SEARCH · PubMed Health
Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.
Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
An epithermal neutron activation method is used to determine the concentration of mineral elements in human dental enamel. A large number (252) of samples from ancient and modern origins are analyzed. The analytical results are mathematically processed using a statistical multivariant method. This allows to differentiate deciduous from permanent teeth and decayed from sound enamel. It is also possible to distinguish the teeth coming from two different necropoles. The origin and the localization of determined elements in the mineralized part, or in the aqueous-organic part, of enamel is suggested. Their role, as witnessed in the physiopathological phenomena of dental enamel, is discussed.
Multielemental analysis, using neutron activation, was carried out on the urine, whole blood, pubic hair and toenails of thirty subjects occupationally exposed to hard metal dusts. A high concentration of Co, W and Cr was observed in all samples analysed. The concentrations determined, when subjected to statistical analysis using pattern recognition techniques (e.g. cluster analysis), indicated a positive correlation, at p = 0.001, for the pair (Co, W) in urine and blood, as well as a possible influence of Cr on this pair.
Multi-element neutron activation analysis method was applied to the determination of metallic foreign bodies which penetrated into the eyes of workers while engaged in grinding and cutting work. A total of 23 small pieces ranging in size from 1 to 10(2) mg were surgically obtained and then analyzed non-destructively with only simple washing treatment. The components of 21 samples were mainly iron and the others were hard pieces of wolfram compound. Elements determined in samples over one weight percent were iron, manganese, chromium, wolfram, and cobalt. All the samples were divided into five classes according to their own elemental composition. It was considered that foreign bodies were composed of carbon steel, steel alloy, and tungsten carbide. These results are regarded to be useful in studying the mechanism of accidents and their effects on eyes.
Multi-element analysis by neutron activation analysis (NAA) in respect to medical applications is discussed. Examples of trace element determinations in pathological human liver tissues, human serum, and rat liver are given. A very sensitive method for determining fluorinated drug in very small samples of human serum by neutron activation is also described. Each biological samples (ca. 100-200 mg, lyophilized matter) was irradiated for short time (10 s or 5 min.) and for long time (24 hrs) in Rikkyo University Research Reactor or Musashi Institute of Technology Research Reactor. Concentration of 12 elements (127I, 55Mn, 26Mn, 65Cu, 23Na, 41K, 37Cl, 27Al, 48Ca, 36S, 58Fe, 64Zn) in human pathological liver, Futraful (19F) (anti-cancer fluorinated drug) clearance of human serum, and calcium uptake (48Ca) in liver of rats were determined by NAA.
Neutron activation analysis was applied to determine the 232Th activity in different matrices. Since in nature thorium consists of almost 100% of the long-lived 232Th, the instrumental trace element analysis method of neutron activation analysis can be applied to determine the thorium content in a sample. which can then be converted into the corresponding specitic activity. For the analysis about 100 mg of the sample was irradiated at a thermal neutron flux of phi(th) = 8 x 10(13) n.cm(-2) x s(-1). After irradiation the activity of the indicator nuclid 232Pa--produced by the (n,gamma) reaction--was measured by gamma spectrometry. The content of thorium was calculated using the activation equation and the isotope-related ki constant. Finally, the concentration of thorium in the sample was converted into the specific activity. The activities of 232Th measured by applying neutron activation analysis in different samples were compared with the results found by a spectrometry and gamma spectrometry for the daughter nuclides 228Ac and 224Ra.
Cyclic and pseudocyclic instrumental neutron activation analysis (INAA) has been used to determine the Se content of 40 Libyan food items. The selected samples include different varieties of local and imported foods such as wheat and barley products (bran and flours), rice, bread, almond, peanuts, vegetables as bean and peas, tea, coffee, sugar, and commonly used spices such as red and black paper, curry, cumin, mixture of spices, thyme, coriander, and fenugreek. Both conventional and anticoincidence gamma-ray spectrometry techniques have been employed. Pseudocyclic INAA in conjunction with anticoincidence counting has been found to provide the most reliable results. The precision of the method has been significantly improved by recycling the samples up to three times. The accuracy has been evaluated by analyzing a number of certified reference materials of varied Se levels. The detection limit has been found to vary between 26 and 90 ppb Se depending on the sample composition. The range of daily dietary intake has been calculated as 13-44 microg of Se per day.
The Leeds facility for in vivo neutron activation analysis has been modified and calibrated for the simultaneous measurement of nitrogen, potassium, sodium, chlorine, phosphorus and calcium in obese patients weighing up to 210 kg. The effects of body size and shape were incorporated into the calibration by measuring 14 anthropomorphic phantoms of known composition representing individual patients being treated for obesity. The phantoms were constructed from tissue substitutes representing lean, skeletal and adipose tissues, arranged to simulate the distributions of the corresponding tissues within the patients, as visualised by CT scanning. The precision of the method, determined by measuring a single phantom ten times over a period of ten weeks, is between two and three per cent for all elements except calcium, for which it is 11.3%. Accuracy is estimated to be similar to precision. The procedure has been used to study changes in body composition of patients undergoing therapeutic starvation.
