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[Assessment of the distribution in the body and the dose on the respiratory tract and organs after single, short-term and long-term inhalation of americium-241].

On the basis of comparison of publications on accidental human intake of americium-241 and animal experimental studies dosimetric characteristics were obtained reflecting the dynamics of accumulation, formation of the dose on the organs and parts of the respiratory tract, as well as of the 24-hour elimination from the organism of the mentioned radionuclide following single, short- and long-term administration of americium-241 from the air. Results were obtained with the use of computers for quantitative modelling of the most complete metabolic transport scheme of americium.

Americium↗

Apoptosis of rat kidney cells after 241-americium administration.

Tumors induction by americium is well known but there are no data on the biological effects of this radionucleide at subcellular level. In order to study the possible ultrastructural lesions induced by this element, a group of rats were injected with 241-Americium-citrate (9 kBq), once a week for five weeks and sacrificed 7 days after the last injection. We describe the alterations observed in the cortex kidney using cytochemical (TUNEL reaction) and histochemical (PAS staining) methods for light microscopy as well as electron microscopy techniques. Various types of lesions were detected: condensation of nuclear chromatine, fragmentation of the nuclei, swollen mitochondria, disappearance of mitochondrial crests and skrinking of the cytoplasm. This study clearly demonstrated the induction of apoptosis by americium in rat cortex kidney cells.

Americium↗

Transfer of environmental plutonium and americium across the human gut.

Data on gut transfer factors for environmental forms of radionuclides are essential for estimates of public radiation exposures following ingestion, and thus in decisions on controlling waste discharges. Dose estimates for transuranic nuclides are particularly sensitive to uncertainties stemming from gut transfer data being related to non-environmental forms and/or derived from animal experiments. We have measured human gut transfer factors for plutonium and americium in two experiments using marine foods obtained near Sellafield, Cumbria. Firstly, the urine of volunteer members of the critical group of shellfish consumers was analysed for transuranics and the results related to their consumption rates. Secondly, remotely-based volunteers ate single quantities of shellfish obtained near Sellafield, and their urine was analysed. An overall result for the gut transfer factor for environmental plutonium of 0.8 X 10(-4) indicates no need to increase the value of 1 X 10(-4), currently used by the International Commission on Radiological Protection (ICRP) for soluble forms. Results for americium show that the ICRP value of 5 X 10(-4) is maximising, and that a value of 1 X 10(-4) would be supportable. The results from the study of critical group members provide confidence in our habits survey techniques and reassurance that there are no significant pathways for intake of transuranics by these people that have not been recognised.

Adult↗

Plutonium and americium uptake in rats fed with Cumbrian shellfish--implications for estimates of dose to man.

Winkles (Littorina littorea) and mussels (Mytilus edulis) collected on the Cumbrian coast contain americium-241 and isotopes of plutonium discharged from the nuclear-fuel reprocessing plant at Sellafield. Shellfish have been fed to rats and measurements made of the gastrointestinal absorption of the actinides. For shellfish collected over a 1-year period from March 1983 to February 1984, the average values for the fractional absorption of plutonium and americium were 9 x 10(-4) and 3 x 10(-4), respectively, for winkles and 1.5 x 10(-3) and 6 x 10(-4), respectively, for mussels. Comparisons with results for winkles collected in December 1981 and mussels collected in July 1982 suggest that there may be considerable seasonal variation in the availability of the actinides for absorption. The results suggest that in calculations of doses to individuals consuming shellfish in west Cumbria, it may be prudent to examine the effect of using the new ICRP gut transfer factor of 1 x 10(-3) for both actinides, in comparison with the value of 5 x 10(-4) recommended previously by NRPB. The use of 1 x 10(-3) would increase the estimate of the committed effective dose equivalent for 1985 intakes, from the value of 0.73 mSv calculated by the Ministry of Agriculture, Fisheries and Food, to 1.29 mSv. However, taking into account up-to-date estimates of the retention of the actinides in liver and bone would reduce this value to 1.07 mSv. If, in addition, allowance is made for the effect of the burial and recycling of actinides in bone, a significant reduction in the dose estimate could result; for example, the use of one proposed dynamic bone model would reduce the value from 1.07 to 0.54 mSv.

Americium↗

The biodistribution and toxicity of plutonium, americium and neptunium.

