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Mr. Sagar Kishor Savale
(Department of pharmaceutics)
avengersagar16@gmail.com
2015-016
4/21/2016 sagar kishor savale 1
CONTENTS
1. INTRODUCTION
2. SURFACTANTS
3. TYPES OF SURFACTANTS
4. HLB SYSTEM
5. ADSORPTION PHENOMENON OF SURFACTANTS
6. PROPERTIES OF SURFACTANTS
7. CRITICAL MICELLE CONCENTRATION
8. APPLICATIONS
9. CONCLUSION
10. REFERENCES
4/21/2016 sagar kishor savale 2
INTRODUCTION
1,2
oSurfactants are known to play a vital role in many processes of
interest in both fundamental and applied science.
oOne important property of surfactants is the formation of colloidal-
sized clusters in solutions, known as micelles.
oMicelles have particular significance in pharmacy because of their
ability to increase the solubility of sparingly soluble substances in
water.
oSurfactants are widely used in molecular biology in formulating new
and in modifying existing medical preparations, in the production of
proprietary medicines, in the production of chemical preparations
aimed for the domestic use, etc.
4/21/2016 sagar kishor savale 3
SURFACTANTS
2
• Hydrophilic- Water loving / Oil hating
• Hydrophobic- Water hating / Oil loving
• Surfactants are amphiphilic molecules composed of a
hydrophilic or polar moiety known as head and a hydrophobic
or nonpolar moiety known as tail.
• The nature and number of polar and nonpolar groups –
Hydrophilic, Lipophillic or somewhere in between.
• Example - Alcohols, Amines and Acids Changes from
hydrophilic to Lipophillic as carbons atoms increasing in their
alkyl chain.
4/21/2016 sagar kishor savale 4
TYPES OF SURFACTANTS
1,2
• Ionic
a. Anionic
1. Fatty acid salts (‘‘soaps’’)
2. Sulfates: Sodium dodecyl sulfate (SDS), ammonium lauryl
sulfate, sodium lauryl ether sulfate (SLES)
3. Ether sulfates: Alkyl ether sulfates
4.Phosphate esters
5. Sulphonates: Alkyl benzene sulphonates
b. Cationic
1. Amine salt
• Alkyl amine salt, Alkyl diamine salt
2.Ammonium Salt
• Alkyl trimethyl ammonium salt
3.Benzalkonium chloride (BAC)
4/21/2016 sagar kishor savale 5
c. Zwitterionic (amphoteric)
1. Quaternary amine group and a carboxyl group containing
surfactant
• Alkyl betaine
• Alkyl imidazoline
2. Quaternary amine group and a sulfonic group containing
surfactant
• Alkyl sulphobetaine
3. Phospholipids surfactant
• Phosphatidyl serine
• Phosphatidyl choline
• Phosphatidyl ethanolamine
4. Carbohydrate-based surfactant
• Alkyl Polyglucoside
• Alkyl Glucamide
4/21/2016 sagar kishor savale 6
• Nonionic
• Alkyl ethoxylate
• Nonylphenolethoxylate
• Amine ethoxylate
• Alkyl poly(ethylene oxide)
HLB SYSTEM1,3
• HLB value – If high -> more polar –> more hydrophilic.
• E.g. polyoxyethelene derivatives of the spans
(Tweens)(9.6-16.7)
• HLB value- If low -> less polar -> more lipophilic.
• E.g. sorbitan esters ( spans)(1.8 -8.6)
4/21/2016 sagar kishor savale 7
4/21/2016 sagar kishor savale 8
 Types of emulsion formation
whether o/w or w/o depends on the
emulsifying agents used.
 O/W- HLB 9-12 – surfactant
Soluble in water
 W/O – HLB 3-6 – surfactant
Insoluble in water
ADSORPTION PHENOMENON OF
SURFACTANTS2
1) Adsorption at liquid-liquid interface-
4/21/2016 sagar kishor savale 9
Fig.-Alignment Of Surfactant At A Liquid-
Liquid Interface
2) Adsorption at liquid-gas interface-
4/21/2016 sagar kishor savale 10
Fig.-Alignment of Surfactant At A Liquid- Gas Surface
Properties of surfactants
1,2
I. Wetting of Solids
II. Solubilization
III. Emulsification
IV. Dispersion of solid in solution
V. Micellization
VI. Detergency
 Wetting of solid-
Three types of wetting phenomena have been described:
1) Adhesional wetting
2) Spreading wetting
3) Immersional wetting.
