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Results for “Electron Probe Microanalysis”

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At least 19 recordsLinked to original sources

Silicon in rat liver organelles: electron probe microanalysis.

Electron probe microanalysis of unfixed freeze-substituted rat liver tissue embedded in Spurr's low viscosity epoxy resin demonstrated the occurrence of Si as well as P, S, and Cl in the nucleus, nucleolus, mitochondria, and rough endoplasmic reticulum. Chemical analysis confirmed that the Si in the organelles did not originate from instrumental contaminants. This suggests that Si may be involved in the biochemistry of these subcellular organelles.

Cell Nucleolus↗

Detection of iodine, sulphur and phosphorus in histological thyroid sections by using electron probe microanalysis.

Electron probe microanalysis for iodine, sulphur and phosphorus was performed in histological frozen sections from thyroid tissue of 5 patients undergone thyroid surgery for benign disease. Iodine seemed to be localized in the colloid of the thyroid follicles. Phosphorus localized in areas which corresponded with the epithelium of the follicles. Sulphur showed a strong association with iodine both in localization and in relative amounts. It was suggested that iodine and sulphur reflect the presence of thyroglobulin in the colloid of thyroid follicles.

Electron Probe Microanalysis↗

Electron microscopy of human melanosomes in unstained, fresh air-dried hair bulbs and their examination by electron probe microanalysis.

Electron microscopy of unstained, fresh air-dried spreads of plucked human hair bulbs revealed relatively well preserved melanocytes and dense storage granules of melanin. Energy dispersive X-ray microanalysis of melanosomes and premelanosomes from black facial hair bulbs disclosed high peaks for potassium and sulfur, intermediate peaks for magnesium and calcium, and low but distinct ones for phosphorus and chlorine. No peaks for magnesium were found in the central portion of mature melanosomes, but at their edges and in premelanosomes conspicuous peaks for this element were obtained.

Electron Probe Microanalysis↗

Cryofixation methods for ion localization in cells by electron probe microanalysis: a review.

Electron probe microanalysis data on the intracellular content and distribution of electrolyte ions depends critically on the functional state of the cells at the moment of cryofixation. Whereas tissue specimens often require special in-situ freezing techniques, isolated and cultured cells can be frozen within their environmental medium under physiologically controlled conditions. Thus, they represent a feasible system to study functional ion-related intracellular parameters such as the K/Na ratio. Specifically modified freezing devices allow the study of ion shifts related to dynamic processes in cells, for example, locomotion and exocytosis. The time resolution achieved by time-controlled cryofixation is approximately 1 ms.

Amoeba↗

Intranuclear sites of Np 237 in mammalian cells: a study using electron microscopy and electron probe microanalysis.

Two methods, electron microscopy and wavelength dispersive electron probe microanalysis, were used to determine the intracellular sites and chemical form of concentrations of neptunium nitrate 237 after chronic intoxication by the intraperitoneal route in two organs in the rat known to concentrate this element (kidney, liver). Abnormal intranuclear formations in the form of clusters of dense granules containing neptunium, phosphorus, sulphur, and calcium were found in the nuclei of kidney proximal tubule cells and hepatocytes. These formations had a maximum diameter of the order of 2 microns and were located in the central part of the nucleus, away from the nucleolus and peripheral chromatin. Serious nuclear and cytoplasmic ultrastructural lesions are often associated in cells containing neptunium inclusions. The absorbed doses in the kidney and the liver were very low. A relationship between these abnormal intranuclear structures and the carcinogenic effect of neptunium remains to be clarified. This effect is related more probably to the chemical toxicity of Np 237.

Animals↗

[Assessment of the interface reaction of endosseous implanted bio-sinterceramics by electron probe microanalysis].

The electron ray microanalysis (ESMA) showed an intimate bone-implant-compound already 4 weeks postoperatively. This compound was detectable in all sinter variants after 78 weeks. An area with changed material contrast was prepared on the surface of the implant with an extent of 45-55 micron until the 24th week and over 100 micron after 78 weeks. A surface stratum relatively rich in calcium and absolutely rich in phosphorus was formed in the immediate contact to the regenerated bone opposite to the implant nucleolus. This stratum had an approximate consistent extent of 20-35 micron from the 12th week. The relative intensity of the stratum rich in calcium and phosphorus corresponded to that of the bone around the implant. The stabilization of the reactive surface stratum can become assumed by that.

