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PloS One 2023Data on the vertical distribution of radionuclides in the soil is necessary to fully understand the radioecological situation around ecosystems, give predictive...
Data on the vertical distribution of radionuclides in the soil is necessary to fully understand the radioecological situation around ecosystems, give predictive estimates to how safe crop products are and justify a rehabilitation strategy for radioactively contaminated areas. A study was conducted to investigate the vertical distribution of radionuclides in soils of the former Semipalatinsk Test Site (STS) territory beyond its testing sites, that is, in areas in which no nuclear weapons or nuclear effects of radiological warfare agents were tested. Soil was sampled layerwise all over the Semipalatinsk Test Site down to 30 cm deep at a 5-cm spacing. Most of high activity concentrations of radionuclides all over the study area were detected in the 0-5 cm soil layer. Activity concentrations of the major man-made radionuclides were determined in soil samples collected by γ-, β and α-spectrometry. As a result, ranges of activity concentrations of 137Cs, 241Am, 90Sr and 239+240Pu were determined in 0-5, 5-10, 10-15, 15-20, 20-25, 25-30 cm soil layers. In the conventionally 'background' area, the 0-5 cm soil layer, on average, contains (the percentage of total activity concentration across the soil profile depth): 137Cs- 83%, 239+240Pu- 87% and 90Sr- 38%. For the 1953 plume, these values were 92%, 83% and 73%, respectively. Values for the 1951 plume in the 0-5 cm soil layer were: 137Cs- 93%, 239+240Pu- 93% and 90Sr- 59%. The minimum concentration of radionuclides are observed 20-30 cm deep in all areas studied. 90Sr is the most mobile radionuclide from the perspective of its ability to travel deep down the soil. The study found out that the nuclide vertical migration rates downward in soils based on detected activity were as follows (in descending order): 90Sr- 137Cs- 239+240Pu- 241Am. Coefficients that determine the ratio of the activity concentration of the radionuclide in the 0-20 and 0-30 cm soil cover layers to that of this radionuclide in the 0-5 cm topsoil were calculated. These coefficients enable to estimate the radionuclide inventory at each soil sampling point from their activity concentration in the 0-5 cm soil layer.
Topics: Humans; Cesium Radioisotopes; Strontium Radioisotopes; Americium; Plutonium; Soil; Ecosystem; Soil Pollutants, Radioactive
PubMed: 36607986
DOI: 10.1371/journal.pone.0278581 -
Chemosphere May 2021Nuclear reprocessing plants are sources of environmental contamination by gaseous or liquid discharges. Numerous radionuclides are of concern, with actinides and Sr...
Nuclear reprocessing plants are sources of environmental contamination by gaseous or liquid discharges. Numerous radionuclides are of concern, with actinides and Sr being the most radiotoxic. Environmental radioactivity survey programs mostly use γ-spectrometry to track contaminations because γ-spectrometry is very cost effective and can be carried out on raw samples. On the other hand, the determination of β- or α-emitting radionuclides in environmental samples requires rather sophisticated analytical methods, and are thus dedicated to specific goals. However, measuring radionuclides such as Pu, Am, and Sr often provides more information about the presence of a current or prior contamination and on its origin, based on the isotopic composition of the samples. We found that the analysis of Pu, Pu, Am, and Sr of a few selected soil samples taken near the nuclear reprocessing plant of La Hague, France, revealed the presence of a previous environmental contamination originating from several incidents in La Hague site involving atmospheric transfer and leaks in flooded waste pits. The Am-Pu dating method indicated a contamination period prior to 1983. The presence of elevated levels of light non-radioactive lanthanides and yttrium in the soil samples confirmed the involvement of cold fuel. Our results demonstrate how long-lived actinides are likely to reveal a long-term contamination of the environment by spent fuel. Our study indicates that there is a requirement to use more sophisticated tools than γ-spectrometry when surveying the environments surrounding industrial plants for nuclear power and nuclear reprocessing with a potential for the accidental release of radioactivity into the environment.
Topics: France; Plutonium; Radioactivity; Soil; Soil Pollutants, Radioactive; Strontium Radioisotopes; Water Pollutants, Radioactive
PubMed: 33422999
DOI: 10.1016/j.chemosphere.2020.129332 -
Military Medical Research Jan 2021In radiological emergencies with radionuclide incorporation, decorporation treatment is particularly effective if started early. Treating all people potentially...
BACKGROUND
In radiological emergencies with radionuclide incorporation, decorporation treatment is particularly effective if started early. Treating all people potentially contaminated ("urgent treatment") may require large antidote stockpiles. An efficacious way to reduce antidote requirements is by using radioactivity screening equipment. We analyzed the suitability of such equipment for triage purposes and determined the most efficient mix of screening units and antidote daily doses.
