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Laboratory Rules and Regulation: Brief History of Siwes
Laboratory Rules and Regulation: Brief History of Siwes
Laboratory Rules and Regulation: Brief History of Siwes
IV. Expose student to the kind of work experience they will encounter when they
graduate
V. Expose students to know the operation and function of the instruments involved
in their course of study.
VI. It makes students know how to manage difficult in work when they graduate.
Introduction:
Malaria parasite is a disease caused by a bacteria plasmodium, resulting from the female
mosquito’s bite popularly known as Anopheles mosquito. This mosquito is the carrier of
malaria parasite when she bites an infected person and releases the infected blood into the
blood system of a healthy individual. Malaria parasites are of various types these are:
Plasmodium vivax, Plasmodium malaria, Plasmodium valve and Plasmodium falcipurum.
However, it is a disease prevalent in the continent of Africa and has claimed millions of lives
yearly.
Apparatus: Glass slide leishman’s stain, microscope, distilled water, dropper, blood sample,
lancet or tourniquet and swab.
Procedure:
A drop of patient’s sample collected with sterilized hypodermic syringe is placed on a
glass slide and smeared for film making, which could be thick or thin. After smearing, the
film was allowed to dry, then placed on a stain rack and flooded with leishman’s stain for
about three minutes and diluted with distilled water. The dilution lasted for five (5) minutes
the flooded was washed with clean water and allowed to dry. Then a drop of emission oil was
placed on the film and presence or absence of plasmodium in the patient.
Observation:
The pink, blue or brown spots in the slide shows the presence of malaria parasite in the
patient, and colorless film indicates absence of malaria parasite in the patient.
Conclusion:
Spots or stains in the film confirms malaria parasite in the patient.
Introduction:
This is one of the viral disease and very active indeed. When infected, it attacks the
immune system of a patient and reduces his or her immunity against any infection within or
outside the body.
HIV test is the antibody screening test (imonuassay) which test the antibody that your body
makes against HIV the imonoassay may be performed on blood
The several test are being used more commonly that can detect both antibodies and antigen.
these test can find recent infection earlier than test that detect antibody .these antigen
Antibody combination test can find HIV a soon as 3 weeks after exposure to the virus but is
only available to the blood testing .
HIV can be done by following serial algorithm steps i.e when the first test is positive then
you go to the next step.
Determine
Unigold
HIV
Determine
Negative
Unigold
Positive
Positive
Stat PaK
Negative
Test Result
The cassette has two line (i.e. Test line and Control line). When both two red lines appeared
in the window the result indicates Positive while when only one line appeared, either in the
control line, which indicates Negative.
Introduction:
Urinalysis test is the routine physical chemical and microscopic examination of the
urine, the microscopy has to be observed first, if the urine is pale amber or amber in colour
only. This is done to detect the presence of substance in the urine whose quantity would lead
to diagnosis of certain abnormalities e.g. the specific gravity, protein, glucose ketones,
urobilinogen, Bilirubine, Blood, and PH.
Procedure:
Urine sample collected from the patient in a clean sterile container, immerse test areas of
the strip completely in urine and remove immediately to avoid dissolving of reagents. Tap
excess urine at the edge of the container. Hold the strip in a horizontal position. Compare the
test result with the colour chart on the container label, and it has to be done in a good light.
Record the result.
Observation:
The optional reading time of each test parameters varies from 30 seconds up to 60
seconds, changes in colour that appear black printed on the contain label at the specified time.
This is to measure the volume of the red blood cells (erythrocytes) in the blood.
Apparatus: Capillary tube, EDTA bottles, syringe and needle, hand gloves, centrifuge, blood
samples, cotton wool and tourniquet.
Procedure:
Result:-
Normal range
Male: 47-54%
Female: 36-46%
Children: 40-60%
HEPATITIS TEST
This is by the use of rapid immune chromographic strip embedded specific antigens being
used to detect Hepatitis “B” and “C” in the serum.
Procedure:
Collection of blood sample was made. It’s was transfer into anticoagulant bottle and is
spin it to separate serum from whole blood. The strip is dipped into the patient serum, but not
expects the maximum level. It was allowed to stay for 5 to 10 seconds. Result is read after
band line appeared.
Observation:
One band line on the control line indicates negative result and double band line means
the result is positive.
Introduction:
HB hemoglobin estimation, Hemoglobin is the main transport of oxygen and carbon dioxide
in the blood it is composed of globin a group of amino acid that for a protein and heme which
contains iron atoms and the red pigment, porphyrine. As with Hematocrit, it is an important
determinant of anemia. A protein-iron compound in red blood cells carries oxygen from the
lungs to body cells, the normal levels in the blood are 12 to 16g/dL in woman and 13.5 to
18g/dL in men less than 7g/dL is considered as Anemia.
