been reported to cause damaging effects on different body organs. This study was designed to evaluate the protective effect of resveratrol (RSV) against arsenic trioxide (ATO)–induced intoxication in experimental animals. Twenty-four Wistar rats were allocated in 4 groups: group 1: control group, received normal diet; group 2: received ATO (3 mg/kg); group 3: received RSV (8 mg/kg) 30 minutes before administration of ATO; and group 4: received ascorbic acid (25 mg/kg) 30 minutes before administration of ATO. Treatments were given to experimental rats daily for consecutive 8 days. At the end of experimental period, bioaccumulation of arsenic in liver and kidney was assessed by hydride generation-atomic absorption spectrophotometer to investigate the association of arsenic accumulation with histological aberrations. Following parameters were also investigated: serum biochemical profile (alanine aminotransferase, aspartate transaminase, alkaline phosphatase, blood urea nitrogen, and creatinine) for evaluation of liver and kidney functions and lipid peroxidation and oxidative stress (malondialdehyde, glutathione, superoxide dismutase, catalase, and glutathione peroxidase) in tissue homogenates of liver and kidney for estimation of oxidative status. The findings of this study indicate that RSV remarkably ameliorated the hepatic and renal toxicity in arsenic-exposed rat model due to its strong antioxidant potential.

Analysis of total arsenic content in purchased rice from Ecuador

Natural and anthropogenic sources contribute to arsenic contamination in water and human food chain in Andean countries. Human exposure to arsenic via rice consumption is of great concern in countries where this crop is the dominant staple food, and limited information is available on the arsenic contamination on rice in Ecuador. This work was to contribute to the lack of knowledge analysing total arsenic by hydride generation-atomic absorption spectrometry in the samples of white, brown and parboiled rice purchased in Ecuadorian markets and produced in the two main rice wetlands in Ecuador, Guayas and Los Ríos, were carried out. For the samples from Guayas, arsenic concentration in white, brown and parboiled rice were 0.174 ± 0.014, 0.232 ± 0.021, and 0.186 ± 0.017 mg/kg respectively, whereas samples of white rice from Los Ríos showed a total arsenic level of 0.258 ± 0.037 mg/kg. This last arsenic concentration exceeds recommended maximum permissible limit by the FAO/WHO. Obtained data have available to estimate the Ecuadorian dietary exposure revealing serious health risk for population.

Innovative and practical deep eutectic solvent based vortex assisted microextraction procedure for separation and preconcentration of low levels of arsenic and antimony from sample matrix prior to analysis by hydride generation-atomic absorption spectrometry

Considering the negative impacts on human health and the environment, determinations of arsenic (As) and antimony (Sb), is of unquestionable importance. The present study describes the development of innovative and practical deep eutectic solvent (DES) based vortex assisted microextraction (DES-VAME) method for preconcentration of As and Sb from environmental waters, honey and rice prior to analysis by hydride generation-atomic absorption spectrometry (HG-AAS). The use of As(III) and Sb(III) in presence of dithizone at pH 10.5 by means of donor–acceptor mechanism were decided as analytes. Total As and Sb were determined after reduction process. The analytical properties obtained following optimization were as follows. Limit of detection (LOD), precision (as RSD%), recoveries and enhancement factor for As and Sb were calculated as 7.5 ng L−1/15.6 ng L−1, 2.1% /2.7%, 93.5%/96.2% and 104/85, respectively. Following validation with certified reference material, the method was successfully applied to the analysis of real samples.

Assessment of Arsenic content in water, soil and plant samples of Patna

The aim of present study was to develop a database of Arsenic (As) in ground water, soil, vegetables, cereal and forage crops to evaluate the potential human health risks posed by higher level of As, in Maner block of Patna,Bihar. The total concentration of arsenic in various samples under study was determined by hydride generator atomic absorption spectrophotometer.The concentration of Arsenic in ground water, soil and plant samples exceeded the WHO guideline values (10 ppb). Concentration of As in groundwater (tubewell) used for irrigation and agricultural soil samples ranged between 11.07 to 91.72 ppb and 82.2-135.5 ppb,respectively, which was on an average above the permissible limit of WHO guideline value. Soil of the study area was slightly acidic to alkaline in nature with low range of nitrogen and medium range of P and K.Crops were sampled from the selected sites and result showed that in vegetables As content varied in the range of 50.8 ppb to 289.1 ppb, in forage/pulse in the range of 90.3 ppb to 241.5 ppb and in cereal (Maize)crop in the range of 40.1 ppb to 265.4 ppb. Above ground concentration of arsenic in vegetables (consumable portion) was found to be higher than cereal and forage crops.

