Investigation of trace element concentration in diabetic rat's tissues

Diabetes is one of the most frequent diseases in developing countries and thus there is a significant interest in diabetes related studies. It was found that vanadium compounds have glucose-lowering properties in diabetes and therefore it is very important to estimate the vanadium dose in diabetes treatment. On the other hand, the proper estimation of vanadium concentration is important due to side effects that occur in vanadium supplementation. In this study the influence of V(IV) and V(V) compounds with different ligands on the concentration of K, Ca, Mn, Fe, Cu, and Zn in selected rat’s tissues was investigated by means of proton induced X-ray emission technique. As a result of the measurements it was found that the concentration of vanadium depends on the organ. The highest value was determined in spleen while the lowest in pancreas. It was also found that the concentration of other elements depends on the presence of vanadium and its concentration. The most meaningful influence of vanadium presence was on iron concentration in spleen, on copper and zinc in kidney, and on manganese in pancreas

Hydrothermal synthesis of euhedral Co3O4Co_{3}O_{4} nanocrystals via nutrient-assisted topotactic transformation of the layered Co(OH)2Co(OH)_{2} precursor under anoxic conditions : insights into intricate routes leading to spinel phase development and shape perfection

Euhedral cobalt spinel cubes, octahedra, and cuboctahedra with narrow size dispersions have been synthesized in a one-pot hydrothermal reaction, using cobalt(II) nitrate and sodium hydroxide at variable concentrations as the only reagents, while their ratio was kept constant at $c_{Co^2+}/c_{OH^–}$ = 2.7. Three main reaction stages, including parent reactive template (PRT) formation, nutrient mediated topotactic nucleation (NTN), and morphogenesis of nanocrystals (MNC), were distinguished. In the NTN step, the primary spinel grains development occurs with the [100] and [111] directions of the $Co_{3}O_{4}$ facets inheriting the [1-11] direction of the elongated PRT plates (formation of cubes) or the [001] direction of the hexagonal PRT plates (formation of octahedra). In an anoxic environment, the excess nitrate anions play a critical role as the $Co^{2+}$ to $Co^{3+}$ oxidants and oxygen donors required to attain the $Co_{3}O_{4}$ stoichiometry. The nucleated $Co_{3}O_{4}$ primary nanocrystals are spontaneously assembled into sub-micrometer spinel mesocrystals via imperfectly oriented attachments and then consolidated into euhedral bulk nanocrystals by a hydrothermal treatment (nanocubes) or via dissolution and reentrant recrystallization processes (octahedra and cuboctahedra)

Selectivity of mixed iron-cobalt spinels deposited on a N,S-doped mesoporous carbon support in the oxygen reduction reaction in alkaline media

One of the practical efforts in the development of oxygen reduction reaction (ORR) catalysts applicable to fuel cells and metal-air batteries is focused on reducing the cost of the catalysts production. Herein, we have examined the ORR performance of cheap, non-noble metal based catalysts comprised of nanosized mixed Fe-Co spinels deposited on N,S-doped mesoporous carbon support (N,S-MPC). The effect of the chemical and phase composition of the active phase on the selectivity of catalysts in the ORR process in alkaline media was elucidated by changing the iron content. The synthesized materials were thoroughly characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), and Raman spectroscopy (RS). Detailed S/TEM/EDX and Raman analysis of the phase composition of the synthesized ORR catalysts revealed that the dominant mixed iron-cobalt spinel is accompanied by minor fractions of bare cobalt and highly dispersed spurious iron oxides (Fe2O3 and Fe3O4). The contribution of individual phases and their degree of agglomeration on the carbon support directly influence the selectivity of the obtained catalysts. It was found that the mixed iron-cobalt spinel single phase gives rise to significant improvement of the catalyst selectivity towards the desired 4e− reaction pathway, in comparison to the reference bare cobalt spinel, whereas spurious iron oxides play a negative role for the catalyst selectivity

Effects of vanadium complexes supplementation on V, Cu, Mn, K, Fe, Zn, and Ca concentration in STZ diabetic rats pancreas

The objective of the study was to assess the effects of Na[V V O(O 2 ) 2 (2,2í-bpy)] ◊ 8 H 2 O (complex 1), Na[V V O(O 2 ) 2 (1,10í-phen)] ◊ 5 H 2 O (complex 2 ), Na[V V O(O 2 ) 2 (4,4í-Me-2,2í-bpy)] ◊ 8 H 2 O (complex 3 ), [ V IV O(SO 4 )(1,10í-phen)] ◊ 2 H 2 O, (complex 4 ), [ V IV O(SO 4 )(2,2í-bpy)] ◊ H 2 O (complex 5 ), where: 2,2í-bpy = 2,2í-bipyridine, 1,10í-phen = 1,10í-phenanthroline, 4,4í-Me-2,2í-bpy = 4,4í-dimethyl-2,2í-bipyridine and a small insulin injection on V, Cu, Mn, K, Fe, Zn, and Ca concentration in the STZ (streptozotocin) diabetic rats pancreas during a 5-week treatment with the tested complexes. In all groups of animals metal concentration in the pancreas was investigated by means of Proton Induced X-ray Emission (PIXE) method. Maximum con- centration of vanadium was observed in the pancreas for complex 5 (1.69 ± 0.09 mg/kg dry weight), lower for complex 3 (1.51 ± 0.10 mg/kg dry weight), and the lowest for complex 1 (1.21 ± 0.27 mg/kg dry weight) sup- plementation. The influence of vanadium administration on other metalsí concentration in the ratsí pancreas was also investigated. All vanadium-tested complexes showed an increase of zinc concentration in the exam- ined pancreas in comparison to the diabetic animals not treated with vanadium. The results were the highest for complex 1 and the lowest for complex 5. The concentration of Fe, Cu, Mn, K and Ca in the pancreas is not evi- dently influenced by administration of the vanadium complexe

On the optimal Cs/Co ratio responsible for the N2ON_2O decomposition activity of the foam supported cobalt oxide catalysts

Structured foam catalysts for N2O decomposition containing Co and Cs were prepared via conventional and organic-assisted impregnation method (acetic acid, citric acid, glycerol, glycine, urea). Organic-assisted impregnation caused higher abundance of smaller particles and different faceting. Glycerol usage leads to increase of specific rate constant for N2O decomposition, urea leads to its decrease. The optimal amount of Cs in Co3O4 deposited on the foam was 2–3 times higher than in the bulk Co3O4-Cs due to the dispersion of part of the Cs species over the bare support. The use of glycerol caused a better surface coverage by spinel phase, thus leaving less space for spreading the cesium on the support instead of on the spinel phase. The positive effect of glycerol on the performance of the catalysts with optimized cesium content was attributed to refaceting of the spinal nanocrystals, and greater resistance of the (1 0 0) planes to gaseous NO/H2O contaminates.Web of Science1612art. no. 10531