Chemotopological study of positron emitter radionuclides used in PET diagnostic imaging: physical, physico-chemical, dosimetric, quantum and nuclear properties

We carried out a chemotopological study of two groups of positron emitter radionuclides of current and potential use in positron emission tomography (PET) diagnostic imaging. The aim was to look for potential β⁺ radionuclides not yet in use for PET imaging, taking into account the similarities of these radionuclides with radionuclides already used in PET imaging. The similarity was studied through physical, physico-chemical, dosimetric, quantum and nuclear properties of the radionuclides. We applied cluster analysis (two similarity functions and three grouping methodologies) and generated six dendrograms. One dendrogram was selected in each group, which was used to build up a basis for a topology. From the calculation of topological properties of several subsets of interest, we propose β⁺ radionuclides ⁴⁷V, ⁴⁸V, ⁶³Zn, ⁷⁰As, ⁹⁰Nb, ¹⁰⁶Ag, ¹¹⁵Sb, ¹¹⁶Sb, ¹²⁰Sb, ¹³⁰Cs, ¹³⁴La and ¹⁴⁰Pr, as potential new radionuclides of use in PET imaging.     

Radionuclide, Metal and Non-metal Levels in Percolated Water from Soils Fertilized with Phosphogypsum

Phosphogypsum (PG) is a by-product of the phosphate fertilizer industry, which is produced by precipitation during the wet process of phosphate rocks. While commercial uses, in agriculture and in manufacturing gypsum board and Portland cement, consume less than a few percent of this by-product, the vast majority is disposed of on land in gypsum. In Brazil, three main industries are responsible for the production and storage of about 5.5 × 10⁶ tons per year. PG may contain trace metals, non-metals, fluorides and natural radionuclides. Since, in Brazil, PG has been used for many years as soil amendment, it is important to know its availability, mainly in aquatic environments used for human consumption. In this case, more restrictive limits must be adopted. This work aimed to evaluate the mobility of metals in sand and clayey soils and, consequently, the contamination of drainage water through greenhouse-scale leaching and transport of toxic elements and radionuclides from soils fertilized with PG to crops. In general, it was observed that elemental concentrations were below the actual detection limit of the equipment for all conditions of interest, indicating a low mobility of the analyzed elements in the soil.     

Radiohalogens for imaging and therapy

Radiohalogens play a very important role in radiopharmaceuticals used for medical imaging (now referred to as molecular imaging) and therapy applications. Development of new radiopharmaceuticals that have radiohalogens incorporated requires an understanding of parameters that are unique to chemistry involving these radionuclides. Those parameters include requirement for production and purification of the halogen radionuclides, as well as development of reaction conditions for use with high specific activity short-lived radionuclides. In this tutorial review, several radiohalogens, their radiolabeling chemistry and their application to medical imaging and therapy are discussed.     

Environmental dose assessment using Ecolego: case study of soil from Japan

From the Fukushima incident, a number of radionuclides were released, causing radioactive contamination to the environment. Depending on their own half-lives, the radionuclides, however, will decay over time. During the decay, those radionuclides can be transferred to the ecosystem and, eventually, to humans. As part of the environmental surveillance and restoration program, radiological dose assessments have been carried out in response to the incident to prevent a potentially unacceptable dose to the public. This study focuses on the deposition of certain radionuclides in soil and their transport through the terrestrial food chain. Soil from two sites, Namie and Iitate, where radioactive contamination is evident was used as the source term. The assessment has been conducted using Ecolego, a simulation software used for conducting dose assessments of complex dynamic systems evolving over time especially in the field of radiology. Possible pathways from the soil used as the source term to humans as well as crops, forage, livestock products, and milk, for specific radioactive species have been studied. The dose assessment results of I-131, Cs-134, Cs-137, Sr-89, and Sr-90 in each compartment of the food chain are presented in this literature. The concentrations of the studied radionuclides vary from one medium to another, resulting from the characteristic of the medium itself along with other factors, such as the half-lives and transfer factors. Due to the fact that the concentrations of the radionuclides are affected by the depth of soil, there may be some uncertainty of the dose assessment results from the model.     