4/21/2016 sagar kishor savale 11
 Emulsification-
 This is the property of surfactants to form a stable
emulsion of two or more immiscible liquids.
 This is a little like micelle solubilization, but the resultant
solubilizing particles are much bigger.
 Emulsification have following mechanisms-
a) Interfacial tension
b) Interfacial double layer
c) Electrical double layer
Fig.-The Electrical Double Layer At En Oil Water Interface
4/21/2016 sagar kishor savale 12
Micellization-
• A micelle is an aggregate of surfactant molecules dispersed in a
liquid colloid. The process of forming micelle is known as
micellization.
• Micelle formations in polar and non-polar solvent depend on the
concentration of the surfactant in the particular solvent.
CRITICAL MICELLE CONCENTRATION (CMC)
• The concentration of monomer at which the micelles are start
to form in solvent at particular temperature.
• Micelles form only when the concentration of surfactant is
greater than the critical micelle concentration (CMC).
4/21/2016 sagar kishor savale 13
Micelles are divided into three types
2
I. Monomeric micelles-
Fig.-The Formation Of Micelle Form Monomer (Surfactant)
 Individual surfactant molecules that are in the system
but are not part of a micelle are called "monomers."
4/21/2016 sagar kishor savale 14
• In micelle, the hydrophobic tails of several surfactant molecules
assemble into an oil-like core the most stable form of which has
no contact with water.
II. Reverse micelle-
• In a non-polar solvent, the lipophilic "tails" of surfactant
molecules have less contact with water or the exposure of
the hydrophilic head groups to the surrounding solvent that is
energetically unfavorable.
• Therefore, the head groups are pulls at the centre with the
tails extending out called as Inverse Reverse micelle (water-
in-oil micelle).
Fig.- Reverse Micelle
• (In Non Polar Solvent)
4/21/2016 sagar kishor savale 15
III. In polar solvent-
The hydrophilic "heads" of surfactant molecules are always in
contact with the sequestering solvent and the hydrophobic single
tail regions in the micelle centre called normal micelle (oil-in-
water micelle).
4/21/2016 sagar kishor savale 16
Fig.- Micelle In Polar
Solvent
Applications of surfactants
2,3,4
• Liquid systems
i. Formulation of solution
ii. Formulation of suspension
iii. Formulation of emulsions
• Formulation of aerosols
• Formulation of semisolid system
i. Formulation of ointment
ii. Formulation of shampoo
• In naturally occurring surfactants
i. Phospholipids & bile salts
• Antimicrobial activity
4/21/2016 sagar kishor savale 17
Conclusion
• Micelle is very good solution on weakly soluble drug which enhances
their bioavailability.
• Recent work on cancer therapy shows that micelle is a good carrier
for drug used in cancer therapy.
• Micelle doesn’t harm to other system of our body and also having
patient compliances.
• By considering all things, micelle is beneficial in drug delivery
system and more research is expected in future so that this wonderful
phenomena can be used in new drug delivery system.
4/21/2016 18sagar kishor savale
References
• Alfred Martin,James swarbrick,Arthur Cammarata et.al,Varghese
publishing House, 3rd edition,1992,page no-355-384
• www.pharmatutor.org/articles/surfactants&it’s
Application in pharmaceuticals overview.
• C.V.S Subhramanyam, A textbook of Physical pharmaceutics,
Vallabh Prakashan, Second Edition, 2000, page no-128 to 153
• Swarbrick James,Boylan James C. “Encyclopedia of Pharmaceutical
Technology,” 2nd edition (2002), published by Mar cel Dekker,USA.