METHODS
The committed effective doses corresponding to activities within the detection limits of monitoring portals and mobile whole-body counters were used to assess their usefulness as triage tools. To determine the optimal resource mix, we departed from a large-scale scenario (60,000 victims) and based on purchase prices of antidotes and screening equipment in Germany, we calculated efficiencies of different combinations of medical countermeasure resources by data envelopment analysis. Cost-effectiveness was expressed as the costs per life year saved and compared to risk reduction opportunities in other sectors of society as well as the values of a statistical life.
RESULTS
Monitoring portals are adequate instruments for a sensitive triage after cesium-137 exposure with a high screening throughput. For the detection of americium-241 whole-body counters with a lower daily screening capacity per unit are needed. Assuming that 1% of the potentially contaminated patients actually need decorporation treatment, an efficient resource mix includes 6 monitoring portals and 25 mobile whole-body counters. The optimum mix depends on price discounts and in particular the fraction of victims actually needing treatment. The cost-effectiveness of preparedness for a "dirty bomb" attack is less than for common health care, but costs for a life year saved are less than for many risk-reduction interventions in the environmental sector.
CONCLUSION
To achieve economic efficiency a high daily screening capacity is of major importance to substantially decrease the required amount of antidote doses. Among the determinants of the number of equipment units needed, the fraction of the potentially contaminated victims that actually needs treatment is the most difficult to assess. Judging cost-effectiveness of the preparedness for "dirty bomb" attacks is an issue of principle that must be dealt with by political leaders.
Topics: Humans; Mass Screening; Medical Countermeasures; Nuclear Weapons; Radiation Injuries; Radiation-Protective Agents; Terrorism
PubMed: 33455578
DOI: 10.1186/s40779-020-00291-3 -
Gels (Basel, Switzerland) Mar 2023The removal of radionuclide/radioactivity from laboratory and environmental water samples under ambient conditions was investigated via batch-type experiments using...
The removal of radionuclide/radioactivity from laboratory and environmental water samples under ambient conditions was investigated via batch-type experiments using polyurea-crosslinked calcium alginate (X-alginate) aerogels. Water samples were contaminated with traces of U-232 and Am-241. The removal efficiency of the material depends strongly on the solution pH; it is above 80% for both radionuclides in acidic solutions (pH 4), while it decreases at about 40% for Am-241 and 25% for U-232 in alkaline solutions (pH 9). This is directly associated with the presence of the radionuclide species in each case; the cationic species UO and Am prevail at pH 4, and the anionic species UO(CO) and Am(CO) prevail at pH 9. Adsorption on X-alginate aerogels is realized by coordination of cationic species on carboxylate groups (replacing Ca) or other functional groups, i.e., -NH and/or -OH. In environmental water samples, i.e., ground water, wastewater and seawater, which are alkaline (pH around 8), the removal efficiency for Am-241 is significantly higher (45-60%) compared to that for U-232 (25-30%). The distribution coefficients () obtained for the sorption of Am-241 and U-232 by X-alginate aerogels are around 10 L/kg, even in environmental water samples, indicating a strong sorption affinity of the aerogel material for the radionuclides. The latter, along with their stability in aqueous environments, make X-alginate aerogels attractive candidates for the treatment of radioactive contaminated waters. To the best of our knowledge, this is the first study on the removal of americium from waters using aerogels and the first investigation of adsorption efficiency of an aerogel material at the sub-picomolar concentration range.
PubMed: 36975660
DOI: 10.3390/gels9030211 -
Iranian Biomedical Journal Nov 2022Introduction: Chemotherapy, biotherapy, and radiotherapy play a limited but important role in treating breast cancer. For more efficient treatment, combination therapy...
INTRODUCTION
Introduction: Chemotherapy, biotherapy, and radiotherapy play a limited but important role in treating breast cancer. For more efficient treatment, combination therapy could be an appropriate option. In this study, radiotherapy using neutron radiation emitted from a 241Am-Be neutron source, as well as biotherapy using curcumin (80 μM) was combined to investigate the efficiency of treatment towards MCF-7 breast cancer in a three dimensional (3D) culture medium.
METHODS
Methods: MTT, neutral red uptake assay, nitric oxide, glutathione assay, catalase, cytochrome c, comet assay, and caspase-3 were used to determine the effect of neutron radiation and also neutron and curcumin combination on the viability of cancer cells.
RESULTS
Results: The results of cytotoxicity test showed that neutron irradiation with or without curcumin at 5, 10, 15, and 20 h reduced the survival of tumor cells. Moreover, the rate of apoptosis due to the neutron effect at different irradiation times enhanced with the increasing time.
