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RAJGAD DNYANPEETH COLLEGE OF PHARMACY, BHOR, PUNE
(412206)
Presented by :
Pund Suraj Babanrao
M. Pharm 1st Year (Pharmaceutics)
R.D’s, college of Pharmacy, Bhor, Pune
INTRODUCTION
The Buccal mucosa lines the inner cheek
Placed between the upper gingivae and cheek
Treat local and systemic conditions
Typically large, hydrophilic and unstable proteins, oligonucleotides
and polysaccharides
An ideal dosage regimen in the drug
therapy of any disease is the one, which
immediately attains the desired
therapeutic concentration of drug in
plasma (or at the site of action) and
maintains it constant for the entire
duration of treatment
ADVANTAGES
 Avoids first pass effect
 Abundance of blood vessel
 Less hostile environment than GIT
 Ease of administration and termination
 Fast cellular recovery
 Directly & easily modify microenvironment
 Lower intersubject variability as compared to
transdermal patches
Contd…
 Permeability enhancers
 Rapid absorption possible & hence relatively
rapid onset of action
 In comparison to TDDS, mucosal surfaces do
not have a stratum corneum thus, the major
barrier layer is absent
DISADVANTAGES
 Relatively small absorptive surface area (0.01
sq m vs 100 sq m for GIT)
 Movement affects mucoadhesive systems
 Less permeable than the small intestine
 Salivation and swallowing
 Taste of the drug
BUCCAL MUCOSA: ENVIRONMENT
The cells of the oral epithelia are surrounded by
an intercellular ground substance, mucus
The oral cavity is marked by the presence of
saliva produced by the salivary glands
Mucus which is secreted by the major and minor
salivary glands as part of saliva
• Continuous mineralization / demineralization of
the tooth enamel
• Protective fluid for all tissues of the oral cavity
• To hydrate oral mucosal dosage forms
Role of Saliva
• Bioadhesion of mucoadhesive drug delivery
systems
• Made up of proteins and carbohydrates
• Cell-cell adhesion
• Lubrication
Role of Mucus
DRUG DELIVERY PATHWAYS
Two possible routes of drug absorption through
oral mucosa
BUCCAL DRUG DELIVERY AND
MUCOADHESIVITY
Mucoadhesion of the device is a key element
The term ‘mucoadhesive’ is commonly used for
materials that bind to the mucin layer of a
biological membrane
Achieve systemic delivery of drugs include
tablets, patches, tapes, films, semisolids and
powders
BIOADHESIVE DDS
FOR MUCOSAL DRUG DELIVERY
MUCOADHESIVE POLYMERS
GENERAL PHYSIOCHEMICAL FEATURES
Predominantly anionic hydrophilicity with numerous hydrogen
bond-forming groups
Suitable surface property for wetting mucus/mucosal tissue
surfaces and
Sufficient flexibility to penetrate the mucus network or tissue
crevices
POLYMER
Carboxymethyl
cellulose
Carbopol Polycarbophil
Sodium Alginate Hydroxyethyl cellulose Hydroxypropyl
methylcellulose
Chitosan Gelatin Pectin
CONSIDERATION
The drug must resist, or be protected by salivary
and tissue enzymes
The drug and adhesive materials must not
damage the teeth, oral cavity
No keratinolysis, discoloration, and irritation
FACTORS AFFECTING DRUG
DELIVERY VIA BUCCAL ROUTE
 Hydrophilic macromolecules such as peptides,
absorption enhancers have been used
 Smaller molecules greater transport
 No ionized forms have greater transport
 More lipid soluble higher its permeability
 More partition coefficient more permeability
 Lipid-soluble drug stores in Obese individuals
DESIGN OF BUCCAL DOSAGE FORM
Matrix type: The Buccal patch designed in a matrix configuration
contains drug, adhesive, and additives mixed together
Bi-directional patches release drug in both the mucosa and
the mouth
Drug + Mucoadhesive Matrix
………………………………………………………………….
………………………………………………………………….
