Arsenic speciation in aqueous samples using a selective As(III)/As(V) preconcentration in combination with an automatable cryotrapping hydride generation procedure for monomethylarsonic acid and dimethylarsinic acid

1994 ◽  
Vol 179 (2) ◽  
pp. 211-219 ◽  
Author(s):  
J. T. Van Elteren ◽  
H. A. Das ◽  
C. L. De Ligny ◽  
J. Agterdenbos ◽  
D. Bax
Keyword(s):  
Arsenic Speciation ◽  
Hydride Generation ◽  
Dimethylarsinic Acid ◽  
Aqueous Samples ◽  
Monomethylarsonic Acid ◽  
Generation Procedure

scholarly journals Arsenic speciation in beverages by direct injection-ion chromatography hydride generation atomic fluorescence spectrometry

2000 ◽  
Vol 22 (2) ◽  
pp. 33-39 ◽  
Author(s):  
E. Moreno ◽  
C Cámara ◽  
W. T. Corns ◽  
D. W. Bryce ◽  
P. B. Stockwell
Keyword(s):  
Certified Reference Materials ◽  
Arsenic Speciation ◽  
Direct Injection ◽  
Hydride Generation ◽  
Standard Addition ◽  
Atomic Fluorescence Spectrometry ◽  
Dimethylarsinic Acid ◽  
Atomic Fluorescence ◽  
Matrix Interferences ◽  
Monomethylarsonic Acid

The procedure developed allows the direct speciation of arsenic in these samples with good sensitivity, selectivity, precision and accuracy. Detection limits determined using the optimized conditions were found to be between 0.16 and 2.9 ng ml−1for arsenite, dimethylarsinic acid, monomethylarsonic acid and arsenate, while standard addition studies showed that the procedure is free from matrix interferences. As no certified reference materials are available for these analytes or matrices, validation was carried out by studying spike recoveries and by comparison of results with an alternative technique.

scholarly journals The arsenic speciation transformation in artificially arsenic-contaminated fluvo-aquic soil (Beijing, China)

2011 ◽  
Vol 57 (No. 3) ◽  
pp. 108-114 ◽  
Author(s):  
X. Zeng ◽  
Q. He ◽  
L. Bai ◽  
L. Li ◽  
S. Su
Keyword(s):  
Arsenic Speciation ◽  
Experimental Results ◽  
Agricultural Area ◽  
Dimethylarsinic Acid ◽  
Aqueous Extracts ◽  
Batch Experiments ◽  
Monomethylarsonic Acid ◽  
And Behaviors ◽  
Adsorption Desorption ◽  
Beijing China

Arsenic (As) speciation transformation often accompanies adsorption-desorption when exogenous arsenide is poured into soil. Disregarding the speciation transformation when evaluating adsorption-desorption of As can greatly influence the experimental results. In this study, batch experiments were conducted, and the results indicated that exogenous monomethylarsonic acid (MMA) or dimethylarsinic acid (DMA) added to fluvo-aquic soil collected from agricultural area in Beijing of China, was completely converted into As(V) after cultivated for<br />60 or 90 days. However, when exogenous As(V) was added to the soil, no speciation transformation of As(V) was observed. Furthermore, although the total As concentration, which was 6.55 or 11.55 mg/kg in aqueous extracts of the soil to which MMA or DMA had been added, respectively, remained stable after cultivated for 30 or 60 days, the As speciation transformation of MMA or DMA into As(V) in soil still occurred. Differences in As speciation can result in different fates and behaviors of As in soil, and As speciation transformation should be taken into account when evaluating the adsorption-desorption of As.

Arsenic Speciation in Urine from Humans Intoxicated by Inorganic Arsenic Compounds

1985 ◽  
Vol 4 (2) ◽  
pp. 203-214 ◽  
Author(s):  
M.A. Lovell ◽  
J.G. Farmer
Keyword(s):  
Arsenic Trioxide ◽  
Suicide Attempts ◽  
Human Subjects ◽  
Arsenic Speciation ◽  
Inorganic Arsenic ◽  
Arsenic Species ◽  
Dimethylarsinic Acid ◽  
Monomethylarsonic Acid ◽  
Detoxification Mechanism