Leaching of uranium,radium and thorium from vertisol soil by ground water

Shallow land burial is routinely used for the disposal of low-level radioactive waste. Natural processes causing leaching of radionuclides can lead to contamination of surrounding ground water and soil by the radionuclides. The comparative leachability of radionuclides U_(nat), ²²⁶Ra, ²²⁸Ra and Th_(nat) from the soil of a radioactive waste disposal site, by ground water was evaluated. The probability of leaching was obtained in the following order Ra (≈77%) > U (≈40%) > Th (≈20%). Observed ratios (OR) were calculated to correlate leachability of radionuclides to that of major cations Ca²⁺ and Mg²⁺. The leaching of the radionuclides was seen to be dependent on Ca²⁺ and SO₄²⁻ leached from the soil. This study provides sitespecific leachability of radionuclides, that can be used as indicator of the tendency for migration or retention in soil. It can play an important role during an unforeseen accident like breach of containment at the waste disposal site leading to contamination of soil and ground water and causing hazard to public via drinking water route.     

Field testing of collection and measurement of radioxenon for the Comprehensive Test Ban Treaty

Pacific Northwest National Laboratory, with guidance and support from the U.S. Department of Energy's NN-20 Comprehensive Test Ban Treaty (CTBT) Research and Development program, has developed and demonstrated a fully automatic sampler-analyzer (ARSA) for the collection and quantitative measurement of the four xenon radionuclides,^131mXe (11.9 d),^133mXe (2.19 d),¹³³Xe (5.24 d), and¹³⁵Xe (9.10 h), in the atmosphere. These radionuclides are important signatures in monitoring for compliance to a CTBT, and may have applications in stack monitoring and other areas where xenon radionuclides are present. The activity ratios between certain of these radionuclides permit discrimination between radioxenon originating from nuclear detonations and that from nuclear reactor operations, nuclear fuel reprocessing, or from medical isotope production and usage. With the ARSA system, xenon is continuously and automatically separated from the atmosphere at flow rates of about 100 lpm by sorption-bed techniques. Samples collected in 8 hours are automatically analyzed by electron-photon coincidence spectrometry to provide detection sensitivities as low as 100 μBq/m³ of air. This sensitivity is about 10-fold better than achieved with reported laboratory-based procedures¹ for the short time collection intervals of interest. Gamma-ray energy spectra and gas analysis data are automatically collected.     

IAEA Programme of natural matrix reference materials for the determination of radionuclides

Summary The International Atomic Energy Agency has been providing analytical quality control services (AQCS) to its Member States since the 1960's. The AQCS programme distributes reference materials (RMs), organizes intercomparison runs, and provides training courses for quality assurance in chemical analysis and radioactivity measurements of food, biological, environmental and marine materials. This paper focusses on those aspects of the subject dealing with reference materials and intercomparison runs for the determination of radionuclides. Nineteen natural matrix reference materials are available for the determination of radionuclides. Twelve new intercomparison and reference materials are in preparation or under consideration. The radionuclides of interest include: K-40, Mn-54, Co-60, Sr-90, Tc-99, Ru-106, Ba-133, Cs-134, Cs-137, Pb-210, Ra-226, Th-228, Th-232, Pu-238, Pu-239+240.     

Sorbent extraction behavior of a nonionic surfactant,Triton X-100, onto commercial charcoal from low level radioactive waste

In nuclear power plants and nuclear laboratories, laundry wastewater is generated from decontaminating polluted instruments, worker’s clothes and taking shower after work. Laundry wastewater contains radionuclides and surfactants. The surfactants included in laundry wastewater affect the extraction of radionuclides. Therefore, surfactants should be removed before extraction of radionuclides. The objective of the present work is to assess the ability of commercial charcoal for the removal of nonionic surfactants, where, commercial charcoal is a commonly available adsorbent for treatment. Charcoal was characterized using different analytical techniques. The isotherm models and thermodynamic parameters were evaluated. Charcoal was applied to the removal of surfactant from liquid radioactive waste. The data obtained can be used for designing a plant for treatment of surfactant rich water and wastewater economically.     

Automated separation and measurement of radioxenon for the Comprehensive Test Ban Treaty

A fully automatic radioxenon sampler/analyzer (ARSA) has been developed and demonstrated for the collection and quantitative measurement of the four xenon radionuclides,^131mXe(11.9 d),^133mXe(2.2 d),¹³³Xe(5.2 d), and¹³⁵Xe(9.1 hr), in the atmosphere. These radionuclides are important signatures in monitoring for compliance to a Comprehensive Test Ban Treaty (CTBT). Activity ratios of these radionuclides permit source attribution. Xenon, continuously and automatically separated from the atmosphere, is automatically analyzed by electron-photon coincidence spectrometry providing a lower limit of detection of about 100 μBq/m³. The demonstrated detection limit is about 100 times better than achievable with reported laboratory-based procedures for the short-time collection intervals of interest.     

