Arsenic-Related Health Risk Assessment of Realgar-Containing NiuHuangJieDu Tablets in Healthy Volunteers Po Administration

Realgar, an arsenic-containing traditional Chinese medicine of As2S2, has significant therapeutic effects for hundreds of years. NiuHuangJieDu tablets (NHJDT) is one of the most commonly prescribed realgar-containing preparations for the treatment of sore throat, swelling, and aching of gums. However, realgar-containing TCMs raise great safety concerns due to the adverse effects reported by arsenic poisoning. In this study, the arsenic-related health risk assessment of NHJDT was conducted in healthy volunteers after single and multiple doses oral administration. Blood, plasma, and urine samples were collected after dosing at predetermined time points or periods. Simple, rapid, and sensitive methods were established for the quantification of total arsenic and arsenic speciation in biological samples. The total arsenic and arsenic speciation were determined by hydride generation-atomic fluorescence spectrometry (HG-AFS) and high-performance liquid chromatography–hydride generation–atomic fluorescence spectrometry (HPLC-HG-AFS), respectively. No significant fluctuation of total arsenic was observed in human blood, and no traces of arsenic speciation were found in human plasma. Dimethylarsenic acid was detected as the predominated arsenic species in human urine after dosing. Therapeutic dose administration of NHJDT was relatively safe in single dose for the limited blood arsenic exposure, but long-term medication may still pose health risks due to the accumulation of arsenics in blood and its extremely slow excretion rate. Therefore, arsenic exposure should be carefully monitored during realgar-containing TCM medication, especially for long-term regimen. The results obtained in this study will provide scientific references for the clinical application of realgar and its-containing TCMs.

Arsenic speciation and sorption in acid mine drainage and the polluted water of the Kosva river basin, Russia

Acid mine drainage (AMD) of the abandoned coal mines of the Kizelovsky coal basin (the Urals, Russia) is one of the worst natural disasters in the region. Acidic sulphate waters with a high content of metals freely flow into the surface water bodies. Arsenic, found in elevated concentrations in AMD, is an element of concern due to its potential toxicity to humans and animals. The aim of this work is determination of chemical speciation of inorganic arsenic in AMD as well as the surface water and groundwater affected by mine drainage, and assessment the natural removal of As from mine drainage due to adsorption on precipitated hydrous ferric oxide (HFO). Geochemical speciation (PHREEQC) revealed that arsenic occurs in all water samples as As(V). Surface complexation model shows that, HFO induced by the natural attenuation process may remove 46–85% of total arsenic in AMD and only 28% in polluted groundwater (on average).

Determination of arsenic, cadmium, selenium, zinc and other trace elements in Bangladeshi fish and arsenic speciation study of Hilsa fish flesh and eggs: Implications for dietary intake

Exposure to As from drinking water and its impact on the health of the Bangladeshi population has received much attention. However, very little information is available regarding As exposure through consumption of fish, which is the main source of animal protein for the majority of Bangladeshis. In this study, concentrations of As, Cd, Pb, Mn Se and Zn in different types of fish, consumed by Bangladeshis, were determined using Inductively Coupled Plasma Mass Spectrometry. Daily intakes of the toxic elements As, Cd and Pb through fish consumption were estimated to be 31.8, 0.4 and 4.8 μg/day, respectively. Hilsa (Tenualosa ilisha) contained the highest concentrations of total As (mean ± SD was 2.55 ± 1.3 mg/kg; n = 15) among the fish analysed. However, toxic inorganic As species were not detected. The dominant As species in Hilsa fish were: dimethylarsenic acid, arsenobetaine and arsenosugars, at 69, 11 and 20% of total As, respectively. The high concentration of Cd detected in Hilsa eggs (average 278 ± 518 μg/kg; range 7.4–1725 μg/kg; n = 10) is of concern since this may have harmful effects on the development of embryos and lead to a decline in the Hilsa population or the quality of the fish. It can also be harmful to those who consume Hilsa eggs on a regular basis. Selenium was found to be highest in Shoal (Micropterus cataractae) fish and a type of small fish, and lowest in Mrigal (Cirrhinus cirrhosis). Small fish species contained Mn and Zn at 7.1- and 4.3-fold higher concentrations, respectively, compared to big fish species. Keski (Corica soborna), a small fish species, contained by far the highest concentrations of Mn (52 mg/kg) and Zn (140 mg/kg), although the concentration of As (1.4 mg/kg) in this fish was lower than that of several other fish species. Small fish species are often consumed whole, including the bones, and therefore the essential trace elements present are potentially bioavailable for cellular metabolism. Our study shows that the Bangladeshi population can easily meet their daily requirement of Se and Zn from consumption of fish such as Shoal fish (Se and Zn), Hilsa fish (Se and Zn) and Keski fish (Se and Zn). Consumption of small fish (such as Keski) and big fish (such as Hilsa) from Bangladesh can provide valuable sources of essential trace elements as part of a balanced diet and thus negate the need for supplements and biofortification of certain foods. Ours is a small study and a detailed total dietary intake and human biomonitoring studies, that includes coverage of different socio-economic groups, are needed in Bangladesh before giving people supplements or biofortified foods.

