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At least 19 recordsLinked to original sources
PubMed1984

Long term effects of thorium dioxide (thorotrast) administration on human liver. Ultrastructural localization of thorium dioxide in human liver by analytical electron microscopy.

The ultrastructual localization of thorium dioxide was examined in liver biopsy specimens from two patients injected more than 30 years before with thorotrast. An energy dispersive X-ray microanalysis spectrometer (Kevex 5100) was used to identify thorium in the liver tissue. By electron microscopy, most of the thorium particles were found in the cells of the reticuloendothelial system, such as macrophages of the portal triad and Kupffer cells in the hepatic sinusoid. Thorium dioxide particles were mainly located within the phagosomes, but larger aggregates existed in the cytoplasma with no visible limiting membrane. In addition, the deposition of thorium granules in a few hepatocytes was also confirmed by electron microscopy. This fact indicates that two main pathways of elimination are still functioning in the late period, but the hepatocytic pathway appears to be less effective than the reticuloendothelial system.

Biopsy↗
PubMed1998

[Thorium: analysis and dosimetry of thorium welding electrodes].

The use of thoriated tungsten electrodes may be at the origin of a potential hazard for the personnel involved in the use of electrodes, as well as the general population. To assess this hazard, the electrode radioactivity measurements by alpha and beta counting has been conducted. The radioelements were identified by alpha and gamma spectromety. It appeared that there was a radioactive disequilibrium between thorium-232 (Th-232) and it daughters atoms. Additionally, some thorium 230 (Th-230) belonging to the uranium chain, was present. The chemical separation and the milling processing had affected the radioactive composition and the thorium in the electrodes, doesn't exactly corresponds to natural thorium. Radiation doses were also assessed: film and photoluminescence dosimetry were undertaken. Finally smears method showed a alpha removable area contamination. Even if the hazard is weak. As a matter of fact, it must not be neglected because it was complex, for the thorium was always accompanied by Th-232 progeny, alpha emitters but also beta and gamma emitters.

Humans↗
PubMed1985

[Uranium, thorium and potassium contents and radioactive equilibrium states of the uranium and thorium series nuclides in phosphate rocks and phosphate fertilizers].

Uranium, thorium and potassium contents and radioactive equilibrium states of the uranium and thorium series nuclides have been studied for 2 phosphate rocks and 7 phosphate fertilizers. Uranium contents were found to be rather high (39-117 ppm) except for phosphate rock from Kola. The uranium series nuclides were found to be in various equilibration states, which can be grouped into following three categories. Almost in the equilibrium state, 238U approximately 230Th greater than 210Pb greater than 226Ra and 238U greater than 230Th greater than 210Pb greater than 226Ra. Thorium contents were found to be, in general, low and appreciable disequilibrium of the thorium series nuclides was not observed except one sample. Potassium contents were also very low (less than 0.3% K2O) except for complex fertilizers. Based on the present data, discussions were made for the radiation exposure due to phosphate fertilizers.

Alpha Particles↗
PubMed2002

XAFS investigation of the structure of aqueous thorium(IV) species, colloids, and solid thorium(IV) oxide/hydroxide.

X-ray absorption fine structure (XAFS) spectroscopy at the Th L3 edge is applied for the characterization of crystalline, anhydrous ThO(2)(cr), microcrystalline ThO(2).xH(2)O(s), amorphous ThO(n)(OH)(4-2n).xH(2)O(am), aqueous Th(IV) solutions, and colloidal suspensions up to p(c)H 3.7. The microcrystalline, possibly hydrated thorium dioxide, is formed at p(c)H 1.5-2.5 by precipitation from suspensions of 16-23 nm thorium dioxide colloids. The solubility data determined for this solid is several orders of magnitude lower than the values for amorphous Th(IV) hydroxide or hydrous oxide. The EXAFS spectrum of the isolated microcrystalline particles shows that their structure is different from that of anhydrous crystalline ThO(2)(cr) and amorphous ThO(n)(OH)(4-2n).xH(2)O(am) precipitated at higher pH and dried at room temperature. The solubility measured for the amorphous Th(IV) precipitate is comparable to that previously reported for a solid prepared in a similar manner. In other solubility studies with amorphous Th(IV) hydroxide or hydrous oxide, considerably higher thorium concentrations are measured at p(c)H 3.5-5. The aqueous speciation is made by EXAFS for solutions prepared by careful coulometric titration under comparable conditions (p(c)H and thorium concentration). The spectra of these solutions demonstrate the presence of a large amount of Th(IV) polynuclear species or colloids of small size, having a highly asymmetric Th-O coordination. The EXAFS spectrum of these colloids is similar to that of the amorphous solid.

