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RESEARCH FRONT

Two Novel Thio-Arsenosugars in Scallops Identified with HPLC–ICPMS and HPLC–ESMS

Markus Kahn A , Reingard Raml A , Ernst Schmeisser A , Birgit Vallant A , Kevin A. Francesconi A and Walter Goessler A B
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A Institute of Chemistry—Analytical Chemistry, University Graz, Universitaetsplatz 1, A-8010 Graz, Austria.

B Corresponding author. Email: walter.goessler@uni-graz.at

Environmental Chemistry 2(3) 171-176 https://doi.org/10.1071/EN05045
Submitted: 10 June 2005  Accepted: 12 August 2005   Published: 27 September 2005

Environmental Context. A new group of arsenic compounds, namely thio-arsenosugars, has recently been discovered in some marine samples, including seafood products. We do not yet understand how these arsenic compounds are produced by living organisms, nor do we know their implications for human health. Their unusual chromatographic properties are the reason that they are difficult to detect by existing methods. We present a new method for finding these thio-arsenosugars, and we also report two new thio-arsenosugars.

Abstract. Two new thio-arsenosugars were identified in aqueous and methanol extracts from the gonad and the muscle of the great scallop by using high-performance liquid chromatography–inductively coupled plasma mass spectrometry (HPLC–ICPMS) and HPLC–electrospray ionization mass spectrometry (ESMS). The gonad of the scallops contained thio-arsenosugar–sulfonate [0.067 mg (As) kg−1; dry mass ± 3.7%] and thio-arsenosugar–sulfate [0.267 mg (As) kg−1; dry mass ± 1.2%]. The muscle also contained both thio-arsenosugar–sulfonate [0.030 mg (As) kg−1; dry mass ± 2.6%] and thio-arsenosugar–sulfate [0.200 mg (As) kg−1; dry mass ± 2.6%]. Methanol increased the extraction efficiency threefold for the two thio-arsenosugars as compared to water. Fresh and freeze-dried samples from both parts of the scallop showed no significant difference with respect to the concentration of the two thio-arsenosugars. In order to confirm the presence of the thio-arsenosugars, a new method for their determination with HPLC–ESMS was developed. Under optimized conditions [Hamilton PRP-X100; 150 by 1.0 mm; 20 mM NH4HCO3 with 55% (v/v) methanol at pH 10.3] we succeeded in determining the pseudomolecular ions of thio-arsenosugar–glycerol, thio-arsenosugar–phosphate, thio-arsenosugar–sulfonate, and thio-arsenosugar–sulfate at concentrations less than 5 µg (As) dm−3 in standard solutions and real samples.

Keywords. : arsenic — bioavailability — contaminant uptake — speciation (nonmetals)


Acknowledgments

Financial support from the Austrian Science Fund, FWF project P16088-N03 and EC project No. QLK4-CT-2001-00264 is gratefully acknowledged.


References


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[12]   Kahn M., Raml R., Goessler W., Schmeisser E., Francesconi K. A., A New Thio-arsenosugar Identified with HPLC–ICPMS as a Significant Compound in the Kidney of the Giant Clam Tridacna derasa; Poster presentation at the European Winter Conference on Plasma Spectrochemistry 2005 (Organiser: Peter Fodor, Corvinus University, Budapest, Hungary).

[13]   Kanaki K., Nischwitz V., Pergantis S. A., High Performance Liquid Chromatography with Inductively Coupled Plasma Mass Spectrometry Detection for the Determination of Novel Thio-Arsenosugars; Poster presentation at the European Winter Conference on Plasma Spectrochemistry 2005 (Organiser: Peter Fodor, Corvinus University, Budapest, Hungary).