Determination of ultratrace tellurium in water by hydride generation atomic absorption spectrometry using online separation and pre-concentration with nano-TiO2 microcolumn

Silica gel loaded with nano-TiO2 was used as solid phase extraction materials to prepare a microcolumn for the online enrichment of trace tellurium in water and then determined by hydride generation atomic absorption spectrometry (HG-AAS). The effect of pH and the flow rate of sample on the extraction efficiency, NaOH concentration on the elution efficiency and other factors influencing hydride generation efficiency of tellurium were carefully investigated. Under the optimized experimental conditions, the sensitivity and the limit of detection (LOD) of this method were 0.009 L/μg and 0.04 μg L−1, respectively, which were 1000 and 850 times better than those obtained by the traditional flame atomic absorption spectrometry (FAAS); and the LOD for tellurium was improved by 45 times in this work, when compared with that by hydride generation-atomic absorption spectrometry (HG-AAS) without any separation and pre-concentration. This method was found to be interference-free of transitional metal ions, probably because of the surface of the nano-TiO2 was positively charged under acidic conditions, and it does not adsorb their cations. This method was successfully applied to the determination of tellurium in water samples.

Arsenic in Playground Soils from Kindergartens and Green Recreational Areas of Bratislava City (Slovakia): Occurrence and Gastric Bioaccessibility.

In this study, playground soils of kindergartens and green recreational zones in Bratislava were investigated for the occurrence and gastric bioaccessibility of arsenic (As) in the < 150μm soil size fraction. Eighty topsoil (0-10cm) samples were collected from playgrounds in kindergartens and green recreational zones throughout the urban area. Bioaccessibility measurements of As were performed using the Simple Bioaccessibility Extraction Test that mimics the human gastric environment, and resulting extracts were analyzed by hydride generation-atomic absorption spectrometry to assess bioaccessible As concentrations in the collected playground soils. Single selective chemical extractions using hydroxylamine hydrochloride-hydrochloric acid and dithionite-citrate-bicarbonate solutions also were used to determine the amount of As associated with amorphous and amorphous/crystalline Fe oxy-hydroxides in soils, respectively. The results showed that the spatial distribution of total As concentrations was related to the historical development of the city, with higher soil concentrations of As found in the old city centre and related urban zones and the lower ones on the outskirts of Bratislava. There was a variation in the values of bioaccessible concentrations and fractions of As, with ranges from 0.40 to 5.60mg/kg and 7.29 to 56.1%, respectively. Correlation and multivariable linear regression analyses revealed that bioaccessible concentrations of As were linearly related to its total concentrations in the soils, whereas dithionite-citrate-bicarbonate extractable Fe (FeDCB) was the main soil property, controlling the bioaccessibility of As. When the amount of FeDCB in the soils increased, As bioaccessibility decreased, confirming an importance of Fe bound to amorphous and crystalline iron oxy-hydroxides to the limitation of As bioaccessibility in urban playground soils of Bratislava. Additionally, single selective extractions showed that As concentrations extracted by hydroxylamine hydrochloride (AsHH) and dithionite-citrate-bicarbonate (AsDCB) were positively correlated with its bioaccessible concentrations (Spearman r = 0.75 and 0.62, respectively; p < 0.001).

Speciation of As in environmental samples using the nano-TiO2/PCHG-FAAS online system

ABSTRACTThis work presents an alternative method for arsenic speciation using the nano-TiO2 hydride generation photocatalytic hydride generation (PCHG) system, which is easily separated from the medium. Nano-TiO2 was studied as photocatalyst to reduction of arsenic species by UV-induced with formic acid and atomic absorption detection of different forms of arsenic [As (III), As (V), dimethylarsinic acid (DMA)] in environmental samples (water, sediment and plant). The effect of the average pH, the organic acid concentration, the ultraviolet irradiation time and their amount were investigated. With the presence of formic acid, the process was more effective in the reduction of arsenic when compared to other organic acids, mainly acetic acid. In addition, the photocatalytic hydride generation and flame atomic absorption spectrometry (nano-TiO2/PCHG-FAAS) increased the identification and quantification of different arsenic species. The ultrasound extraction procedure was used as a method to prepare samples with solutions of 1.0 mol L−1 phosphoric acid. The accuracy of the measurements (n = 12), calculated as relative standard deviation, was less than 8.6%. The detection limits for As (III) and As (total) in samples were 0.418 and 0.574 μg g−1, respectively.