Trends in the urinary concentrations of the four arsenic species, pentavalent [As (V)] and trivalent [As (III)] inorganic arsenic, monomethylarsonic acid (MMAA) and dimethylarsinic acid (DMAA), were followed for several days subsequent to the acute intoxication of two human subjects by arsenic trioxide [As (III)2O3] and sodium orthoarsenate [Na2HAs(V)O4.7H2O], respectively, in unsuccessful suicide attempts. Total arsenic concentrations ranged from 1.6 to 18.7 mg/l. The increasing predominance of the less toxic methylated species, especially DMAA, after 3 or 4 days supports the concept of methylation as a natural detoxification mechanism as part of an overall reduction/methylation sequence involved in the biotransformation of inorganic arsenic by the human body. However, the additional possibility of oxidation of As(III) to As(V) in vivo under extreme immediate postingestion conditions is suggested by initial high urinary As(V) after arsenic trioxide intoxication. Relative proportions of As(V), As(III), MMAA and DMAA in both cases probably reflect species-dependent differences in rates of direct elimination and reactivity with tissues as well as the efficiency of methylation.

scholarly journals Sample Preparation and Storage Can Change Arsenic Speciation in Human Urine

1999 ◽  
Vol 45 (11) ◽  
pp. 1988-1997 ◽  
Author(s):  
Jörg Feldmann ◽  
Vivian W-M Lai ◽  
William R Cullen ◽  
Mingsheng Ma ◽  
Xiufen Lu ◽  
...  
Keyword(s):  
Human Urine ◽  
Arsenic Speciation ◽  
Speciation Analysis ◽  
Arsenic Species ◽  
Urine Samples ◽  
Dimethylarsinic Acid ◽  
Detection Techniques ◽  
Monomethylarsonic Acid ◽  
The Stability ◽  
And Storage

Abstract Background: Stability of chemical speciation during sample handling and storage is a prerequisite to obtaining reliable results of trace element speciation analysis. There is no comprehensive information on the stability of common arsenic species, such as inorganic arsenite [As(III)], arsenate [As(V)], monomethylarsonic acid, dimethylarsinic acid, and arsenobetaine, in human urine. Methods: We compared the effects of the following storage conditions on the stability of these arsenic species: temperature (25, 4, and −20 °C), storage time (1, 2, 4, and 8 months), and the use of additives (HCl, sodium azide, benzoic acid, benzyltrimethylammonium chloride, and cetylpyridinium chloride). HPLC with both inductively coupled plasma mass spectrometry and hydride generation atomic fluorescence detection techniques were used for the speciation of arsenic. Results: We found that all five of the arsenic species were stable for up to 2 months when urine samples were stored at 4 and −20 °C without any additives. For longer period of storage (4 and 8 months), the stability of arsenic species was dependent on urine matrices. Whereas the arsenic speciation in some urine samples was stable for the entire 8 months at both 4 and −20 °C, other urine samples stored under identical conditions showed substantial changes in the concentration of As(III), As(V), monomethylarsonic acid, and dimethylarsinic acid. The use of additives did not improve the stability of arsenic speciation in urine. The addition of 0.1 mol/L HCl (final concentration) to urine samples produced relative changes in inorganic As(III) and As(V) concentrations. Conclusions: Low temperature (4 and −20 °C) conditions are suitable for the storage of urine samples for up to 2 months. Untreated samples maintain their concentration of arsenic species, and additives have no particular benefit. Strong acidification is not appropriate for speciation analysis.

scholarly journals Importance of monitoring arsenic methylation metabolism in acute promyelocytic leukemia patients receiving the treatment of arsenic trioxide

2021 ◽  
Vol 10 (1) ◽  
Author(s):  
Yu Zheng ◽  
Yuan-Fei Mao ◽  
Hui-Jin Zhao ◽  
Li Chen ◽  
Li-Ning Wang ◽  
...  
Keyword(s):  
Arsenic Trioxide ◽  
Acute Promyelocytic Leukemia ◽  
Arsenic Speciation ◽  
Promyelocytic Leukemia ◽  
Chronic Liver ◽  
Dimethylarsinic Acid ◽  
Metabolic Pattern ◽  
Methylation Index ◽  
Arsenic Methylation

