Histology: Clearing and Impregnation

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1
Alternative term (AKA) for Clearing is
Dealcoholization
2
Definition of Clearing (Dealcoholization) is
The process whereby alcohol or a dehydrating agent is removed from the tissue and replaced by a fluid (clearing agent) that will dissolve the wax with which the tissue must be impregnated
3
Primary optical reason why the process is named "clearing" is
In addition to removing alcohol, many of these substances have the property of making tissues transparent due to their high index of refraction (RI) approximately equal to that of tissues
4
List of common clearing agents includes
Xylene/Xylol, Toluene/Toluol, Benzene, Chloroform, Cedarwood oil, Carbon disulfide, Oil of bergamot, Clove oil, Carbon tetrachloride, Aniline oil, Tetrahydrofuran, Petroleum ether, Cedar oil, Creosote
5
List of other clearing agents includes
Terpineol, Phenol in alcohol, Dioxane, Carboxylol
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Key characteristics of a good clearing agent include
Miscible with alcohol, miscible with melted paraffin wax/mounting medium, does not produce excessive shrinkage/hardening, does not dissolve aniline dyes, does not evaporate quickly in wax bath, makes tissues transparent
7
Ideal volume ratio of clearing agent to tissue specimen is
At least 10x the volume of the tissue
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Clearing agents used directly from water for frozen sections are
Gum syrup & Glycerin
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Clearing time and general quality of Xylene (Xylol) are
½ to 2 hours (usual; 15-30 minutes for urgent biopsies); excellent and true clearing agent, most rapid clearing agent
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Advantages of Xylene include
Cheap, does not extract out aniline dyes, miscible with absolute alcohol and paraffin, can be used with celloidin sections
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Disadvantages of Xylene include
Highly flammable, becomes milky when dehydration is incomplete, NOT recommended for nervous tissues and lymph nodes (causes hardening and tissue shrinkage)
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Clearing time and substitute nature of Toluene (Toluol) are
1-2 hours; substitute for xylene or benzene, acts slower than benzene and is expensive
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Safety warnings for Toluene include
Not carcinogenic, but highly concentrated fumes are toxic upon prolonged exposure
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Clearing time and characteristics of Benzene are
15-60 minutes; rapid acting, recommended for urgent biopsies and routine purposes, highly flammable
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Primary health hazard/carcinogenic risk associated with Benzene exposure is
Carcinogenic or may damage bone marrow (Aplastic anemia)
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Clearing time and tissue suitability for Chloroform are
6-24 hours; slower in action than xylene but causes less brittleness; best of traditional clearing agents for routine use, gives widest latitude
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Tissue indications for Chloroform include
Recommended for tough (skin, fibroid, decalcified tissues), large tissue specimens, nervous tissue, lymph nodes, granulation tissue, and fetal/delicate specimens
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Disadvantages of Chloroform include
Does not make tissues transparent, toxic to the liver after prolonged inhalation
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Clearing time and tissue indications for Cedarwood Oil are
2-3 days; clears both Paraffin and Celloidin sections, recommended for CNS tissues and cytological studies (especially smooth muscles and skin)
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Disadvantages of Cedarwood Oil include
Very expensive, requires 2 changes, quality not always uniform, extremely slow, becomes milky on prolonged storage
21
Tissue indication and feature of Aniline Oil are
Recommended for clearing embryos, insects, and very delicate specimens; clears 70% alcohol without excessive tissue shrinkage/hardening
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Disadvantages and properties of Clove Oil are
Removes aniline dyes, dissolves Celloidin, tissues become brittle, quality not guaranteed (tends to be adulterated), not suitable for routine purposes (expensive)
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Property and health hazard of Carbon Tetrachloride are
Properties very similar to chloroform, but cheaper; toxic on prolonged exposure
24
Dual processing action of Tetrahydrofuran as a clearing agent is
Dehydrates and clears at the same time since it is miscible in both water and paraffin
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Features and usage of Methyl Benzoate / Methyl Salicylate are
Slow-acting clearing agents that can be used when double embedding techniques are required
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Alternative term (AKA) for Impregnation is
Infiltration
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Definition of Impregnation (Infiltration) is
The process whereby the clearing agent is completely removed from the tissue and replaced by a medium that will fill all natural cavities, spaces, and interstices of the tissues, setting to a sufficiently firm consistency for cutting thin sections