Page no.-2639-2653
4/21/2016 sagar kishor savale 19
4/21/2016 sagar kishor savale 20

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Surfactant

  • 1. Mr. Sagar Kishor Savale (Department of pharmaceutics) avengersagar16@gmail.com 2015-016 4/21/2016 sagar kishor savale 1
  • 2. CONTENTS 1. INTRODUCTION 2. SURFACTANTS 3. TYPES OF SURFACTANTS 4. HLB SYSTEM 5. ADSORPTION PHENOMENON OF SURFACTANTS 6. PROPERTIES OF SURFACTANTS 7. CRITICAL MICELLE CONCENTRATION 8. APPLICATIONS 9. CONCLUSION 10. REFERENCES 4/21/2016 sagar kishor savale 2
  • 3. INTRODUCTION 1,2 oSurfactants are known to play a vital role in many processes of interest in both fundamental and applied science. oOne important property of surfactants is the formation of colloidal- sized clusters in solutions, known as micelles. oMicelles have particular significance in pharmacy because of their ability to increase the solubility of sparingly soluble substances in water. oSurfactants are widely used in molecular biology in formulating new and in modifying existing medical preparations, in the production of proprietary medicines, in the production of chemical preparations aimed for the domestic use, etc. 4/21/2016 sagar kishor savale 3
  • 4. SURFACTANTS 2 • Hydrophilic- Water loving / Oil hating • Hydrophobic- Water hating / Oil loving • Surfactants are amphiphilic molecules composed of a hydrophilic or polar moiety known as head and a hydrophobic or nonpolar moiety known as tail. • The nature and number of polar and nonpolar groups – Hydrophilic, Lipophillic or somewhere in between. • Example - Alcohols, Amines and Acids Changes from hydrophilic to Lipophillic as carbons atoms increasing in their alkyl chain. 4/21/2016 sagar kishor savale 4
  • 5. TYPES OF SURFACTANTS 1,2 • Ionic a. Anionic 1. Fatty acid salts (‘‘soaps’’) 2. Sulfates: Sodium dodecyl sulfate (SDS), ammonium lauryl sulfate, sodium lauryl ether sulfate (SLES) 3. Ether sulfates: Alkyl ether sulfates 4.Phosphate esters 5. Sulphonates: Alkyl benzene sulphonates b. Cationic 1. Amine salt • Alkyl amine salt, Alkyl diamine salt 2.Ammonium Salt • Alkyl trimethyl ammonium salt 3.Benzalkonium chloride (BAC) 4/21/2016 sagar kishor savale 5
  • 6. c. Zwitterionic (amphoteric) 1. Quaternary amine group and a carboxyl group containing surfactant • Alkyl betaine • Alkyl imidazoline 2. Quaternary amine group and a sulfonic group containing surfactant • Alkyl sulphobetaine 3. Phospholipids surfactant • Phosphatidyl serine • Phosphatidyl choline • Phosphatidyl ethanolamine 4. Carbohydrate-based surfactant • Alkyl Polyglucoside • Alkyl Glucamide 4/21/2016 sagar kishor savale 6
  • 7. • Nonionic • Alkyl ethoxylate • Nonylphenolethoxylate • Amine ethoxylate • Alkyl poly(ethylene oxide) HLB SYSTEM1,3 • HLB value – If high -> more polar –> more hydrophilic. • E.g. polyoxyethelene derivatives of the spans (Tweens)(9.6-16.7) • HLB value- If low -> less polar -> more lipophilic. • E.g. sorbitan esters ( spans)(1.8 -8.6) 4/21/2016 sagar kishor savale 7
  • 8. 4/21/2016 sagar kishor savale 8  Types of emulsion formation whether o/w or w/o depends on the emulsifying agents used.  O/W- HLB 9-12 – surfactant Soluble in water  W/O – HLB 3-6 – surfactant Insoluble in water
  • 9. ADSORPTION PHENOMENON OF SURFACTANTS2 1) Adsorption at liquid-liquid interface- 4/21/2016 sagar kishor savale 9 Fig.-Alignment Of Surfactant At A Liquid- Liquid Interface
  • 10. 2) Adsorption at liquid-gas interface- 4/21/2016 sagar kishor savale 10 Fig.-Alignment of Surfactant At A Liquid- Gas Surface
  • 11. Properties of surfactants 1,2 I. Wetting of Solids II. Solubilization III. Emulsification IV. Dispersion of solid in solution V. Micellization VI. Detergency  Wetting of solid- Three types of wetting phenomena have been described: 1) Adhesional wetting 2) Spreading wetting 3) Immersional wetting. 4/21/2016 sagar kishor savale 11
