The serum selenium levels in 367 healthy adult (25-64 yr) Central Bohemia residents, 176 men and 191 women, were determined using atomic absorption spectrometry. An extremely wide range of values was found in the whole population sample (< 20-296 micrograms/L) as well as in each sex or age category studied. The mean selenium concentration and 95% confidence interval calculated after logarithmic transformation of the data were 74 micrograms/L (71-77) for the whole population sample, 72 micrograms/L (67-76) for men, and 76 micrograms/L (72-81) for women. About 10% of the residents exhibited serum selenium level below 45 micrograms/L. There was no significant correlation between serum selenium and sex, age, or smoking status of participants. However, the lowest average level was found in the group of heavy smoking women: 66 micrograms/L. The selenium status of the Central Bohemia population seems to be below European average. Groups of residents having a very low nutritional selenium intake may be expected to occur in this population.
As the concentration of methylmercury (MeHg) in the environment is insignificant, hair can be used as a suitable matrix to estimate endogenous MeHg exposure. A validated analytical method with AMA 254 spectrometer was used for the determination of inorganic mercury and methylmercury species in the hair of dentists, workers in fish industry and professionally non-exposed adults. ANOVA and QC Expert software was used for statistical evaluation. The number of amalgam fillings in oral cavity, consumption of fish, gender, smoking habits and age of the subjects were taken into account. A significantly higher level of inorganic bound mercury (Hg in) was found in the hair of dentists. The number of amalgam fillings had a slightly significant effect on Hg in ; fish consumption had a significant influence on MeHg and slightly also on Hg in. Other parameters were not significant.
A sampling procedure appropriate for the determination of mercury in whole blood was tested by using both inactive controls and a 197Hg mercury radio-indicator. To exclude the influence of the instrumental device (an AMA 254 single-purpose mercury atomic absorption spectrometer) on the determination of mercury in whole blood, the function of the instrument was checked by using rat blood with metabolised 197Hg. The measurement procedure was found to be free of errors. However, the study showed that the material used for the sampling vessels is a crucial parameter for obtaining accurate analytical results. The stability of solutions and samples was tested towards polyethylene (PE) and polypropylene (PP) vessels. PE displayed a time-dependent increase in the mercury content both in the samples and in the blood control material. The probable cause of this increase was direct contamination from the material of the vessel and/or diffusion of mercury from the environment through the vessel walls related to a strong complexing affinity of the sample matrix. This assumption was confirmed by supplying the vessels with the complexing agent Na2EDTA (0.05 mol L(-1)). Commercial PP vessels for blood sampling (Sarstedt S-Monovette Metall Analytik) did not give rise to statistically significant variations in mercury content in the samples and blood control material over a 30-day period.
The determination of trace amounts of mercury in biological materials is described. Vanadium pentoxide-catalysed digestion in nitric acid under pressure in a PTFE autoclave was used for destruction of the samples. Satisfactory destruction was achieved in the absence of sulphuric acid. Mercury was determined in the digest solution by atomic-absorption spectrophotometry using a cold vapour circulating in a closed system The detection limit was optimally 1 ng g-l. No losses of mercury occurred. The accuracy of the determination was confirmed by the close agreement of certified and determined concentrations of mercury in reference materials.
Contents of selenium (Se) were determined in human skeletal remains of prehistoric populations by in situ trapping of Se hydride by ET AAS (atomic absorption spectrometry with electrothermal atomisation). Dr Korunová worked out a method of determination of Se in preparation. The method of determination of Se was verified by means of radioactive indicator 75 Se incorporated in the tissues of laboratory animals. Detection limit of the method was 23 pg Se.Se is another element suitable for dietary reconstruction in past populations as it relates to the consumption of meat in a similar way to zinc. Through the analysis of Se, we were able to distinguish between Eneolithic archaeological cultures (Corded Ware ceramic, Bell Beaker culture) and Bronze Age cultures (Protouně tice, Starouně tice, Uně tice cultures).Significant differences were found in the levels of Se in the bones of individuals derived from the Bell Beaker and Uně tice Cultures, to the 95% confidence interval.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.