ABSTRACT
As the concentration of methylmercury (MeHg) in the environment is insignificant, hair can be used as a suitable matrix to estimate endogenous MeHg exposure. Avalidated 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.
Subject(s)
Fishes , Hair/chemistry , Methylmercury Compounds/analysis , Occupational Exposure , Adolescent , Adult , Aged , Animals , Case-Control Studies , Czech Republic/epidemiology , Dentists , Environmental Monitoring , Epidemiological Monitoring , Feeding Behavior , Female , Fresh Water , Humans , Male , Middle Aged , Young AdultABSTRACT
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.