Journal Article↗
PubMed1999

Organ distribution of thorium in thorium workers: good agreement with new models of the International Commission on Radiological Protection.

Higher than environmental levels of (232)Th have been found in autopsy samples of lungs and other organs from four former employees of a thorium refinery. Working periods of the subjects ranged from 3 to 24 years, and times from end of work to death ranged from 6 to 31 years. Examination of the distribution of thorium among the organs showed that concentrations in the lung relative to pulmonary lymph nodes, bone or liver were much higher calculated from the dosimetric models in Publication 30 of the International Commission on Radiological Protection (ICRP). Much better agreement was found with more recently proposed models in Publications 68 and 69 of the ICRP. Radiation doses estimated from the amounts of thorium in the autopsy samples were compatible with health studies that found no significant difference in mortality from that of the general population of men in the U.S.

Administration, Inhalation↗
PubMed2000

Thorium isotopes in autopsy samples from thorium workers.

Concentrations of 232Th and activity ratios of 228Th to 232Th and 230Th to 232Th were determined in autopsy samples from five former employees of a thorium refinery. The ranges of 232Th activity concentrations (mBq per gram of wet tissue) were 0.17-94 in lungs, 3.9-1210 in pulmonary lymph nodes, 0.14-1.19 in bones, 0.015-0.68 in liver, 0.97-5.8 in spleen, and 0.009-0.068 in kidneys. These concentrations are 10 to 1,000 times greater than have been reported for persons not occupationally exposed to thorium. In most of the samples, the ratios of 228Th to 232Th and 230Th to 232Th activity at death of the subject were 0.2-0.4 and 0.1-0.2, respectively. 228Th to 228Ra activity ratios (+/- standard errors) of 0.86 +/- 0.11 in lungs and 1.18 +/- 0.13 in lymph nodes of one subject were obtained by calculation from ratios of 228Th to 232Th.

Autopsy↗
PubMed2001

Current research activity in the measurement of thorium and the identification of future research needs.

A pre-requisite in the setting and enforcement of regulatory limits for exposure to thorium in the workplace is that thorium and its progeny can be accurately measured. Literature surveys have shown that the majority of thorium measurements were performed using either a radiochemical technique, such as alpha or gamma spectroscopy, or ICP-MS. For many methods. there was a separation step to isolate and pre-concentrate thorium from the sample matrix. Thorium was most commonly measured in geological matrices and industrial materials. A survey of current research activity was performed through distribution of a questionnaire to laboratories and national centres. From the rcsponses, four areas of current activity were identified: (i) development of methods for low level thorium determination, (ii) biological monitoring and metabolism of thorium, (iii) environmental monitoring for thorium, and (iv) health risks from X ray contract media. Two key areas for priority research were identified by the thorium Thematic Network: namely sample preparation methods and for traceable standards and reference materials for thorium analysis.

Environmental Exposure↗
PubMed1988

Microanalytical study of thorium 232 deposits in bone marrow and liver.

Analytical microscopy was used to study the distribution and chemical composition of thorium deposits in bone marrow and liver after injection of thorium dioxide and thorium nitrate. Thorotrast (thorium dioxide) was identified as being localized in bone marrow macrophages of a patient who had undergone cerebral arteriography forty two years ago. Large thorotrast deposits were also present in liver cells. We show that non-colloidal thorium (thorium nitrate) injected in rats concentrates in a non soluble form in bone marrow macrophages, hepatocytes and Kupffer cells. These deposits of thorium associated with phosphorus can be explained by the formation of thorium phosphate in lysosomes and we demonstrate that they remain in tissue for a long time. Microanalysis was performed with ion microscopy, and electron probe microanalysis by X ray spectrometry, which can identify and localize thorium and associated elements at cellular or intracellular level.

Animals↗
PubMed1993

Thorium metabolism and bioassay of mineral sands workers.