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Ideal volume ratio of impregnating medium to tissue specimen is
At least 25x the volume of the tissue
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Three general methods of impregnation used in histology are
1. Paraffin wax impregnation, 2. Celloidin (Collodion) impregnation, 3. Gelatin impregnation
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Simplest, most common, and best routine impregnation medium is
Paraffin wax impregnation
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Melting point range for standard paraffin wax used for impregnation is
54-58°C
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Protocol for Manual Processing paraffin wax impregnation is
Requires at least 4 changes of wax with 15 minutes interval
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Mechanism of Automatic Processing (e.g., Autotechnicon) is
Makes use of an automatic tissue processing machine which fixes, dehydrates, clears, and infiltrates tissues, decreasing time and labor
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Principles and pressure conditions for Vacuum Embedding are
Impregnation under negative atmospheric pressure using a vacuum of up to 760 mmHg applied via a water or mechanical pump
35
Tissue indications for Vacuum Embedding are
Recommended for urgent biopsies and delicate tissues such as lung, brain, connective tissues, decalcified bones, eyes, spleen, and CNS
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Time reduction achieved by Vacuum Embedding is
Reduces 25-75% of impregnation time
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Melting point and composition of Paraplast are
MP: 56-57°C; mixture of highly purified paraffin wax and synthetic plastic polymers, more elastic and resilient than paraffin
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Melting point and properties of Embeddol are
MP: 56-58°C; synthetic wax substitute similar to paraplast, less brittle and less compressible than paraplast
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Melting point and tissue application for Bioloid are
MP: 38-42°C or 45-56°C (Ester wax: 46-48°C); semisynthetic wax recommended for embedding eyes
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Solubility characteristics of Ester Wax are
Harder than paraffin, not soluble in water, but soluble in 95% ethyl alcohol and other clearing agents
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Composition and properties of Water Soluble Waxes (Carbowax) are
Mostly polyethylene glycols; solid at room temperature, soluble in water (does not require dehydration/clearing), suitable for enzyme histochemical studies
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Tissue outcome caused by infiltration in overheated paraffin (above 60°C) is
Produces shrinkage and hardening of tissues
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Temperature maintenance requirement for a paraffin oven is
Maintained at a temperature 2-5°C above the melting point of the wax
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Effect of reused wax containing water on tissue blocks and its remedy are
Impairs impregnating capacity and prevents formation of a good tissue block; remedied by heating wax to 100-105°C to evaporate water
45
Maximum usage limit for paraffin wax before replacing with fresh wax is
Paraffin wax may be used only twice
46
Definition and chemical nature of Celloidin are
Purified form of nitrocellulose soluble in many solvents
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Tissue indications for Celloidin impregnation include
Specimens containing large cavities or hollow spaces which tend to collapse, hard/dense tissues (bones and teeth), large tissue sections of whole embryos, and whole organs like eyes
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Major advantage of Celloidin over paraffin wax is
Causes much less shrinkage and distortion than paraffin wax
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Disadvantages of Celloidin impregnation include
1. Slow and tedious, 2. Serial sections are difficult to prepare, 3. Very thin sections (<10 µm) are difficult to cut
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Tissue indications and cutting conditions for the Wet Celloidin Method are
Recommended for bones, teeth, large brain sections, and whole organs; tissues must be cut wet (knife & block kept moist with 70% alcohol)
51
Tissue indications and block composition of the Dry Celloidin Method are
Preferred for processing whole eye sections; uses Gilson's mixture (equal parts chloroform and cedarwood oil) in block, allowing cutting without alcohol
52
Solvent mixture used to dissolve Low Viscosity Nitrocellulose (L.V.N.) is
Soluble in equal concentration of Ether and Alcohol
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Primary conditions where Gelatin Impregnation is utilized are
Rarely used except when dehydration is to be avoided and when tissues are to be subjected to histochemical and enzyme studies
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Specimen types for which Gelatin impregnation is specifically indicated are
Delicate specimens and frozen tissue sections (prevents fragmentation of tough and friable tissues)
55
Solubility and melting point properties of Gelatin as an impregnating medium are
Water soluble (does not require dehydration and clearing), low melting point so it does not overharden tissue
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