3. Introduction
• Lateral flow tests also known as lateral
flow immunochromatographic assays, are
simple devices intended to detect the
presence (or absence) of a target analyte in
sample (matrix) without the need for
specialized and costly equipment
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4. Principal of immunochromatography
kit
• Principal of immunochromatography is the
same as ELISA sandwich method,
only difference is in that immunological
reaction is carried out on the chromato-
graphic paper by capillary action.
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5. • For this system, two kinds of specific antibodies
against antigen are used.
• One of the antibodies is immobilized on
the chromatographic paper
• other is labeled with colloidal gold and
infiltrated into sample pad
• An imunochromatographic unit is completed by
attaching the sample pad at the end of the
membrane.
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6. • Liquid sample is dropped on the sample pad
• The antigen in the sample forms an
immunocomplex with the antibody labeled with
colloidal gold.
• Its complex moves along with the liquid sample
• and makes a contact with the antibody
immobilized on the membrane
• followed by forming an immuno- complex with
the immobilized antibody,
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7. • Resulting in generating a colored red purple
line.
• Appearance of red purple line on the
membrane indicates the presence of antigen
of interest in the sample
• Liquid of the sample migrates through the
membrane very fast, it makes it possible to
detect the presence or absence of antigen
within 15 minutes
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9. Sample pad: Acts as a sponge and holds an excess
of sample fluid. Once soaked, the fluid migrates
to the second element
Conjugate pad:A dried format of bio-active particles
in a salt-sugar matrix that contains everything to
guarantee an optimized chemical reaction
between the target molecule (e.g., an antigen)
and its chemical partner (e.g., antibody) that has
been immobilized on the particle's surface
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10. • Control:It contains an antibody that picks up
free latex/gold in order to confirm the test has
operated correctly.
• Test: It contains a specific capture molecule
and only captures those particles onto which
an analyte molecule has been immobilized
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11. Procedure
• Take an alcohol swab and disinfect the site of
prick.
• Take a pricker and puncture the area below
finger tip.
• Ooze the blood .
• Take two drops with sucker and dispensed in
sample hole of strip.
• Add buffer to sample.
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12. • Wait for 10-15 min
• Observe result and interpret accordingly
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15. Good and Bad of ICTs
• ICTs are a promising tool for reliable level of
diagnostic performance.
• Simple
• Rapid assays that can be completed in 10-15
min.
• They reduce the need for trained examiners
and costly equipment.
• It can be used under harsh field conditions.
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16. • ICT assays are not as sensitive as other
immunoassays
• Note that the results should be confirmed by
other reference tests
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