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OCULAR DRUG DELIVER SYSTEMS
By
Sai Dhatri Arige
V. V. Institute of Pharmaceutical Sciences
1
CONTENTS
Introduction
Physiology of eye
Diseases of eye
Ocular drug delivery systems
Advantages of ocular drug delivery systems
Conclusion
References
2
INTRODUCTION
These ocular drug delivery systems
were mainly developed to treat eye
locally.
The problem with other dosage forms
is eye irritation ( due to drug particle
size &shape).
It mainly leads to the lacrimation.
3
4
Physiology of Eye
DISEASES OF EYE
Eye is a sensitive sensory organ
which is located on the surface of
the body.
It is easily prone for many injuries
and infections .
Ocular disorders are classified as 2
Types
1 Periocular diseases.
2 Intraocular diseases.
5
I. PERIOCULAR DISEASES
 Conjuctivitis:- Redness of the eye and
the presence of a foreign body.
It is mainly caused due to acute
infection or allergy.
Bacterial conjuctivitis is the other most
common ocular infection.
6
Keratitis:-
It is the condition in which patient feel
decreased vision,ocular pain, red eye and
cloudy/opaque cornea.
It is mainly caused due to bacteria, viruses,
fungi, protozoa and parasites.
7
II. INTRAOCULAR DISEASES
Infection in the inner eye includes
aqueous humor ,iris ,vitreous humor ,
and retina.
These are majorly effects the eye and
also afford the possibility of spread of
infections.
Glaucoma is the common intraocular
disease present in the world.
8
OCULAR DRUG DELIVERY SYSTEMS
Ideal characteristics of ocular drug
delivery system
 It should not induce a foreign body
sensation or long lasting blurring.
 It must possess more local activity
 It must deliver drug to the right place
 It should be easy for self- administration.
OPTHALMIC SOLUTIONS
Viscous solutions and Hydrogels
 Mucoadhesive Formulations
i.Cationic polymers
ii.Anionic polymers
Dispersed system
i.Liposomes
ii.Nanoparticles
Non-erodible ocular insert
Erodible ocular insert
10
VISCOUS SOLUTIONS & HYDROGELS
The principle involved in the formulation
of viscous solutions and hydrogels is
addition of hydrocolloids to aqueous drug
solutions.
Polymers used in these formulations are
cellulose derivatives carbomers
polysaccharides, polyvinyl alcohol and
polyvinyl pyrrolidone.
Gels permit longer residence time in the
precorneal area than viscous solutions. 11
MUCOADHESIVE FORMULATIONS
These are based up on entaglement of non
covalent bonds between polymers and
mucous.
The polymers used in these formulations are
many high molecular weight polymers with
different functional groups like carboxyl,
hydroxyl, aminosulphates which are
capable of forming hydrogen bonds and
they will not crossing biological membrane.
12
Anionic polymers: Sodium alginate,
Poloxamers, Carbomers, Sodium
Carboxy Methyl Cellulose.
Cationic polymers: Chitosan.
These formulation helps in increasing
the residence time of drug in the eye.
13
DISPERSED SYSTEMS
 Lipsomes: The potential advantages
achieved with the liposomes are control of
the rate of encapsulated drug and protection
of the drug from the metabolic enzymes
present at the tear corneal epithelium
interface.
Liposomes are vesicles composed of lipid
membrane enclosing an aqueous volume.
14
NANOPARTICLES
 This approach is considered mainly for the water
soluble drugs. Nanoparticles are particulate drug
delivery systems 10-1000 nm in the size in
which the drug may be dispersed, encapsulated
or absorbed.
 The materials mainly used for the preparation of
ophthalmic nanoparticles are
polyalkylcyanoacrylates.
 The polymers used for the preparation of
ophthalmic nanoparticles are rapidly bio-
degradable.
15
IMPLANTS
Scleral and vitreal implants are
developed for treatment of
endophthalmitis. Implants made from
polylactide/glycolide polymers can result
in drug release over 5-6 month period
without the need for replacement.
Retisert and intravitreal implants are able
to delivers the drug over a period of six
months. 16
ADVANTAGES OF OCULAR DRUG DELIVERY
 Ocular contact time increases.
 Accurate dose is possible.
 Constant and predictable rate of drug
release can be achieved.
 Systematic absorption can be reduced and
side effects can be reduced.
 Shelf life increased
 Better patient compliance
17
CONCLUSION
The novel advanced delivered systems
offer more protective and effective means
of the therapy for all inaccessible diseases
or syndromes of eyes.
These ocular drug delivery has been
established with controlled loading and
sustained release.
18
REFERENCES:
 Controlled drug delivery – Concepts and Advances, by
S.P. Vyas and Roop K. Khar.
 Ansel’s Pharmaceutical dosage forms and drug delivery
systems, by Loyd V. Allen, Nicholas G. Popovich and
Howard c. Ansel.
 Advances in Controlled and Novel drug delivery, edited
by N.K. Jain.
 Textbook of Industrial Pharmacy, edited by Shobharani
R. Hiremath.
 Novel drug delivery systems, by Y.W. Chein, published
by Marcel Dekker, volume 50.