CONCLUSION
Conclusion: Due to the significant anticancer effect of curcumin in 3D culture, using this molecule before or after neutron therapy is recommended.
Topics: Humans; Female; Curcumin; Breast Neoplasms; Americium; Apoptosis; Neutrons; Cell Line, Tumor
PubMed: 36380684
DOI: 10.52547/ibj.3756 -
Health Physics Sep 2010Self-assembled monolayer on mesoporous supports (SAMMS) are hybrid materials created from attachment of organic moieties onto very high surface area mesoporous silica....
Self-assembled monolayer on mesoporous supports (SAMMS) are hybrid materials created from attachment of organic moieties onto very high surface area mesoporous silica. SAMMS with surface chemistries including three isomers of hydroxypyridinone, diphosphonic acid, acetamide phosphonic acid, glycinyl urea, and diethylenetriamine pentaacetate (DTPA) analog were evaluated for chelation of actinides ((239)Pu, (241)Am, uranium, thorium) from blood. Direct blood decorporation using sorbents does not have the toxicity or renal challenges associated with traditional chelation therapy and may have potential applications for critical exposure cases, reduction of nonspecific dose during actinide radiotherapy, and for sorbent hemoperfusion in renal insufficient patients, whose kidneys clear radionuclides at a very slow rate. Sorption affinity (K(d)), sorption rate, selectivity, and stability of SAMMS were measured in batch contact experiments. An isomer of hydroxypyridinone (3,4-HOPO) on SAMMS demonstrated the highest affinity for all four actinides from blood and plasma and greatly outperformed the DTPA analog on SAMMS and commercial resins. In batch contact, a fifty percent reduction of actinides in blood was achieved within minutes, and there was no evidence of protein fouling or material leaching in blood after 24 h. The engineered form of SAMMS (bead format) was further evaluated in a 100-fold scaled-down hemoperfusion device and showed no blood clotting after 2 h. A 0.2 g quantity of SAMMS could reduce 50 wt.% of 100 ppb uranium in 50 mL of plasma in 18 min and that of 500 dpm mL(-1) in 24 min. 3,4-HOPO-SAMMS has a long shelf-life in air and at room temperature for at least 8 y, indicating its feasibility for stockpiling in preparedness for an emergency. The excellent efficacy and stability of SAMMS materials in complex biological matrices suggest that SAMMS can also be used as orally administered drugs and for wound decontamination. By changing the organic groups of SAMMS, they can be used not only for actinides but also for other radionuclides. By using the mixture of these SAMMS materials, broad spectrum decorporation of radionuclides is very feasible.
Topics: Actinoid Series Elements; Adsorption; Americium; Chelating Agents; Decontamination; Humans; Isomerism; Pentetic Acid; Plutonium; Porosity; Pyridones; Radiation Injuries; Radioactive Hazard Release; Terrorism; Thorium; Time Factors; Uranium
PubMed: 20699706
DOI: 10.1097/HP.0b013e3181ce5f3e -
RSC Advances Jul 2020Development of efficient extractants for the separation of actinides and lanthanides in the technologies of nuclear fuel cycle is one of the most urgent and complex...
Development of efficient extractants for the separation of actinides and lanthanides in the technologies of nuclear fuel cycle is one of the most urgent and complex tasks in modern nuclear energetics. New family of 4,7-dichloro-1,10-phenanthroline-2,9-dicarboxylic acid diamides based on cyclic amines was synthesized and shown to exhibit high selectivity in the La/Am pair separation (SF (Am/La ≈ 10)) and in the Am/Eu pair separation (SF (Am/Eu ≈ 12)). It was shown that pyrrolidine derived diamide is more efficient extractant for americium, curium and lanthanides from highly acidic HNO solution than its non-cyclic ,,','-tetraalkyl analogues. The structures of synthesized compounds were studied in details by IR, NMR spectroscopy, and single crystal X-ray diffraction. According to spectroscopy data, incorporation of aromatic rings to the amide fragment of ligand leads to complex dynamic behavior in solutions what is believed to strongly affect the extraction ability of synthesized ligands.