Procedure: The blood sample was collected from the patient, 0.05 micro litre was dropped
into the cartradge hole and put it in a hemocue machine, for about 2 minutes and count the
percentage of the hemoglobin (blood). When using the tallquist paper, is compeering
analysis. When the amount of blood cross match the colour, then you take your reading from
the matching colour.
Result:
Normal Zone
Normal Zone
Boarder Line
Anemia: Men
Boarder Line to
Normal: Women
Boarder Line
Anemia
Frank Anemia
Frank Anemia
Frank Anemia
Frank Anemia
CHAPTER FOUR
5.1 SUMMARY
Based on the training conducted, this report can be summarized as follows:-
1. The Student Industrial Work Experience Scheme (SIWES) can be seen as the only vital tool
for bridging the gap between the theoretical knowledge and the practical aspect.
2. All analysis conducted on the human body fluid require sound knowledge of the body system
by the professional to ensure accurate data analysis.
3. The report indicate an over view of the various challenges the student may likely encounter in
the course of practicing the chosen professions.
4. During this period, some basic things which ordinarily I would have not been aware of in the
class rooms have been made plain as my doubts are cleared on some issues relating to the
health of man.
5. Through this SIWES practice more experience have been gained far beyond what I learned in
the theory classes, as I moved from theoretical to the practical aspect.
1. CONCLUSION
Having carried out this training successfully, it can be concluded that the SIWES remain the
only medium for completing the theoretical training. Medical laboratory science remain the
only medium of determining the actual cause of illness in the human body before
prescriptions are made.
LIMITATION
Having undergone the four (4) months mandatory SIWES training, it is important to note that
the training was not all-round smooth as there were problems arising from the use of some
laboratory equipment/apparatus, cost of transportation to training site and personal
relationship.
RECOMMENDATION
It is recommended that:
1. Facilities used for the training should be upgraded to modern days equipment so as to aid
better training experience.
2. Also organizations and SIWES should make more effort and work hard in the development
and training of student without difficulty in other to get the standard of education.
3. Fund should be made available to the organization giving SIWES training to enable the
students have access to off-set the cost of transportation in the training site.
REFERENCES:
Baker and Silverton, introduction to Medical Laboratory technology page 6, 31, 293, 335, 339
and 360.
Sarojini .T. Ramlingam (1993) modern bilogy for senior secondary school science series,
New (Ed), published by Africa-Fep Publisher Limited 1993.
Information and Guideline for SIWES, 2002.
Clinical chrmistry, Richard J. Henry, Donal C. Cannan. James W. Winklman, (1974),
2nd Eddition, New York.
Textbook of Medical Physiology, (1996) MC Grawthll Inc.com.panya, 4th Eddition.
Oxford Advance Dictionary (2000) Oxford University Press 6th Eddition
0 CHAPTER THREE
3.1 WATER TREATMENT:
The source of water that is being using in De
–
ShalomPharmaceutical Lab. is
bore hole.
The water is treated in order to get rid of some micro-organism and metals like
magnesium ion (Mg
2+
), Calcium ion (Ca
2+
) etc.
METHOD:
-
The water is pumped from the bore hole into a 1,500Litre surface tank.
-
The first treatment is chlorination (chlorine disinfection) which is done by thea
ddition of 6% De
–
Shalom chlorine solution to the water that has been pumpedinto the surface ta
nk. This is done to make the water microbial free and to introduceoxidation.
-
Add of 100g sodium bicarbonate (Na
2
CO
3
) to soften the water and to shift the pHvalue from acidic towards neutral or ba
sic medium.
-
The water is allowed to pass through sand bed filtration. There are two types o
f sand bed filtration, they are.
1.
Rapid sand bed filtration.2.
Slow sand bed filtration by composite filter.
The water is transferred into the holding tank of 10,000L and then pass throug
hseries of micron filters ranging from 5 micron to 0.5 micron.5micron 2micron
2micron 1micron 0.5microndeionizer
-
The water is passed through the deionizer (an ion exchange resin i.e Na
+
and K
+
exchange resin) which remove all ions except Na
+
and K
+
.
-
The water is then exposed to ultra violet sterilizer so as to screen and to kill an
ymicrobe that may be present.
Water source 1500L Surface tank Sand bed 5micron filter 10000LStorage tank Series
of micron filters ranging from 5micron filter to0.5micronfilter Deionizer with ion e
xchange resin Ultra Violet sterilizer.