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Biomedical subjects

Ewa Bulska

Publications and source records attributed to Ewa Bulska.

10 recordsLinked to original sources

In vivo investigation of the distribution and the local speciation of selenium in Allium cepa L. by means of microscopic X-ray absorption near-edge structure spectroscopy and confocal microscopic X-ray fluorescence analysis.

In this work, microscopic X-ray absorption near-edge structure spectroscopy (mu-XANES) and confocal microscopic X-ray fluorescence analysis (mu-XRF) were used for the in vivo determination of the distribution of total selenium and for the local speciation of selenium in roots and leaves of onion. Selected Allium cepa L. plants were grown hydroponically in a standard medium containing inorganic selenium compounds (selenite or selenate). The measurements were performed in vivo, that is, on living plants without the need for any form of sampling or sample pretreatment and without the necessity for cutting plant tissues into pieces. Distinct energy differences of the XANES spectra of various selenium reference compounds having different oxidation states allow adjusting the excitation energies used for mu-XRF mapping in such a manner that the distribution of selenium in various oxidation states is obtained with a spatial resolution of a few tens of micrometers within the virtual cross section of the onion tissues. We find that the ratio of inorganic to amino acid selenium compounds differs in various subparts of the plant. Detailed in vivo investigation of the distribution of various selenium species in virtual cross sections of root tips and green leaf shows that the selenium transport takes place via different mechanisms, depending on the nature of the selenium compounds originally taken up.

Amino Acids↗

Laser ablation inductively coupled plasma mass spectrometry assisted insight into ion-selective membranes.

Laser ablation inductively coupled plasma mass spectrometry was used to evaluate ion depth profiles across ion-selective membranes. Advantageously, this approach does not require incorporation of additional components (e.g., chromoionophore) in the membrane composition, as compared to that used in typical potentiometric applications. Moreover, comparison of the distribution of ions in differently pretreated membranes is possible. Concentration profiles of primary and interfering agent (Na+) ions were recorded, for example, of Pb2+-selective poly(vinyl chloride)-based membranes. It was found that the contents and the distribution of Pb(2+) and Na+ ions across the membrane is strongly dependent on the composition of the solutions to which both sides of the membrane are exposed during preconditioning and on the plasticizer included in the membrane formulation. Typical plasticizers, bis(2-ethylhexyl sebacate) (DOS) and the more polar 2-nitrophenyl octyl ether (o-NPOE), were used. It was found that faster ion transport occurs for o-NPOE, and the membrane saturation with Pb2+ ions was achieved within less than 20 h for a 400-microm-thick membrane. In the case of the less polar plasticizer DOS, due to slower rate of ion transport, even after 20 h, the Pb2+ concentration gradients were still visible within the membrane. On the basis of concentration profiles, primary ion diffusion coefficients in both membranes were calculated, and the value obtained for o-NPOE containing membrane was found to be approximately 2 times higher than for its DOS-plasticized counterpart.

Decanoic Acids↗

[Low zinc and high copper levels in mothers of children with isolated cleft lip and palate].

UNLABELLED: Changes in orofacial development have been reported in offspring of animals treated with copper injections or low zinc diet during pregnancy. The aim of our study was to determine serum levels of zinc and copper in mothers of children with non-syndromic orofacial clefts and in women who gave birth to healthy children. Ninety six healthy women participated in the study: 35 mothers of children with cleft lip and cleft palate (CLP), 30 mothers of children with cleft palate (CP) and 31 control mothers of healthy children. Serum zinc and copper concentrations were determined by the use of inductively coupled plasma-mass spectrometry (ICP-MS). RESULTS: Between CLP and controls there were significant differences in mean zinc levels (511 +/- 121 microg/L vs 572 +/- 76 microg/L, p = 0.012) and copper levels (991 +/- 388 microg/L vs 810 +/- 201 microg/L, p = 0.02). In CP mean serum zinc and copper levels were 540 +/- 130 microg/L and 846 +/- 291 microg/L. The ratio of serum zinc to copper levels was significantly lower in CLP comparing to CP and controls (0.57 +/- 0.19 vs 0.67 +/- 0.18 and 0.74 +/- 0.19, p = 0.003). CONCLUSION: Our results suggest that trace elements may play a role in facial clefting in humans.

Adult↗

Structure of YAG crystals doped/substituted with erbium and ytterbium.

