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SOLUBILITY
PRESENTED BY:-              GUIDED BY:-
TARUN POKHARIYAL             MISS. STUTI SINGH
M.PHARM.(PHARMACEUTICS)      JAIPUR NATIONAL
JAIPUR NATIONAL UNIVERSITY UNIVERSITY (JAIPUR)
JAIPUR
                 DATE- 29 AUG 2011
CONTENTS
 INTRODUCTION
 EXPRESSION OF SOLUBILITY
 MECHENISM OF SOLUBILITY
 SOLVENTS FOR SOLUBILISATION
 SOLUBILITY SYSTEM
 FACTORS AFFECTING SOLUBILITY
 APPROCHES OF SOLUBILITY ENHANCEMENT
 REFERENCES
INTRODUCTION:-PROPERTY OF A SOLID, LIQUID
  OR GAS TO DISSOLVE IN SOLID, LIQUID OR GAS.
o IN QUANTITATIVE TERM
o IN QUALITATIVE TARM


EXPRESSION OF SOLUBILITY:-
  ACCORDING TO USP AS NUMBER OF MILILETRES OF
SOLVENT IN WHICH 1 GRAM OF SOLUTE WILL DISSOLVE
TERMS USED              PART OF SOLVENT
                        REQUIRED FOR ONE PART
                        OF SOLUTE
VERY SOLUBLE            LESS THAN 1 PART
FREELY SOLUBLE          1-10 PARTS
SOLUBLE                 10-30 PARTS
SPARINGLY SOLUBLE       30-100 PARTS
SLIGHTLY SOLUBLE        100-1000 PARTS
VERY SLIGHTLY SOLUBLE   1000-10000
PRACTICAL Y             MORE THAN 10000
INSOLUBLE/INSOLUBLE
OTHER TERMS TO EXPRESS THE SOLUBILITY:-
1. MOLARITY
2. MOLALITY
3. %




RELATED TERMS OF SOLUBILITY:-
1. SATURATED SOLUTION
2. SUBSATURATED SOLUTION
3. SUPERSATURATED SOLUTION
SOLUBILITY CAN BE DESCRIBED BY THE GIBBS
PHASE RULE AS FOLLOW:-


             F=C-P+2
WHERE
F= NO. OF DEGREE FREEDOM
C=SMALLEST NO. OF COMPONENT THAT
   DESCRIBE THE CHEMICAL COMPOSITION OF
   EACH PHASE
P=NUMBER OF PHASE
• HILDEBRAND& SCOTT APPROACH:-

SOLVENT POWER OF A LIQUID IS INFLUENCED BY
ITS INTERMOLECULAR COHESIVE FORCES &
THAT THE STRENGTH OF THESE FORCES.
MECHENISM OF SOLUBILITY

SOLUTE –SOLVENT INTERACTION:-       FOR THE
SOLUBILIZATION INTERMOLECULAR FORCES MUST
EXIST.
1.   REPULSIVE AND ATTRACTIVE FORCES
2.   VAN DER WAAL FORCE
3.   ION DIPOLE & ION INDUCED DIPOLE
4.   HYDROGEN BONDS
VAN DER WAAL FORCES:- MOLECULE TEND TO
ALIGN THEMSELVES WITH THEIR NEIGHBOUR SO THAT
NEGATIVE POLE OF ONE MOLECULE POINT TOWARD
THE OPPOSIT

ION DIPOLE AND ION INDUCED DIPOLE:- CATION
ATTRACT THE NEGATIVE OXYGEN ATOM OF WATER
AND ANION ATTRACTING HYDROGEN ATOM OF
WATER MOLECULE
SOLVENTS FOR SOLUBILIZATION:-
• POLAR SOLVENT
• NONPOLAR SOLVENTS
• SEMIPOLAR SOLVENTS
• POLAR SOLVENTS:- THESE DISSOLVE IONIC SOLUTES
    AND OTHER POLAR SUBSTANCES
MECHENISM:-
I. REDUCE FORCE OF ATTRACTION BETWEEN
      OPPOSITELY CHARGED ION IN CRYSTAL.
II. SOLVENTS BREAK COVALENT BONDS OF
      POTENTIALLY STRONG ELECTROLYTE BY ACID BASE
      REACTION
                     HCL+H2O      H3O +CL⁻
III. FINALLY POLAR SOLVENTS ARE CAPABLE OF
     SOLVATING MOLECULES THROUGH DIPOLE
      INTERACTION FORCES WHICH LEAD TO SOLUBILITY
      OF COMPOUND.
• NONPOLAR SOLVENTS:- DISSOLVE NONPOLAR
  SOLUTE WITH SIMILAR INTERNAL PRESSURE
  THROUGH INDUCED DIPOLE INTERACTION.
  eg.oil in benzene

