Section Cutting and Staining: A practical introduction to histological methods for students and practitioners — John Shaqi
Section Cutting and Staining: A practical introduction to histological methods for students and practitionersColman, Walter S.
Science
Section Cutting and Staining: A practical introduction to histological methods for students and practitioners
Colman, Walter S.
Microscopy
*Chromic and nitric fluid.*--This is made as follows:--
Chromic acid 1 gramme 45 grains.
Nitric acid 2 grammes 1-1/2 drachms.
Water 200 c.c. 1 pint.
If the bone is not very compact the fluid may be used diluted with an
equal quantity of water. A large quantity of fluid should be used, and
like all decalcifying fluids, it should be frequently changed.
As soon as the specimen is sufficiently flexible, it should be
thoroughly washed in running water for some hours, and then transferred
to spirit until it is convenient to cut sections.
*Von Ebner’s solution*:--
Hydrochloric acid 1 gramme 1-1/2 drachms.
Common salt 10 grammes 2 ounces.
Water to 100 c.c. 1 pint.
It is a very useful decalcifying agent, but causes the fibrous elements
to swell up rather more than chromic and nitric fluid. A large quantity
of the fluid must be used, and it should be changed daily. It must be
very thoroughly washed out in running water when the decalcification is
completed.
*Bleaching solution* (eau de Javelle).
(1) “Chloride of lime” (bleaching powder) 20 1/2 oz.
Water 100 2-1/2 oz.
Shake up well.
(2) Carbonate of potassium 20 1/2 oz.
Water 100 2-1/2 oz.
Mix the two solutions. Allow them to stand for an hour and filter.
It is used chiefly for clearing vegetable sections but may also be used
for sections containing a large quantity of pigment. It is particularly
useful in decolourizing sections of “madura foot” due to the presence
of a black fungus.
CHAPTER III.
SECTION CUTTING.
*Embedding of sections.*--Before sections are made the tissues require
to be embedded in some fluid, which will permeate their interstices,
and is capable of being rendered firm so as to support the most
delicate parts when the knife passes through the tissue.
The most generally useful substances are:--
(1) gum, (2) celloidin, (3) paraffin or wax.
*Gum.*--_Picked_ colourless gum arabic 2 parts, cold water 3 parts.
Leave with frequent stirring until dissolved. Add ten drops of carbolic
acid to each ounce of the mucilage.
Specimens are thoroughly freed from all trace of the hardening fluid by
washing in water, and the tissue is then placed in the gum solution for
at least twelve hours, or if enough carbolic acid be added, it may be
left there for an indefinite time.
When frozen, gum forms a firm non-crystalline mass, which supports the
tissue on all sides. It must not be frozen too deeply, or it becomes
hard and rather brittle and is apt to injure the razor. If this have
occurred the surface can be softened sufficiently by breathing gently
on it.
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