Contd…
• Reserviour type: The buccal patch designed in a
reservoir system contains a cavity for the drug and
additives separate from the adhesive
Impermeable backing is applied to control the direction of drug
delivery; to reduce patch deformation and disintegration while in
the mouth; and to prevent drug loss
Backing Layer
Drug + Mucoadhesive Matrix
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
BUCCAL MUCOADHESIVE DOSAGE FORMS
Three types based on their geometry
Type-l
• single layer device with multidirectional release
• significant drug loss due to swallowing
Type-ll
• impermeable backing layer is superimposed
• preventing drug loss into the oral cavity
Type-lll
• unidirectional release device, drug loss is minimal
• achieved by coating every face except contact face
BUCCAL FORMULATION
Buccal tablets
• Most commonly investigated
dosage form for Buccal drug
• Tablets are small, flat, and oval,
with a diameter of approximately
5–8 mm
• Tablets can be applied to different
sites in the oral cavity
• Drawback : lack of physical
flexibility, poor patient
compliance
Buccal patches
• laminates consisting of an
impermeable backing layer, a
drug-containing reservoir layer, a
bioadhesive surface for mucosal
attachment
• similar to those used in
transdermal drug delivery
• Backing layer control the
direction of drug release, prevent
drug loss, minimize deformation
and disintegration
Contd…
Buccal films
• Most recently developed dosage
form for Buccal administration
• Preferred over adhesive tablets in
terms of flexibility and comfort
• Flexible, elastic, and soft, yet
adequately strong
• Effective in oral disease
Buccal gels
• Semisolid dosage forms, have the
advantage of easy dispersion
throughout the oral mucosa
• may not be as accurate as from
tablets, patches, or films
• Poor retention of the gels at the
site of application has been
overcome by using bioadhesive
formulations
EXPERIMENTAL METHODOLOGY FOR
BUCCAL PERMEATION STUDIES
EVALUATION
In vitro
Methods
In vivo
Methods
IN VITRO EVALUATION
 Percentage increase in weight
 Swelling properties of films
 Shear stress method
 Folding endurance
 Diffusion study
 Thickness study
IN VIVO EVALUATION
1 2 3 4 5 Intelli Drug Device
ACTIVE INGREDIENTS DELIVERED
VIAA BUCCAL ROUTE
Insulin nicotin nifedipine Flurbiprofen
Acyclovir pindolol oxytocin Diclofenac sodium
Arecoline Propolis Omeprazole Melatonin
Carbamazepine Fluride Danazol Testosterone
Chlorhexidine
diacetate
Metoprolol
tartrate
Chlorhexidine
diacetate
Morphine sulphate
RECENT & FUTURE OF BDDS
 Buccal nitroglycerin, can use for acute therapy for an
anginal attack as well as for chronic prophylaxis
 Novel liquid aerosol formulation of insulin
 Development of suitable delivery devices, permeation
enhancement, and Buccal delivery of drugs that
undergo a first-pass effect, such as cardiovascular
drugs, analgesics, and peptides
 Research yield some successes
 Promote further research; more companies
 Rest depend on delivery technology
CONCLUTION
Buccal drug delivery is a promising area for
systemic delivery of orally inefficient
drugs as well as an attractive alternative
for noninvasive delivery of potent peptide
and perhaps protein drug molecules
REFERENCES
 Michael J Rathbone, in: Oral Mucosal Drug Delivery
 M.S. Wani*, Dr. S.R. Parakh, Dr. M.H. Dehghan, S.A.
