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At least 19 recordsLinked to original sources
PubMed1991

The determination of platinum in biological tissue by instrumental neutron activation analysis.

Neutron activation analysis was used to determine platinum in the tissues of rats that had received doses of the tumor chemotherapy agent cis-Pt. Two elements causing spectral interference were identified as 47Sc from 46Ca, a natural component of tissue, and tin (117mSn), an element introduced inadvertently during necropsy and sample work-up. A protocol was devised to correct for interference, using emission lines from 47Ca and 113Sn, respectively, with appropriate consideration for relative detector efficiencies, decay times and half-lives.

Animals↗
PubMed1979

Cadmium analysis by radiochemical neutron activation analysis.

Radiochemical neutron activation analysis (RNAA) has been routinely used at the National Bureau of Standards to analyze Cd in a variety of environmentally important matrices. The method used to separate Cd from other neutron-activated products is solvent extraction. Zinc diethyldithiocarbamate [Zn(DDC)2] in chloroform will quantitatively extract Cd from an aqueous solution over a pH range from 1 to 12. In addition to the extraction of Cd, Zn(DDC)2 will also extract Cu, which can interfere with the Cd analysis by producing a high background level of radiation. This can be avoided by first extracting with Bi(DDC)3 in chloroform which removes Cu, but not Cd. Copper concentrations can, therefore, be determined in addition to Cd. This two extraction radiochemical separation procedure is very versatile and is often used as part of a larger multi-element analysis scheme. One such scheme involves the use of an inorganic-ion exchanger, Hydrated Manganese Dioxide (HMD), to retain As, Sb, Se, and Cr prior to extraction. The eluted fraction is then extracted with Bi(DDC)3 to remove Cu, and then with Zn(DDC)2 to remove Cd.

Activation Analysis↗
PubMedDate not supplied

Determination of inorganic components in Brazilian medicinal plants by neutron activation analysis.

Instrumental neutron activation analysis (INAA) has been applied to multielemental determinations of medicinal extracts obtained from the plants. Cordia Verbenacea DC, Folidago Microglossa DC, and Petiveria Alliacea. Concentrations of the elements Al, Br, Ca, Cl, Co, Cs, Fe, K, La, Mg, Mn, Na, Rb, Sb, and Zn have been determined in dried extracts of these herbs by short and long irradiations under a thermal neutron flux of 10(11)-10(13) n/cm2s in the IEA-R1 nuclear reactor. The NBS Tea Leaves (1572) and NIES Pepperbush (1) reference materials were analyzed simultaneously with the plant extracts. The results obtained in these analyses have shown a good accuracy and reproducibility of the method. The relative errors and the relative standard deviations were less than 10% for most of the elements analyzed.

Brazil↗
PubMed1978

Measurement of chromium VI and chromium III in stainless steel welding fumes with electrom spectroscopy for chemical analysis and neutron activation analysis.

Electron Spectroscopy for Chemical Analysis (ESCA) was explored as a means of studying the oxidation state of chromium in SMAC (coated electrode) stainless steel welding fume collected on Nucleopore filters in the laboratory. Chromuim VI and III (as a percent of the total chromium) obtained from ESCA analysis was applied to results from Neutron Activation Analysis (NAA) to yield an average of 69 microgram chromium VI per sample. Diphenylcarbazide/atomic absorption (DPC/AA) results are reported for samples submitted to an industrial laboratory. Possible chemical species and solubility of chromium VI in stainless steel fumes is discussed in light of analogy between the SMAC process and the manufacturing process for chromates.

Air Pollutants↗
PubMed1978

Determination of certain selected bulk and trace elements in the bovine liver matrix using neutron activation analysis.

Effective utilisation of neutron activation analysis (NAA) for the elemental analysis of biomedical samples with or without a radiochemical separation, especially when optimal Ge(Li) well type detectors are employed for the acquisition of complex spectra, is demonstrated by determining normal values for 25 elements in bovine liver. Optimal conditions for the determination of Ag, Br, Cl, Co, Cs, Fe, I, K, Mn, Na, P, Rb, Sb, Sc, Se and Zn with the aid of instrumental thermal neutron activation analysis (INAA) by varying the irradiation and decay time are presented. Where INAA was inadequate, simple post irradiation separation based on ion-exchange has been used to determine such elements as Au, Ca, Cd, Ce, Cr, Cu, La, Mo and W. Results from the IAEA intercomparison run for animal muscle (H-4) are also given. The influence of sample size with respect to within-tissue variation of the bulk and trace elements in liver and the contamination of liver samples from the interfering components such as residual blood are also discussed.

