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Determination of selenium and its compounds in marine organisms.

Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS) (2014-12-04)
Małgorzata Anita Bryszewska, Amund Måge
ABSTRACT

In this study, we investigate the type and quantity of selenium compounds in fish and marine organisms, using ion-pair reversed phase LC–ICP-MS, developed and applied for the analysis of Atlantic cod, Atlantic salmon, Greenland halibut, Atlantic herring, blue mussel, common crab, scallop, calanus, and Euphasia super. Of the samples examined, the lowest level of selenium was found in farmed Atlantic salmon (0.17 mg Se kg(−1) dm). The total selenium extraction efficiency by phosphate buffer was 2.5 times higher in sea plankton and shellfish samples than in fish samples. Analysis of Se species in each hydrolysate obtained by proteolysis showed the presence of selenomethionine, which constituted 41.5% of the selenium compounds detected in hydrolysates of Atlantic herring and 98.4% of those in extracts of Atlantic salmon. Inorganic compounds, such as selenates and selenites, were detected mainly in sea plankton and shellfish samples (<0.13 mg Se kg(−1) wm), although no correlation was found between the presence of inorganic compounds and total selenium concentration. The accuracy of the total selenium determination was validated using a certified reference material (oyster tissue (NIST 1566b)). A lyophilised powder of cod (Gadus morhua) was used to validate speciation analysis, enzymatic hydrolysis of lyophilised powder of cod recovered 54 ± 6% of total selenium, and SeMet constituted 83.5 ± 5.28% of selenium detected in hydrolysates. The chromatographic detection limits were, respectively, 0.30 ng mL(−1), 0.43 ng mL(−1), 0.54 ng mL(−1), 0.55 ng mL(−1), 0.57 ng mL(−1) and 0.72 ng mL(−1) for selenate, selenomethionine, selenite, Se-methyl-selenocysteine, selenocystine and selenomethionine selenoxide.The data on selenium concentrations and speciation presented here could be useful in estimating levels of selenium intake by seafood consumption.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Nitric-14N acid solution, ~10 N in H2O, 99.99 atom % 14N
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Ammonium-14N2,sulfate-16O4, 99.99 atom % 16O, 99.99 atom % 14N
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Tetrabutylammonium hydroxide solution, 40 wt. % in H2O
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Selenium, pellets, <5 mm, ≥99.99% trace metals basis
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Selenium, pellets, <5 mm particle size, ≥99.999% trace metals basis
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Ammonium-14N2 sulfate solution, 40 wt. % in H2O, 99.99 atom % 14N
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Triethylamine, ≥99.5%
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Phosphoric acid solution, 85 wt. % in H2O, FCC, FG
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Ammonium sulfate-14N2 solution, 40 wt. % in H2O, 99.99 atom % 14N
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Tetrabutylammonium hydroxide solution, technical, ~40% in H2O (~1.5 M)
Millipore
Hydrogen peroxide solution, 3%, suitable for microbiology
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Triethylamine, puriss. p.a., ≥99.5% (GC)
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Triethylamine, BioUltra, ≥99.5% (GC)
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Tetrabutylammonium hydroxide solution, ~40% in water, suitable for ion chromatography
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Tetrabutylammonium hydroxide solution, 1.0 M in methanol
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Triethylamine, ≥99%
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2-Thiobarbituric acid, ≥98%
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Triethylamine, ≥99.5%
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Sodium selenite, BioReagent, suitable for cell culture, ≥98%
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Selenium, powder, −100 mesh, 99.99% trace metals basis
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Hydrogen peroxide solution, contains ~200 ppm acetanilide as stabilizer, 3 wt. % in H2O
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Hydrogen peroxide solution, contains inhibitor, 30 wt. % in H2O, ACS reagent
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Hydrogen Peroxide Solution, 30% (w/w), puriss. p.a., reag. ISO, reag. Ph. Eur.
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Nitric acid concentrate, 0.1 M HNO3 in water (0.1N), eluent concentrate for IC
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Ammonium sulfate, analytical standard, for Nitrogen Determination According to Kjeldahl Method, traceable to NIST SRM 194
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Phosphoric acid-16O4 solution, 70 wt. % in D2O, 99.9 atom % 16O
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Ammonium hydroxide solution, BioUltra, ~1 M NH3 in H2O (T)
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Ammonium sulfate, for molecular biology, ≥99.0%
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Phosphoric acid, puriss. p.a., crystallized, ≥99.0% (T)
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Ammonium sulfate, ACS reagent, ≥99.0%