Polshettiwar, V.V. Chopade, V.V. Pande, in: Current
Status In Buccal Drug Delivery System: A review
Amir H Shojaei, Faculty of Pharmacy and Pharmaceutical
Sciences, University of Alberta, Edmonton, Alberta,
Canada T6G 2N8, in: Buccal Mucosa As A Route For
Systemic Drug Delivery: A Review
 Yie W. Chien, in: Novel Drug Delivery System
Hitesh R. Patel*, Dr. M.M. Patel, in: Draw Attention
Towards Mucoadhesive Buccal Drug Delivery System
 Bio-Images Research Ltd, in: Applications of gamma
scintigraphy in oral drug delivery
Buccal dds suraj seminar2

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Buccal dds suraj seminar2

  • 1. RAJGAD DNYANPEETH COLLEGE OF PHARMACY, BHOR, PUNE (412206) Presented by : Pund Suraj Babanrao M. Pharm 1st Year (Pharmaceutics) R.D’s, college of Pharmacy, Bhor, Pune
  • 2. INTRODUCTION The Buccal mucosa lines the inner cheek Placed between the upper gingivae and cheek Treat local and systemic conditions Typically large, hydrophilic and unstable proteins, oligonucleotides and polysaccharides
  • 3. An ideal dosage regimen in the drug therapy of any disease is the one, which immediately attains the desired therapeutic concentration of drug in plasma (or at the site of action) and maintains it constant for the entire duration of treatment
  • 4. ADVANTAGES  Avoids first pass effect  Abundance of blood vessel  Less hostile environment than GIT  Ease of administration and termination  Fast cellular recovery  Directly & easily modify microenvironment  Lower intersubject variability as compared to transdermal patches
  • 5. Contd…  Permeability enhancers  Rapid absorption possible & hence relatively rapid onset of action  In comparison to TDDS, mucosal surfaces do not have a stratum corneum thus, the major barrier layer is absent
  • 6. DISADVANTAGES  Relatively small absorptive surface area (0.01 sq m vs 100 sq m for GIT)  Movement affects mucoadhesive systems  Less permeable than the small intestine  Salivation and swallowing  Taste of the drug
  • 7. BUCCAL MUCOSA: ENVIRONMENT The cells of the oral epithelia are surrounded by an intercellular ground substance, mucus The oral cavity is marked by the presence of saliva produced by the salivary glands Mucus which is secreted by the major and minor salivary glands as part of saliva
  • 8. • Continuous mineralization / demineralization of the tooth enamel • Protective fluid for all tissues of the oral cavity • To hydrate oral mucosal dosage forms Role of Saliva • Bioadhesion of mucoadhesive drug delivery systems • Made up of proteins and carbohydrates • Cell-cell adhesion • Lubrication Role of Mucus
  • 9. DRUG DELIVERY PATHWAYS Two possible routes of drug absorption through oral mucosa
  • 10. BUCCAL DRUG DELIVERY AND MUCOADHESIVITY Mucoadhesion of the device is a key element The term ‘mucoadhesive’ is commonly used for materials that bind to the mucin layer of a biological membrane Achieve systemic delivery of drugs include tablets, patches, tapes, films, semisolids and powders
  • 11.
  • 13. MUCOADHESIVE POLYMERS GENERAL PHYSIOCHEMICAL FEATURES Predominantly anionic hydrophilicity with numerous hydrogen bond-forming groups Suitable surface property for wetting mucus/mucosal tissue surfaces and Sufficient flexibility to penetrate the mucus network or tissue crevices
  • 14. POLYMER Carboxymethyl cellulose Carbopol Polycarbophil Sodium Alginate Hydroxyethyl cellulose Hydroxypropyl methylcellulose Chitosan Gelatin Pectin
  • 15. CONSIDERATION The drug must resist, or be protected by salivary and tissue enzymes The drug and adhesive materials must not damage the teeth, oral cavity No keratinolysis, discoloration, and irritation
  • 16. FACTORS AFFECTING DRUG DELIVERY VIA BUCCAL ROUTE  Hydrophilic macromolecules such as peptides, absorption enhancers have been used  Smaller molecules greater transport  No ionized forms have greater transport  More lipid soluble higher its permeability  More partition coefficient more permeability  Lipid-soluble drug stores in Obese individuals
  • 17. DESIGN OF BUCCAL DOSAGE FORM Matrix type: The Buccal patch designed in a matrix configuration contains drug, adhesive, and additives mixed together Bi-directional patches release drug in both the mucosa and the mouth Drug + Mucoadhesive Matrix …………………………………………………………………. ………………………………………………………………….