Activation Analysis↗
PubMedDate not supplied

Study of physiopathological phenomena in dental enamel by neutron activation analysis.

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.

Bone Density↗
PubMedDate not supplied

Nondestructive determination of arsenic in urine by epithermal neutron activation analysis and Compton suppression.

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.

Arsenic↗
PubMed1975

[Investigations of contact tissues of Blount vitallium staples using the instrumental neutron activation analysis (author's transl)].

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.

Activation Analysis↗
PubMed1990

Neutron activation analysis of manganese contents in ordinary hospital meals.

Neutron activation analysis (NAA) was applied to measurement of manganese (Mn) content in food as an example of ordinary hospital meals. The results showed that: 1. NAA permits measurement of Mn with a simple pretreatment procedure in comparison with AAS (atomic absorption analysis). 2. Daily Mn intake was estimated to be about 3 mg from food, and about 4 mg from green tea. Neutron activation analysis (NAA) has been used for measuring various elements under the conditions appropriate for the irradiated or radioactivated subject of analysis. We presently applied NAA to measurement of manganese (Mn) contents in food as an example of ordinary hospital meals with an estimation of daily Mn intake.

Food Analysis↗
PubMed1978

[Studies on the presence of metal traces in tissue surrounding A.O. angle plates, based on neutron activation analysis (author's transl)].

Using instrumental neutron activation analysis, 11 samples of tissue in contact with A.O. angle plates and 8 samples of fascial tissue were examined for their content of trace elements, half a year to 5 1/2 years after hip joint intertrochanteric osteotomies. Significant increases in the concentrations of the elements Cr, Fe, Co, Ni and Mo, all of which are contained in the A. O. steel plates (V4A steel), were found both in the contact tissue and in the tissue of the fascia lata femoris about 4--8 cm away from the angle plates, whereas the levels of concentration of elements not specific for the alloy in question, namely, Zn, Se, Rb and Cs, were normal or just subnormal. It was possible to prove by means of element correlations that the elements Cr, Co, Ni and Mo are present in constant ratios in those tissue samples which are loaded with traces of metals foreign to the body. However, only the Mo:Cr ratio corresponds to that of the angle plates. The authors considered Ni to be a useful indicator for the degree of metal loading of a tissue, since Ni will normally occur in human tissue in very low concentrations (less than or equal to 10(-6) g/g dry substance) and was identified by the authors--contrary to previous studies--even in the fascial tissue located up to 8 cm away from the contact tissue. Non-linear correlations were found between iron and the other components of the steel, reflecting the complicated regulatory mechanisms governing the presence of iron in the organism. The results of the analysis are discussed in respect of possible long-term action of the implantate components liberated by corrosion, which, in case of long-term implantates might place an overall burden of foreign ions on the body.

Chromium↗
PubMed1979

Neutron activation analysis of selenium and 17 elements in sediment.

Instrumental neutron activation analysis was performed to determine Na, Mg, Al, Cl, Sc, V, Cr, Mn, Fe, Co, Ni, Rb, Sb, Cs, Ba, Ce and Eu in the Pacific core sediment. Selenium was also determined by neutron activation analysis, by applying a solvent extraction method with 2,3-diaminonaphthalene (DAN) as a post-irradiation procedure, after the wet-ashing of the sediment. Homogeneity of trace constituents in the sediment and neutron flux corrections for accurate determination were also investigated.

Activation Analysis↗
PubMed1978

A two-way scanning method for total body in vivo neutron activation analysis.

When determining the total body content of many elements by neutron activation analysis, irradiation and whole body counting by scanning along the length of the body has significant advantages. A neutron source of lower output and a whole body counter using smaller detectors and shielding (than otherwise needed) can provide a high, uniform response for many elements throughout the body. This was previously achieved by making the speed and direction of scanning identical in irradiation and counting (one-way scanning). A simple theoretical model for scanned irradiation and counting is described. The model is used to show that a scanning regime in which both scanning directions are used (two-way scanning) can provide acceptably uniform response for elements having induced activities of a wide range of half-life. This is supported by measurements made using an existing scanning facility for total body in vivo neutron activation analysis. The two-way scanning regime offers the advantages of increased patient comfort, simpler operation and more efficient use of the time available for counting induced activity.

