Affiliation: Division of Pharmacology, Dept. Of Pharmaceutical Sciences, Birla Institute of Technology, Mesra, Ranchi, Pin - 835 215, India Date Added: 2009-02-02 Date Modified: 2009-02-02 Procedure - After deep ether anesthesia, dissect the rat’s liver (Wistar albino
rats, 200 – 250 g) by cutting on the ventral side.
- Fix 2 – 3 mm. of the liver tissue in neutral buffered formalin (10%
formaldehyde in Phosphate buffered saline) over night.
- After fixation, place the tissues in 70% isopropyl alcohol for 3 hours
and then in each ascending strength (80%, 90%, 100% isopropyl alcohol) for 2
hours each. The amount of alcohol used should be 15 times of the size of the
tissue.
- Then dip the tissues in acetone for a period of 1 – 2 h with periodical
shaking.
- After removing the acetone, add xylene to check for the appearance of
milkyness. If milkyness appears then repeat the dehydration procedure.
- Impregnate the dehydrated tissue in paraffin wax (m.p. = 56°C)
for a period of 1h at 58 – 60 °C.
- Pour the molten paraffin into L-block along with the tissues and allow
it to become hard.
- Section the tissue into very thin (2–8 or 5 – 10 micrometer) sections
using a microtome.
- Mount the tissue on the slides with Mayer’s albumin solution (a mixture
of equal parts of egg white and glycerin, beaten and filtered with the
addition of 1% sodium salicylate) and keep in warm oven for 2 h at 60°C.
- Place slides containing paraffin sections on a slide holder.
- Deparaffinize with Xylene for 20 – 30 minutes and blot the excess xylene.
- Rehydrate the tissue successively with 100%, 90%, 80% isopropyl alcohol
for 2 – 3 min. each and put it into water for 3 min.
- Blot the excess water; put the tissue into Hematoxylin stain for 1 – 2
min.
- Remove it from Hematoxylin stain and then again put it into tap water
for 1 – 2 min.
- Dip the slides containing tissue sections into 1N HCl followed by
Scott’s water ( Sodium Bicarbonate 3.5 g, Magnesium sulphate 20 g, distilled
water 1 litre ) for 1 min each.
- Immerse the tissue in Eosin stain for 30 secs.
- Dehydrate the tissue successively with 80%, 90%, 100% isopropyl alcohol
and finally with Xylene for 20 – 30 min.
- Place coverslip on the slides using one drop of DPX, taking care to
leave no bubbles and dry overnight to make the permanent slide.
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