  • 18. Contd… • Reserviour type: The buccal patch designed in a reservoir system contains a cavity for the drug and additives separate from the adhesive Impermeable backing is applied to control the direction of drug delivery; to reduce patch deformation and disintegration while in the mouth; and to prevent drug loss Backing Layer Drug + Mucoadhesive Matrix ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
  • 19. BUCCAL MUCOADHESIVE DOSAGE FORMS Three types based on their geometry Type-l • single layer device with multidirectional release • significant drug loss due to swallowing Type-ll • impermeable backing layer is superimposed • preventing drug loss into the oral cavity Type-lll • unidirectional release device, drug loss is minimal • achieved by coating every face except contact face
  • 20.
  • 21. BUCCAL FORMULATION Buccal tablets • Most commonly investigated dosage form for Buccal drug • Tablets are small, flat, and oval, with a diameter of approximately 5–8 mm • Tablets can be applied to different sites in the oral cavity • Drawback : lack of physical flexibility, poor patient compliance Buccal patches • laminates consisting of an impermeable backing layer, a drug-containing reservoir layer, a bioadhesive surface for mucosal attachment • similar to those used in transdermal drug delivery • Backing layer control the direction of drug release, prevent drug loss, minimize deformation and disintegration
  • 22. Contd… Buccal films • Most recently developed dosage form for Buccal administration • Preferred over adhesive tablets in terms of flexibility and comfort • Flexible, elastic, and soft, yet adequately strong • Effective in oral disease Buccal gels • Semisolid dosage forms, have the advantage of easy dispersion throughout the oral mucosa • may not be as accurate as from tablets, patches, or films • Poor retention of the gels at the site of application has been overcome by using bioadhesive formulations
  • 23. EXPERIMENTAL METHODOLOGY FOR BUCCAL PERMEATION STUDIES EVALUATION In vitro Methods In vivo Methods
  • 24. IN VITRO EVALUATION  Percentage increase in weight  Swelling properties of films  Shear stress method  Folding endurance  Diffusion study  Thickness study
  • 25. IN VIVO EVALUATION 1 2 3 4 5 Intelli Drug Device
  • 26. ACTIVE INGREDIENTS DELIVERED VIAA BUCCAL ROUTE Insulin nicotin nifedipine Flurbiprofen Acyclovir pindolol oxytocin Diclofenac sodium Arecoline Propolis Omeprazole Melatonin Carbamazepine Fluride Danazol Testosterone Chlorhexidine diacetate Metoprolol tartrate Chlorhexidine diacetate Morphine sulphate
  • 27. RECENT & FUTURE OF BDDS  Buccal nitroglycerin, can use for acute therapy for an anginal attack as well as for chronic prophylaxis  Novel liquid aerosol formulation of insulin  Development of suitable delivery devices, permeation enhancement, and Buccal delivery of drugs that undergo a first-pass effect, such as cardiovascular drugs, analgesics, and peptides  Research yield some successes  Promote further research; more companies  Rest depend on delivery technology
  • 28. CONCLUTION Buccal drug delivery is a promising area for systemic delivery of orally inefficient drugs as well as an attractive alternative for noninvasive delivery of potent peptide and perhaps protein drug molecules
  • 29. REFERENCES  Michael J Rathbone, in: Oral Mucosal Drug Delivery  M.S. Wani*, Dr. S.R. Parakh, Dr. M.H. Dehghan, S.A. Polshettiwar, V.V. Chopade, V.V. Pande, in: Current Status In Buccal Drug Delivery System: A review Amir H Shojaei, Faculty of Pharmacy and Pharmaceutical Sciences, University of Alberta, Edmonton, Alberta, Canada T6G 2N8, in: Buccal Mucosa As A Route For Systemic Drug Delivery: A Review  Yie W. Chien, in: Novel Drug Delivery System Hitesh R. Patel*, Dr. M.M. Patel, in: Draw Attention Towards Mucoadhesive Buccal Drug Delivery System  Bio-Images Research Ltd, in: Applications of gamma scintigraphy in oral drug delivery