Staining plastic blocks with triiodide to image cells and soft tissues in backscattered electron SEM of skeletal and dental tissues

Backscattered electron scanning electron microscopy (BSE SEM) is an invaluable method for studying the histology of the hard, mineralised components of poly-methyl methacrylate (PMMA) or other resin embedded skeletal and dental tissues. Intact tissues are studied in micro-milled or polished block fa...

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Main Author: A Boyde
Format: Article
Language:English
Published: AO Research Institute Davos 2012-07-01
Series:European Cells & Materials
Subjects:
Online Access:http://www.ecmjournal.org/journal/papers/vol024/pdf/v024a11.pdf
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spelling doaj-7456cf42aa06410cbb5344eecb5c167d2020-11-24T21:43:45Zeng AO Research Institute DavosEuropean Cells & Materials1473-22622012-07-0124154161Staining plastic blocks with triiodide to image cells and soft tissues in backscattered electron SEM of skeletal and dental tissuesA BoydeBackscattered electron scanning electron microscopy (BSE SEM) is an invaluable method for studying the histology of the hard, mineralised components of poly-methyl methacrylate (PMMA) or other resin embedded skeletal and dental tissues. Intact tissues are studied in micro-milled or polished block faces with an electron-optical section thickness of the order of a half to one micron and with the area of the section as big as a whole – large or small – bone organ. However, BSE SEM does not give information concerning the distribution of uncalcified, ‘soft’, cellular and extracellular matrix components. This can be obtained by confocal microscopy of the same block and the two sorts of images merged but the blocks have to be studied in two microscope systems. The present work shows a new, simple and economic approach to visualising both components by using the triiodide ion in Lugol's iodine solution to stain the block surface prior to the application of any conductive coating – and the latter can be omitted if charging is suppressed by use of poor vacuum conditions in the SEM sample chamber. The method permits the use of archival tissue, and it will be valuable in studies of both normal growth and development and pathological changes in bones and joints, including osteoporosis and osteoarthritis, and tissue adaptation to implants. http://www.ecmjournal.org/journal/papers/vol024/pdf/v024a11.pdfBonecartilageosteoidhistopathologyimplant interface
collection DOAJ
language English
format Article
sources DOAJ
author A Boyde
spellingShingle A Boyde
Staining plastic blocks with triiodide to image cells and soft tissues in backscattered electron SEM of skeletal and dental tissues
European Cells & Materials
Bone
cartilage
osteoid
histopathology
implant interface
author_facet A Boyde
author_sort A Boyde
title Staining plastic blocks with triiodide to image cells and soft tissues in backscattered electron SEM of skeletal and dental tissues
title_short Staining plastic blocks with triiodide to image cells and soft tissues in backscattered electron SEM of skeletal and dental tissues
title_full Staining plastic blocks with triiodide to image cells and soft tissues in backscattered electron SEM of skeletal and dental tissues
title_fullStr Staining plastic blocks with triiodide to image cells and soft tissues in backscattered electron SEM of skeletal and dental tissues
title_full_unstemmed Staining plastic blocks with triiodide to image cells and soft tissues in backscattered electron SEM of skeletal and dental tissues
title_sort staining plastic blocks with triiodide to image cells and soft tissues in backscattered electron sem of skeletal and dental tissues
publisher AO Research Institute Davos
series European Cells & Materials
issn 1473-2262
publishDate 2012-07-01
description Backscattered electron scanning electron microscopy (BSE SEM) is an invaluable method for studying the histology of the hard, mineralised components of poly-methyl methacrylate (PMMA) or other resin embedded skeletal and dental tissues. Intact tissues are studied in micro-milled or polished block faces with an electron-optical section thickness of the order of a half to one micron and with the area of the section as big as a whole – large or small – bone organ. However, BSE SEM does not give information concerning the distribution of uncalcified, ‘soft’, cellular and extracellular matrix components. This can be obtained by confocal microscopy of the same block and the two sorts of images merged but the blocks have to be studied in two microscope systems. The present work shows a new, simple and economic approach to visualising both components by using the triiodide ion in Lugol's iodine solution to stain the block surface prior to the application of any conductive coating – and the latter can be omitted if charging is suppressed by use of poor vacuum conditions in the SEM sample chamber. The method permits the use of archival tissue, and it will be valuable in studies of both normal growth and development and pathological changes in bones and joints, including osteoporosis and osteoarthritis, and tissue adaptation to implants.
topic Bone
cartilage
osteoid
histopathology
implant interface
url http://www.ecmjournal.org/journal/papers/vol024/pdf/v024a11.pdf
work_keys_str_mv AT aboyde stainingplasticblockswithtriiodidetoimagecellsandsofttissuesinbackscatteredelectronsemofskeletalanddentaltissues
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