Determination of total arsenic in fish by hydride-generation atomic absorption spectrometry: method validation, traceability and uncertainty evaluation

Fish containing arsenic compound is one of the important indicators of arsenic contamination in water monitoring. The high level of arsenic in fish is due to absorption through food chain and accumulated in their habitat. Hydride generation (HG) coupled with atomic absorption spectrometric (AAS) detection is one of the most popular techniques employed for arsenic determination in a variety of matrices including fish. This study aimed to develop a method for the determination of total arsenic in fish by HG-AAS. The method for sample preparation from American of Analytical Chemistry (AOAC) Method 999.10-2005 was adopted for acid digestion using microwave digestion system and AOAC Method 986.15 – 2005 for dry ashing. The method was developed and validated using Certified Reference Material DORM 3 Fish Protein for trace metals for ensuring the accuracy and the traceability of the results. The sources of uncertainty of the method were also evaluated. By using the method, it was found that the total arsenic concentration in the fish was 45.6 ± 1.22 mg.Kg-1 with a coverage factor of equal to 2 at 95% of confidence level. Evaluation of uncertainty was highly influenced by the calibration curve. This result was also traceable to International Standard System through analysis of Certified Reference Material DORM 3 with 97.5% of recovery. In summary, it showed that method of preparation and HG-AAS technique for total arsenic determination in fish were valid and reliable.

Determination of sub-ng g–1 levels of total inorganic arsenic and selenium in foods by hydride-generation atomic absorption spectrometry after pre-concentration

ABSTRACTA new and simple ultrasonic-assisted extraction (UAE) procedure was developed for the determination of inorganic arsenic and selenium in foods by hydride-generation atomic absorption spectrometry (HG-AAS). The various analytical variables affecting complex formation and extraction efficiency were investigated and optimised. The method is based on selective complex formation of As(III) and Se(IV) in the presence of excess As(V) and Se(VI) with toluidine red in the presence of tartaric acid at pH 4.5, and then extraction of the resulting condensation products into the micellar phase of non-ionic surfactant, polyethylene glycol dodecyl ether, Brij 35. Under optimised conditions, good linear relationships were obtained in the ranges of 4–225 and 12–400 ng l–1 with limits of detection of 1.1 and 3.5 ng l–1 for As(III) and Se(IV), respectively. The repeatability was better than 3.9% for both analytes (n = 10, 25 ng l–1) while reproducibility ranged from 4.2% to 4.8%. The recoveries of As(III) and Se(IV) spiked at 25–100 ng l–1 were in the range of 94.2–104.8%. After pre-concentration of a 5.0 ml sample, the sensitivity enhancement factors for As(III) and Se(IV) were 185 and 140, respectively. Accuracy was assessed by analysis of two standard reference materials (SRMs) and spiked recovery experiments. The method was successfully applied to the accurate and reliable determination of total As and total Se by HG-AAS after pre-reduction with a mixture of L-cysteine and tartaric acid. Finally, the method was shown to be rapid and sensitive, with good results for extraction, pre-concentration and determination of total As and Se contents (as As(III) and Se(IV)) from food samples.

Low-level arsenic exposure via drinking water consumption and female fecundity - A preliminary investigation

High level arsenic exposure is associated with reproductive toxicity in experimental and observational studies; however, few data exist to assess risks at low levels. Even less data are available to evaluate the impact of low level arsenic exposure on human fecundity. Our aim in this pilot study was a preliminary evaluation of associations between low level drinking water arsenic contamination and female fecundity. This retrospective study was conducted among women previously recruited to a hospital-based case-control study of spontaneous pregnancy loss in Timiṣ County, Romania. Women (n=94) with planned pregnancies of 5–20 weeks gestation completed a comprehensive physician-administered study questionnaire and reported the number of menstrual cycles attempting to conceive as the time to pregnancy (TTP). Drinking water samples were collected from residential drinking water sources and we determined arsenic levels using hydride generation-atomic absorption spectrometry (HG-AAS). Multivariable Cox-proportional hazards regression with Efron approximation was employed to evaluate TTP as a function of drinking water arsenic concentrations among planned pregnancies, adjusted for covariates. There was no main effect for drinking water arsenic exposure, yet the conditional probability for pregnancy was modestly lower among arsenic exposed women with longer TTPs, relative to women with shorter TTPs, and relative to unexposed women. For example, 1µg/L average drinking water arsenic conferred 5%, 8%, and 10% lower likelihoods for pregnancy in the 6th, 9th, and 12th cycles, respectively (P=0.01). While preliminary, our results suggest that low level arsenic contamination in residential drinking water sources may further impair fecundity among women with longer waiting times; however, this hypothesis requires confirmation by a future, more definitive study.

