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EVALUATION SEMINAR
SUBJECT:
     MODERN PHARMACEUTICAL                 ANALYSIS


TOPIC: ELECTROPHORESIS

               Presented by
                 DEVI. S
                   I M. Pharm,
            Department of Pharmaceutics,
                    M.S.R.C.P,
                  Bangalore-54.
CONTENTS
¤ Introduction
¤ Definition and Principle
¤ Theory
¤ Factors affecting the
  migration of ions
¤ Types of electrophoresis
 o   Moving boundary electrophoresis
 o        Zone electrophoresis
INTRODUCTION
 Electrophoresis is a physical method of analysis
  which involves separation of the compounds that
  are capable of acquiring electric charge in
  conducting electrodes.
 ELECTROPHORESIS (Greek word)=BORNE BY ELECTRICITY



 It is a separation technique in which the components are
  separated due to their varying behavior under the
  influence of an applied electric field.
 The technique was pioneered in 1937 by the Swedish
  chemist Arne Tiselius for the separation of proteins.
DEFINITION AND PRINCIPLE
Electrophoresis is defined as the “migration of
  charged molecules under the influence of an
  external electric field”

 In practical terms, a positive (anode) and negative (cathode)
  electrode are placed in a solution containing ions.
 Then, when a voltage is applied across the electrodes, solute
  ions of different charge, i.e., anions (negative) and cations
  (positive), will move through the solution towards the
  electrode of opposite charge.
THEORY
Ion migration velocity can be expressed as:
                V=µeE




The applied field (Fef) (driving force) : Fef=qE
The friction (Ffr) drag is given by: Ffr=6ήπrv
At equilibrium: Fef=Ffr
Therefore: qE=6ήπrv
FACTORS AFFECTING THE MIGRATION OF
IONS
   Factors related to the sample
   Charge
   Size
   Shape
   Properties of electric field
   Potential difference
   Current
   Resistance
   Environmental characteristics
   pH
   Temperature
   Electrolyte concentration
   Composition and nature of supporting medium
   Buffer
   Supporting medium
TYPES OF
    ELECTROPHORESIS
Free solution / frontal / moving boundary
electrophoresis:               supporting medium is absent


Zone electrophoresis: supporting medium is present
1) Paper electrophoresis

2) Gel electrophoresis

3) Capillary electrophoresis

4) Continuous electrophoresis

5) Isotachophoresis

6) Iso electric focusing
MOVING BOUNDARY ELECTROPHORESIS
ZONE ELECTROPHORESIS
  Paper electrophoresis
a) Open strip Paper Electrophoresis




       Horizontal               Vertical
b) Closed strip Paper Electrophoresis




       Horizontal                 Vertical
c. Immersed strip Paper Electrophoresis
                      -   +
            Cooling
            liquid

      Filter paper

      Buffer



d. Enclosed strip Paper Electrophoresis
GEL ELECTROPHORESIS
CAPILLLARY ELECTROPHORESIS
CONTINUOUS ELECTROPHORESIS
ISOTACHOPHORESIS
 Iso-equal , tachos- speed, phoresis-migration
 The technique of Isotachophoresis depends on the
  development of potential gradient.
Principle:
 A leading electrolyte(chloride) with a higher mobility than the
  analytes and a trailing electrolyte(glycinate) with a lower
  mobility are used.
 After application of an electric potential a low electrical field
  is created in the leading electrolyte and a high electrical field
  in the terminating electrolyte.
 The pH at sample level is determined by the counter-ion of
  the leading electrolyte that migrates in the opposite direction.
ISO ELECTRIC FOCUSINNG(IEF)
» Proteins carry both positive and negative charges, which is the PH when
  molecule has no net charge.
» The pH which gives zero net charge is the isoelectric point or pH.
» Generally proteins readily crystallize at the isoelectric point.
» Most of the proteins have isoelectric point of 5-9.
» When electrophoresis is run in a solution buffered at constant PH
  ,   proteins having a net charge will migrate towards the opposite
  electrode so long as the current flows.
» The use of PH gradient across the supporting medium causes each
  protein to migrate to an area of specific PH
» Proteins are found at the point of the gradient where they carry no net
  charge.
» The PH of the protein equals the PH of the gradient, thus resulting in
  sharp well defined protein bands.
REFERENCES
1. Instrumental methods of chemical analysis by B.K. sharma
   pg.no C269-c281.
2. Electrophoresis by Melvin wiley publications.
3. http://en.wikipedia.org/wiki/Electrophoresis.
4. www.pharmainfo.net.
5. Theory of Electrophoresis-K.S. Pitre, Dr. Harisingh Gour
   University, Sagar, India, Encyclopedia of Analytical
   Science.
6. http://books.google.co.in
7. Fundamentals of Analytical chemistry-Skoog (pg.no-1003)
‘winning doesn’t always mean
  being first, means ur doing
  better than you have done
  before’
                    Bonnie
  Blair

