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Recent Advancement in
Ocular Drug Delivery System
A Systematic Review
Manshi rana
1st Year
M.Pharm
(Pharmaceutics)
INTRODUCTION
Since its introduction in the field of biomedicine, microtechnology has been making
rapid progress into the realm of pharmaceutical sciences and technology .
It offers completely new opportunities to develop very sophisticated and precise drug
delivery tools .
A significant number of concepts and implemented projects, which is reflected in a
large number of scientific papers, continually pushes pharmaceutical technology to a
new level of coping with various diseases, including those related to the eye.
• Inserts are another form of administration that is possible for ophthalmic
medications.
• their primary purpose is to be inserted into the conjunctival sac. They are made up
of a reservoir for the active substance along with a matrix structure or a film that
controls the rate at which the active ingredient is released.
• Inserts are used less commonly since their application is difficult, they may cause
visual abnormalities, and the feeling of the presence of a foreign body in the eye .
RECENT DEVELOPMENTS IN OCULAR DRUG
DELIVERY SYSTEMS
• Goal - improving the efficacy of drugs administered intraocularly.
Based on the intraocular drug dose increase performed in the HARBOR
and SAVE clinical trials for neovascular AMD, limiting intravitreal
injections has been advocated to decrease the socioeconomic treatment
load.
Aim to summarize
(1) Intraocular pharmacokinetics of current intravitreal drugs.
(2)Efforts to enhance the intraocular pharmacokinetics and pharmacodynamics of
intravitreal drugs: dose escalation of intravitreal drugs, increasing the molecular
weight of intravitreal drug molecules, sustained-release intravitreal implants, micro-
and nanoparticles, hydrogels, combination drug delivery systems, port delivery
systems.
(3) Drug administration routes besides the intravitreal route.
Figure 1: The following is a schematic representation of the many ways of ocular drug administration: (1) the topical route, (2) the subconjunctival route, (3) the suprachoroidal
route with microcannula and microneedle, (4) the subretinal route, and (5) the intravitreal injection and port delivery system.
OCULAR GENE THERAPY
• Gene treatments in this sector have been on the rise over the past few decades,
driven by developments in viral vector technology and discoveries in the
genetic foundation for ocular ailments.
• This trend culminated in the FDA approval of LuxturnaTM in 2017, the first
medicine of its kind to treat ocular conditions using gene therapy.
• This landmark achievement strengthens the research and clinical interests in
gene therapy for a wider variety of ocular illnesses than it had previously. There
are about 350 hereditary ocular illnesses, including a wide variety of genetic
loci, such as retinitis pigmentosa, choroideremia, Stargardt disease, and Leber's
congenital amaurosis (LCA) . Some of these diseases include retinitis
pigmentosa, Stargardt disease, and Leber's congenital amaurosis (LCA).
• The engineering of vectors and the packaging of transgenes have made
significant contributions to the enhancement of transgene expression and
the phenotypic rescue following intraocular administration. Even though
viral vectors have been used successfully in ocular gene therapy, there are
still concerns regarding the heterogeneity of viral genomes throughout the
manufacturing process, as well as packaging capacity and immunological
reactions. In order to circumvent these constraints, non-viral vectors are
currently in the process of being designed for gene therapy.
• In this article, we take a look at the growing corpus of research and clinical
trials that include gene therapy for hereditary and acquired eye illnesses. We
also discuss the recent developments in viral and non-viral vectors that have
been made in this area of research.
OCULAR STRUCTURE & ITS BARRIERS
• The front part known as the anterior segment and the back section known
as the posterior segment, make up the eye.
anterior segment
1. cornea
2. Conjunctiva
3. iris
4. ciliary body
5. crystalline lens
6. aqueous humour
posterior segment
1. sclera
2. choroid
3. Retina
4. vitreous humour
They are the most significant obstacles in the way of ocular medication
administration.
NANO BASED DRUG DELIVERY SYSTEM FOR
GLUCOMA
• Glaucoma is a group of eye diseases that damage the optic nerve,
leading to progressive vision loss and blindness. It is the leading cause
of irreversible blindness globally. To this day, intraocular pressure
(IOP) management is the cornerstone of treatment for glaucoma.
With the aim of reducing intraocular pressure (IOP), there has been a
recent surge in the use of nanocarriers to enhance ocular drug
delivery. This development is particularly significant as the long-term
use of conventional IOP-lowering agents, which are based on poorly
penetrating molecules, can cause frequent ocular toxicity and
intolerance due to their adverse effects on the corneal epithelium.