In the nuclear fuel cycle the transuranic radionuclides plutonium-239, americium-241 and neptunium-237 would probably present the most serious hazard to human health if released into the environment. Despite differences in their solution chemistry the three elements exhibit remarkable similarity in their biochemical behaviour, apparently sharing similar transport pathways in blood and cells. After entering the blood the elements deposit predominantly in liver and skeleton, where retention appears to be prolonged, with half-times of the order of years. The principal late effects of all three radionuclides are the induction of cancers of bone, lung or liver. For the latter tumours the induction risk per unit radiation dose appears similar for the three radionuclides. But in bone there are indications that, due to microscopic differences in the distribution of the alpha-particle radiation dose, the efficiency of bone cancer induction may increase in the order americium-241 less than plutonium-239 less than neptunium-237. No case of human cancer induced by these radionuclides is known.

Americium↗

Environmental and human monitoring of Americium-241 utilizing extraction chromatography and alpha-spectrometry.

Recent developments in extraction chromatography have simplified the separation of americium from complex matrices in preparation for alpha-spectroscopy relative to traditional methods. Here we present results of procedures developed/adapted for water, air, and bioassay samples with less than 1 g of inorganic residue. Prior analytical methods required the use of a complex, multistage procedure for separation of americium from these matrices. The newer, simplified procedure requires only a single 2 mL extraction chromatographic separation for isolation of Am and lanthanides from other components of the sample. This method has been implemented on an extensive variety of "real" environmental and bioassay samples from the Los Alamos area, and consistently reliable and accurate results with appropriate detection limits have been obtained. The new method increases analytical throughput by a factor of approximately 2 and decreases environmental hazards from acid and mixed-waste generation relative to the prior technique. Analytical accuracy, reproducibility, and reliability are also significantly improved over the more complex and laborious method used previously.

Americium↗

Colloid-borne americium migration in Gorleben groundwater: significance of iron secondary phase transformation.

The mobility of actinides in natural water may be enhanced by colloid-mediated transport. In this context the reversibility of actinide colloid interaction is a key factor. Iron is an element that can generate colloids under conditions found in natural waters. In this paper, the impact of hematite and the low-crystalline precursor 2-line ferrihydrite on colloid-mediated transport of americium(III) is investigated. Am(III)-containing iron colloids are generated from two different approaches, namely contact between the two in aqueous solution or coprecipitation of Am(III) during iron colloid generation. Dissolved organic carbon (DOC), especially humic substances, has a strong influence on the stability of inorganic colloids. In addition, humic substances interfere in the distribution and kinetics of exchange between groundwater and sediments. Four groundwaters from the Gorleben aquifer system are used with DOC concentrations varying between 0.9 and 81.6 mgC/L together with Pleistocene Aeolian quartz sand from this site. Batch and column experiments are conducted under near-natural conditions (Ar + 1% CO2). To study the influence of kinetics, contact times up to one month are studied. The dynamic light-scattering investigations show that the colloidal stability of the 2-line ferrihydrite increases with increasing DOC concentration. The low-crystalline iron colloids have a marginal influence on the Am(III) transport due to reversibility of americium sorption. Contrary to this, the crystalline hematite generated from coprecipitation of Am(III) leads to an increase of unretarded colloid-mediated Am(III) transport up to a factor of almost five. Chemical characterization of these hematite colloids shows that Am(III) is structurally entrapped in the hematite. The distribution of Am(III) and 2-line ferrihydrite between groundwater and sand sediment remained in disequilibrium even after one month. This shows that the kinetics of Am(III) distribution between the different phases (bulk solution/colloidal form/ sediment) is a key issue.

Americium↗

The gastrointestinal absorption of plutonium and americium in the hamster.

Plutonium-239 and americium-241 were administered to adult hamsters in various chemical forms and their absorption from the gut was measured. The results have been compared with published data on other species in order to derive values for the estimated absorption of these actinides in man. On the basis of current knowledge, the best values for adults would appear to be: 0.05% for americium, 0.01% for plutonium ingested in soluble form, and 0.0001% for plutonium ingested as the dioxide. Plutonium dioxide should be considered as soluble if a significant proportion (greater than 5%) of the activity is in particles less than 25 nm in diameter.