Abstract Background Arsenic trioxide [ATO, inorganic arsenite (iAsIII) in solution] plays an important role in the treatment of acute promyelocytic leukemia (APL). However, the long-term adverse effects (AEs) and the retention of arsenic among APL patients are rarely reported. In this study, we focused on arsenic methylation metabolism and its relationship with chronic hepatic toxicity, as we previously reported, among APL patients who had finished the treatment of ATO. Methods A total of 112 de novo APL patients who had completed the ATO-containing treatment were enrolled in the study. Arsenic species [iAsIII, inorganic arsenate (iAsV), and their organic metabolites, monomethylarsonic acid (MMA) and dimethylarsinic acid (DMA)] in patients’ plasma, urine, hair and nails were detected by high-performance liquid chromatography combined with inductively coupled plasma mass spectrometry (HPLC-ICP-MS). Eighteen single nucleotide polymorphisms (SNPs) of the arsenic (+ 3 oxidative state) methylation transferase (AS3MT) gene, which was known as the main catalyzer for arsenic methylation, were tested with the polymerase chain reaction method. Results The study showed the metabolic pattern of arsenic in APL patients undergoing and after the treatment of ATO, in terms of total arsenic (TAs) and four species of arsenic. TAs decreased to normal after 6 months since cessation of ATO. But the arsenic speciation demonstrated significantly higher portion of iAsIII in patient’s urine (40.08% vs. 1.94%, P < 0.001), hair (29.25% vs. 13.29%, P = 0.002) and nails (30.21% vs. 13.64%, P = 0.003) than the healthy controls’, indicating a decreased capacity of arsenic methylation metabolism after the treatment of ATO. Urine primary methylation index (PMI) was significantly lower in patients with both chronic liver dysfunction (0.14 vs. 0.28, P = 0.047) and hepatic steatosis (0.19 vs. 0.3, P = 0.027), suggesting that insufficient methylation of arsenic might be related to chronic liver disorders. Two SNPs (A9749G and A27215G) of the AS3MT gene were associated with impaired urine secondary methylation index (SMI). Conclusions The long-term follow-up of arsenic speciation indicated a decreased arsenic methylation metabolism and a probable relationship with chronic hepatic disorders among APL patients after the cessation of ATO. Urine PMI could be a monitoring index for chronic AEs of ATO, and the SNPs of AS3MT gene should be considered when determining the dosage of ATO.

scholarly journals Arsenic Speciation in Drinking Tea Samples by Hydride Generation Atomic Fluorescence Spectrometry

2013 ◽  
Vol 25 (14) ◽  
pp. 8169-8172 ◽  
Author(s):  
Longfei Cai ◽  
Chunxiu Xu ◽  
Minghua Zhong ◽  
Yunying Wu ◽  
Shufen Zheng
Keyword(s):  
Arsenic Speciation ◽  
Hydride Generation ◽  
Fluorescence Spectrometry ◽  
Atomic Fluorescence Spectrometry ◽  
Atomic Fluorescence

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

2022 ◽  
Vol 12 ◽  
Author(s):  
Xiao Wu ◽  
Ruoning Yan ◽  
Rong Guan ◽  
Yi Du ◽  
Yuexin Liu ◽  
...  
Keyword(s):  
Risk Assessment ◽  
Health Risk ◽  
Healthy Volunteers ◽  
Arsenic Speciation ◽  
Arsenic Exposure ◽  
Hydride Generation ◽  
Atomic Fluorescence Spectrometry ◽  
Total Arsenic ◽  
Atomic Fluorescence

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.

scholarly journals The use of L-ascorbic acid in speciation of arsenic compounds in drinking water

2009 ◽  
pp. 165-175 ◽  
Author(s):  
Aleksandar Stanic ◽  
Sasa Jovanic ◽  
Nikola Marjanovic ◽  
Zvonimir Suturovic
Keyword(s):  
Ascorbic Acid ◽  
Atomic Absorption Spectrometry ◽  
Atomic Absorption ◽  
Ph Value ◽  
Arsenic Speciation ◽  
Hydride Generation ◽  
Reaction Medium ◽  
Absorption Spectrometry ◽  
Arsenic Content ◽  
Arsonic Acid

Arsenic speciation, besides total arsenic content determination, is very important in analysis of water, foodstuffs, and environmental samples, because of varying degrees of toxicity of different species. For such purpose hydride generation atomic absorption spectrometry can be used based on the generation of certain types of hydride, depending on the pH value and pretreatment in different reaction media. In this study, we have investigated the effect of L-ascorbic acid as the reaction medium as well as the pre-reducing agent in speciation of arsenic by hydride generation-atomic absorption spectrometry in order to determine monomethyl arsonic acid (MMA) in the presence of inorganic forms of arsenic.

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