Silver ions are responsible for memory impairment induced by oral administration of silver nanoparticles.

Increasing use of silver nanoparticles (AgNPs) results in increased human exposure. AgNPs are able to cross brain-blood barrier and are a risk factor for the brain. Thus, we hypothesized that AgNPs exposure might affect hippocampal dependent memory, which required cognitive coordination processes. To verify the assumption, in this study we evaluated the effects of orally administered bovine serum albumin (BSA)-coated AgNPs on spatial memory, which engage cognitive coordination processes for on-going stimuli segregation. Rats following 28 days of oral administration with 1 mg/kg (n = 10) or 30 mg/kg (n = 10) BSA-AgNPs or saline, a control groups (n = 10, n = 8), were tested with an active place avoidance task in the Carousel Maze test. The study revealed significant impairment of long- and short-term memory, irrespectively of dose of AgNPs, whereas non-cognitive activity was on a similar level. We found significantly higher content of silver in the hippocampus in comparison to the lateral cortex. No silver was found in the cerebellum and the frontal cortex. The nanoSIMS analysis reveal a weak signal of silver in the hippocampus of AgNPs treated animals that should be attributed to the presence of silver in ionic form rather than AgNPs. Our findings indicate that oral exposure to a low dose AgNPs induces detrimental effect on memory and cognitive coordination processes. The presence of silver ions rather than AgNPs in different brain regions, in particular the hippocampus, suggests crucial role of silver ions in AgNPs-induced impairment of the higher brain functions.

Preparation of water samples for proficiency testing on radionuclides.

The Institute of Nuclear Chemistry and Technology (INCT) procedure for preparation of water samples for proficiency testing on determination of (241)Am, (137)Cs, (239)Pu, (226)Ra and (90)Sr in water is presented. Natural waters were applied as the raw materials and spiked with the aforementioned radionuclides. The procedure of spiking water allows to prevent losses of the radionuclides and to assign property values from formulation. The main advantages of this procedure are (i) similarity of the test materials to the water samples routinely analysed by radioanalytical laboratories, and (ii) traceable assigned values with low uncertainties.

Metrological assessment of the high-accuracy RNAA method for determination of cobalt in biological materials.

The paper summarizes work on the development of the high-accuracy RNAA method for the determination of trace amounts of cobalt in biological materials. The method is based on a combination of neutron activation with selective and quantitative isolation of the analyte in a state of high radiochemical purity by use of column chromatography followed by gamma-ray spectrometric measurements. The method was devised according to a set of rules, which were formulated to obtain high accuracy of the method. The procedure has been also equipped with several criteria as key factors in quality assurance. Qualification of the high-accuracy RNAA method as a primary ratio method has been demonstrated and its usefulness in the certification of the candidate reference materials tea leaves and mixed Polish herbs is presented.

Some difficult problems still existing in the preparation and certification of CRMs.

Differences between particle size measurements of CRMs by various methods are discussed and the importance of the reliability of such data for proper estimation of the homogeneity of the material is emphasized. On the basis of a very simple model, the dependence of the Ingamells' sampling constant on the average mass of a single particle of the material is derived, and theoretical predictions are compared with the experimental results. Various approaches to the certification of the candidate RMs are briefly reviewed. The merits of the approach being used in this laboratory to evaluate data obtained in the interlaboratory comparison, and to assign certified and information values, is discussed. The conclusions are supported by results obtained for selected trace elements by use of "definitive" (primary) and "very accurate" methods. Some observations on the unusual resistance of some biological materials to wet ashing and the resulting possibility of making analytical errors are mentioned.

A comprehensive study on the contents and leaching of trace elements from fly-ash originating from Polish hard coal by NAA and AAS methods.

In order to assess the environmental risks associated with the emission of fly-ash into the atmosphere and its storage on waste heaps, the trace element contents of fly-ashes from burning Polish hard coal were determined by a newly developed INAA method. Leaching of trace elements from the fly-ash by water and H2SO4 solution (pH approximately 2.5) simulating acid rain, respectively, was studied using AAS and spectrophotometric methods. Analogous experiments were done with neutron-irradiated fly-ash, following the composition of the eluate gamma-spectrometrically. The new fine fly-ash (CTA-FFA-1) candidate reference material was prepared, and the certification was undertaken on the basis of an international intercomparison run. Preliminary evaluation of results shows that at least 38 elements will be certified and, in addition, the "information values" for at least 12 elements will be given.