1
C) Electrical properties
Most surfaces acquire a surface electric charge
when brought into contact with an aqueous
medium due to either ionization of functional
groups on the drug molecules and/or adsorption
of ions to the surface of the particles.
                                                             2
                      Ionization
Surface charge of colloidal particle is controlled by the
 ionization of surface groups
Examples:
 Amino acids & proteins have carboxyl & amino groups
 whose ionization depend on the pH as follow;
NH2-R-COO           NH3-R-COO               NH3-R-COOH
at high pH            zwitter ion               at low pH
alkaline medium      iso-electric point       acidic medium
Negatively charged   zero charge              positively charged
A protein is least soluble at its iso-electric point and is
 readily precipitated
                                                      3
•    Iso electric point:
    1. pH at which +ve charges = -ve charges,
    2. i.e. net charge of the amino acid = zero.
    3. It is a definite pH specific for each protein.
    4. At this pH protein is least soluble&
       precipitated.
Q; How can you precipitate insulin???
By adjusting the pH of the solution to the iso electric point
    of insulin (pH 5.2).
                                                    4
                  Ion adsorption
• Ions may be adsorbed on the surface of the colloidal
  particle following immersion in an aqueous solution
  containing electrolyte.
• In the absence of added electrolytes, preferential
  absorption of hydroxyl ions onto the surface of particles
  will occur.
• Hydronium ions are more hydrated than hydroxyl ions
  and are therefore more likely to remain within the bulk
  medium.
• Surfaces of sol in water are more often –ve charged than
  +ve charged because cations are more hydrated than
  anions so cations reside in the bulk while less hydrated
  anions adsorbed on the surface.
                                                 5
            The electrical double layer
• The charged particles is surrounded by
  an ionic cloud containing charges of
  opposite sign to that of the particles (the
  whole system is electrically neutral)
• Development of a net charge at the
  particle surface affects the distribution of
  ions in the surrounding interfacial region,
• As a result: concentration of counter ions
  increase at the surface,
  Thus, an electrical double layer exists
  around each particle.
                                                 6
     Electro-kinetic phenomenon
• The movement of charged particles with respect to an
 adjacent liquid phase is the base principle underlying
 four electro-kinetic phenomena:
  1. Electrophoresis
  2. Electro-osmosis
  3. Sedimentation potential
  4. Streaming potential
                                                  7
1- Electrophoresis:
The movement of colloidal particles under the influence
    of electric field is called Electrophoresis.
In the electrophoresis cell, when an electric field is
    applied across the colloidal solution, the colloidal
    particles migrate to oppositely charged electrode.
• The velocity of the particles will
  depend on their size and charge.
• Therefore electrophoresis can be
  used to determine size and zeta
  potential of colloidal particles.
• Used generally for separation of
  protein           using         paper
  electrophoresis
                                                          8
1- Electrophoresis:
• The movement rate of protein is dependent on zeta potential,
 molecular size and potential gradient where a mixture of
 proteins can be resolved into separate zones if the mobilities of
 the individual proteins are different
# The electrophoretic mobility of a protein at the iso-electric
 point is zero
2. Electro-osmosis
▪ The opposite in principle to electrophoresis
▪ Is the movement of the liquid with respect to the particles
  under the influence of potential gradient
▪ The dispersion medium itself begins to move in an electric
  field
▪ Also used to determine zeta potential of colloidal particles.
                                                           9
3. Sedimentation potential:
• The reverse of electrophoresis
• The creation of a potential when particles undergo
 sedimentation.
• Also used to determine zeta potential of colloidal
 particles
4. Streaming potential:
▪ The reverse of electro-osmosis
▪ Forcing a liquid to flow through a charged plug or bed of
  particles creates the potential.
▪ Also used to determine zeta potential of colloidal particles
                                                         10
     Pharmaceutical applications of
              colloids
1) Colloidal silver iodide, silver chloride & silver protein are
 effective germicides & not cause irritation as ionic silver
 salts.
2) Colloidal copper used in cancer.
3) Colloidal gold used as diagnostic agent.
4) Colloidal mercury used in syphilis.
5) Association colloids (SAA) are used to increase solubility &
 stability of certain compounds in aqueous & oily
 pharmaceutical preparations e.g. water soluble vitamins A, D
 and K also essential oils and phenols of low water solubility.
                                                      11
     Pharmaceutical applications of
              colloids
6) Efficiency of certain substances is increased when used in
 colloidal form due to large surface area.
 e.g. efficiency of kaolin in adsorbing toxins from GIT.
 e.g. efficiency of aluminum hydroxide as antacid.
7) Blood plasma substitutes as dextran, PVP & gelatin are
 hydrophilic colloids used to restore or maintain blood
 volume.
8) Iron - dextran complex form non-ionic hydrophilic sols
used for treatment of anemia.