  • 12.  Emulsification-  This is the property of surfactants to form a stable emulsion of two or more immiscible liquids.  This is a little like micelle solubilization, but the resultant solubilizing particles are much bigger.  Emulsification have following mechanisms- a) Interfacial tension b) Interfacial double layer c) Electrical double layer Fig.-The Electrical Double Layer At En Oil Water Interface 4/21/2016 sagar kishor savale 12
  • 13. Micellization- • A micelle is an aggregate of surfactant molecules dispersed in a liquid colloid. The process of forming micelle is known as micellization. • Micelle formations in polar and non-polar solvent depend on the concentration of the surfactant in the particular solvent. CRITICAL MICELLE CONCENTRATION (CMC) • The concentration of monomer at which the micelles are start to form in solvent at particular temperature. • Micelles form only when the concentration of surfactant is greater than the critical micelle concentration (CMC). 4/21/2016 sagar kishor savale 13
  • 14. Micelles are divided into three types 2 I. Monomeric micelles- Fig.-The Formation Of Micelle Form Monomer (Surfactant)  Individual surfactant molecules that are in the system but are not part of a micelle are called "monomers." 4/21/2016 sagar kishor savale 14
  • 15. • In micelle, the hydrophobic tails of several surfactant molecules assemble into an oil-like core the most stable form of which has no contact with water. II. Reverse micelle- • In a non-polar solvent, the lipophilic "tails" of surfactant molecules have less contact with water or the exposure of the hydrophilic head groups to the surrounding solvent that is energetically unfavorable. • Therefore, the head groups are pulls at the centre with the tails extending out called as Inverse Reverse micelle (water- in-oil micelle). Fig.- Reverse Micelle • (In Non Polar Solvent) 4/21/2016 sagar kishor savale 15
  • 16. III. In polar solvent- The hydrophilic "heads" of surfactant molecules are always in contact with the sequestering solvent and the hydrophobic single tail regions in the micelle centre called normal micelle (oil-in- water micelle). 4/21/2016 sagar kishor savale 16 Fig.- Micelle In Polar Solvent
  • 17. Applications of surfactants 2,3,4 • Liquid systems i. Formulation of solution ii. Formulation of suspension iii. Formulation of emulsions • Formulation of aerosols • Formulation of semisolid system i. Formulation of ointment ii. Formulation of shampoo • In naturally occurring surfactants i. Phospholipids & bile salts • Antimicrobial activity 4/21/2016 sagar kishor savale 17
  • 18. Conclusion • Micelle is very good solution on weakly soluble drug which enhances their bioavailability. • Recent work on cancer therapy shows that micelle is a good carrier for drug used in cancer therapy. • Micelle doesn’t harm to other system of our body and also having patient compliances. • By considering all things, micelle is beneficial in drug delivery system and more research is expected in future so that this wonderful phenomena can be used in new drug delivery system. 4/21/2016 18sagar kishor savale
  • 19. References • Alfred Martin,James swarbrick,Arthur Cammarata et.al,Varghese publishing House, 3rd edition,1992,page no-355-384 • www.pharmatutor.org/articles/surfactants&it’s Application in pharmaceuticals overview. • C.V.S Subhramanyam, A textbook of Physical pharmaceutics, Vallabh Prakashan, Second Edition, 2000, page no-128 to 153 • Swarbrick James,Boylan James C. “Encyclopedia of Pharmaceutical Technology,” 2nd edition (2002), published by Mar cel Dekker,USA. Page no.-2639-2653 4/21/2016 sagar kishor savale 19