THANKYOU

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Recent Advancement in Ocular Drug Delivery System.pptx

  • 1. Recent Advancement in Ocular Drug Delivery System A Systematic Review Manshi rana 1st Year M.Pharm (Pharmaceutics)
  • 2. INTRODUCTION Since its introduction in the field of biomedicine, microtechnology has been making rapid progress into the realm of pharmaceutical sciences and technology . It offers completely new opportunities to develop very sophisticated and precise drug delivery tools . A significant number of concepts and implemented projects, which is reflected in a large number of scientific papers, continually pushes pharmaceutical technology to a new level of coping with various diseases, including those related to the eye. • Inserts are another form of administration that is possible for ophthalmic medications. • their primary purpose is to be inserted into the conjunctival sac. They are made up of a reservoir for the active substance along with a matrix structure or a film that controls the rate at which the active ingredient is released. • Inserts are used less commonly since their application is difficult, they may cause visual abnormalities, and the feeling of the presence of a foreign body in the eye .
  • 3. RECENT DEVELOPMENTS IN OCULAR DRUG DELIVERY SYSTEMS • Goal - improving the efficacy of drugs administered intraocularly. Based on the intraocular drug dose increase performed in the HARBOR and SAVE clinical trials for neovascular AMD, limiting intravitreal injections has been advocated to decrease the socioeconomic treatment load.
  • 4. Aim to summarize (1) Intraocular pharmacokinetics of current intravitreal drugs. (2)Efforts to enhance the intraocular pharmacokinetics and pharmacodynamics of intravitreal drugs: dose escalation of intravitreal drugs, increasing the molecular weight of intravitreal drug molecules, sustained-release intravitreal implants, micro- and nanoparticles, hydrogels, combination drug delivery systems, port delivery systems. (3) Drug administration routes besides the intravitreal route.
  • 5. Figure 1: The following is a schematic representation of the many ways of ocular drug administration: (1) the topical route, (2) the subconjunctival route, (3) the suprachoroidal route with microcannula and microneedle, (4) the subretinal route, and (5) the intravitreal injection and port delivery system.
  • 6. OCULAR GENE THERAPY • Gene treatments in this sector have been on the rise over the past few decades, driven by developments in viral vector technology and discoveries in the genetic foundation for ocular ailments. • This trend culminated in the FDA approval of LuxturnaTM in 2017, the first medicine of its kind to treat ocular conditions using gene therapy. • This landmark achievement strengthens the research and clinical interests in gene therapy for a wider variety of ocular illnesses than it had previously. There are about 350 hereditary ocular illnesses, including a wide variety of genetic loci, such as retinitis pigmentosa, choroideremia, Stargardt disease, and Leber's congenital amaurosis (LCA) . Some of these diseases include retinitis pigmentosa, Stargardt disease, and Leber's congenital amaurosis (LCA).
  • 7. • The engineering of vectors and the packaging of transgenes have made significant contributions to the enhancement of transgene expression and the phenotypic rescue following intraocular administration. Even though viral vectors have been used successfully in ocular gene therapy, there are still concerns regarding the heterogeneity of viral genomes throughout the manufacturing process, as well as packaging capacity and immunological reactions. In order to circumvent these constraints, non-viral vectors are currently in the process of being designed for gene therapy. • In this article, we take a look at the growing corpus of research and clinical trials that include gene therapy for hereditary and acquired eye illnesses. We also discuss the recent developments in viral and non-viral vectors that have been made in this area of research.
  • 8. OCULAR STRUCTURE & ITS BARRIERS • The front part known as the anterior segment and the back section known as the posterior segment, make up the eye. anterior segment 1. cornea 2. Conjunctiva 3. iris 4. ciliary body 5. crystalline lens 6. aqueous humour
  • 9. posterior segment 1. sclera 2. choroid 3. Retina 4. vitreous humour They are the most significant obstacles in the way of ocular medication administration.
  • 10. NANO BASED DRUG DELIVERY SYSTEM FOR GLUCOMA • Glaucoma is a group of eye diseases that damage the optic nerve, leading to progressive vision loss and blindness. It is the leading cause of irreversible blindness globally. To this day, intraocular pressure (IOP) management is the cornerstone of treatment for glaucoma. With the aim of reducing intraocular pressure (IOP), there has been a recent surge in the use of nanocarriers to enhance ocular drug delivery. This development is particularly significant as the long-term use of conventional IOP-lowering agents, which are based on poorly penetrating molecules, can cause frequent ocular toxicity and intolerance due to their adverse effects on the corneal epithelium.