Animals↗

Electron probe microanalysis: its present, its future.

Electron probe microanalysis (EPM) is a method of elemental ultramicroanalysis based on the spectrometry of the characteristic X rays which are emitted when a target sample is excited by an electron beam. In the same sample many more elements (from carbon and up in the periodic table) in much smaller volumes (less than 1 micronm3 or 10(-15) liter) can be analyzed with EPM than with any other ultramicroanalytical method. Quantitation down to 10(-15) g is relatively easy. Any application of EPM in biology depends on the development of suitable methods for biological sample preparation. Liquid droplets of 10(-11)-liter volumes are routinely analyzed. Elemental content in isolated cells can be quantitated. The analysis of cellular, extracellular, and intercellular content in the same preparation is in sight: a general method for the analysis of diffusible elements in different compartments in tissue relies on the manipulation of frozen hydrated tissue near liquid nitrogen temperature. Localization in the same preparation of several organic compounds at high resolution will be possible by use of appropriate tags. All fields of microphysiology are likely to benefit from this new discipline.

Cells↗

Electron probe microanalysis of biological soft tissues: principle and technique.

Electron probe microanalysis is a method based upon X-ray spectrometry used for analyzing the chemical element content of very small amounts of material. The concentration of electrolytes in the microenvironment of cells, in cells, and in intracellular organelles can be measured. The main difficulties in using this method in biological soft tissue lie in sample preparation and in proper interpretation of the data. Best tissue preparation seems to be to quench the sample and to analyze it either freeze dried in thin or ultrathin sections, or frozen hydrated in thin sections or bulk samples. In all cases analysis should be performed using a cold stage and an ultra clean vacuum in order to minimize mass loss due to beam damage and mass gain due to contamination trapping. Interpretation of the data relies upon the knowledge of both the localization of the volume excited by the electron beam and the origin of the continuum and characteristic X-ray signals received by the X-ray spectrometer. This knowledge can be complicated by two facts: 1) when the electron beam is used in an analytical mode, viewing of the analyzed microarea can be lost, and 2) the X-ray signals received by the spectrometer can originate not only from the volume directly excited by the electron beam but from areas that can be far apart, excited by the electron beam tail, scattered electrons or secondary fluorescence, particularly when using energy dispersive spectrometers. Theoretical quantitation of the results is well developed. Practical quantitation could be complicated by the possibility of mass gain, mass loss, standard inhomogeneity, non-uniformity of sample thickness, possibility of shrinkage during freeze drying and, when using energy dispersive spectrometry, by the low signal over background for low atomic number elements (Na), the possibility of overlap of characteristic X-ray lines, and the use of complex and empirical methods for background stripping and peak deconvolution. All these difficulties can be overcome, making electron probe microanalysis one of the most powerful tools available to the biologist.

Animals↗

Frontiers in electron probe microanalysis: application to cell physiology.

The application of electron probe microanalysis techniques, using X-ray and electron energy loss instruments, to problems in cell physiology is reviewed. The details of the special methodological requirements for the analysis of cryosections at high spatial resolution in an analytical electron microscope are discussed together with a comprehensive review of data obtained on major organ systems and cell types.

Animals↗

Application of Electron Probe Microanalysis to the Study of Geological and Planetary Materials.

The impact of electron probe microanalysis on the study of geological and planetary materials has been tremendous. Electron microprobes evolved into routine analytical instruments in geological research laboratories as instrument capabilities improved and applications to geologic/planetary materials expanded. The contributions of electron probe microanalysis to the characterization of minerals, both terrestrial and extraterrestrial, and to other significant geological research, such as light element analysis, trace element analysis, and element mapping, is described.

Journal Article↗

Electron probe microanalysis of cytoplasmic concentrations of elements in a single cell in culture and suspension.