Explore the source record for details and available documents.
The method of instrumental neutron activation analysis (NAA) has been improved for air filter samples in the determination of low level heavy metals in indoor air. By using the techniques of epithermal neutron irradiation in conjunction with Compton suppression, the detection limits of cadmium, arsenic and antimony measurements have been dramatically reduced to 2 ng for Cd, 0.2 ng for As, and 0.03 ng for Sb. The determination of these heavy metals in particulate material generated from cigarette smoking in indoor environments has been conducted. Other elements, Br, Cl, Na, K, Zn were also found at elevated levels.
In this study, instrumental neutron activation analysis was applied to the determination of Sc, La, Ce, Nd, Sm, Eu, Tb, Yb, Lu, Hf, Th, and U in lung samples from miners working in coal mines located in the state of Santa Catarina, Brazil. These results were compared to those from a control group constituted of healthy individuals. The results showed that the elements determined exhibit considerable intersubject variability within a single group of individuals and the mean values of concentrations in miners' lungs were higher than those of normal individuals. Lung samples presented U concentrations varying from 11 to 890 micrograms/kg. Therefore, for some samples, the contribution of the uranium fission products in the analysis of La, Ce, Nd, and Sm was considered by determining the interference correction factors. The accuracy of the results was evaluated by analyzing certified reference materials.
Epithermal neutron activation analysis, in conjunction with Compton suppression, has been employed to determine arsenic levels in artificially doped urine samples. Typical detection limits were of the order of 10 ng/g. Replicate determinations gave precision values between 2 and 12%, whereas accuracy measurements were between +/- 1 and +/- 20%. Biological and geological reference materials from the National Institute of Standards and Technology (NIST) were also analyzed for arsenic content. Typically, the precision achieved again was between 2 and 12%, whereas the accuracy measurements were in excellent agreement with the certified values.
Instrumental neutron activation analysis with Gamma-spectroscopy is a very sensitive method for testing trace elements. Specimens of contact tissue around 5 Blount's vitallium clamps were, after preparation at the Nuclear Research Institute Jülich irradiated with thermic neutrons and their element-specific gamma spectra were measured after 33 and 125 days. In contact tissue a significant rise in concentration of the alloy-specific elements cobalt and chromium was found. The unspecific elements silver, caesium, iron, rubidium, antimon, scandium and zink were either within or very close to the normal. The metallosis of contact tissue is due to corrosion of the surfaces of cobalt-chromium implants.
The technique of instrumental neutron activation analysis was applied as a sensitive nondestructive analytical tool for the determination of heavy metals and rare earth elements in phosphate fertilizer ingredients. The contents of heavy metals Fe, Zn, Co, Cr and Sc as well as rare earth elements La, Ce, Hf, Eu, Yb and Sm were determined in four samples representing the phosphate fertilizer components (e.g. rock phosphate, limestone and sulfur). These samples were collected from the Abu-Zabal phosphate factory in El-Qalubia governarate, Egypt. The aim of this study was to determine the elemental pattern in phosphate ingredients as well as in the produced phosphate fertilizer. Fair agreement was found between the results obtained for the standard reference material Soil-7 and the certified values reported by the International Atomic Energy Agency. The results for the input raw materials (rock phosphate, limestone and sulfur) and the output product as final fertilizer are presented and discussed.
Explore the source record for details and available documents.
An instrumental neutron activation analysis was applied to the multielemental analysis of the Stenopsyche griseipennis taken from the head water area and the lower of Tama river. The dry Stenopsyche griseipennis were irradiated for 3 minutes and 12 hours in a thermal neutron flux 1.5 X 10(12) n . cm-2 . sec-1 of TRIGA-II reactor of Rikkyo University. Thus, Al, Ca, Cl, Mg, V, Na, K, Br, La, Sm, Se, Cr, Ba, Cs, Sc, Rb, Zn, Co, Fe, and Sb could be analyzed. Analysis of the river water samples taken from the sampling points of the Stenopsyche griseipennis was carried out by the method given in the author's previous paper. The analytical results of Na, K, Zn and Se for the Stenopsyche griseipennis showed constant value independently of the river water quality, and Mn showed the different concentration between at the head water area and at the lower. On the other hand, the analytical results of Al, Fe, Sc, V, As, Sb, etc. showed wide range values. It can be considered that these elements were affected by taking up river sediment, and V, As and Sb concentrations in the Stenopsyche griseipennis at head water area showed larger values than those at the lower.