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Effect Of Fluoride And Cobalt On Forming Enamel: Scanning Electron Microscope And X-Ray Microanalysis Study, S. H. Ashrafi, D. R. Eisenmann, A. E. Zaki, R. Liss
Effect Of Fluoride And Cobalt On Forming Enamel: Scanning Electron Microscope And X-Ray Microanalysis Study, S. H. Ashrafi, D. R. Eisenmann, A. E. Zaki, R. Liss
Scanning Microscopy
The forming surfaces of enamel of rat incisors were examined by scanning electron microscope one hour after injection of either 5 mg/100 g body weight of sodium fluoride or 12 mg/100 g body weight of cobalt chloride. The cell debris from the surfaces of the separated incisors was either gently wiped off with soft facial tissues or chemically removed by treating with NaOH, NaOCl or trypsin. Best results to remove cell debris were obtained from 0.25% trypsin treatment.
SEM studies revealed that the surface of the normal secretory enamel was characteristic in appearance with well-developed smooth prism outlines. In fluoride …
Proton Microprobe And Particle Induced X-Ray Emission (Pixe) Analysis For Studies Of Pathological Brain Tissue, K. G. Malmqvist, A. Brun, K. Inamura, E. Martins, L. G. Salford, B. K. Siesjö, U. A. S. Tapper, K. Themner
Proton Microprobe And Particle Induced X-Ray Emission (Pixe) Analysis For Studies Of Pathological Brain Tissue, K. G. Malmqvist, A. Brun, K. Inamura, E. Martins, L. G. Salford, B. K. Siesjö, U. A. S. Tapper, K. Themner
Scanning Microscopy
Particle Indiced X-ray Emission and proton microprobe analyses have been applied for the investigation of regional elemental distributions in connection with various pathological states in the brain. Malignant brain tumours and adjacent histologically intact tissue removed during surgery were analysed with PIXE. Systematic elemental variations, e.g., for calcium and selenium, were observed in the tumour front. The proton microprobe was applied to study the Ca and K concentrations in various cell strata in hippocampus following transient ischaemia in rat brain. Significant increases in the Ca level occurred in selectively vulnerable cells within 48 h after the ischaemia.