Activation Analysis↗
PubMed1977

Determination of gold in plasma and plasma fractions by atomic absorption spectrometry and by neutron activation analysis.

Three techniques of gold analysis, flame and electrothermal atomic absorption spectrometry and neutron activation analysis, have been compared, using plasma and plasma fractions (derived by gel chromatography) from rheumatoid patients receiving aurothiomalate therapy and from plasma samples incubated with aurothiomalate in vitro. The three methods correlated well in the analysis of gold in whole plasma, but only neutron activation analysis was suitable for the assay of all the plasma fractions. The susceptibility of the two atomic absorption methods to interference by sodium chloride was investigated.

Gold↗
PubMedDate not supplied

Bone mineral measurements of the central skeleton by in vivo neutron activation analysis for routine investigation os osteopenia.

In vivo neutron activation analysis has been used to measure bone mineral content in the central skeleton where osteoporotic fractures occur. To be of diagnostic value, the results must be normalized for body size. From data obtained from 74 healthy children and adults up to 55 years of age, we have found that the calcium in the central skeleton is approximately proportional to the cube of the subject's height. The correlation for the adults alone has an r value of 0.81. When data from both adults and children are used, r = 0.95. The validity of this cubic height relationship to the Ca concentration measurements has been further substantiated by studies on rats. The total femur calcium content of 110 rats from weanling to 25 weeks of age was proportional to the overall femur (length) 3.6 (or (length)2.6 per unit length) with r = 0.99. When the level of Ca content is related to data on normal subjects of the same body size (giving the Calcium Bone Index or CaBI) a good separation is obtained between normal volunteers and osteoporotic subjects. Volunteers who were 20 to 55 years of age had CABI 1.0 "/- .12 (SD) while osteoporotics had CaBI 0.69 +/- .10 (SD). When the calcium content as determined by in vivo activation analysis is expressed as a CaBI, it provides a powerful tool for the diagnosis of osteopenia. We suggest that all bone measurements, including peripheral ones, be normalized for body size in order to increase their diagnostic value.

Activation Analysis↗
PubMedDate not supplied

Determination of trace elements in aerosol samples by instrumental neutron activation analysis.

Two nuclear techniques, Energy-Dispersive X-Ray Fluorescence Analysis (EDXRF) and Instrumental Neutron Activation Analysis (INAA), were used to analyze aerosol samples collected in the city of São Paulo, Brazil. Na, Cl, Mn, V, Al, Sm, Mo, W, La, As, Br, Sb, K, Ba, Se, Th, Cr, Rb, Ca, Fe, Ce, and Sc were determined by INAA, and Al, Si, P, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Ga, As, Se, Br, Rb, Sr, Hg, and Pb were determined by EDXRF. A preliminary identification of the main source of the atmospheric aerosol was performed based on enrichment factor and correlation coefficient calculations.

Aerosols↗
PubMed1979

Neutron activation analysis of biological materials by the monostandard method.

Instrumental neutron activation analysis by the monostandard method has been applied to the analyses of biological NBS standard reference materials; 1571 Orchard Leaves and 1577 Bovine Liver. Aluminum foils containing 0.100% gold or 2.00% cobalt were used as the monostandards. The gamma-ray spectral data were recorded on punched paper tape and were analyzed by a computer assisted data processing. The following 25 elements were determined: Al, Ca, Cl Cu, Mg, Mn, V (by short period irradiation), As, Ba, Br, Co, Cr, Cs, Eu, Fe, Hg, K, La, Na, Rb, Sb, Sc, Se, Sm and Zn (by long period irradiation). The results were compared with the certified values by NBS and the reported values in literatures to prove the reliability and accuracy of the monostandard method.

Activation Analysis↗
PubMed1978

Neutron uniformity studies related to clinical total body in vivo neutron activation analysis.

Methods of assessing the uniformity of thermal and fast neutron fluence in relation to total body in vivo neutron activation analysis are described. Results are presented for 14 MeV neutrons emitted by sealed tube generators housed in a massive concrete shield, representing a substantial source of neutrons degraded in energy. Optimisation of conditions for patient irradiations is discussed and it is shown that acceptable uniformity of fluence can be achieved with little or no premoderation of the incident neutrons.

Activation Analysis↗