The concentration of thorium in the blood serum and urine of Western Australian mineral sands workers was studied to complement estimates of radiation dose derived from air sampling measurements. The concentration of thorium in urine samples from occupationally unexposed persons and pooled serum samples was also investigated. The concentration of thorium in the urine of the workers varied from 3-210 ng L-1 (geometric mean = 31 ng L-1, n = 34) while the concentration of thorium in the serum varied from 170-2,000 ng L-1 (geometric mean = 480 ng L-1, n = 25). No correlation was found between the bioassay results and cumulative airborne thorium exposure. The geometric mean ratio of daily excretion of thorium in urine to total thorium in the serum pool was 2.5%, considerably lower than the value of 10% proposed by the ICRP. These data indicate that more information is required to clarify the biokinetic models for thorium and that doses assessed from air sampling data must be interpreted with caution.

Air Pollutants, Radioactive↗
PubMed2003

Simultaneous spectrophotometric determination of uranium and thorium by flow injection analysis using selective masking.

A flow injection system for the simultaneous determination of uranium and thorium has been developed by using selective masking and a spectrophotometric detector with two flow cells aligned with the same optical path. The injected sample solution was first mixed with a reagent solution containing Chromazurol S (CAS) and cetyltrimethylammonium chloride (CTMAC), and the total absorbance of uranium- and thorium-CAS complexes was measured in the first flow cell at 620 nm. The sample stream was then mixed with an EDTA solution in order to convert the thorium-CAS complex to a thorium-EDTA complex, and the absorbance of the uranium-CAS complex was measured in the second flow cell. The detection limits were 10 microg dm(-3) for uranium and 7 microg dm(-3) for thorium. The calibration graphs were linear (r < 0.9998) at least over the ranges of 0.1 to 10 mg dm(-3) for uranium and 0.08 to 8 mg dm(-3) for thorium. The RSDs were less than 1.5% (n = 3) in the calibration range. Uranium and thorium of up to the 6-fold concentration to each other could be determined in admixtures with relative errors of less than 3.3%. The sample throughput was 24 per hour. The proposed system was successfully applied to the analysis of a uranium-thorium ore mock solution by coupling with anion-exchange in a magnesium nitrate medium to eliminate interference from coexisting elements.

Journal Article↗
PubMed1999

Determination of thorium in organs from thorotrast patients by inductively coupled plasma mass spectroscopy and x-ray fluorescence.

Concentrations of thorium were determined by inductively coupled plasma mass spectroscopy in various organs collected from Japanese Thorotrast autopsy subjects to provide information on dosimetry for Thorotrast patients. Duplicate analyses were performed for 98 samples, and data for thorium in 27 different organs were obtained. The highest thorium level was found in spleen (mean: 16,000 microgram/g wet weight), followed by liver (2100 microgram/g wet weight) and bone marrow (600 microgram/g wet weight). The other concentrations decreased in the following order: lymph node, gallbladder, testis, lung, small intestine, adrenal gland, pancreas, dura, esophagus, muscle, thyroid, large intestine, stomach, fat, kidney, urinary bladder, main artery, prostate, diaphragm, trachea, heart, cerebellum, cerebrum and intervertebral disk. The last four organs showed markedly low concentrations of 2-7 microgram/g wet weight. Compared to the background thorium levels reported in the literature for human organs, the values for the organs from Thorotrast patients (even in the organs with the lowest concentrations) were at least several thousand times higher, suggesting the importance of also considering organs with minor deposition in dosimetry. Distributions of thorium in some selected organs were studied by microbeam X-ray fluorescence. The thorium conglomerates could be identified, and images of microdistributions of thorium in the organ slices were obtained.

Humans↗
PubMed2001

The in vivo assessment of thorium body burden by gamma ray sepctrometry.

Thorium is used in many different industrial technologies and is widely found in nature. Internal contamination with thorium is considered as highly hazardous because of its radiological and chemical toxicities, which depend on the chemical form in which thorium appears. The assessment of the thorium body burden is then of primary importance in detecting the risks of personal contamination, and for appropriate counteractions when contamination is detected. The in vivo assessment of the thorium lung burden is commonly achieved by gamma ray spectrometry of its progeny. Three methods for the assessment of thorium in the lungs are compared. In the first method, the radionuclide examined is 208Tl, measured with a Nal(TI) detector. This simple method can be affected by systematic errors due to 220Rn exhalation and because of the assumption of equilibrium between 232Th and 228Th. The second method, based on the measurement of the gamma rays emitted by 228Ac, requires the use of high-resolution gamma spectrometry (HPGe detectors). The accuracy of the thorium quantification is better with this technique. The third method is based on the measurement of exhaled 220Rn.

Body Burden↗