19
20
20

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Ocular drug deliver systems

  • 1. OCULAR DRUG DELIVER SYSTEMS By Sai Dhatri Arige V. V. Institute of Pharmaceutical Sciences 1
  • 2. CONTENTS Introduction Physiology of eye Diseases of eye Ocular drug delivery systems Advantages of ocular drug delivery systems Conclusion References 2
  • 3. INTRODUCTION These ocular drug delivery systems were mainly developed to treat eye locally. The problem with other dosage forms is eye irritation ( due to drug particle size &shape). It mainly leads to the lacrimation. 3
  • 5. DISEASES OF EYE Eye is a sensitive sensory organ which is located on the surface of the body. It is easily prone for many injuries and infections . Ocular disorders are classified as 2 Types 1 Periocular diseases. 2 Intraocular diseases. 5
  • 6. I. PERIOCULAR DISEASES  Conjuctivitis:- Redness of the eye and the presence of a foreign body. It is mainly caused due to acute infection or allergy. Bacterial conjuctivitis is the other most common ocular infection. 6
  • 7. Keratitis:- It is the condition in which patient feel decreased vision,ocular pain, red eye and cloudy/opaque cornea. It is mainly caused due to bacteria, viruses, fungi, protozoa and parasites. 7
  • 8. II. INTRAOCULAR DISEASES Infection in the inner eye includes aqueous humor ,iris ,vitreous humor , and retina. These are majorly effects the eye and also afford the possibility of spread of infections. Glaucoma is the common intraocular disease present in the world. 8
  • 9. OCULAR DRUG DELIVERY SYSTEMS Ideal characteristics of ocular drug delivery system  It should not induce a foreign body sensation or long lasting blurring.  It must possess more local activity  It must deliver drug to the right place  It should be easy for self- administration.
  • 10. OPTHALMIC SOLUTIONS Viscous solutions and Hydrogels  Mucoadhesive Formulations i.Cationic polymers ii.Anionic polymers Dispersed system i.Liposomes ii.Nanoparticles Non-erodible ocular insert Erodible ocular insert 10
  • 11. VISCOUS SOLUTIONS & HYDROGELS The principle involved in the formulation of viscous solutions and hydrogels is addition of hydrocolloids to aqueous drug solutions. Polymers used in these formulations are cellulose derivatives carbomers polysaccharides, polyvinyl alcohol and polyvinyl pyrrolidone. Gels permit longer residence time in the precorneal area than viscous solutions. 11
  • 12. MUCOADHESIVE FORMULATIONS These are based up on entaglement of non covalent bonds between polymers and mucous. The polymers used in these formulations are many high molecular weight polymers with different functional groups like carboxyl, hydroxyl, aminosulphates which are capable of forming hydrogen bonds and they will not crossing biological membrane. 12
  • 13. Anionic polymers: Sodium alginate, Poloxamers, Carbomers, Sodium Carboxy Methyl Cellulose. Cationic polymers: Chitosan. These formulation helps in increasing the residence time of drug in the eye. 13
  • 14. DISPERSED SYSTEMS  Lipsomes: The potential advantages achieved with the liposomes are control of the rate of encapsulated drug and protection of the drug from the metabolic enzymes present at the tear corneal epithelium interface. Liposomes are vesicles composed of lipid membrane enclosing an aqueous volume. 14
  • 15. NANOPARTICLES  This approach is considered mainly for the water soluble drugs. Nanoparticles are particulate drug delivery systems 10-1000 nm in the size in which the drug may be dispersed, encapsulated or absorbed.  The materials mainly used for the preparation of ophthalmic nanoparticles are polyalkylcyanoacrylates.  The polymers used for the preparation of ophthalmic nanoparticles are rapidly bio- degradable. 15
  • 16. IMPLANTS Scleral and vitreal implants are developed for treatment of endophthalmitis. Implants made from polylactide/glycolide polymers can result in drug release over 5-6 month period without the need for replacement. Retisert and intravitreal implants are able to delivers the drug over a period of six months. 16
  • 17. ADVANTAGES OF OCULAR DRUG DELIVERY  Ocular contact time increases.  Accurate dose is possible.  Constant and predictable rate of drug release can be achieved.  Systematic absorption can be reduced and side effects can be reduced.  Shelf life increased  Better patient compliance 17
  • 18. CONCLUSION The novel advanced delivered systems offer more protective and effective means of the therapy for all inaccessible diseases or syndromes of eyes. These ocular drug delivery has been established with controlled loading and sustained release. 18
  • 19. REFERENCES:  Controlled drug delivery – Concepts and Advances, by S.P. Vyas and Roop K. Khar.  Ansel’s Pharmaceutical dosage forms and drug delivery systems, by Loyd V. Allen, Nicholas G. Popovich and Howard c. Ansel.  Advances in Controlled and Novel drug delivery, edited by N.K. Jain.  Textbook of Industrial Pharmacy, edited by Shobharani R. Hiremath.  Novel drug delivery systems, by Y.W. Chein, published by Marcel Dekker, volume 50. 19
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