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 — John Shaqi
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
point has been exceeded, the tissue will have become so brittle as to
crumble before the knife. For the purpose of hardening animal tissues,
the student has at his command two principal agents, namely, alcohol and
chromic acid, each of which possesses advantages of its own, but the use
of each of which is also attended by its own inconveniences. Thus, by
the use of alcohol, there is very much less risk of overhardening the
specimen than if chromic acid had been employed. Alcohol, however,
though a capital indurating agent in some instances, does not answer so
well in many others. Chromic acid is, therefore, to be preferred for
general use. It is, however, a very delicate agent to manage, for unless
the greatest care be taken it is exceedingly likely to overharden
tissues submitted to its action, and when this happens the specimen
becomes utterly useless for cutting, as there is no known means of
removing the extreme brittleness which it has acquired. By taking the
precautions now to be given, this overhardening may generally be
avoided. Let us harden a portion of some viscus, say the kidney, for
instance. Suppose we cut from the organ five or six small pieces (from
half to three-quarters of an inch square, _not larger_). These must be
placed in a mixture of equal parts of methylated spirit and water for
three days, at the end of which period they may be transferred to a
solution of chromic acid, made by dissolving twenty grains of the pure
acid in sixteen ounces of distilled water. The solution should be kept
in a wide-necked bottle furnished with a glass stopper. At the
expiration of seven days, pour off the solution and replace it by fresh.
At the end of another week, carefully examine the immersed tissues, and
by means of a sharp razor see if they have acquired the necessary degree
of hardness to allow of a section of _moderate_ thinness being made. If
so, remove the pieces and put them into a stoppered bottle containing
from six to eight ounces of methylated spirit. If, however, the
hardening be found not to be sufficiently advanced, the chromic acid
solution is to be poured off and again replaced by fresh. It will now be
necessary to examine the tissues at intervals of about two days, until
they are found to be sufficiently hard, when they must be transferred to
the spirit. Under no circumstances, however, should they be permitted to
remain in the chromic acid longer than the end of the third week, and
though they should at this time appear not to have undergone sufficient
induration, yet it will be advisable to transfer them to the methylated
spirit, which in a short time will _safely_ complete the process of
hardening, without any risk being run of the tissue becoming ruinously
brittle. It will be noticed, that when the specimens have been
transferred to spirit, the latter will in a day or two become of a deep
yellow color, whilst a thick flocculent deposit falls to the bottom of
the bottle.
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