Strategy for the determination of mixtures of alpha and beta emitters in water samples with a combination of rapid methods

Journal of Radioanalytical and Nuclear Chemistry - Quantification of several alpha and beta emitters in mixtures of radionuclides arouses great interest in many fields such as surveillance around...     

Characterization of an extraction chromatographic resin for the separation and determination of 36Cl and 129I

The monitoring of long-lived radionuclides is of great importance in the context of the surveillance of nuclear facilities, during their operation as well as during their decommissioning. This is especially true for radionuclides of rather volatile elements, such as chlorine and iodine, the main interest being in ³⁶Cl and ¹²⁹I. Liquid Scintillation Counting (LSC) is a widely used measurement technique especially for the determination of ³⁶Cl that requires a thorough and selective sample preparation in order to give accurate results. Sample preparation methods frequently employed such as volatilization and/or repeated precipitation steps can be rather elaborate and time consuming. Therefore, an attempt has been made to develop an ‘easy to use’ extraction chromatographic resin that allows extraction, and subsequent separation, of chloride and iodide from pretreated environmental and decommissioning samples for their determination via LSC. First results of the characterization of the resin including D _w values of Cl^?, I^? and potential interferents, and of the method development are presented as well as the result of the analysis of a simulated real sample.     

Sequential radioanalytical method for the determination of U and Th isotopes, <Superscript>226</Superscript>Ra and <Superscript>210</Superscript>Po using alpha spectrometry in samples of the Brazilian phosphate industry

The phosphate rocks used for the production of phosphate fertilizers present in their composition radionuclides of the U and Th series. During the chemical attack, the radionuclides are distributed to final products and phosphogypsum. A sequential radiochemical procedure was implemented to determine the content of radionuclides alpha emitters in samples of fertilizers and phosphogypsum produced in Brazil. The results obtained show that the levels of radioactivity present in the fertilizers are of the same order of magnitude on those found in the phosphogypsum, reaching values up to 1158 and 457 Bq kg⁻¹, for the U and Th series, respectively.     

Measurement of macroscopic and microscopic thermal neutron cross sections of V,Co, Cu,In, Dy and Au using neutron self-absorption properties

In this study, the total thermal neutron macroscopic and microscopic cross sections of V, Co, Cu, In, Dy and Au were measured using neutron self-absorption properties. Pure foils of these elements with various thicknesses were irradiated using a 5 Ci²³⁸Pu–Be source. After the irradiation, the gamma-spectra of their radionuclides were recorded by an HpGe detector. The gamma-photopeak areas of interest were determined by evaluating the gamma-spectra obtained from the foils. They were plotted as a function of foil thickness for each element. Then a non-linear least-squares fitting method was applied to the functions, and the total thermal neutron macroscopic and microscopic cross sections of V, Co, Cu, In, Dy and Au were obtained.     

Methodology for the U.S. Food and Drug Administration's radionuclides in foods program

The U.S. Food and Drug Administration (FDA) is responsible for the wholesomeness of the nation's food supply. The FDA modified its food monitoring program in January, 1973, to include radioactive isotopes. The methodology used to perform, analyses on these food products are taken from the standerd setting societies such as the AOAC International, American Society for Testing Materials and American Public Health Association Standard Methods. In addition, methods not tested by these societies are taken from the literature or from Department of Energy manuals such as the Health and Safety Laboratory and also from Environmental Protection Agency, Public Health Service, and Food and Agricultural Organization manuals. These include the methods for long-lived radionuclides such as tritium, strontium-90, cesium-137 and plutonium. Also, the short-lived radionuclides such as iodine-131, radiocesium, radiocerium and radioruthenium. In addition, they include the natural occurring radionuclides such as radium and uranium isotopes. The activity concentrations of gamma-emitters such as radiocesium, iodine-131 and radioruthenium are determined by gamma-ray spectrometry. This is done using intrinsic germanium detectors with the appropriate hardware and software. The alpha and “pure” beta-emitters are determined by various radiochemical methods and techniques. The radiochemical methodology and equipment used in analyzing these radionuclides are described and discussed. Also, the methodology and equipment for the gamma-emitters are described in more detail in this paper. In addition, the limits of detection for the methods used will be discussed.     