Two series of yttrium aluminum garnets doped with erbium and ytterbium ions have been studied by single-crystal X-ray diffraction. The single crystals were obtained by the Czochralski method. The concentration of doping ions was established by the plasma emission spectroscopy method. For the Er series, it is equal to 23.4, 46.7, 72.5, and 100%, whereas, for Yb-doped YAGs, it equals 26.5, 48.2, 75.9, and 100%. The results are supplemented by the data obtained for pure YAG. The X-ray data for all samples were collected at two temperatures: 295(2) and 102(2) K. Additionally, for YAGs doped with ca. 50% of doping ions, some more detailed temperature measurements were performed. Pure single crystals of ErAG and YbAG were also studied as a function of diffraction angles. Careful single-crystal measurements utilizing a CCD diffractometer revealed the unit cell parameters, which slightly-but significantly-deviate from cubic symmetry. The average unit cell parameters change linearly with the amount of substituting Er and Yb cations, with two different slopes related to the ionic radii. Both of the dodecahedral distances depend linearly on the concentration of the substituting ions, but the longer dodecahedral distance also changes with temperature contrary to the shorter one. There is no correlation between the octahedral interatomic distance [Al(VI)...O] and the unit cell parameter or temperature; however, weak trends appear for the tetrahedral [Al(IV)...O] distance. Such weak trends are just the secondary consequences of the ion substitution taking place at the dodecahedral site. The dependences between the unit cell parameters and the concentration of doping ions allow us to establish concentrations of particular doping ions in mixed (Er, Yb) doped YAGs just on the basis of the measured unit cell parameters and knowledge of the amount of Y.

Journal Article↗

[Urinary trace elements excretion in patients with cystine calculosis].

UNLABELLED: Not all cystinuric patients develop urinary calculi. There is the need to identify modulating factors. In recent years the role of trace elements in the mechanism of stone formation has received a steadily increasing attention. The aim of our study was to determine urinary excretion of trace elements in patients with recurrent cystine calculosis. MATERIAL AND METHODS: 11 patients with recurrent cystine calculosis and 15 healthy volunteers participated in the study. Urinary zinc, copper, chromium, boron and arsenic concentrations were determined by use of inductively coupled plasma-mass spectrometry (ICP-MS). RESULTS: There was a statistically significant difference between the patients with cystinuria and controls in mean arsenic urinary excretion (0.625+/-0.6 microg/kg body weight/24 h vs. 1.264+/-0.635 microg/kg b.w./24 h, p=0.02). There was also a noticeable difference in urinary chromium, the mean concentration of which was higher in case of the patients with cystinuria (3.32+/-3.59 microg/kg/24 h) than in the controls (1.38+/-0.69 microg/kg/24 h). The mean urinary excretion of zinc, copper, and boron (in microg/kg b.w./24 h) were respectively 7.40+/-7.98; 1.33+/-0.48; 26.55+/-15.81 in the patients with cystinuria and 9.84+/-5.33; 1.16+/-0.84; 35.87+/-13.76 in the controls. CONCLUSION: It seems that a decreased excretion of arsenic may contribute to the development of cystine calculosis.

Adolescent↗

Use of solid-phase extraction to eliminate interferences in the determination of mercury by flow-injection CV AAS.

Solid-phase extraction with two-step elution has been developed for effective elimination of copper and iron interference with mercury determination by flow-injection cold vapour atomic absorption spectrometry (CV AAS). Sodium tetrahydroborate(III) was used as reducing agent. Cation-exchanger Dowex 50Wx4 was applied for the sorption of mercury and both interfering ions. In the first step elution of Cu(II) and Fe(III) was performed using 0.5 mol L(-1) KF solution. Then mercury was eluted with 0.1% thiourea in 8% HCl. The detection limit (3 delta) for Hg(II) was 27 ng L(-1). The expanded uncertainty estimated for the whole procedure was about 6%. The accuracy of the proposed method was evaluated by determination of the recovery of known amount of mercury added to mineral, spring, and tap waters, and by analysis of a certified reference material BCR-144R (sewage sludge).

Journal Article↗

Comparison of the potentiometric, (31)P NMR, and zero-point titration methods of determining ionized magnesium in erythrocytes.

A simple and rapid method of determining ionized magnesium in erythrocytes using a potentiometric clinical analyzer, Microlyte 6 (Kone, Finland), was investigated. The erythrocyte cell membranes were destroyed using ultrasound. The results were compared with those obtained with the (31)P nuclear magnetic resonance spectroscopy method and the zero-point titration method using atomic absorption spectrometry. The results obtained from potentiometry and from the other methods did not differ significantly (Student t test, alpha = 0.01). Total magnesium concentration was determined using atomic absorption spectrometry.

Adult↗