Electron probe microanalysis is a method for evaluation of concentrations of elements at the subcellular level, effective in studies of an individual cell in culture or suspension. Intracellular concentrations of cytoplasmic ions (K+, Na+, Cl-) most rapidly and markedly reacting to changes is an adequate criterion for evaluating the traumatism of manipulations used in cell technologies. Using electron probe microanalysis it will be possible to develop special procedures (for example, therapeutic cloning) for reprogramming or cryopreservation, when intactness of intracellular balance of element serves as the criterion of cell status.

Animals↗

Correlated microradiography, X-ray microbeam diffraction and electron probe microanalysis of calcifications in an odontoma.

Using microradiography, X-ray microbeam diffraction and electron probe microanalysis, a correlated morphologic crystallographic study was performed on dysplastic enamel in a compound odontoma. The tumor was found in the lateral incisor-canine region of the left mandible of a 36-year-old woman. A conspicuous feature was the presence of hypomineralized areas, which were situated in the proximity of enamel surface and distinctly demarcated from the adjacent enamel. X-ray microbeam diffraction and electron probe microanalysis showed that these lesions have a lower crystallinity and a higher concentration of magnesium as compared with the adjacent enamel. In addition, the present study revealed the presence of two other types of calcifications: (1) calcified structures within the fissure or on the enamel surface, which include lacunae of varying size and which resemble a form of coronal cementum, and (2) spherical calcifications which may be an epithelial product.

Adult↗

Performance and limitations of electron probe microanalysis applied to the characterization of coatings and layered structures.

Electron probe microanalysis (EPMA) at low electron energies (typically 3-10 keV) has been used to study the composition of coatings with a film thickness of 0.1-1.3 microm ("bulk" analysis). The accuracy of quantification, including the most critical situation of low atomic number elements (boron-oxygen), is about 5% relative by use of pure element or arbitrary compound standards. A special procedure of data processing ("thin film" analysis) enables the simultaneous determination of film thickness and composition, provided that the substrate is known. The film thickness may be in the range of 2 nm to 5 microm. EPMA can be also applied in the mode of "non-destructive in-depth analysis", which is based on the combined evaluation of experiments at different electron energies. The quantitative characterization of layered structures and implantation zones is demonstrated.

Journal Article↗

Quantitative electron probe microanalysis of acetylcholinesterase activity in rat brain sections.

In this study we determined acetylcholinesterase (AChE) activity by electron probe microanalysis (EPMA). AChE was localized in rat brain sections by a histochemical reaction that produced a Cu-ferricyanide precipitate. This reaction is based on the hydrolysis of acetylcholine substrate with AChE. The copper (iron) concentration in the deposit is proportional to acetylcholine involved in the hydrolysis reaction. Absolute determination of the size of the reaction was calculated from EPMA measurements compared with those made from a dextran standard containing a known amount of Cu(Fe). Electron probe microanalysis allows AChE activity to be assayed quantitatively on thick brain sections with a spatial resolution of 10 microns.

Acetylcholinesterase↗

Grazing exit electron probe microanalysis of submicrometer inclusions in metallic materials.

Grazing exit electron probe microanalysis (GE-EPMA) is a new method of EPMA in which characteristic X-rays emitted from only near-surface regions of a specimen are detected at extremely low exit angles near 0 degrees (the grazing exit condition). This technique requires the analytical objects exist on a flat surface. Therefore, the GE-EPMA analysis has been used only for the analysis of particles or a thin film on a flat substrate so that there were only few applications for practical analysis. As a new application, we have carried out GE-EPMA analysis of approximately 0.2-microm inclusions on stainless steel, which appeared to be a projection on the specimen surface with chemical etching. The GE-EPMA quantitative results were in excellent agreement with those of inclusions that were extracted from the stainless steel and analyzed by EPMA with conventional exit condition (30 degrees). This method could be, therefore, applied to the analysis of the submicrometer inclusion in a wide variety of metallic materials if the inclusion appears to be a projection with chemical etching treatment.

Journal Article↗