Distribution and dynamics of radionuclides and stable elements in the coastal waters off Rokkasho Village, Japan, prior to the opening of a nuclear reprocessing facility

The suspended particles floating in the seawater have the ability to biologically, as well as physically adsorb radionuclides and other elements dissolved in seawater. We have studied the distribution and composition of suspended particles, as well as the state of eluted of radionuclides in the decomposition process, in the coastal waters off Rokkasho Village, where radionuclides will be discharged from a nuclear fuel reprocessing plant in the near future.     

Ligands for molecular imaging: the synthesis of bis(thiosemicarbazone) ligands

Bis(thiosemicarbazones) have been of interest to chemists for over fifty years; they display antitumour, antibiotic and antiviral properties. Recently it has become apparent that they may also provide a convenient way of labelling biologically active molecules by using metallic radionuclides and/or fluorescence. Although apparently simple, the synthesis of bis(thiosemicarbazone) ligands can be problematic. This article provides a summary of the published literature, based on the synthetic strategies used and indicates some of the difficulties that may arise.     

Actinides and Long-Lived Radionuclides in Tissues of the Japanese Population: Summary of the Past 20-Year Studies

Radioactive fallout constitutes the major source of contamination of the environment with fission products. Our primary interest was in selected fission products, such as ¹³¹I, ⁸⁹Sr, ⁹⁰Sr, and ¹³⁷Cs, and neutron activation products, such as ³H and ¹⁴C. Plutonium-239,240, ²⁴¹Am and ⁹⁰Tc are generated from nuclear tests, and they are important by-products of nuclear industries. Polonium-210, ²¹⁰Pb and ²³²Th, ²³⁰Th and ²²⁸Th occur widely in nature. These radionuclides enter the human body through inhalation and the ingestion through food and water. These nuclides may cause radiation doses to certain organs of the body. Assessment of the resulting health hazards is an essential public health activity, which demands reliable techniques for the assay of the various radionuclides in man and his environment. In this paper, we present the accumulation of radionuclides from man-made sources and primordial radionuclides in various tissues of the Japanese population. The studies were performed at the Department of Public Health, Akita University School of Medicine, during the periods from 1973 to 1995.     

Study of 137Cs, 90Sr, 239,240Pu, 238Pu and 241Am behavior in the Chernobyl soil

The vertical distribution of ¹³⁷Cs, ⁹⁰Sr, ^239,240Pu, ²³⁸Pu and ²⁴¹Am was determined in soil samples collected from the Chernobyl exclusion zone in 1994. The results show very close distribution profiles for all radionuclides, with about 90% of the total activity of each nuclide lying between the surface and the fourth centimeter. Sequential extraction methods were used to determine the association of radionuclides in soil. The data on vertical distribution of radionuclide species were used to calculate their vertical migration parameters.     

Relating β+ radionuclides’ properties by order theory

We studied 27 β⁺ radionuclides taking into account some of their variants encoding information of their production, such as integral yield, threshold energy and energy of projectiles used to generate them; these radionuclides are of current use in clinical diagnostic imaging by positron emission tomography (PET). The study was conducted based on physical, physico-chemical, nuclear, dosimetric and quantum properties, which characterise the β⁺ radionuclides selected, with the aim of finding meaningful relationships among them. In order to accomplish this objective the mathematical methodology known as formal concept analysis was employed. We obtained a set of logical assertions (rules) classified as implications and associations, for the set of β⁺ radionuclides considered. Some of them show that low mass defect is related to high and medium values of maximum β⁺ energy, and with even parity and low mean lives; all these parameters are associated to the dose received by a patient subjected to a PET analysis.     

Analyse par activation non destructive: Contribution a l'etude des conditions d'analyses exactes

In non destructive activation analysis, either relative measurements or parametric counting techniques are used. However, in so complex media as biological or geological samples, where a lot of radionuclides are produced, an accurate determination of an element, must take into account, the “background shape and height effect” due to the other radionuclides. To achieve accuracy in such determinations, a new method is developed.