• SEMIPOLAR SOLVENTS:- eg KETONE AND
  ALCOHOL.
  CAN INDUCE CERTAIN DEGREE OF POLARITY IN
   NONPOLAR SOLVENTS.
    eg. ACETONE INCREASE SOLUBILITY OF ETHER IN
        WATER.
 HOLES OPEN IN THE SOLVENT



 MOLECULES OF SOLID BREAK AWAY
 FROM THE BULK

FREE MOLECULES INTEGRATED INTO THE
 HOLE IN SOLVENT
SOLUBILITY OF GASES IN LIQUID:-
                           eg. AMMONIUM
WATER.
       CONC.OF DISSOLVED GAS WHEN IT IS IN
EQUILIBRIUM WITH SOME OF THE PURE GAS ABOVE
THE SOLUTION .


SOLUBILITY OF LIQUIDS IN LIQUIDS:-eg.
ALCOHOL+ WATER=HYDROALCOHOLIC WATER
IDEAL OR REAL SOLUTION:-
           RAOULT’S LAW
                           Pi =pi⁰ Xi
  where,
         pi = partial pressure of component in liquid
         pi⁰= vapor pressure in pure state
          xi= mole fraction of component in
               solution
TWO DEVIATION:-
NEGATIVE DEVIATION:-ADHESIVE ATTRACTION B/W MOLECULE OF
DIFFERENT SPECIES EXCEED THE COHESIVE ATTRACTION B/W LIKE
MOLECULE
POSITIVE DEVIATION:-
TYPES OF LIQUIDS –LIQUIDS SYSTEM:-
(1) COMPLETELY MISCIBLE-WATER AND ALCOHOL
(2) PARTIAL MISCIBLE-PHENOL WATER SYSTEM
(3) TERNERY SYSTEM
             addition of third compound in the pair of partialy
miscible liquid
CONJUGATE SOLUTIONS:-
CONTAIN TWO LIQUIDS WHICH ARE PARTIALLY
MISCIBLE THAN LAYER OF SATURATED SOLUTION
FORMED IN LITTLE AMOUNT ON THE BORDERLINE
Eg PHENOL IN WATER.
CRITICAL SOLUTION TEMP:-
1. UPPER CONSOLUTE TEMP.phenol water
    system(66.8O)
2. LOWER CONSOLUTE TEMP.trietylamine& water
    (18.5)
FACTORS AFFECTING SOLUBILITY:-
1. PARTICLE SIZE
2. TEMPERATURE-SOLID↑ GAS↓
3. PRESSURE
  FOR GAS        HENARY LAW:- C=ớP



