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Journal ArticleDOI

Effect of sodium azide on the ultrastructural preservation of tissues

Hassmig Minassian, +1 more
- 01 Nov 1979 - 
- Vol. 117, Iss: 2, pp 243-253
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TLDR
An electron microscopic study was carried out to examine the quality of ultra‐structural preservation of parenchymatous and mesenchym atous tissues and isolated cells fixed in glutaraldehyde with sodium azide (NaN3) as an additive.
Abstract
An electron microscopic study was carried out to examine the quality of ultrastructural preservation of parenchymatous and mesenchymatous tissues and isolated cells fixed in glutaraldehyde with sodium azide (NaN3) as an additive. The dense tissues fixed with conventional glutaraldehyde containing calcium chloride demonstrated only a narrow zone of good tissue preservation on the surface of the specimens. Addition of azide at a concentration of 0.1% greatly improved the cellular preservation in the deeper region of tissues, in particular with respect to the mitochondrial morphology. There was no adverse effect on other cell organelles. The improvement in mitochondrial preservation and the enhancement of penetration of the fixative is presumably due to selective and instantaneous inhibition of mitochondrial metabolic activity by the azide, thus retarding anoxic degenerative effects on cellular structures until permanent fixation is completed by the comparatively slow-acting aldehyde. However, the addition of azide offers no significant improvement in the ultrastructural preservation of isolated lymphocytes and liver cells, or fibroblasts maintained in culture.

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References
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Journal ArticleDOI

THE USE OF LEAD CITRATE AT HIGH pH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPY

TL;DR: The stain reported here differs from previous alkaline lead stains in that the chelating agent, citrate, is in sufficient excess to sequester all lead present, and is less likely to contaminate sections.
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A method for staining epoxy sections for light microscopy.

TL;DR: A technique for staining sections of osmium-fixed, epoxy-embedded tissues for light microscopy using aqueous toluidine blue at pH 11.1 and does not require prior removal of embedding medium, which permits better utilization of the full resolving power of the light microscope.
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Cellular change in human disease: A new method of pathological analysis

TL;DR: Evaluation of cellular alterations as a method for studying the pathogenesis and the manifestations of human disease is presented based on evaluation by chemical and morphologic methods performed with human tissues obtained at immediate autopsy.
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The application of electron microscopy and cellular biochemistry to the autopsy. Observations on cellular changes in human shock.

TL;DR: A method based on the utilization of electron microscopy, morphometric analysis, tissue culture, and biochemical analysis in the study of human autopsies is described in this paper, where rapid sampling immediately following somatic death is conducted in order to make meaningful the application of such techniques.
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