Administration, Oral↗

XAFS study of americium sorbed onto groundwater colloids.

The sorption of americium, as Am(III), onto groundwater colloids obtained from a marl aquifer was studied in 2 x 10(-2)M sodium bicarbonate groundwater and 2 x 10(-2)M sodium chloride bicarbonate-free solutions. At the in situ groundwater pH of 8.6, the americium was strongly sorbed onto the colloids. XAFS analyses were performed on these sorbed Am species to establish the oxidation state and its near-neighbour bonding. These XAFS data, obtained at 400 mg l(-1) colloid concentrations and total Am concentration of 1.53 x 10(-5)M (dissolved and onto colloids), indicated that Am remains trivalent, and that surface complexes are formed with the colloids without surface precipitation. This conclusion is based on the absence of Am-Am interactions in the second or third shells. The surface complexes generated by the Am(III) sorbed onto active sites are described on the basis of the XAFS data. They include the presence of about seven water molecules around the ternary surface complexes of this trivalent actinide.

Adsorption↗

Metabolism of americium-241 in man: an unusual case of internal contamination of a child and his father.

The metabolism of americium-241 has been studied during an 8-year period in an adult male and his son who, at the ages of 50 and 4 years, respectively, were accidentally and unknowingly contaminated within their home by means of inhalation. Chelation therapy with calcium trisodium pentetate was more effective in enhancing the removal of americium-241 from the child than from the father.

Age Factors↗

[Study of the influence of peroral zincacin on the removing of ingested Americium].

Effect of different cincacine doses was studied in rats ingesting americium citrate during 2 weeks. As a result new data showing the possibility and efficacy of per oral cincacine administration at americium intake into digestive tract have been obtained. Dose dependence of cincacine efficacy has been stated for per oral 241Am intake. Preparation administration at a dose of 25 mumol/kg reduces amount of 241Am in skeleton, liver and kidney by 93, 90 and 33%, respectively and is optimum for radionuclide removal from the body and for the prevention of its deposition in organs. Digestive system organs and kidney structure at cincacine administration at a dose of 150 and 300 mumol/kg) to the rats ingesting 241Am have been studied.

Administration, Oral↗

Task-specific ionic liquids bearing 2-hydroxybenzylamine units: synthesis and americium-extraction studies.

The synthesis of two task-specific ionic liquids (TSILs) bearing 2-hydroxybenzylamine entities is described. These compounds are based on an imidazolium substructure onto which one hydrobenzylamine-complexing moiety is grafted. We have demonstrated that, whether pure or diluted, TSIL is able to extract americium ions. Furthermore, recovery of americium from the IL phase into a receiving phase can be achieved under acidic conditions. A possible mechanism for the metal-ion partitioning is presented, in which the extraction system is driven by an ion-exchange mechanism.

Journal Article↗

The movement of plutonium, americium, and curium through the food chain.

The actinides, plutonium, americium and curium, are being produced in increasing quantites as the nuclear programme is expanded. As these alpha-particle-emitting elements are hazardous to man there is considerable concern about the movement of these elements through the environment; The uptake of these elements from soil into the plants is low, as is the gastrointestinal concentration factor. Although there are complexing agents in the environment which have been shown to complex these elements there is no evidence that these complexing agents might bring about a concentration of actinides in the food chain of man.

Actinoid Series Elements↗

The uptake of plutonium-238, 239, 240, americium-241, strontium-90 and caesium-137 into potatoes.

Transfer factors have been measured for 239 Pu + 240 Pu, 241 Am, 90 Sr and 137 Cs into potatoes grown in a blend of soil which included silt polluted with radioactive waste discharged into the Irish Sea. The experiment has been carried out over four seasons and attempts to assess the radiological consequences to the consumer which would arise if potatoes were to be grown in land heavily contaminated with the silt. During the course of the experiment plutonium and americium became less available for uptake, 90 Sr became slightly more available and 137 Cs remained nearly constant in its availability. The values of the transfer factors are among the lowest reported for these radionuclides into potatoes.

Americium↗

Measurements of the gastrointestinal absorption and tissue distribution of plutonium, americium and polonium in experimental animals.