C= CONC. OF DISSOLVED GAS
P= PARTIAL PRESSURE
SIGMA= SOLUBILITY CONSTANT
4.NATURE OF THE SOLUTE AND SOLVENT
 eg.1 GM OF LEAD CHLORIDE DISSOLVE IN 100 gm. Of WATER
AT ROOM TEMP. 200GM OF ZINC CHLORIDE CAN DISSOLVE
5.MOLECULAR SIZE:-
6EFFECT OF CHEMICAL REACTION:-. eg. HCL IS
10000 TIMES MORE SOLUBLE IN WATER THAN IS
OXYGEN
7.POLARITY:-
8.POLYMORPH:-
9.SALTING OUT:-
10.pH.:-as pH increase OF SOLUTION THE
QUANTITY OF DRUG IN SOLUTION INCREASE BCZ
THE WATER SOLUBLE IONIZABLE SALT IS FORMED
                 HA↔H+ A-
APPROACHES OF SOLUBILITY ENHANCEMENT:-
PHYSICAL MODIFICATION.
1. PARTICLE SIZE REDUCTION
I.   MICRONIZATION
II. NANO SUSPENSION
2. MODIFICATION OF CRYSTAL HABIT
CRYSTALLINE FORM, AMORPHOUS FORM
ANHYDROUS FORM,HYDRATES
3. DRUG DISPERSION IN CAREEIERS:-
1. EUTECTIC MIXTURE:-poorly soluble drug with
     highly water soluble carrier.eg.urea with
     chloramphanicol
2. SOLID DISPERSION:drug in an inert carrier. Eg
     pvp, polyethylene glycol.
3. SOLID SOLUTION
4.COMPLEXATION:
I. STACHING COMPLEXATION:overlap of planar
     region.
II. INCLUSION COMPLEXATION:insertion of
     nonpolar molecule into host.eg cyclodextrin
5.BY USING SURFACTANTS:-
I. ANIONIC
II. CATIONIC
III. NONIONIC
6. MICROEMULSION:-IS A FOUR COMPONENT
SYSTEM COMPOSED OF EXTERNAL
PHASE,INTERNAL PHASE,SURFACTANT AND
COSURFACTANT
DROPLET DIAMETER 0.1 MICRON
CHEMICAL MODIFICATION:-
1. ADJUST THE PH
2. CHANGE DIELECTRIC CONSTANT
eg.nonionizable and hydrophobic substances
3. USE OF SALT FORM
OTHER TECHNIQUES:-
1.CO-CRYSTALLIZATION- CO-CRYSTALS ARE
CRYSTALLINE MATERIAL THAT CONSIST TWO OR MORE
MOLECULAR (ELECTRICALLY NEUTRAL) SPECIES HELD
TOGETHER BY NON COVALENT FORCES.eg.sacchrin,
nicotinamide ,acetic acid
2. CO-SOLVANCY:-solubilisation of drug into co-
solvent
    weak electrolyte and non nonpolar molecules
have poor water solubility can be improve by altering
 polarity of solvents.
Solubility enhancement as high as 500 fold achieved
using 20% 2-pyrollidone.
3. HYDROTROPHY:-it increase the solubility in
water due to presence of large amount of additives.
eg. sodium benzoate, urea.
4.SOLUBILISING AGENTS:- eg PEG 400
IMPROVES SOLUBILITY OF HYDROCHLORTHIAZIDE
5.NANOTECHNOLOGY APPROACHES:-
1. NANOCRYSTALS:-particle size 1-1000 nm
2. NANOMORPH
REFERENCES
1) PHYSICAL PHARMACY-ALFRED MARTIN
2) REVIEW ARTICLE ( THE PHARMA RESEARCH )
3) ADVANCE PHARMACEUTICS –CHERNG-JUKIM
4) PHYSICAL PHARMACY –DR. SHYAMLA
   BHASKARAN
5) MODERN PHARMACEUTICS-GILBERT S.
   BANKER
6) AULTON’S PHARMACEUTICS- MICHAEL E.
   AULTON
1

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Solubility Factors and Enhancement Techniques

