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Presentation on Penetration
                           enhancers




Dr. Sanjula Baboota                 Abdul Muheem
Deptt of pharmaceutics              M.Pharma(pharmaceutics)
JAMIA HAMDARD                       F/O PHARMACY
                                    JAMIA HAMDARD
Introduction
• Permeation of drugs throughout epithelial
  barriers could be promoted by ‘penetration
  enhencers’capable     of    decreasing   barrier
  properties of the mucosa by different
  mechanisms.
• Enhancement is founded on different techniques
  that are usually divided in chemical or physical
  methods.
Chemical methods-
chemical enhancers are through to improve
absorption without irritation or damage the
mucosa by-
• Alteration the rheology of the mucus layer.
• Transiently altering the lipid bilayer membrane.
• Increasing cell membrane fluidity.
• Extracting structural lipids.
• Altering cellular proteins.
• Increasing the thermodynamics activity of          the
  permeate.
• Overcoming the enzymatic barrier.

-chemical enhancers could be added to a formulation,
alone or in combination ;their efficacy depends on the
physiochemical properties of both the drug & vehicle.
-various chelators ,surfactants, bile salts &fatty acids,
have been used as permeation enhancers ;chitosan & its
derivatives have been used as enhancers of small polar
moiety & hydrophobic large molecules.
 recently lysalbinic acid ,a product of egg albumin
,hydrolysis ,has been successfully used as enhancers for
protein & peptides.
Enzymatic drug inactivation is neither rapid nor extensive
as the enzymatic activity of buccal mucosa is relatively
low .
Nevertheless ,enzymes of the oral cavity could degrades
some peptide & protein drugs
Co- administration of enzyme inhibitors such as aprotinin
,could be effective as they reduce the activity of
proteolytic enzymes.
S.No   Penetration Enhancers     S.No   Penetration Enhancers

1      Aprotinin                 8      Phosphotidyl choline

2      Azone                     9      Polyoxyethylene

3      Lauric acids              10     Sod. Glycocholate

4      Glycol                    11     Sod. Taurocholate

5      Cyclodextrin              12     Sod.glycodeoxycholate

6      Cetyltrimethyl ammonium   13     Sod.EDTA
       bromide
7      Polysrbate 80             14     Sod.taurodeoxycholine
S.N. Drug         Enhancers                 results                  Methods


1    Insulin      Sod.glycocholate          F=0.5%                   Dog in-vivo


2    Glucose      SLS, polysorbate 80       SLS increased the        Rat in-vivo
                                            permeability,
                                            polysorbate 80 less
                                            effective
3    Insulin      5% sod. Glycocholate      Increased F buccal       Rat in vivo
                                            from 0.7% -26%

4    insulin      5% laureth-9,aprotinin,   Increased F from 0.7-    Rat in vivo
                  sod.salicylate            3.6% ,laureth-9 ,other
                                            had no effect
5    Calcitonin   Various bile salts        Increased                Rat in vivo
                                            pharmacologic effect,
                                            increased stability
6    Interferon   1-4% sod.taurocholate     Increased F from         Rat in vivo
                  ,5% cyclodextrin          0.014% to 0.25% with
                                            sod.taurocholate,
                                            other have less effect
Penetration enhencers

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Penetration enhencers

  • 1. Presentation on Penetration enhancers Dr. Sanjula Baboota Abdul Muheem Deptt of pharmaceutics M.Pharma(pharmaceutics) JAMIA HAMDARD F/O PHARMACY JAMIA HAMDARD
  • 2. Introduction • Permeation of drugs throughout epithelial barriers could be promoted by ‘penetration enhencers’capable of decreasing barrier properties of the mucosa by different mechanisms. • Enhancement is founded on different techniques that are usually divided in chemical or physical methods. Chemical methods- chemical enhancers are through to improve absorption without irritation or damage the mucosa by-
  • 3. • Alteration the rheology of the mucus layer. • Transiently altering the lipid bilayer membrane. • Increasing cell membrane fluidity. • Extracting structural lipids. • Altering cellular proteins. • Increasing the thermodynamics activity of the permeate. • Overcoming the enzymatic barrier. -chemical enhancers could be added to a formulation, alone or in combination ;their efficacy depends on the physiochemical properties of both the drug & vehicle.
  • 4.
  • 5. -various chelators ,surfactants, bile salts &fatty acids, have been used as permeation enhancers ;chitosan & its derivatives have been used as enhancers of small polar moiety & hydrophobic large molecules. recently lysalbinic acid ,a product of egg albumin ,hydrolysis ,has been successfully used as enhancers for protein & peptides. Enzymatic drug inactivation is neither rapid nor extensive as the enzymatic activity of buccal mucosa is relatively low . Nevertheless ,enzymes of the oral cavity could degrades some peptide & protein drugs Co- administration of enzyme inhibitors such as aprotinin ,could be effective as they reduce the activity of proteolytic enzymes.
  • 6. S.No Penetration Enhancers S.No Penetration Enhancers 1 Aprotinin 8 Phosphotidyl choline 2 Azone 9 Polyoxyethylene 3 Lauric acids 10 Sod. Glycocholate 4 Glycol 11 Sod. Taurocholate 5 Cyclodextrin 12 Sod.glycodeoxycholate 6 Cetyltrimethyl ammonium 13 Sod.EDTA bromide 7 Polysrbate 80 14 Sod.taurodeoxycholine
  • 7. S.N. Drug Enhancers results Methods 1 Insulin Sod.glycocholate F=0.5% Dog in-vivo 2 Glucose SLS, polysorbate 80 SLS increased the Rat in-vivo permeability, polysorbate 80 less effective 3 Insulin 5% sod. Glycocholate Increased F buccal Rat in vivo from 0.7% -26% 4 insulin 5% laureth-9,aprotinin, Increased F from 0.7- Rat in vivo sod.salicylate 3.6% ,laureth-9 ,other had no effect 5 Calcitonin Various bile salts Increased Rat in vivo pharmacologic effect, increased stability 6 Interferon 1-4% sod.taurocholate Increased F from Rat in vivo ,5% cyclodextrin 0.014% to 0.25% with sod.taurocholate, other have less effect