Novel Preservation Methods for Inorganic Arsenic Speciation in Model and Natural Water Samples by Stripping Voltammetric Method

In this study, the preservation of As(III) in model solutions and natural groundwater samples from four locations in Croatia was conducted. Model laboratory samples were spiked with As(III) and As(V), and different complexing agents. Solutions were analysed in intervals of 24, 48 h and during ten days after preparation. Model samples containing citric acid, sodium citrate, sodium oxalate and potassium sodium tartrate in combination with acetic acid, spiked with As(III)and As(V), showed good species preservation. As(III), in model samples, was preserved for 7 days with citric acid, and citric acid in combination with acetic acid, as well as with tartrate. As(III), in natural samples, was preserved for 6 to 12 days with potassium sodium tartrate, citric acid, and citric acid in combination with acetic acid and showed improvement, compared with unpreserved samples (oxidation in 3 days). The results showed that acetic acid alone was not successful in preserving As speciation. Good resolution of inorganic arsenic species was achieved using differential pulse anodic stripping voltammetry technique (DPASV). Since this technique is comparatively cheaper and more convenient to use than other available techniques it could become a method of choice for arsenic speciation in water.

Occurrence, Geochemistry and Speciation of Elevated Arsenic Concentrations in a Fractured Bedrock Aquifer System

The presence of elevated arsenic concentrations (≥ 10 µg L−1) in groundwaters has been widely reported in areas of South-East Asia with recent studies showing its detection in fractured bedrock aquifers is occurring mainly in regions of north-eastern USA. However, data within Europe remain limited; therefore, the objective of this work was to understand the geochemical mobilisation mechanism of arsenic in this geologic setting using a study site in Ireland as a case study. Physicochemical (pH, Eh, d-O2), trace metals, major ion and arsenic speciation samples were collected and analysed using a variety of field and laboratory-based techniques and evaluated using statistical analysis. Groundwaters containing elevated dissolved arsenic concentrations (up to 73.95 µg L−1) were characterised as oxic-alkali groundwaters with the co-occurrence of other oxyanions (including Mo, Se, Sb and U), low dissolved concentrations of Fe and Mn, and low Na/Ca ratios indicated that arsenic was mobilised through alkali desorption of Fe oxyhydroxides. Arsenic speciation using a solid-phase extraction methodology (n = 20) showed that the dominant species of arsenic was arsenate, with pH being a major controlling factor. The expected source of arsenic is sulphide minerals within fractures of the bedrock aquifer with transportation of arsenic and other oxyanion forming elements facilitated by secondary Fe mineral phases. However, the presence of methylarsenical compounds detected in groundwaters illustrates that microbially mediated mobilisation processes may also be (co)-occurring. This study gives insight into the geochemistry of arsenic mobilisation that can be used to further guide research needs in this area for the protection of groundwater resources.

Arsenic Speciation Techniques in Soil Water and Plant: An Overview

There are more than 100 different arsenic with different characteristics in the soil-water-plant ecosystem. The identification and quantification of individual arsenic species is essential for understanding the distribution, environmental fate and behavior, metabolism and toxicity of arsenic. Due to the hazardous nature of arsenic, people have a high interest in the measurement of arsenic species. The reaction of the formation of arsenic speciation in the soil-water-plant environment is briefly studied. There is little information on methods used to quantify arsenic forms and species in contaminated soil, water and plant. The purpose of this article is to understand the available sample pretreatment, extraction, separation, detection and method validation techniques for arsenic speciation analysis of arsenic species in soil, water and plant. The performances of various sample preparation and extraction processes, as well as effective separation techniques, that contribute greatly to excellent sensitivity and selectivity in arsenic speciation when coupling with suitable detection mode, and method validity are discussed. The outlines of arsenic speciation techniques are discussed in view of the importance to the completeness and accuracy of analytical data in the soil-water-plant samples. To develop cheap, fast, sensitive, and reproducible techniques with low detection limits, still needed to confine research on arsenic speciation present in environmental matrices.