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Fluorimetry
Yogeeta
M.Pharma (Ist year)
Pharmacolgy
CONTENT:
• INTRODUCTION
• PRINCIPLE
• FACTORS AFFECTING FLUORESCENCE
• QUENCHING
• INSTRUMENTATION
• APPLICATION
 Introduction of Fluorimetry:
• Absorption of UV/visible radiation causes transition of electrons from
one state to another. (i.e. ground state to excited state).
• At the excited state, electron is not stable, so it emits the energy in
the form radiation to returns to ground state.
• The study of this transition is called as fluorimetry.
Terminology related to state of electrons
• Singlet ground state : A state in which all the electrons in a molecule are
paired.
• Doublet state: A state in which an unpaired electron is present . E.g. free
radical or
• Triplet state: A state in which unpaired electrons of same spin are present
(unpaired and same spin)
• Singlet excited state: A state in which electrons are unpaired but of
opposite spin
 Principle of fluorimetry:
• Fluorescence is the phenomena of emission of radiation when there
is transition from singlet ground state to singlet excited state .
• wavelength of absorbed radiation is called Excitation wavelength
• wavelength of emitted radiation is called Emission wavelength.
• Phosphorescence is also a related phenomenon, which is the study
of emitted radiation when electrons undergo transition from triplet
state to singlet ground state
Jablonski diagram
Electronic transition Effect produced
π → π*
Only absorption but no fluorescence
π → π* (and singlet transition) Fluorescence
π → π*(and triplet transition) Phosphorescence
 Factors affecting Fluorescence:
1. Conjugation (i.e. unsaturated molecule with π electrons)
• So conjugation molecule absorb UV/visible radiation which predominantly
leads to more fluorescence
2. Nature of substituent group
• (electron donating groups like (NH2, OH) enhance fluorescence; whereas
electrons withdrawing groups like (NO2,COOH) reduce fluorescence intensity)
3. Rigidity of structure
• (Rigid structure gives more fluorescence intensity, whereas Flexible structure
gives less fluorescence intensity)
4. Effect of temperature
• increase in temp leads to more collision as a results decrease fluorescence
intensity; & decrease in temp. leads to less collisions and results in increased
fluorescence intensity
5. Viscosity
• increase in viscosity leads to decreased collision of molecule, which leads to
enhancement of fluorescence intensity . Decrease in viscosity causes
increased collision of molecule , which results in decrease fluorescence
intensity.
6. Effect of pH
• eg: aniline in neutral or alkaline medium gives visible fluorescence but in
acidic condition gives fluorescence in UV region only.
7. Oxygen:
It can decrease the fluorescence in two ways:
 it oxidises fluorescent substance to non fluorescent substance
 it quenches (decrease)fluorescence, because of the paramagnetic properties
of molecule energy, as it has triplet ground state
 Quenching:
• Fluorescence quenching is a physicochemical process that lowers the
intensity of emitted light from fluorescent molecules.
• A variety of factors affect fluorescence- due to concentration, pH, pressure of
chemical substance, temperature, viscosity etc.
• Types of Quenching:
Self quenching
Chemical quenching
Static quenching
Collision quenching
1. Static quenching:
• This occurs because of complex formation in molecule(in ground state
that is before excited state)
• Gain property like nonfluorescent for .eg_-caffeine reduces the
fluorescence intensity of riboflavin by complex formation.
2.Collision quenching:
• It results of several factors like presence of halides, heavy metals,
increased temp. and decrease in viscosity, where no. of collisions are
increased. And quenching take place.
3. Chemical Quenching:
It is due to various factors like change in pH, presence of oxygen,
halides and electrons, withdrawing groups, heavy metals etc.
-change in pH: aniline in neutral or alkaline medium gives
visible fluorescence at 290 nm but in acidic condition gives
fluorescence.
-Oxygen: oxidation leads to fluorescent substance to non fluorescent
substance
3. Concentration Quenching or self quenching:
It is a kind of self quenching. It occurs when the concentration of the
fluorescence molecule increases in a sample solution the fluorescence
intensity is reduced in highly concentrated solution
Fluorimetry:
 Instrumentation:
1. Source of light: In Fluorimetry there are mainly three types of lamps are
used
A. Mercury vapour lamp :-
-At high pressure Mercury lamp give 350 nm to 734 nm region radiation.
-At low pressure Mercury vapour give addition line at 254 nm is used as
source in filter type of Fluorimetry.
B. Xenon arc lamp :- It give a more intensity radiation when compared to
Mercury lamp.
C. Tungsten lamp :- when molecule are excited in visible region tungsten
lamp are used.
2. Filter and monochromator: In Fluorimetry there are mainly two filter are
present
-Primary filter :– absorbed visible radiation and transmit uv radiation.
-Secondary filter :– absorbed uv radiation and transmit visible radiation.
Continue…….
• Mainly two monochromator are used in flourimetry.
