Arsenobetaine is a significant arsenical constituent of the red Antarctic alga Phyllophora antarctica

2008 ◽  
Vol 5 (3) ◽  
pp. 171 ◽  
Author(s):  
Marco Grotti ◽  
Francesco Soggia ◽  
Cristina Lagomarsino ◽  
Walter Goessler ◽  
Kevin A. Francesconi

Environmental context. Although arsenic occurs in marine animals at high concentrations, the pathways by which it is biotransformed and accumulated remain largely unknown. The observation that some species of algae can contain significant concentrations of arsenobetaine, a major marine arsenic species, is relevant to explanations of the source of this compound to marine animals and its transport through the marine food web. Abstract. Significant amounts of arsenobetaine (up to 0.80 μg As g–1 dry mass, representing 17% of the extractable arsenic) were found in the extracts of all four samples of the red alga Phyllophora antarctica collected from two sites in Antarctica (Terra Nova Bay and Cape Evans). The assignment was made with high performance liquid chromatography–inductively coupled plasma mass spectrometry (HPLC-ICPMS) based on exact cochromatography with a standard compound with two chromatographic systems (cation-exchange and ion-pairing reversed-phase), each run under two sets of mobile phase conditions. Particular care was taken during sample preparation to ensure that the arsenobetaine was of algal origin and did not result from epiphytes associated with the alga. Another red alga, Iridaea cordata, collected from Terra Nova Bay, did not contain detectable concentrations of arsenobetaine. For both algal species, the majority of the extractable arsenic was present as arsenosugars. Confirmation that marine algae can contain significant amounts of arsenobetaine allows a simpler explanation for the widespread occurrence of this arsenical in marine animals.


Foods ◽  
2021 ◽  
Vol 10 (12) ◽  
pp. 2925
Author(s):  
Jędrzej Proch ◽  
Aleksandra Orłowska ◽  
Przemysław Niedzielski

In this work, a methodology for determination of As(III), As(V), dimethylarsinic acid (DMA), Fe(II) and Fe(III) in fifty-eight samples (forty-nine products of thirteen brands from three countries) commercial yerba mate (Ilex paraguariensis) was performed. The hyphenated high performance liquid chromatography inductively coupled plasma optical emission spectrometry (HPLC-ICP OES) technique was used. Arsenic was determined below the quantification limit in 38 samples of yerba mate. As(III) was found at the level 0.09 and 0.08 mg kg−1. The As(V) content was in the range: 0.21 to 0.28 mg kg−1. The content of DMA was found the highest of the three arsenic species in the range: 0.21 to 0.47 mg kg−1. The content of Fe(II) and Fe(III) was found in the range: 0.61 to 15.4 mg kg−1 and 0.66 to 43.1 mg kg−1, respectively and the dominance of Fe(III) was observed. Moreover, total and extractable content of 16 elements were determined. The results have been subjected to statistical analysis in order to establish relationships between samples of the same origin (country), kind (type) and composition (purity).



2020 ◽  
Vol 12 (3) ◽  
pp. 837
Author(s):  
Katarzyna Nocoń ◽  
Wioletta Rogula-Kozłowska ◽  
Grzegorz Majewski ◽  
Patrycja Rogula-Kopiec

This paper presents results of the research on soluble inorganic As(III) and As(V) bound to submicron atmospheric particles (PM1) in two Polish urban background sites (Zabrze and Warsaw). The purpose of the research was to give some insight on the susceptibility to leaching of PM1-bound arsenic species from easily water-soluble compounds, i.e., considered potentially bioavailable based on its daily and seasonal changes. Quantitative analysis for 120 PM1 samples (collected from 24 June 2014 to 8 March 2015) was performed by using a high-performance liquid chromatography in combination with inductively coupled plasma mass spectrometry. The mean seasonal concentrations of dominant soluble As specie—As(V)—ranged from 0.27 ng/m3 in the summer season in Warsaw to 2.41 ng/m3 in the winter season in Zabrze. Its mean mass shares in total As were 44% in Warsaw and 75% in Zabrze in the winter and 18% and 48%, respectively, in the summer. Obtained results indicated fossil fuel combustion as the main source of PM1-bound As(V) and road traffic emission as its minor sources. In opposite to As(V), soluble As(III) was not clearly seasonally variable. In both seasons, its mean concentrations were higher in Zabrze than in Warsaw. As(III) concentrations were not preferentially shaped by an exact emission from road traffic in both cities.