  • 1. SOLUBILITY PRESENTED BY:- GUIDED BY:- TARUN POKHARIYAL MISS. STUTI SINGH M.PHARM.(PHARMACEUTICS) JAIPUR NATIONAL JAIPUR NATIONAL UNIVERSITY UNIVERSITY (JAIPUR) JAIPUR DATE- 29 AUG 2011
  • 2. CONTENTS  INTRODUCTION  EXPRESSION OF SOLUBILITY  MECHENISM OF SOLUBILITY  SOLVENTS FOR SOLUBILISATION  SOLUBILITY SYSTEM  FACTORS AFFECTING SOLUBILITY  APPROCHES OF SOLUBILITY ENHANCEMENT  REFERENCES
  • 3. INTRODUCTION:-PROPERTY OF A SOLID, LIQUID OR GAS TO DISSOLVE IN SOLID, LIQUID OR GAS. o IN QUANTITATIVE TERM o IN QUALITATIVE TARM EXPRESSION OF SOLUBILITY:- ACCORDING TO USP AS NUMBER OF MILILETRES OF SOLVENT IN WHICH 1 GRAM OF SOLUTE WILL DISSOLVE
  • 4. TERMS USED PART OF SOLVENT REQUIRED FOR ONE PART OF SOLUTE VERY SOLUBLE LESS THAN 1 PART FREELY SOLUBLE 1-10 PARTS SOLUBLE 10-30 PARTS SPARINGLY SOLUBLE 30-100 PARTS SLIGHTLY SOLUBLE 100-1000 PARTS VERY SLIGHTLY SOLUBLE 1000-10000 PRACTICAL Y MORE THAN 10000 INSOLUBLE/INSOLUBLE
  • 5. OTHER TERMS TO EXPRESS THE SOLUBILITY:- 1. MOLARITY 2. MOLALITY 3. % RELATED TERMS OF SOLUBILITY:- 1. SATURATED SOLUTION 2. SUBSATURATED SOLUTION 3. SUPERSATURATED SOLUTION
  • 6. SOLUBILITY CAN BE DESCRIBED BY THE GIBBS PHASE RULE AS FOLLOW:- F=C-P+2 WHERE F= NO. OF DEGREE FREEDOM C=SMALLEST NO. OF COMPONENT THAT DESCRIBE THE CHEMICAL COMPOSITION OF EACH PHASE P=NUMBER OF PHASE
  • 7. • HILDEBRAND& SCOTT APPROACH:- SOLVENT POWER OF A LIQUID IS INFLUENCED BY ITS INTERMOLECULAR COHESIVE FORCES & THAT THE STRENGTH OF THESE FORCES.
  • 8. MECHENISM OF SOLUBILITY SOLUTE –SOLVENT INTERACTION:- FOR THE SOLUBILIZATION INTERMOLECULAR FORCES MUST EXIST. 1. REPULSIVE AND ATTRACTIVE FORCES 2. VAN DER WAAL FORCE 3. ION DIPOLE & ION INDUCED DIPOLE 4. HYDROGEN BONDS
  • 9. VAN DER WAAL FORCES:- MOLECULE TEND TO ALIGN THEMSELVES WITH THEIR NEIGHBOUR SO THAT NEGATIVE POLE OF ONE MOLECULE POINT TOWARD THE OPPOSIT ION DIPOLE AND ION INDUCED DIPOLE:- CATION ATTRACT THE NEGATIVE OXYGEN ATOM OF WATER AND ANION ATTRACTING HYDROGEN ATOM OF WATER MOLECULE SOLVENTS FOR SOLUBILIZATION:- • POLAR SOLVENT • NONPOLAR SOLVENTS • SEMIPOLAR SOLVENTS
  • 10. • POLAR SOLVENTS:- THESE DISSOLVE IONIC SOLUTES AND OTHER POLAR SUBSTANCES MECHENISM:- I. REDUCE FORCE OF ATTRACTION BETWEEN OPPOSITELY CHARGED ION IN CRYSTAL. II. SOLVENTS BREAK COVALENT BONDS OF POTENTIALLY STRONG ELECTROLYTE BY ACID BASE REACTION HCL+H2O H3O +CL⁻ III. FINALLY POLAR SOLVENTS ARE CAPABLE OF SOLVATING MOLECULES THROUGH DIPOLE INTERACTION FORCES WHICH LEAD TO SOLUBILITY OF COMPOUND.
  • 11. • NONPOLAR SOLVENTS:- DISSOLVE NONPOLAR SOLUTE WITH SIMILAR INTERNAL PRESSURE THROUGH INDUCED DIPOLE INTERACTION. eg.oil in benzene • SEMIPOLAR SOLVENTS:- eg KETONE AND ALCOHOL. CAN INDUCE CERTAIN DEGREE OF POLARITY IN NONPOLAR SOLVENTS. eg. ACETONE INCREASE SOLUBILITY OF ETHER IN WATER.
  • 12.  HOLES OPEN IN THE SOLVENT  MOLECULES OF SOLID BREAK AWAY FROM THE BULK FREE MOLECULES INTEGRATED INTO THE HOLE IN SOLVENT
  • 13. SOLUBILITY OF GASES IN LIQUID:- eg. AMMONIUM WATER. CONC.OF DISSOLVED GAS WHEN IT IS IN EQUILIBRIUM WITH SOME OF THE PURE GAS ABOVE THE SOLUTION . SOLUBILITY OF LIQUIDS IN LIQUIDS:-eg. ALCOHOL+ WATER=HYDROALCOHOLIC WATER
  • 14. IDEAL OR REAL SOLUTION:- RAOULT’S LAW Pi =pi⁰ Xi where, pi = partial pressure of component in liquid pi⁰= vapor pressure in pure state xi= mole fraction of component in solution TWO DEVIATION:- NEGATIVE DEVIATION:-ADHESIVE ATTRACTION B/W MOLECULE OF DIFFERENT SPECIES EXCEED THE COHESIVE ATTRACTION B/W LIKE MOLECULE POSITIVE DEVIATION:-