An analytical method for arsenic in agricultural products using hydride generation-atomic absorption spectrometry

An analytical method for arsenic in agricultural products using hydride generation-atomic absorption spectrometry

Magnesium, zinc, arsenic, selenium and platinum urinary excretion from cancer patients of Antofagasta region, Chile: multi-metal approach.

ObjectivesTo evaluate the short-term 24 h urinary excretion of platinum, arsenic, selenium, magnesium and zinc in patients with lung cancer and with cancer other than lungs treated with cisplatin or/and carboplatin from Antofagasta, Chile.DesignUrine measurements of Pt and Se were made by inductively coupled plasma optical emission spectrometry, As by hydride-generation atomic absorption spectrometry and Mg and Zn by means of flame furnace atomic absorption spectrometry.SettingAll samples were provided by the Oncological Centre of Antofagasta Regional Hospital (Region of Antofagasta, Chile).ParticipantsNinety 24-h urine samples from cancer patients after the infusion of Pt-base drugs and 10 24-h urine samples from cancer patients not treated with metal-base drugs.Main outcome measuresConcentrations of Pt, Se, As, Zn and Mg coming from 24-h urine samples.ResultsPt excreted was not significantly different between patients with lung and other cancers treated with cisplatin. The excretion of Mg, Zn and Se was greater than As. Then, Pt favours the excretion of essential elements. For lung and other types of cancers treated with drugs without Pt, excretion of Mg, Zn and Se was also greater than that of As, suggesting antagonism Mg-Zn-Se–anti-cancer drug relationship.ConclusionsThe amounts of Mg, Zn and Se excreted were greater than for As either with or without Pt-containing drugs, suggesting antagonist Mg-Zn-Se–anti-cancer drug relationships. The excretion of As, Mg, Zn and Se is induced by Pt. Knowledge obtained can contribute to understanding the arsenic cancer mechanism and the As-Mg-Zn-Se-Pt inter-element association for lung cancer and other types of cancer.

Study of Arsenic Impurity in Water of Lahore by Hydride Generation-Atomic Absorption Spectrophotometry

Study of Arsenic Impurity in Water of Lahore by Hydride Generation-Atomic Absorption Spectrophotometry

WITHDRAWN: Use status and metabolism of realgar in Chinese patent medicine

Realgar is widely used in combination with other herbs as Chinese patent medicine to treat a wide range of diseases in China. It is also a well known arsenical toxicant. Chronic arsenic poisoning events caused by long-term usage of realgar-containing medicines have been reported in literatures. Given to the paradoxical role of realgar, comprehensive outline of its usage status in Chinese patent medicine might provide basal data for evaluating its toxicology risks in populations. Unfortunately, the relevant information is limited. Also, a metabolic process after intake of realgar-containing medicine in humans is poorly understood. The Traditional Chinese Patent Medicine Prescription Database was reviewed to get the information on the usage status of realgar. Realgar powder was dissolved in different pH-value solutions (1, 3, 5, 7, 9 and 11) to determine the soluble arsenic concentrations from realgar. Ten volunteers aged 24-26 years old were recruited to take four pills of Niu Huang Jie Du Pian (NHJDP), a very common Chinese patent medicine with realgar, to analyze the arsenic metabolism after exposure to realgar-containing medicine. The four pills were taken according to the medical instruction. Concentrations of soluble arsenic from realgar and urinary arsenic metabolites in humans were determined by hydride generation atomic absorption spectrometry. A total of 191 (2.25%) realgar-containing traditional Chinese patent medicines were obtained from the database, and almost 86.91% of them were for oral application. 73 (38.22%) medicines were found to be available for children. The mass fraction of arsenic in realgar-containing medicine ranged from 0.11% to 27.52%. According to medical instructions, the amount of average daily arsenic intake ranged from 0.47 to 2895.53mg. Nearly 86% medicines with daily intake of arsenic >10mg. Only inorganic arsenic (iAs) was detected from realgar in dissolution experiment and the levels of soluble iAs increased with pH values. After intake NHJDP, arsenic excretion in urine significantly increased, with a maximum excretion of iAs and monomethylarsonic acid at 6h post-ingestion and a peak excretion of dimethylarsinic acid at 9h post-ingestion. Arsenic methylation capacity was decreased after intake NHJDP. Females carried a more efficient arsenic methylation process than males. Realgar is widely used in traditional Chinese medicine. The arsenic solubility from realgar may be enhanced under alkaline conditions. The levels of urinary arsenic metabolites significantly increased while the arsenic methylation capacity significantly decreased after intaking realgar-containing medicine, which may suggest that a potential health hazard exists if people use arsenical medicines for long-term.