2019 ◽  
Vol 2019 ◽  
pp. 1-6 ◽  
Author(s):  
Hongfang Hou ◽  
Wanjing Cui ◽  
Qing Xu ◽  
Zhanhui Tao ◽  
Yafei Guo ◽  
...  

A sensitive and accurate simultaneous continuous analysis for six arsenic species including arsenobetaine (AsB), arsenocholine (AsC), monomethylarsonic acid (MMA), dimethylarsinic acid (DMA), arsenite (AsIII), and arsenate (AsV) has been developed by high performance liquid chromatography with inductively coupled plasma mass spectrometry (HPLC-ICP-MS). An anion-exchange column of Hamilton PRP-X100 (Switzerland) was applied for separation of the six arsenic species with gradient elution of 1.25 mmol/L Na2HPO4 and 11.0 mmol/L KH2PO4 as the mobile phase A and 2.5 mmol/L Na2HPO4 and 22.0 mmol/L KH2PO4 as the mobile phase B. The linearity ranges for AsB, AsC, MMA, DMA, AsIII, and AsV were between 0.5 and 50.0 μg/L, and the detection limits of the six arsenic species were all within 0.01–0.35 ng/L. The relative standard deviations (RSDs) were within 2.26–3.68% and the recovery rates of samples ranged from 95 to 103%. The proposed method was applied for the arsenic speciation analysis of sediment pore-water samples, which were taken from the supernatant after centrifugation and filtration.



Molecules ◽  
2019 ◽  
Vol 24 (2) ◽  
pp. 241 ◽  
Author(s):  
Qiaoli Shi ◽  
Mingyan Ju ◽  
Xiaoxia Zhu ◽  
Hui Gan ◽  
Ruolan Gu ◽  
...  

A rapid and sensitive method was established for arsenic (As) speciation based on high performance liquid chromatography coupled to inductively coupled plasma mass spectrometry (HPLC-ICP-MS). This method was validated for the quantification of four arsenic species, including arsenite (AsIII), arsenate (AsV), monomethylarsonic acid (MMAV) and dimethylarsinic acid (DMAV) in cynomolgus macaque plasma. Separation was achieved in just 3.7 min with an alkyl reverse phase column and highly aqueous mobile phase containing 20 mM citric acid and 5 mM sodium hexanesulfonate (pH = 4.3). The calibration curves were linear over the range of 5–500 ng·mL−1 (measured as As), with r > 0.99. The above method was validated for selectivity, precision, accuracy, matrix effect, recovery, carryover effect and stability, and applied in a comparative pharmacokinetic study of arsenic species in cynomolgus macaque samples following intravenous and intragastrical administration of arsenic trioxide solution (0.80 mg·kg−1; 0.61 mg·kg−1 of arsenic); in addition, the absolute oral bioavailability of the active ingredient AsIII of arsenic trioxide in cynomolgus macaque samples was derived as 60.9 ± 16.1%.



2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Abiodun A. Ojo ◽  
Amos Onasanya

The closed anaerobic decomposition extracts of Fucus distichus incubated with seawater and sediment, and without sediment as control, were subjected to extractions and isolation on Sephadex LH 20 and Cellulose Thin Layer Chromatography. The decomposition extracts and isolates were analyzed by using both the Hydride Generation Gas Chromatography Atomic Absorption Spectrometry (HG-GC-AAS) and High Performance Liquid Chromatography Inductively Coupled Plasma Mass Spectrometry (HPLC-ICPMS) to identify the arsenic species in the equilibrium mixtures of the seaweed and filtrates separately. In the methanol seaweed extract, equilibrium mixture of arsenosugars (AS) AS1 and AS2 and their biotransformation products of dimethylarsinoylethanol (DMAE) and dimethylarsinic acid (DMAA) were identified. In the methanol filtrate extract of the mixture, only DMAE and DMAA were identified. However, in the control methanol filtrate extract five organoarsenic species, AS1 and AS2, one unidentified hidden organoarsenic species, DMAE and DMAA were identified in the equilibrium mixture. This result confirmed that the hidden organoarsenic species in Fucus distichus, AS1 and AS2, and an unidentified organoarsenic compounds are biotransformed to only DMAE and DMAA under an anaerobic condition. This also suggests that DMAE and DMAA are strong intermediate candidates for the generation of arsenobetaine, from arsenoribosides in the marine food webs.



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