  • 15. TYPES OF LIQUIDS –LIQUIDS SYSTEM:- (1) COMPLETELY MISCIBLE-WATER AND ALCOHOL (2) PARTIAL MISCIBLE-PHENOL WATER SYSTEM (3) TERNERY SYSTEM addition of third compound in the pair of partialy miscible liquid CONJUGATE SOLUTIONS:- CONTAIN TWO LIQUIDS WHICH ARE PARTIALLY MISCIBLE THAN LAYER OF SATURATED SOLUTION FORMED IN LITTLE AMOUNT ON THE BORDERLINE Eg PHENOL IN WATER. CRITICAL SOLUTION TEMP:- 1. UPPER CONSOLUTE TEMP.phenol water system(66.8O) 2. LOWER CONSOLUTE TEMP.trietylamine& water (18.5)
  • 16.
  • 17. FACTORS AFFECTING SOLUBILITY:- 1. PARTICLE SIZE 2. TEMPERATURE-SOLID↑ GAS↓ 3. PRESSURE FOR GAS HENARY LAW:- C=ớP C= CONC. OF DISSOLVED GAS P= PARTIAL PRESSURE SIGMA= SOLUBILITY CONSTANT 4.NATURE OF THE SOLUTE AND SOLVENT eg.1 GM OF LEAD CHLORIDE DISSOLVE IN 100 gm. Of WATER AT ROOM TEMP. 200GM OF ZINC CHLORIDE CAN DISSOLVE
  • 18. 5.MOLECULAR SIZE:- 6EFFECT OF CHEMICAL REACTION:-. eg. HCL IS 10000 TIMES MORE SOLUBLE IN WATER THAN IS OXYGEN 7.POLARITY:- 8.POLYMORPH:- 9.SALTING OUT:- 10.pH.:-as pH increase OF SOLUTION THE QUANTITY OF DRUG IN SOLUTION INCREASE BCZ THE WATER SOLUBLE IONIZABLE SALT IS FORMED HA↔H+ A-
  • 19. APPROACHES OF SOLUBILITY ENHANCEMENT:- PHYSICAL MODIFICATION. 1. PARTICLE SIZE REDUCTION I. MICRONIZATION II. NANO SUSPENSION 2. MODIFICATION OF CRYSTAL HABIT CRYSTALLINE FORM, AMORPHOUS FORM ANHYDROUS FORM,HYDRATES 3. DRUG DISPERSION IN CAREEIERS:- 1. EUTECTIC MIXTURE:-poorly soluble drug with highly water soluble carrier.eg.urea with chloramphanicol 2. SOLID DISPERSION:drug in an inert carrier. Eg pvp, polyethylene glycol. 3. SOLID SOLUTION
  • 20. 4.COMPLEXATION: I. STACHING COMPLEXATION:overlap of planar region. II. INCLUSION COMPLEXATION:insertion of nonpolar molecule into host.eg cyclodextrin 5.BY USING SURFACTANTS:- I. ANIONIC II. CATIONIC III. NONIONIC 6. MICROEMULSION:-IS A FOUR COMPONENT SYSTEM COMPOSED OF EXTERNAL PHASE,INTERNAL PHASE,SURFACTANT AND COSURFACTANT DROPLET DIAMETER 0.1 MICRON
  • 21. CHEMICAL MODIFICATION:- 1. ADJUST THE PH 2. CHANGE DIELECTRIC CONSTANT eg.nonionizable and hydrophobic substances 3. USE OF SALT FORM OTHER TECHNIQUES:- 1.CO-CRYSTALLIZATION- CO-CRYSTALS ARE CRYSTALLINE MATERIAL THAT CONSIST TWO OR MORE MOLECULAR (ELECTRICALLY NEUTRAL) SPECIES HELD TOGETHER BY NON COVALENT FORCES.eg.sacchrin, nicotinamide ,acetic acid
  • 22. 2. CO-SOLVANCY:-solubilisation of drug into co- solvent weak electrolyte and non nonpolar molecules have poor water solubility can be improve by altering polarity of solvents. Solubility enhancement as high as 500 fold achieved using 20% 2-pyrollidone. 3. HYDROTROPHY:-it increase the solubility in water due to presence of large amount of additives. eg. sodium benzoate, urea.
  • 23. 4.SOLUBILISING AGENTS:- eg PEG 400 IMPROVES SOLUBILITY OF HYDROCHLORTHIAZIDE 5.NANOTECHNOLOGY APPROACHES:- 1. NANOCRYSTALS:-particle size 1-1000 nm 2. NANOMORPH
  • 24. REFERENCES 1) PHYSICAL PHARMACY-ALFRED MARTIN 2) REVIEW ARTICLE ( THE PHARMA RESEARCH ) 3) ADVANCE PHARMACEUTICS –CHERNG-JUKIM 4) PHYSICAL PHARMACY –DR. SHYAMLA BHASKARAN 5) MODERN PHARMACEUTICS-GILBERT S. BANKER 6) AULTON’S PHARMACEUTICS- MICHAEL E. AULTON
  • 25. 1