Nanoparticulate Transscleral Ocular Drug Delivery
Jigar N Shah
1
, Hiral J Shah
2
, Anastasia Groshev
3
, Anjali A Hirani
3
, Yashwant V Pathak
3
and Vijaykumar B Sutariya
3*
1
Department of Pharmaceutics, Institute of Pharmacy, Nirma University, Gujarat, India
2
Department of Pharmaceutics, Arihant School of Pharmacy & BRI, Adalaj, Gujarat, India
3
Department of Pharmaceutical Sciences, USF College of Pharmacy, University of South Florida, Tampa, USA
*
Corresponding author: Vijaykumar B Sutariya, Department of Pharmaceutical Sciences, University of South Florida College of Pharmacy, 12901 Bruce B. Downs
Blvd, MDC 30, Tampa, FL 33612, USA, Tel: (813) 974-5289; Fax: (813) 905-9890; E-mail: vsutariy@health.usf.edu
Rec date: Mar 20, 2014; Acc date: Jun 2, 2014; Pub date: Jun 4, 2014
Copyright: © 2014 Sha et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use,
distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
Ocular drug delivery is one of the most challenging areas of drug delivery due to the unique mostly avascular
nature of the major eye structures and presence of two blood barriers. Effectiveness of a more conventional
systemic delivery falls short due to low drug levels in the eye tissue. Periocular approaches require penetration of
fibrous sclera and present their own limitations. Utilization of nanotechnology presents new avenue of drug system
development with potential to penetrate protective barriers and sustain ample tissue saturation. More specifically,
transscleral delivery permits a range of applications in targeted delivery, gene, stem cell, protein and peptides,
oligonucleotide, and ribozyme therapies. The exciting range of current applications is expounded in this review.
Keywords: Ocular delivery; Transscleral delivery; Drug delivery
systems; Nanotechnology; Nanoparticle; Drug delivery; Macular
degeneration; Retina
Introduction
Ocular drug delivery has remained one of the most challenging
tasks for pharmaceutical researchers. The unique and complex
structure of the eye restricts the entry of drug molecules at the
required site of action. The eye is anatomically divided into the
anterior and posterior segments with the lens–iris barrier roughly
demarcating the two segments. The anterior segment consists of the
front one-third of the eye that mainly includes pupil, cornea, iris,
ciliary body, aqueous humor, and lens while the posterior segment
consists of the back two-thirds of the eye that includes vitreous humor,
retina, choroid, macula, and optic nerve (Figure 1) [1,2]. Further, the
anatomy of the eye presents a unique system with two barriers that
prevents penetration of substances from the blood, namely, the blood-
aqueous and blood-retinal barrier [3].
There are a large number of major diseases affecting the eye
including Age-Related Macular Degeneration (AMD), Diabetic
Macular Edema (DME), cataract, Proliferative Vitreoretinopathy
(PVR), uveitis, Cytomegalovirus (CMV), and glaucoma. Table 1
highlights the classification, signs and symptoms and current
treatment options for these diseases [4-38].
Ocular drug delivery methods to treat anterior segment disease
include topical (i.e. eye drops, ointment), systemic, and periocular (i.e.
subconjunctival injections, implants) administration routes.
Figure 1: Schematic representation of major structure of the eye.
The anterior segment includes pupil, cornea, iris, ciliary body, and
aqueous humor. The lens separates anterior portion from posterior,
which includes vitreous humor, retina, choroid, macular, and optic
nerve. Sclera encasing the whole eye protects it impedes penetration
of majority external agents. Reprinted with permission from
reference [1]
Disease Classification Signs and symptoms Treatment
AMD Dry AMD (non-exudative)
Break down of photoreceptors,
retinal pigment epithelium (RPE)
and choriocapillaries
Specific high dose formulation containing
antioxidants, zinc and vitamin supplements
Shah JN et al., J Biomol Res Ther 2014, 3:3
DOI: 10.4172/2167-7956.1000116
Review Open Access
J Biomol Res Ther
ISSN:2167-7956 JBMRT, an open access journal
Volume 3 • Issue 3 • 1000116
Journal of
Biomolecular Research & Therapeutics
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ISSN: 2167-7956