The Elements of Bacteriological Technique: A Laboratory Guide for Medical, Dental, and Technical Students. Second Edition Rewritten and Enlarged.Eyre, J. W. H. (John William Henry)
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The Elements of Bacteriological Technique: A Laboratory Guide for Medical, Dental, and Technical Students. Second Edition Rewritten and Enlarged.
Eyre, J. W. H. (John William Henry)
Bacteriology -- Technique
For use in these laboratory methods of diagnosis it is most convenient
to prepare hæmolytic serum specific for human blood--whether the
laboratory is isolated or attached to a large hospital. Ox blood, sheep
blood or goat blood if readily obtainable, may however be used instead,
and although the following method is directed to the preparation of
human hæmolysin the same procedure serves in all cases.
THE PREPARATION OF HÆMOLYTIC SERUM.
_Apparatus Required:_
Small centrifuge, preferably electrically driven, with two
receptacles for tubes, and enclosed in a safety shield (Fig. 162).
Sterile centrifuge tubes (10 c.c. capacity), Fig. 163.
Sterile pipettes (10 c.c. graduated) in case.
Sterile glass capsules (in case).
Sterile test-tubes.
Sterile all glass syringe (5 c.c. or 10 c.c. capacity)
and needle.
[Illustration: FIG. 162.--Small electrical centrifuge.]
[Illustration: FIG. 163.--Centrifuge tube.]
_Reagents Required:_
Normal saline solution.
10 per cent. sodium citrate solution in normal saline.
Human blood (_vide infra_).
METHOD.--
1. Select a healthy full-grown rabbit of not less than 2500 grammes
weight in accordance with the directions already given (page 322) and
prepare it for intraperitoneal inoculation.
2. Measure out 2 c.c. citrated human blood (collected at a surgical
operation or a venesection, or withdrawn by venipuncture from the median
basilic or median cephalic vein of a normal adult) into a centrifuge
tube and centrifugalise thoroughly.
3. Wash with three changes of normal saline (_vide_ also page 388).
4. Transfer the washed cells to a sterile capsule by means of a sterile
pipette. Add 5 c.c. of normal saline and mix thoroughly.
5. Take up the mixture of cells and saline in the all-glass syringe and
inject into the peritoneal cavity of the rabbit.
6. Seven days later inject intraperitoneally the washed cells from 5
c.c. human blood mixed with 5 c.c. normal saline.
7. Seven days later inject the washed cells from 10 c.c. human blood
mixed with 5 c.c. normal saline.
8. After a further interval of seven days repeat the injection of washed
cells from 10 c.c. human blood mixed with 5 c.c. normal saline.
NOTE.--Better results are obtained if the second and
subsequent injections are made intravenously, even when
smaller quantities of washed red cells are employed. If,
however, the intravenous route is selected exceeding great
care must be exercised to avoid the introduction of air into
the vein--an accident which is followed, within a few
minutes, by the death of the rabbit from pulmonary embolism.
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