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Pannoramic midi whole slide scanner

Manufactured by 3DHISTECH

The Pannoramic MIDI whole slide scanner is a high-performance digital pathology scanner designed for efficient digitization of glass slides. It captures high-resolution images of entire microscope slides, enabling digital review and analysis of pathological samples.

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3 protocols using pannoramic midi whole slide scanner

1

Histological Analysis of Lung Architecture

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The left lung was fixed in Milloning buffer solution (pH 7.4) with 4% paraformaldehyde to preserve the pulmonary architecture. Lung sections were stained using Sirius Red (pH 10.2) or Masson’s trichrome for the analysis of peribronchiolar leukocyte infiltration and extracellular matrix deposits, respectively, as described previously19 (link),20 (link). The slides stained using Masson’s trichrome were scanned with 3DHISTECH–Pannoramic MIDI whole slide scanner, and the images were captured using a 20× objective lens. The analysis was performed in 10 bronchioles per animal in a double-blind experiment evaluating the use of Image-Pro-Plus® software version 6.2 (Media Cybernetics Inc,). The quantification of eosinophils, neutrophils and mononuclear cells number on the peribronchiolar region was performed under an optical microscope (BX40; Olympus) through an integrating eyepiece. The morphometric reticulum had a known area of 104 μm2 at the final magnification of 1,000× and was randomly positioned over the peribronchiolar regions. Three different fields were analyzed for bronchioles in 7 bronchioles per animal19 (link),20 (link).
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2

Histological Analysis of Pulmonary Silicosis

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The left lung was removed, fixed in Milloning buffer solution (pH 7.4) with 4% paraformaldehyde to preserve pulmonary architecture. Briefly, samples were embedded in paraffin (Sigma-Aldrich), and 4 μm-thick sections were cut and stained with hematoxylin and eosin for quantification of granuloma area, Picrosirius for collagen fibers and Sirius Red (pH 10.2) for neutrophils and eosinophils counted in the parenchyma and in peribronchiolar area, respectively. Slides were scanned with 3DHISTECH–Pannoramic MIDI whole slide scanner (capture with a 20× objective lens) and the resulting images analyzed with CaseViewer 3.3, Pannoramic Viewer 1.15.4, and HistoQuant softwares (3DHISTECH). Silica crystals were analyzed, in 15 independent fields, with a light microscope (Olympus BX50) equipped with polarizing attachment for detecting birefringent particles and Image-Pro Plus Version 4.
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3

Histological Analysis of Lung Tissue

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Left lungs from each experimental group were dissected and placed in Millonig fixative solution (pH = 7.4) with 4% paraformaldehyde for 48 h to preserve tissue architecture. Tissues were dehydrated and clarified in xylene before paraffin embedding. Lung sections of 4 μm were stained with hematoxylin and eosin (H&E), to analyze granulomas, or Picrosirius, to evaluate collagen deposition, in light microscope using 3DHISTECH–Pannoramic MIDI whole slide scanner (capture with a 20× objective lens) and the resulting images analyzed with CaseViewer 3.3, Pannoramic Viewer 1.15.4, and HistoQuant softwares (3DHISTECH). Silica crystals were analyzed, in 15 independent fields, with a light microscope (Olympus BX51) equipped with polarizing attachment for detecting birefringent particles and the quantification were performed using the software Image-Pro Plus Version 6.2 (Media Cybernetics Inc., Rockville, MD, United States).
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