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Nephelometry and
Turbidimetry
introduction
Turbidimetric + nephlometeric
analysis:
When part of incident radiant energy
is dissipated by absorption,
reflection, and refraction, while the
remainder is transmit light as a
function of the concentration of the
dispersed phase is the basis of
turbidimetric analysis
Nephlometer Turbidimeter
Definition the measurement of the intensity of
scattered light at right angles to the
direction of the incident light as a
function of the concentration of the
dispersed phase ,It is most sensitive
for very dilute suspensions (100
mg/L).
Light passing through a
medium with dispersed
particles, so the intensity of
light transmitted is
measured.
Instrument used Nephlometery machine spectrophotometer
Type of light measured Scattered light Transmitted light
Arrangement of
photometer
Measurement of light scattered at
right angle to the direction of the
propagation of light from the source.
It could be movable detectors which
allow operator to vary the angle of
detection
Measurement is made in the
same direction as the
propagation of the light
from the source.
Clinical uses Ag-Ab rxn, immunocomplex rxn,ppts,
lipoprotein
Ag-Ab rxn, immunocomplex
rxn,ppts, liver dis, protein
in urine or CSF
Nephelometry and
Turbidimetry
Instrumentation:
1- light source:
Tungsten its relatively low intensity makes it
less useful for samples with low light
scattering. Alternatives are:
quartz halogen lamp, xenon lamp and laser
which have higher intensities than tungsten
lamp.
2-lens assembly:
Light enter the sample holder through lens
assembly.
3-there is provision for the insertion of filter
between the sample and source of
light(monochromator).
4- detector (photo –cell):
It is shielded to minimize interference from
stray light.
5-Read out device:
Light intensity is converted to an electrical
signal by the detector .
Example:
The turbidity of a dilute barium sulphate suspension.
The concentration of the reactants must be controlled
by adding pure solid barium chloride of definite grain
size.
-NACL and HCL are added before the precipitation in
order to inhibit the growth of microcrystal of barium
sulphate
-A glycerol ethanol solution helps to stabilise the
turbidity.
The reaction vessels is shaken gently in order to obtain
a uniform particle size.
Each vessel should be shaken at the same rate and the
same number of times.
MEASURMENTS:
1-plug the instrument into ground outlet.
2- choose desirable scale from 0-10
starting with the highest conc. (for std 1=scale
10)
3- turn power switch on.
4-selecte desirable range by range selector at
desirable position .
5- select filter required.
6- transfer your standards in the cleaned cell
and place them in cell holder.
7- remove the standards.
8- fill the second cell with blank to set zero .
9- check the reading of the standards again.
10- measure your unkown.
11- draw calibration curve.
Precaution:
 ..
-Number and size of the particles should remain
constant if repeated preparation are made
-clean cell & filter
- avoid air bubbles (high reading).
-dilute sample if there is need.
-prepare the blank ,standards, Sample at the
same time.(to avoid ppt)
Advantages and disadvantages :
Advantages : rapidity of procedure and
simplicity of the measurements.
Disadvantages: lack of accuracy of the
measurements.
Thankyou!!!

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Nephelometry turbidimetry

  • 2. introduction Turbidimetric + nephlometeric analysis: When part of incident radiant energy is dissipated by absorption, reflection, and refraction, while the remainder is transmit light as a function of the concentration of the dispersed phase is the basis of turbidimetric analysis
  • 3.
  • 4. Nephlometer Turbidimeter Definition the measurement of the intensity of scattered light at right angles to the direction of the incident light as a function of the concentration of the dispersed phase ,It is most sensitive for very dilute suspensions (100 mg/L). Light passing through a medium with dispersed particles, so the intensity of light transmitted is measured. Instrument used Nephlometery machine spectrophotometer Type of light measured Scattered light Transmitted light Arrangement of photometer Measurement of light scattered at right angle to the direction of the propagation of light from the source. It could be movable detectors which allow operator to vary the angle of detection Measurement is made in the same direction as the propagation of the light from the source. Clinical uses Ag-Ab rxn, immunocomplex rxn,ppts, lipoprotein Ag-Ab rxn, immunocomplex rxn,ppts, liver dis, protein in urine or CSF
  • 6. Instrumentation: 1- light source: Tungsten its relatively low intensity makes it less useful for samples with low light scattering. Alternatives are: quartz halogen lamp, xenon lamp and laser which have higher intensities than tungsten lamp. 2-lens assembly: Light enter the sample holder through lens assembly.
  • 7. 3-there is provision for the insertion of filter between the sample and source of light(monochromator). 4- detector (photo –cell): It is shielded to minimize interference from stray light. 5-Read out device: Light intensity is converted to an electrical signal by the detector .
  • 8. Example: The turbidity of a dilute barium sulphate suspension. The concentration of the reactants must be controlled by adding pure solid barium chloride of definite grain size. -NACL and HCL are added before the precipitation in order to inhibit the growth of microcrystal of barium sulphate -A glycerol ethanol solution helps to stabilise the turbidity. The reaction vessels is shaken gently in order to obtain a uniform particle size. Each vessel should be shaken at the same rate and the same number of times.
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  • 10. MEASURMENTS: 1-plug the instrument into ground outlet. 2- choose desirable scale from 0-10 starting with the highest conc. (for std 1=scale 10) 3- turn power switch on. 4-selecte desirable range by range selector at desirable position . 5- select filter required.
  • 11. 6- transfer your standards in the cleaned cell and place them in cell holder. 7- remove the standards. 8- fill the second cell with blank to set zero . 9- check the reading of the standards again. 10- measure your unkown. 11- draw calibration curve.
  • 12. Precaution:  .. -Number and size of the particles should remain constant if repeated preparation are made -clean cell & filter - avoid air bubbles (high reading). -dilute sample if there is need. -prepare the blank ,standards, Sample at the same time.(to avoid ppt)
  • 13. Advantages and disadvantages : Advantages : rapidity of procedure and simplicity of the measurements. Disadvantages: lack of accuracy of the measurements.