• Excitation monochromator :– provide a suitable radiation for excited
of molecule.
• Emission monochromator :– Isolates only the radiation emitted by
the flourescent molecule.
3. Sample cell : sample cell are cylindrical or quadrangular
shape. The cell are made up of colour corrected fused glass and
pathlength is normally 10 mm or 1 cm.
Continue….
4. Detector :-
• Mainly photovoltaic cell, Photo multiplier tubes , Photo tube are
used as detector.
• Photo multiplier tubes are the best and accurate.
5. Instruments
• A. Single beam fluorimeter
• B. Double beam fluorimeter
• C. Spectrofluorometer
1. Single beam fluorometer
• Tungsten lamp as source of light.
• The primary filter absorbs visible radiation and transmits UV radiation.
• Emitted radiation measured at 90 degree by secondary filter.
• Secondary filter absorbs UV radiation and transmits visible radiation.
• Advantages
• simple in construction
• Easy to use
• econimical
• Disadvantage:
• It is not possible to use reference solution and sample solution at a time.
• Rapid scanning to obtain excitation and emission spectrum of the compound
is not possible
2. Double beam fluorometer:
• Two incidence beam of light source pass through primary filter
separately and fall on either sample or reference solution.
• The emitted radiation from sample or reference pass separately
through secondary filter.
• Advantages:
• Sample and reference solution can be analysed simultaneously.
• Disadvantage:
• Rapid scanning is not possible due to use of filter.
 Applications:
• Determination of vitamin B1 and B2
• Mainly used in acid base titration:
fluoresce in: colourless - green
quinine sulphate: blue violet
acridine :green –violet
• Pharmaceutical analysis:
compound reagent Excitation
wavelength
fluorescence
hydrocortisone 75%v/v H2So4 460 520
nicotinamide Cyanogen chloride 250 430
• Fluorimetry is employed to carry out both qualitative and
quantitative analyses for various aromatic compounds present in
cigarette smoke, air-pollutant, concentrates, and automobiles
exhaust.
• Measurement of naturally fluorescent compound:
like tyrosine, tryptophan, bilirubin, and vitamins
• Measurement of chemically induced fluorescence:
like chloroquine, heroin, hydrocortisone, isoniazid.
Reference:
• Dr. Ravi Sankar, ‘text book of pharmaceutical Analysis’, Rx
publications, page no. 3.1 to 3.18
• Douglas A Skoog, Principle of instrumental analysis.
• Gurdeep R Chatwal, Instrumental methods of chemical analysis
Thank You…..

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Fluorimetery.

  • 2. CONTENT: • INTRODUCTION • PRINCIPLE • FACTORS AFFECTING FLUORESCENCE • QUENCHING • INSTRUMENTATION • APPLICATION
  • 3.  Introduction of Fluorimetry: • Absorption of UV/visible radiation causes transition of electrons from one state to another. (i.e. ground state to excited state). • At the excited state, electron is not stable, so it emits the energy in the form radiation to returns to ground state. • The study of this transition is called as fluorimetry.
  • 4. Terminology related to state of electrons • Singlet ground state : A state in which all the electrons in a molecule are paired. • Doublet state: A state in which an unpaired electron is present . E.g. free radical or • Triplet state: A state in which unpaired electrons of same spin are present (unpaired and same spin) • Singlet excited state: A state in which electrons are unpaired but of opposite spin
  • 5.  Principle of fluorimetry: • Fluorescence is the phenomena of emission of radiation when there is transition from singlet ground state to singlet excited state . • wavelength of absorbed radiation is called Excitation wavelength • wavelength of emitted radiation is called Emission wavelength. • Phosphorescence is also a related phenomenon, which is the study of emitted radiation when electrons undergo transition from triplet state to singlet ground state
  • 6. Jablonski diagram Electronic transition Effect produced π → π* Only absorption but no fluorescence π → π* (and singlet transition) Fluorescence π → π*(and triplet transition) Phosphorescence
  • 7.  Factors affecting Fluorescence: 1. Conjugation (i.e. unsaturated molecule with π electrons) • So conjugation molecule absorb UV/visible radiation which predominantly leads to more fluorescence 2. Nature of substituent group • (electron donating groups like (NH2, OH) enhance fluorescence; whereas electrons withdrawing groups like (NO2,COOH) reduce fluorescence intensity) 3. Rigidity of structure • (Rigid structure gives more fluorescence intensity, whereas Flexible structure gives less fluorescence intensity)
  • 8. 4. Effect of temperature • increase in temp leads to more collision as a results decrease fluorescence intensity; & decrease in temp. leads to less collisions and results in increased fluorescence intensity 5. Viscosity • increase in viscosity leads to decreased collision of molecule, which leads to enhancement of fluorescence intensity . Decrease in viscosity causes increased collision of molecule , which results in decrease fluorescence intensity. 6. Effect of pH • eg: aniline in neutral or alkaline medium gives visible fluorescence but in acidic condition gives fluorescence in UV region only.
