Lab 2: Tissue Processing - PowerPoint Presentation

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Lab 2: Tissue Processing

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ObjectivesWhat is tissue processing

?What are the major steps in tissue processing?

Identify

types of fixative

.

The

advantage of each fixative

.

The

disadvantage of each fixative

.

What

chemical or alterations

that can be done to

improve tissue processing

?

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OverviewThose who are unfamiliar with histotechnology often ask, “How does a pathologist look at a biopsy under the microscope and diagnose a disease

? ” The process is long and involved, and each sequential step is completely dependent on the previous one.

The majority of surgical tissue is treated with various reagents

used to preserve tissue elements

(such as

nuclei,

cytoplasm, and tissue morphology

) and

prepare the specimen for paraffin embedding and

microtomy

.

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Cont.Preparing fresh tissue samples for microscopic use has many steps, such as

fixation and processing,

embedding

and

microtomy

,

de-

paraffinization

and staining, and finally cover slipping.

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Tissue ProcessingThe term tissue processing refers to

treatment of the tissue necessary to impregnate it into a solid medium, so that the tissue is rendered sufficiently firm yet elastic for the tissue sections of desirable thickness to be cut on microtome.

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Tissue processing can be performed manually (hand processing), but where multiple specimens have to be dealt with it is more convenient and much more efficient to use an

automated tissue processing machine ( a “tissue processor”).

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Cont.These devices have been available since the 1940’s1 and have slowly evolved to be:

1. Safer

in use

,

2.

handle larger specimen numbers,

3. process

more

quickly,

4. produce

better quality outcomes

.

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Types of processors:The

tissue-transfer (or “dip and dunk”) machines where specimens are transferred from container to container

to be

processed.

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The

fluid-transfer

(

or “enclosed”)

types

where specimens

are held

in

a single process chamber or retort and fluids are pumped in and out as required.

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Histopathological TechniqueHistopathological technique deals with the preparation of tissue for microscopic examination.

The aim of good histological technique to preserve microscopic anatomy of tissue and make them hard, so that very thin section (4 to 5 micron) can be made

.

After staining

, the section should represent the anatomy of the tissue as close to as possible to their structure in life.

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These processes are

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1. FixationThis is the process by which the

constituents of cells and tissue are fixed in a physical and partly also in a chemical state so that they will withstand subsequent

treatment with various reagents with minimum loss of architecture

.

This is achieved by

exposing the tissue to chemical compounds, call fixatives

.

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Mechanism of action of fixativesMost fixatives act by biodegradable enzymes that perform a

proteolysis which then form a sponge or meshwork, tending to hold the other constituents.

Good fixative is most important factors

in the production of satisfactory

results in histopathology

.

No fixative will penetrate a piece of tissue thicker than 1 cm.

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Properties of an Ideal Fixative:1. Prevents autolysis and bacterial decomposition. 2. Preserves tissue in their natural state and fix all components.

3. Make the cellular components insoluble to reagent used in tissue processing.

4. Preserves tissue volume.

5. Avoid excessive hardness of tissue.

6. Allows enhanced staining of tissue.

7. Should be non-toxic and non-allergic for user.

8. Should not be very expensive.

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Factor affecting fixation:1. Size and thickness of piece of tissue. 2. Tissue covered by large amount of mucous fix slowly.

3. The same applies to tissue covered by blood or organ containing very large amount of blood.

4. Fatty and

lipomatous

tissue fix slowly.

5.Correct choice of fixatives.

6. Fixation is accelerated by maintaining temperature around 60C

o

.

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Formaldehyde The most commonly used fixative is formalin

.It is prepared by mixing 40% formaldehyde gas in 100w/v of distilled water.

Routinely,

10% formalin

is used.

Mechanism of action

It forms

cross links between amino acids of protein

thereby making them insoluble.

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Cont.Advantages:1. Rapid penetration.2. Easy availability & cheap.

3. Does not overharden the tissue.

4. Fixes lipids for frozen sections

Disadvantages:

1. Irritant to the nose, the eyes and mucus membranes.

2. Formation of precipitate of

paraformaldehyde which can be prevented by adding methanol.

3. Formation of black formalin pigment, Acid formaldehyde

hematin.

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Alcohol (Ethyl Alcohol)

Absolute alcohol alone has very little place in routine fixation for histopathology.It acts as a

reducing agents

, become

oxidized to acetaldehyde

and then to

acetic acid

.