In order to set limits on environmental and occupational intakes of radionuclides, information is needed on their uptake and metabolism in man. Human data are very limited, particularly for long-lived alpha-emitting isotopes such as those of the actinides. Animal experiments are therefore an important source of data on the distribution of radionuclides in tissues, and the effects of factors such as subject age and the chemical form of elements on gastrointestinal absorption. The NRPB performs experimental programs using mainly rats and guinea pigs. In order to study the gastrointestinal absorption and tissue distribution of plutonium, americium and polonium, a variety of analytical techniques are employed. These include ion exchange and solvent extraction leading to alpha spectrometry and liquid scintillation counting. The investigation of low specific-activity environmental or industrial materials, and the very low bioavailability of elements such as the actinides, means that very low levels of activity have to be measured. Contamination at the dissection and tissue separation stage, as well as during the radiochemistry, has to be rigorously avoided. Where very detailed information is needed on the location of radionuclides within tissues, such as in the study of alpha-emitter distribution in the intestine, autoradiography is used. The application and relevance of different measurement techniques to animal studies will be discussed and examples of the results presented.

Aging↗

The assessment of plutonium and americium in contaminated wounds with high energy resolution semiconductor detectors.

A simple to use method was installed for the measurement of wounds contaminated with plutonium and americium by using a semiconductor detector. This technique does not explicitly require the knowledge of the detector efficiency but uses a plant 241Am calibration source. A computer programme has also been developed for the quantification of the contamination according to the shape and the depth of the contaminant in the wound.

Americium↗

Concentrations of plutonium and americium in plankton from the western Mediterranean Sea.

Understanding the transfer of radionuclides through the food chain leading to man and in particular, the uptake of transuranic nuclides by plankton, is basic to assess the potential radiological risk of the consumption of marine products by man. The main sources of transuranic elements in the Mediterranean Sea in the past were global fallout and the Palomares accident, although at present smaller amounts are released from nuclear establishments in the northwestern region. Plankton from the western Mediterranean Sea was collected and analyzed for plutonium and americium in order to study their biological uptake. The microplankton fractions accounted for approximately 50% of the total plutonium contents in particulate form. At Garrucha (Palomares area), microplankton showed much higher 239,240 Pu activity, indicating the contamination with plutonium from the bottom sediments. Concentration factors were within the range of the values recommended by the International Atomic Energy Agency. Continental shelf mesoplankton was observed to efficiently concentrate transuranics. In open seawaters, concentrations were much lower. We speculate that sediments might play a role in the transfer of transuranics to mesoplankton in coastal waters, although we cannot discard that the difference in species composition may also play a role. In Palomares, both 239,240 Pu and 241Am showed activities five times higher than the mean values observed in continental shelf mesoplankton. As the plutonium isotopic ratios in the contaminated sample were similar to those found in material related to the accident, the contamination was attributed to bomb debris from the Palomares accident. Concentration factors in mesoplankton were also in relatively good agreement with the ranges recommended by IAEA. In the Palomares station the highest concentration factor was observed in the sample that showed predominance of the dynoflagellate Ceratium spp. Mean values of the enrichment factors showed, on average, discrimination rather than enrichment in the primary producer trophic chain.

Americium↗

Assessment of the global fallout of plutonium isotopes and americium-241 in the soil of the central region of Saudi Arabia.

A radiochemical technique for determination of plutonium isotopes and 241Am in soil samples is tested against IAEA-standard reference materials to determine its accuracy and precision for reliable results. The technique is then used in the investigation of topsoil samples, collected from the natural environment of the central region of Saudi Arabia, to assess the effect of fallout accumulation of these radionuclides in the region. Plutonium and americium were sequentially separated from all other components of the sample by anion-exchange chromatography and co-precipitated with Nd3+ as fluorides. The precipitates were mounted on membrane filters and measured using a high-resolution alpha-spectrometer. The results of the analysis of the reference materials showed satisfactory sensitivity and precision of the technique. The results of the analyzed soil samples show activity levels ranging from < LLD to 0.089 and from <LLD to 0.50 Bq/kg for 238Pu and 239+240Pu, respectively. 241Am levels ranged from <LLD to 0.49 Bq/kg. 238Pu/239+240Pu and 241Am/239+240Pu activity ratios ranged from 0 to 0.216 and 0.3-1.23, respectively. A discussion based on the observed data is presented.

Americium↗