  • 9. 7. Oxygen: It can decrease the fluorescence in two ways:  it oxidises fluorescent substance to non fluorescent substance  it quenches (decrease)fluorescence, because of the paramagnetic properties of molecule energy, as it has triplet ground state
  • 10.  Quenching: • Fluorescence quenching is a physicochemical process that lowers the intensity of emitted light from fluorescent molecules. • A variety of factors affect fluorescence- due to concentration, pH, pressure of chemical substance, temperature, viscosity etc. • Types of Quenching: Self quenching Chemical quenching Static quenching Collision quenching
  • 11. 1. Static quenching: • This occurs because of complex formation in molecule(in ground state that is before excited state) • Gain property like nonfluorescent for .eg_-caffeine reduces the fluorescence intensity of riboflavin by complex formation. 2.Collision quenching: • It results of several factors like presence of halides, heavy metals, increased temp. and decrease in viscosity, where no. of collisions are increased. And quenching take place.
  • 12. 3. Chemical Quenching: It is due to various factors like change in pH, presence of oxygen, halides and electrons, withdrawing groups, heavy metals etc. -change in pH: aniline in neutral or alkaline medium gives visible fluorescence at 290 nm but in acidic condition gives fluorescence. -Oxygen: oxidation leads to fluorescent substance to non fluorescent substance 3. Concentration Quenching or self quenching: It is a kind of self quenching. It occurs when the concentration of the fluorescence molecule increases in a sample solution the fluorescence intensity is reduced in highly concentrated solution
  • 14.  Instrumentation: 1. Source of light: In Fluorimetry there are mainly three types of lamps are used A. Mercury vapour lamp :- -At high pressure Mercury lamp give 350 nm to 734 nm region radiation. -At low pressure Mercury vapour give addition line at 254 nm is used as source in filter type of Fluorimetry. B. Xenon arc lamp :- It give a more intensity radiation when compared to Mercury lamp. C. Tungsten lamp :- when molecule are excited in visible region tungsten lamp are used. 2. Filter and monochromator: In Fluorimetry there are mainly two filter are present -Primary filter :– absorbed visible radiation and transmit uv radiation. -Secondary filter :– absorbed uv radiation and transmit visible radiation.
  • 15. Continue……. • Mainly two monochromator are used in flourimetry. • Excitation monochromator :– provide a suitable radiation for excited of molecule. • Emission monochromator :– Isolates only the radiation emitted by the flourescent molecule. 3. Sample cell : sample cell are cylindrical or quadrangular shape. The cell are made up of colour corrected fused glass and pathlength is normally 10 mm or 1 cm.
  • 16. Continue…. 4. Detector :- • Mainly photovoltaic cell, Photo multiplier tubes , Photo tube are used as detector. • Photo multiplier tubes are the best and accurate. 5. Instruments • A. Single beam fluorimeter • B. Double beam fluorimeter • C. Spectrofluorometer
  • 17. 1. Single beam fluorometer • Tungsten lamp as source of light. • The primary filter absorbs visible radiation and transmits UV radiation. • Emitted radiation measured at 90 degree by secondary filter. • Secondary filter absorbs UV radiation and transmits visible radiation. • Advantages • simple in construction • Easy to use • econimical
  • 18. • Disadvantage: • It is not possible to use reference solution and sample solution at a time. • Rapid scanning to obtain excitation and emission spectrum of the compound is not possible
  • 19.
  • 20. 2. Double beam fluorometer: • Two incidence beam of light source pass through primary filter separately and fall on either sample or reference solution. • The emitted radiation from sample or reference pass separately through secondary filter. • Advantages: • Sample and reference solution can be analysed simultaneously. • Disadvantage: • Rapid scanning is not possible due to use of filter.
  • 21.
  • 22.  Applications: • Determination of vitamin B1 and B2 • Mainly used in acid base titration: fluoresce in: colourless - green quinine sulphate: blue violet acridine :green –violet • Pharmaceutical analysis: compound reagent Excitation wavelength fluorescence hydrocortisone 75%v/v H2So4 460 520 nicotinamide Cyanogen chloride 250 430
  • 23. • Fluorimetry is employed to carry out both qualitative and quantitative analyses for various aromatic compounds present in cigarette smoke, air-pollutant, concentrates, and automobiles exhaust. • Measurement of naturally fluorescent compound: like tyrosine, tryptophan, bilirubin, and vitamins • Measurement of chemically induced fluorescence: like chloroquine, heroin, hydrocortisone, isoniazid.
  • 24. Reference: • Dr. Ravi Sankar, ‘text book of pharmaceutical Analysis’, Rx publications, page no. 3.1 to 3.18 • Douglas A Skoog, Principle of instrumental analysis. • Gurdeep R Chatwal, Instrumental methods of chemical analysis