SOLUBILIZATION
PRESENTED BY
“SANJAY KUMAR”
DE-073
SUBMITTED TO :
Dr. TAHMINA ADNAN
LECTURER AT HAMDARD
UNIVERSITY,
FACULTY OF PHARMACY
The process whereby something becomes
soluble or more soluble.
Break up of solute-solute
intermolecular bonds.
Break up of solvent-solvent
intermolecular bonds.
Formation of cavity in solvent
phase large enough to
accommodate solute particles.
Transfer of solute into cavity of
solvent phase.
Formation of solute –solvent
intermolecular forces.
o IN QUANTITATIVE WAY:
Concentration of solute ion a saturated solution at a
certain temperature.
o IN QUALITATIVE WAY:
Spontaneous interaction of two or more substances
to form homogenous molecular dispersion
 There are three main factors that control solubility
of a solute.
 Temperature,
 Nature of solute or solvent,
 Pressure.
TEMPERATURE
EXOTHERMIC PROCESS
solubility decreases
with increase in
temperature and vice
versa
ENDOTHERMIC
PROCESS
solubility increases with
increase in temperature
and vice versa.
NATURE OF SOLUTE
AND SOLVENT
A polar solute dissolved in
polar solvent.
Solubility of a non-polar
solute in a solvent is large.
A polar solute has low
solubility or insoluble in a
non-polar solvent
PRESSURE
An increase in pressure
increases of solubility of a gas
in a liquid. The relationship
between pressure and
solubility can be summarized
by combining Le Chatelier's
principle and Henry's Law.
STRUCTURE OF SURFACTANTS
Surfactant molecules are usually
organic compounds that contain
hydrophobic groups or "tails" and
hydrophilic groups or "heads."
Surfactants are chemical species
that act as wetting agents to
lower the surface tension of
a liquid and allow for increased
spread ability
EXAMPLE
Sodium stearate
4-(5-dodecyl) benzenesulfonate
 alkyl ether phosphates
benzalkaonium chloride (BAC)
 There are four types of surfactants.
 Anionic,
 Nonionic,
 Cationic,
 Zwitter (amphoteric) ion.
 Have a negatively charged
end of the molecule that gives it
hydrophilic part .
 These negatively charged
parts of the molecules are
usually sulfonates, sulfates, or
carboxylates .
 Are ionic , made up of two
ions positively charged(metal,
ion )and a negatively
charged(organic ion)
EXAMPLE: sodium alkyl
benzene sulfonates, sodium
stearate (a soap), and
potassium alcohol sulfates
have no ions.
derive their polarity from
having an oxygen rich
portion of the molecule at
one end and a large
organic molecule at the
other end.
EXAMPLE: alcohol
ethoxylates,
nonylphenoxy
polyethylenoxy alcohols,
and ethylene
oxide/propylene oxide
block copolymers
Are positively charged
molecules usually derived from
nitrogen compounds.
Not commonly used as cleaning
agents .
 Many cationic surfactants have
bactericidal or other sanitizing
properties.
Cationic surfactants are usually
incompatible with anionic
surfactants, because they will
react with the negatively charged
anionic surfactant to form an
insoluble or ineffective
compound.
 Change their charge with pH.
 They can be anionic, nonionic,
or cationic depending on pH.
 For the amphoteric
surfactants the charge of the
hydrophilic part is controlled by
the pH of the solution.
They can act as anionic
surfactant in an alkalic solution
or as cationic surfactant in an
acidic solution.
 Are made out of amphipathic molecules.
 A micelle is a ball that forms when amphipathic
molecules are put in a liquid.
 The liquid can be polar like water or non-polar like
butane or octane. Micelles will form because only
one end of the amphipathic molecules will be
compatible with the liquid.
 In the aqueous system the high interfacial energy between
the water molecules and the hydrocarbon chains of the
surfactant is the primary factor in the process, while in a
nonpolar system the attractive interaction between the
polar parts serves as the force governing the association
process.
 The micellization in aqueous solutions may be perceived as
a phase separation that is modified through geometrical
restrictions, while the corresponding phenomenon in oils is
a chemical equilibrium similar to that of alcohols in such
media.
 The consequence of this difference is that the process in
water is highly cooperative and the designation of a critical
micellization concentration (cmc) is justified.
 In the nonpolar environment, on the other hand, the
association process is gradual and the term cmc is not
warranted. In this case the interactions leading to the
micellization are amenable to analysis by spectroscopic
methods.
 Following are three types of micelles
 Spherical micelle,
 Rod shaped micelle,
 Laminar micelle.
 Amphipatic can form bilayers
that sandwich the tails in the
middle, or they can form
spherical micelles.
Phospholipids are amphipathic
molecules that contain two
water-fearing tails.
Phospholipids prefer to form
bilayers.
Fatty acids have only one water-
fearing tail, so forming a micelle is
easier and more stable for them
Monomers are arranged in rod
shape
Rod formation is primarily
governed by the characteristic
Gibbs free energy of rod
formation, ΔG rod.
Geometrically, a rod-shaped
micelle consists of a central
cylindrical part of hydrocarbon
radius r c and of more or less
hemispherical parts at the ends
of hydrocarbon radius r s.
 The model includes
hydrophobic, electrostatic, and
steric interactions.
Are interconvertable.
In this type of micelle
monomers are arranged in
laminar manner.
They are form at higher
concentration.
Initially micelles are of
spherical type but as the
concentration increases
towards higher side leads to
formation of laminar micelle.