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Dev

  • 1. EVALUATION SEMINAR SUBJECT: MODERN PHARMACEUTICAL ANALYSIS TOPIC: ELECTROPHORESIS Presented by DEVI. S I M. Pharm, Department of Pharmaceutics, M.S.R.C.P, Bangalore-54.
  • 2. CONTENTS ¤ Introduction ¤ Definition and Principle ¤ Theory ¤ Factors affecting the migration of ions ¤ Types of electrophoresis o Moving boundary electrophoresis o Zone electrophoresis
  • 3. INTRODUCTION  Electrophoresis is a physical method of analysis which involves separation of the compounds that are capable of acquiring electric charge in conducting electrodes. ELECTROPHORESIS (Greek word)=BORNE BY ELECTRICITY  It is a separation technique in which the components are separated due to their varying behavior under the influence of an applied electric field.  The technique was pioneered in 1937 by the Swedish chemist Arne Tiselius for the separation of proteins.
  • 4. DEFINITION AND PRINCIPLE Electrophoresis is defined as the “migration of charged molecules under the influence of an external electric field”  In practical terms, a positive (anode) and negative (cathode) electrode are placed in a solution containing ions.  Then, when a voltage is applied across the electrodes, solute ions of different charge, i.e., anions (negative) and cations (positive), will move through the solution towards the electrode of opposite charge.
  • 5. THEORY Ion migration velocity can be expressed as: V=µeE The applied field (Fef) (driving force) : Fef=qE The friction (Ffr) drag is given by: Ffr=6ήπrv At equilibrium: Fef=Ffr Therefore: qE=6ήπrv
  • 6. FACTORS AFFECTING THE MIGRATION OF IONS  Factors related to the sample  Charge  Size  Shape  Properties of electric field  Potential difference  Current  Resistance  Environmental characteristics  pH  Temperature  Electrolyte concentration  Composition and nature of supporting medium  Buffer  Supporting medium
  • 7. TYPES OF ELECTROPHORESIS Free solution / frontal / moving boundary electrophoresis: supporting medium is absent Zone electrophoresis: supporting medium is present 1) Paper electrophoresis 2) Gel electrophoresis 3) Capillary electrophoresis 4) Continuous electrophoresis 5) Isotachophoresis 6) Iso electric focusing
  • 9. ZONE ELECTROPHORESIS Paper electrophoresis a) Open strip Paper Electrophoresis Horizontal Vertical b) Closed strip Paper Electrophoresis Horizontal Vertical
  • 10. c. Immersed strip Paper Electrophoresis - + Cooling liquid Filter paper Buffer d. Enclosed strip Paper Electrophoresis
  • 14. ISOTACHOPHORESIS  Iso-equal , tachos- speed, phoresis-migration  The technique of Isotachophoresis depends on the development of potential gradient. Principle:  A leading electrolyte(chloride) with a higher mobility than the analytes and a trailing electrolyte(glycinate) with a lower mobility are used.  After application of an electric potential a low electrical field is created in the leading electrolyte and a high electrical field in the terminating electrolyte.  The pH at sample level is determined by the counter-ion of the leading electrolyte that migrates in the opposite direction.
  • 15.
  • 16. ISO ELECTRIC FOCUSINNG(IEF) » Proteins carry both positive and negative charges, which is the PH when molecule has no net charge. » The pH which gives zero net charge is the isoelectric point or pH. » Generally proteins readily crystallize at the isoelectric point. » Most of the proteins have isoelectric point of 5-9. » When electrophoresis is run in a solution buffered at constant PH , proteins having a net charge will migrate towards the opposite electrode so long as the current flows. » The use of PH gradient across the supporting medium causes each protein to migrate to an area of specific PH » Proteins are found at the point of the gradient where they carry no net charge. » The PH of the protein equals the PH of the gradient, thus resulting in sharp well defined protein bands.
  • 17. REFERENCES 1. Instrumental methods of chemical analysis by B.K. sharma pg.no C269-c281. 2. Electrophoresis by Melvin wiley publications. 3. http://en.wikipedia.org/wiki/Electrophoresis. 4. www.pharmainfo.net. 5. Theory of Electrophoresis-K.S. Pitre, Dr. Harisingh Gour University, Sagar, India, Encyclopedia of Analytical Science. 6. http://books.google.co.in 7. Fundamentals of Analytical chemistry-Skoog (pg.no-1003)
  • 18.
  • 19.
  • 20. ‘winning doesn’t always mean being first, means ur doing better than you have done before’ Bonnie Blair