Potential of microalgae as source of health-beneficial bioactive components in produced eggs.

In line with the growing interest in humans' nutrition, production of microalgae-based functional foods characterized by an increased content of bioactive substances is attractive. The aim of this study was to investigate the potential of microalgae as additives to feed for laying hens, to enrich the eggs with polyunsaturated fatty acids (PUFA) and selenium/carotenoid antioxidants. Our results showed that supplementation of hens by feed containing 1% of Trachydiscus minutus or 1% of Japonochytrium marinum leads to increase of long-chain PUFA in eggs by 26-66%. Addition of 1% of Scenedesmus obliquus to feed causes the increase of lutein and cantaxanthin in eggs by 48% and 18%, respectively, and addition of 0.5% selenium enriched Chlorella vulgaris increases the final content of organic selenium in eggs by 100-152%. As concerns selenium, it is important to notice that its bioavailability has to be considered. Despite the higher concentration of total selenium in Vischeria helvetica than in C. vulgaris, its bioaccessibility in Vischeria was limited, thus out of usage for feeding purposes. Administration of combinations of selenium enriched Chlorella + Japonochytrium and Chlorella + Schizochitrium verified the increased concentrations of organic selenium, PUFA, as well as carotenoids, with no adverse effect on quality and productivity of eggs. The study confirmed the potential of both traditional as well as new microalgae to be used as feed supplements for functional eggs production. The supplementation of hens by specific microalgae combinations could be advantageous in terms of spectrum of bioactive compounds present.

Speciation of Cu, Se, Zn and Fe in blood serum of hemodialysed patients.

The speciation of trace elements in serum samples of hemodialysed patients was investigated using on-line connection of SEC and ICP-MS. The 0.02 mol/l TRIS-HCl buffer of pH 7.5 was used as mobile phase. The results of speciation as well as the total concentration data were compared with those of control group of healthy person. Alterations of total concentration were observed in case of selenium and zinc only. Iron was present in form of transferrin and ferritin, main amount of copper was bound to ceruloplasmin and selenium compounds were identified as selenoproteine P and glutathione peroxidase. The latter compound was detected in samples of control group only. The chromatograms of the other elements were similar and no substantial changes between both investigated groups were observed.

Determination of zinc in plant samples by isotope dilution inductively coupled plasma mass spectrometry.

Determination of zinc involved spiking with (68)Zn enriched solution, digestion by HNO(3)+H(2)O(2) in microwave decomposition unit, off-line separation of zinc on Chelex-100 column and measurement of ((64)Zn+(66)Zn)/(68)Zn isotope ratio on ICP-MS spectrometer with a quadrupole mass filter. After optimization of standard operation procedure (details are given) the method was validated. LOD was found to be 0.3 mug g(-1) for the procedure without zinc separation and 3.6 mug g(-1) for the procedure involving zinc separation, respectively. The accuracy of results was proved by analyses of several CRM and a primary solution of zinc, the concentration of which was verified by gravimetry and complexometric titration. Barium is the only element causing serious interferences and it must be removed from samples. The uncertainty budget is given together with the scheme of combined uncertainty calculation. The main uncertainty components are contamination during zinc separation and uncertainty of isotopic composition of natural zinc.

Custom-made interface between electrothermal vaporiser and inductively coupled plasma-mass spectrometer: determination of nickel by isotope dilution in plant samples.

ICP-mass spectrometer Perkin Elmer Elan 6000 was adapted for ETV analysis by coupling with GBC GF 3000 graphite furnace atomiser. Both instruments were connected by a 25 cm long PTFE tubing of 6 mm i.d. and a custom-made interface. The apparatus was applied to nickel determination using isotope dilution technique. The efficiency of analyte transfer through the interface was approximately 20%, however the incomplete transfer did not influence the blank values. Measured isotope ratio was very stable, whereas the magnitude of ion signal showed a little shift. CRM samples were analysed after microwave decomposition and by slurry technique as well. Obtained results were compared with those of pneumatic sample nebulisation after nickel separation on Chelex column. All tested techniques gave accurate results with comparable precision. However, the slurry technique allowed significant decreasing of the blank values and the limit of detection. The duration of analysis run can also be substantially shortened from several hours to a few minutes.