2003
DOI: 10.1007/s00216-003-1941-y
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Preparation, homogeneity and stability studies of a candidate LRM for Se speciation

Abstract: A laboratory reference material (LRM) was prepared from Brazil nuts (Bertholletia excelsa) for quality control (QC) purposes of selenium speciation. The preparation of this LRM led through the usual operation steps applied during routine reference material production from biota samples-preparation of the raw material, homogenisation, storage design, checking of homogeneity, microbiological status and possible irradiation effects, and monitoring the species stability vs time at different storage temperatures. T… Show more

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Cited by 40 publications
(23 citation statements)
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“…Only one nut of this richest food source of selenium contributed with 288.75 µg of selenium daily, increasing selenium intake to more than the recommended levels (55 µg/day), but not exceeding the tolerable upper intake level (400 µg/day) [45]. Selenium in Brazil nuts is found in selenomethionine and selenocysteine species, and studies show that selenomethionine concentration ranges from 75 to 90 % [46,47]. Despite high selenium content in Brazil nuts, no participants complained of symptoms associated with selenosis, as observed by Lemire et al [48].…”
Section: Discussionmentioning
confidence: 99%
“…Only one nut of this richest food source of selenium contributed with 288.75 µg of selenium daily, increasing selenium intake to more than the recommended levels (55 µg/day), but not exceeding the tolerable upper intake level (400 µg/day) [45]. Selenium in Brazil nuts is found in selenomethionine and selenocysteine species, and studies show that selenomethionine concentration ranges from 75 to 90 % [46,47]. Despite high selenium content in Brazil nuts, no participants complained of symptoms associated with selenosis, as observed by Lemire et al [48].…”
Section: Discussionmentioning
confidence: 99%
“…The usual analytical practice is based on proteolytic enzymes as tools of this process (Bodó et al, 2003;Gilon, Astruc, Astruc, & Potin-Gautier, 1995;Huerta et al, 2003;Kannamkumarath et al, 2002;Yasumoto et al, 1988). One-step enzymatic digestion with the help of two commercially available proteolytic enzymes, pronase E and protease XIV was applied (Bodó et al, 2003;Gilon et al, 1995). The ground and de-fatted sample (350 mg) was placed in a 15 mL polyethylene vial followed by the addition of 30 mg enzyme dissolved in 4.5 mL 50 mM potassium phosphate buffer (pH 7.4).…”
Section: Enzymatic Hydrolysis Procedures For Se-speciationmentioning
confidence: 99%
“…The Se-speciation analysis was carried out with the help of a high performance liquid chromatography-UV photochemical digestion-hydride generation-atomic fluorescence detection system (HPLC-UV-HG-AFS) described elsewhere (Bodó et al, 2003;Ipolyi, Corns, Stockwell, & Fodor, 2001) and only modifications are listed here. The separation was performed on a silica-based strong cationexchange column (Ionospher 5C, Varian BV, Middelburg, The Netherlands) and on a polystyrene-divinylbenzenebased anion-exchange column (Hamilton PRP X-100, Reno, NV, USA).…”
Section: Hplc Measurementsmentioning
confidence: 99%
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