Characterization of an algal extract by HPLC-ICP-MS and LC-electrospray MS for use in arsenosugar speciation studies

A large scale extract of the brown alga Fucus serratus was found to contain four arsenosugars (1–4) together with traces of dimethylarsinate (DMA) and arsenate by HPLC-ICP-MS. The extract was divided into 1500 equal subsamples which were then freeze-dried and stored at –18°C. The homogeneity of this population of subsamples was established by random sampling and quantification of total arsenic by ICP-MS (1.22 µg As ±3.2%, mean ± RSD, n = 32) and hydride generation AAS (1.27 µg As ±2.0%, n = 32), and by quantification with HPLC-ICP-MS of the individual arsenic species in 10 subsamples: arsenosugar 1, 0.10 µg As ±3.6%; arsenosugar 2, 0.086 µg As ±2.9%; arsenosugar 3, 0.62 µg As ±3.8%; arsenosugar 4, 0.40 µg As ±3.1%; dimethylarsinate, 0.005 µg As ±20%; and arsenate ca. 0.001 µg As. The identity of the arsenosugars was confirmed by LC–electrospray (ES) MS with variable fragmenter voltage which provided simultaneous elemental and molecular detection. LC-ESMS was also used to quantify the four arsenosugars, producing values within 5% (2, 3 and 4) or 14% (1) of the ICP-MS data. The subsamples of Fucus extract provide a homogeneous source of natural material containing arsenosugars for use in arsenic speciation studies.

[1]  S. Pergantis,et al.  Identification of arsenosugars at the picogram level using nanoelectrospray quadrupole time-of-flight mass spectrometry. , 2000, Analytical chemistry.

[2]  H. Muntau,et al.  Certification of total arsenic, dimethylarsinic acid and arsenobetaine contents in a tuna fish powder (BCR-CRM 627) , 1999 .

[3]  J. Creed,et al.  Detection of arsenosugars from kelp extracts via IC-electrospray ionization-MS-MS and IC membrane hydride generation ICP-MS , 1999 .

[4]  W. Goessler,et al.  Determination of Arsenic Compounds in Earthworms , 1998 .

[5]  K. Reimer,et al.  Seasonal changes in arsenic speciation in Fucus species , 1998 .

[6]  X. Le,et al.  Effect of arsenosugar ingestion on urinary arsenic speciation. , 1998, Clinical chemistry.

[7]  E. Larsen Method optimization and quality assurance in speciation analysis using high performance liquid chromatography with detection by inductively coupled plasma mass spectrometry , 1998 .

[8]  K. Reimer,et al.  The identification of some water-soluble arsenic species in the marine brown algae Fucus distichus , 1997 .

[9]  W. Goessler,et al.  Arsenic compounds in a marine food chain , 1997 .

[10]  G. A. Pedersen,et al.  Characterization of national food agency shrimp and plaice reference materials for trace elements and arsenic species by atomic and mass spectrometric techniques , 1997 .

[11]  E. Larsen,et al.  Arsenic speciation by liquid chromatography coupled with ionspray tandem mass spectrometry , 1996 .

[12]  E. Larsen Speciation of dimethylarsinyl-riboside derivatives (arsenosugars) in marine reference materials by HPLC-ICP-MS , 1995 .

[13]  R. Rubio,et al.  Extraction method for arsenic speciation in marine organisms , 1995 .

[14]  M. Morita,et al.  Arsenic compounds in tissues of the leatherback turtle, Dermochelys coriacea , 1994, Journal of the Marine Biological Association of the United Kingdom.

[15]  X. Le,et al.  Human urinary arsenic excretion after one-time ingestion of seaweed, crab, and shrimp. , 1994, Clinical chemistry.

[16]  J. Edmonds,et al.  Arsenic compounds from marine organisms , 1993 .

[17]  D. Mcadam,et al.  The Synthesis of (R)-2',3'-Dihydroxypropyl 5-Deoxy-5-Dimethylarsinyl-β-D-Riboside, a Naturally Occurring Arsenic-Containing Carbohydrate , 1987 .

[18]  C. Raston,et al.  Isolation, crystal structure and synthesis of arsenobetaine, a constituent of the western rock lobster, the dusky shark, and some samples of human urine , 1981 .