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Cont.Advantages

:-Alcohol penetrates rapidly in presence of other fixative hence in combination e.g.

Carnoy's

fixative is used to increase the speed of tissue processing

.

-

Ethanol preserves some proteins in relatively

undenatured

state so that it can be used for immunofluorescence or some histochemical methods to detect certain enzymes.-Methyl alcohol is used for fixing blood and bone marrow smears.

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Cont. Disadvantages:

-It is slow to penetrate, hardens and shrinks the tissue.

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AcetoneCold acetone is sometimes used as a fixative for the

histochemical demonstration of some tissue enzymes like

phosphatases

and lipases

.

Its mode of action as fixative is

similar to that of alcohol

.

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Mercuric Chloride (HgCl2)

Advantages: -It penetrates rapidly without destroying lipids.

 

Disadvantages:

-

It causes shrinkage of the tissue if it used alone.

-It brings about precipitation of the proteins.

-It neither fixes nor destroys carbohydrates.

 Note: Treatment of the tissue with mercuric chloride brings out more brilliant staining with most of the dyes.

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Picric acid Advantages: -It penetrates well and fixes rapidly.

Disadvantages:

-It produces marked

cells shrinkage

hence it is not used alone.

-It

precipitates proteins and combines with them to form

picrate's

some of the picrate's

are water-soluble so must be treated with alcohol before further processing where the tissue comes into contact with water.

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Cont. Note: All the tissues fixed in picric acid containing fixatives should be thoroughly washed to remove the yellow discoloration to ensure proper staining of tissue sections.

If the fixative is not removed by washing thoroughly with time even the embedded tissue loses its staining quality.

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Potassium dichromateIt fixes the cytoplasm without precipitation. Valuable in mixtures for the fixation of lipids especially phospholipids. Used for fixing phosphatides and mitochondria.

Note: Thorough washing of the tissue fixed in dichromate is required to avoid forming an oxide in alcohol which cannot be removed later.

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2. DehydrationTissues are dehydrated by using increasing strength of alcohol; e.g. 50%, 70%, 90% and 100%. The duration for which tissues are kept in each

strength of alcohol depends upon the size of tissue,

fixative used and type of tissue

; e.g. after fixation in aqueous fixative delicate tissue need to be dehydrated slowly starting in 50% ethyl alcohol directly whereas most tissue specimens may be put into 70% alcohol.

Delicate tissue

will get

high degree of shrinkage by two great concentration of alcohol

.

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Cont.Note : If the water is one of the fixative components

must be the work of dehydration step after the fixation process while the water was not a contents do not need to perform this step.

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3. ClearingDuring dehydration water in tissue has been replaced by alcohol. The next step alcohol should be

replaced by paraffin wax. As

paraffin wax is not alcohol soluble

, we

replace alcohol with a substance in which wax is soluble

.

This step is call

clearing

.

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Cont.Types of Wax employed for Impregnation:1. Paraffin wax

2. Water soluble wax 3. Other material, like

colloidin

, gelatin,

paraplast

etc.

 

Paraffin wax

is used routinely. It has hard consistency, so section of 7 micron thickness can be cut.

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4. BlockingImpregnated tissues are placed in a mould with their labels and then fresh melted wax is poured in it and allowed to settle and solidify.

Once the block has cooled sufficiently to form a surface skin it should be immersed in cold water to cool it rapidly.

After the block has completely cooled it is

cut into individual blocks and each is trimmed

.

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5. DecalcificationLoss of calcium salts from a bone or tooth OR the process of removing calcareaous matter.

Methods of decalcification:Acid decalcifying agentsIron exchange resins with acid and decalcifying fluids

Electrolytic decalcification

Chelating agents

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Cont. Acid decalcifying agentsThe commonest method of decalcification is dissolving calcium salts in an acid solution.Some of the acid decalcifying agents are (Nitric acid, Formic acid and Trichloroacetic

acid)Iron exchange resins with acid and decalcifying fluidsThe removal of calcium ions from the decalcifying fluid by the resins leads to quicker and more efficient decalcification.

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Cont.Electrolytic decalcificationIt is the speedier decalcification without damage to cytological features and staining.

Chelating agentsEDTA is a chelating agent, it is a white crystalline powder soluble in distilled water to about 20%.As a decalcifying agent it combines with calcium ions to form soluble, non-ionized compound.

The volume of solution for decalcifying should be 150 times that of the tissue.

The solution should be renewed every 5to7 days during decalcification.

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Cont.

Methodology

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GOOD LUCK