PubMed: 35519740
DOI: 10.1039/d0ra05182a -
Health Physics Apr 2015Diethylenetriaminepentaacetic acid (DTPA) is an FDA-approved chelating agent for enhancing the elimination of transuranic elements such as americium from the body. Early... (Comparative Study)
Comparative Study
Diethylenetriaminepentaacetic acid (DTPA) is an FDA-approved chelating agent for enhancing the elimination of transuranic elements such as americium from the body. Early access to therapy minimizes deposition of these radionuclides in tissues such as the bone. Due to its poor oral bioavailability, DTPA is administered as an IV injection, delaying access. Therefore, a diethyl-ester analog of DTPA, named C2E2, was synthesized as a means to increase oral absorption. As a hexadentate ligand, it was hypothesized that C2E2 was capable of binding americium directly. Therefore, the protonation constants and americium stability constant for C2E2 were determined by potentiometric titration and a solvent extraction method, respectively. C2E2 was shown to bind americium with a log K of 19.6. The concentrations of C2E2, its metabolite C2E1, and DTPA required to achieve effective binding in rat, beagle, and human plasma were studied in vitro. Dose response curves for each ligand were established, and the 50% maximal effective concentrations were determined for each species. As expected, higher concentrations of C2E2 were required to achieve the same degree of binding as DTPA. The results indicated that chelation in beagle plasma is more representative of the human response than rats. Finally, the pharmacokinetics of C2E2 were investigated in beagles, and the data was fit to a two-compartment model with elimination from the central compartment, along with first-order absorption. Based on the in vitro data, a 100 mg kg dose of C2E2 can be expected to have an effective duration of action of 3.8 h in beagles.
Topics: Americium; Animals; Binding, Competitive; Biological Availability; Chelating Agents; Dogs; Female; Humans; Injections, Intravenous; Male; Pentetic Acid; Rats; Species Specificity; Tissue Distribution
PubMed: 25706138
DOI: 10.1097/HP.0000000000000230 -
Journal of Environmental Radioactivity Apr 2021Data, despite being crucial for internal dose assessment, is lacking on the transfer of artificial radionuclides from the environment to the food supply. Expanding the...
Data, despite being crucial for internal dose assessment, is lacking on the transfer of artificial radionuclides from the environment to the food supply. Expanding the available information on these factors is important for the improvement of dose models for specific scenarios. This paper describes the results of a 70 day field experiment with broiler chickens on the dynamics of excretion of Cs and Am from the muscle, liver and bone of broilers after a 30 day application of contaminated feed. The radionuclide concentrations in the feed and the thigh muscle, thigh bone and liver of 54 chickens divided between grass meal and soil contaminated feed groups were evaluated by gamma spectrometry for Am and Cs. The obtained results confirm previous data on the dynamics of the excretion of cesium from organs, which can be described with a fast and a slow exponential curve of excretion. On the 70th day, following the 30-days application, 2-8% of the first-day activity concentrations of Cs in organs (muscle, liver, bone) were detected. In the first two days, activity concentration of Am decreases twofold in both liver and bone. 35% of the maximum activity concentration of Am remained in bone and 15% in liver on the last day of the experiment.
Topics: Animal Feed; Animals; Cesium Radioisotopes; Chickens; Radiation Monitoring; Soil Pollutants, Radioactive
PubMed: 33515923
DOI: 10.1016/j.jenvrad.2021.106543 -
Sensors (Basel, Switzerland) Jul 2022Neutrons constitute a significant component of the secondary cosmic rays and are one of the most important contributors to natural cosmic ray radiation background dose....
Neutrons constitute a significant component of the secondary cosmic rays and are one of the most important contributors to natural cosmic ray radiation background dose. The study of the cosmic ray neutrons' contribution to the dose equivalent received by humans is an interesting and challenging task for the scientific community. In addition, international regulations demand assessing the biological risk due to radiation exposure for both workers and the general population. Because the dose rate due to cosmic radiation increases significantly with altitude, the objective of this work was to characterize the thermoluminescent dosimeter (TLDs) from the perspective of exposing them at high altitudes for longtime neutron dose monitoring. The pair of TLD-700 and TLD-600 is amply used to obtain the information on gamma and neutron dose in mixed neutron-gamma fields due to the present difference in 6Li isotope concentration. A thermoluminescence dosimeter system based on pair of TLD-600/700 was characterized to enable it for neutron dosimetry in the thermal energy range. The system was calibrated in terms of neutron ambient dose equivalent in an experimental setup using a 241Am-B radionuclide neutron source coated by a moderator material, polyethylene, creating a thermalized neutron field. Afterward, the pair of TLD-600/700 was exposed at the CERN-EU High-Energy Reference Field (CERF) facility in Geneva, which delivers a neutron field with a spectrum similar to that of secondary cosmic rays. The dosimetric system provided a dose value comparable with the calculated one demonstrating a good performance for neutron dosimetry.
Topics: Altitude; Americium; Humans; Neutrons; Radiation Dosage; Radiation Dosimeters; Thermoluminescent Dosimetry
PubMed: 35957277
DOI: 10.3390/s22155721