solubilization,Solubility and Micelle Formation

  • 1.
    SOLUBILIZATION PRESENTED BY “SANJAY KUMAR” DE-073 SUBMITTEDTO : Dr. TAHMINA ADNAN LECTURER AT HAMDARD UNIVERSITY, FACULTY OF PHARMACY
  • 2.
    The process wherebysomething becomes soluble or more soluble.
  • 3.
    Break up ofsolute-solute intermolecular bonds. Break up of solvent-solvent intermolecular bonds. Formation of cavity in solvent phase large enough to accommodate solute particles. Transfer of solute into cavity of solvent phase. Formation of solute –solvent intermolecular forces.
  • 4.
    o IN QUANTITATIVEWAY: Concentration of solute ion a saturated solution at a certain temperature. o IN QUALITATIVE WAY: Spontaneous interaction of two or more substances to form homogenous molecular dispersion
  • 5.
     There arethree main factors that control solubility of a solute.  Temperature,  Nature of solute or solvent,  Pressure.
  • 6.
    TEMPERATURE EXOTHERMIC PROCESS solubility decreases withincrease in temperature and vice versa ENDOTHERMIC PROCESS solubility increases with increase in temperature and vice versa. NATURE OF SOLUTE AND SOLVENT A polar solute dissolved in polar solvent. Solubility of a non-polar solute in a solvent is large. A polar solute has low solubility or insoluble in a non-polar solvent PRESSURE An increase in pressure increases of solubility of a gas in a liquid. The relationship between pressure and solubility can be summarized by combining Le Chatelier's principle and Henry's Law.
  • 7.
    STRUCTURE OF SURFACTANTS Surfactantmolecules are usually organic compounds that contain hydrophobic groups or "tails" and hydrophilic groups or "heads." Surfactants are chemical species that act as wetting agents to lower the surface tension of a liquid and allow for increased spread ability EXAMPLE Sodium stearate 4-(5-dodecyl) benzenesulfonate  alkyl ether phosphates benzalkaonium chloride (BAC)
  • 8.
     There arefour types of surfactants.  Anionic,  Nonionic,  Cationic,  Zwitter (amphoteric) ion.
  • 9.
     Have anegatively charged end of the molecule that gives it hydrophilic part .  These negatively charged parts of the molecules are usually sulfonates, sulfates, or carboxylates .  Are ionic , made up of two ions positively charged(metal, ion )and a negatively charged(organic ion) EXAMPLE: sodium alkyl benzene sulfonates, sodium stearate (a soap), and potassium alcohol sulfates
  • 10.
    have no ions. derivetheir polarity from having an oxygen rich portion of the molecule at one end and a large organic molecule at the other end. EXAMPLE: alcohol ethoxylates, nonylphenoxy polyethylenoxy alcohols, and ethylene oxide/propylene oxide block copolymers
  • 11.
    Are positively charged moleculesusually derived from nitrogen compounds. Not commonly used as cleaning agents .  Many cationic surfactants have bactericidal or other sanitizing properties. Cationic surfactants are usually incompatible with anionic surfactants, because they will react with the negatively charged anionic surfactant to form an insoluble or ineffective compound.
  • 12.
     Change theircharge with pH.  They can be anionic, nonionic, or cationic depending on pH.  For the amphoteric surfactants the charge of the hydrophilic part is controlled by the pH of the solution. They can act as anionic surfactant in an alkalic solution or as cationic surfactant in an acidic solution.
  • 13.
     Are madeout of amphipathic molecules.  A micelle is a ball that forms when amphipathic molecules are put in a liquid.  The liquid can be polar like water or non-polar like butane or octane. Micelles will form because only one end of the amphipathic molecules will be compatible with the liquid.
  • 14.
     In theaqueous system the high interfacial energy between the water molecules and the hydrocarbon chains of the surfactant is the primary factor in the process, while in a nonpolar system the attractive interaction between the polar parts serves as the force governing the association process.  The micellization in aqueous solutions may be perceived as a phase separation that is modified through geometrical restrictions, while the corresponding phenomenon in oils is a chemical equilibrium similar to that of alcohols in such media.  The consequence of this difference is that the process in water is highly cooperative and the designation of a critical micellization concentration (cmc) is justified.  In the nonpolar environment, on the other hand, the association process is gradual and the term cmc is not warranted. In this case the interactions leading to the micellization are amenable to analysis by spectroscopic methods.
  • 15.
     Following arethree types of micelles  Spherical micelle,  Rod shaped micelle,  Laminar micelle.
  • 16.
     Amphipatic canform bilayers that sandwich the tails in the middle, or they can form spherical micelles. Phospholipids are amphipathic molecules that contain two water-fearing tails. Phospholipids prefer to form bilayers. Fatty acids have only one water- fearing tail, so forming a micelle is easier and more stable for them
  • 17.
    Monomers are arrangedin rod shape Rod formation is primarily governed by the characteristic Gibbs free energy of rod formation, ΔG rod. Geometrically, a rod-shaped micelle consists of a central cylindrical part of hydrocarbon radius r c and of more or less hemispherical parts at the ends of hydrocarbon radius r s.  The model includes hydrophobic, electrostatic, and steric interactions.
  • 18.
    Are interconvertable. In thistype of micelle monomers are arranged in laminar manner. They are form at higher concentration. Initially micelles are of spherical type but as the concentration increases towards higher side leads to formation of laminar micelle.