It is advisable to use an adhesive to promote tissue attachment to the
glass slides used in histological preparation. This is routinely achieved
by the application of a smear of glycerin/albumen mixture to the slide before
the section is mounted and dried. However, this does not always provide a
strong enough bond and the section may become detached from the slide during
the staining procedure. Sections mounted on slides coated by one of the following
methods are much more likely to remain attached during the more "aggressive"
histological techniques. It should be noted that gelatine gives a positive
reaction with some methods and that poly-l-lysine is expensive hence the
routine use of glycerin/albumen. For very fragile sections and some
methods it may be necessary to coat the slide with a protective film of celloidin.
PREPARATION OF POLY - l - LYSINE COATED
SLIDES
Put the slides in racks and wash thoroughly in soapy water, rinse in
tap water and finally rinse in distilled water.
Dilute poly - l - lysine 1:10 in distilled water or allow previously
prepared solution to reach room temperature. (See 5.)
Place racks of slides in the solution leave for 5 mins.
Drain slide racks on blotting paper and either dry at 60oC
for 1 hour (use photographic drying cabinet), or leave to dry for 18 hours
at room temperature covered with foil to keep off dust.
Filter the used poly - l - lysine solution and store at 4oC
for future use. (It is stable for several months. Discard the solution upon
any sign of mould growth). Bring to room temperature before use.
PREPARATION OF GELATINISED SLIDES
Put the slides in racks and wash thoroughly in soapy water, rinse in
tap water and finally rinse in distilled water.
Immerse the slide racks in hot gelatine solution...0.5% gelatine in
distilled water at 60-80oC. Leave for a few seconds for slides
to warm up.
Drain the slide racks on blotting paper and remove excess gelatine
solution by tipping the racks and allowing it to run off the slides.
Dry overnight at 37oC.
Store at room temperature.
PREPARATION OF ORGANOSILANE (AES) TREATED
SLIDES
Put the slides in racks and wash thoroughly in soapy water, rinse in
tap water and finally rinse in distilled water.
Allow the slides to dry completely.
Prepare a 2% solution of 3-aminopropyltriethoxy-silane (AES) in acetone
in a dry staining dish.
Immerse the slides in the AES solution for 2 minutes.
Rinse the slides in two changes of distilled water.
Dry the slides at 37oC for two hours.
Slides may be stored at room temperature.
Note: AES slides can often be used in place of poly-l-lysine
treated slides and are less expensive to prepare.
CELLOIDINIZATION OF SECTIONS
Prepare a 1% solution of celloidin in a mixture of equal parts of ethanol
and ether.
Dewax the sections and rinse in alcohol.
Place the slides in a coplin jar of the celloidin solution and leave
for 5 minutes.
Remove the slides, wipe the backs to remove excess celloidin and place
immediately in 80% alcohol for 5 minutes.
Rinse briefly in water and continue with the chosen technique.
The celloidin film will slowly dissolve in the dehydrating alcohol
step at the end of the method.
If the film proves difficult to remove use a mixture of equal parts
of ethanol and ether.