Section-Cutting: A Practical Guide to the Preparation and Mounting of Sections for the Microscope, Special Prominence Being given to the Subject of Animal SectionsMarsh, Sylvester
Science
Section-Cutting: A Practical Guide to the Preparation and Mounting of Sections for the Microscope, Special Prominence Being given to the Subject of Animal Sections
Marsh, Sylvester
Microscopy; Microscopy -- Technique
As the process just described, however, is both troublesome and tedious,
it is much better for ordinary purposes to have recourse to the
_decalcifying method_, by which means sections in every way suitable for
the examination of the essential structure of bone may be obtained with
ease. To carry out this plan a piece of fresh bone should be cut into
small pieces and placed in a solution made by dissolving 15 grains of
pure chromic acid in 7 ounces of distilled water, to which 30 minims of
nitric acid s. g. 1.420 are afterwards to be added. Here they should
remain for three or four weeks, or until the bone has become
sufficiently soft to cut easily, the fluid being repeatedly changed
during the process. From this solution they must be transferred to
methylated spirit for a few days, when a piece may be selected, imbedded
in paraffine, and cut in the microtome (§ 12). Some of the sections
should be mounted, unstained, in spirit. For this purpose a cell of
gold-size, as above described, must first be prepared and filled _full_
of a mixture of spirit of wine one part, and distilled water three
parts. Into this the section must be carefully placed and the cover
applied, the same precautions for the exclusion of air-bubbles being
taken which were recommended when speaking of mounting in glycerine (§
16). When the cover is in position a ring of gold-size must be laid on,
repeated when dry, and the slide afterwards finished in the ordinary
manner. It will also be advisable to stain some of the sections with
carmine (§ 14), or picro-carmine (§ 42), and mount them in glycerine.
_Teeth_ may also be treated by the decalcifying method, but in this case
it must be remembered that the enamel will dissolve away.
27. _Brain._—The best hardening fluid is that recommended by Rutherford,
and is made by dissolving 15 grains of pure chromic acid and 31 grains
of crystalized bichromate of potash in 43 ounces of distilled water.
Small pieces of brain, which have previously been immersed for
twenty-four hours in rectified spirit, should be placed in about a pint
of this solution, where they must remain for five or six weeks, the
fluid being repeatedly changed during the process. If by this time they
are not sufficiently hard the induration must be completed in alcohol.
Sections are easily cut in the microtome by the paraffine method (§ 12).
These may advantageously be stained in a solution of aniline blue, made
by dissolving 1-1/2 grain of aniline blue in 10 ounces of distilled
water, and adding 1 drachm of rectified spirit (_Frey_). As this stain
acts very rapidly two or three minutes’ immersion will generally be
found long enough. The sections must then be mounted in balsam (§ 23).
Public-domain text, read in full here on John Shaqi.
Reviews
Reviews
No reviews yet
Be the first to share your thoughts on this work.
Join the Discussion
Join the discussion
Sign in to leave a comment or review.
Sign InorCreate an account