Abstract
Age-related macular degeneration (AMD) is a leading cause of permanent blindness
globally. Due to the various obstacles, highly invasive intravitreal (IVT) injections are the primary
method used to deliver medications to the tissues of the posterior eye. An utmost patientfriendly
topical ocular delivery approach has been extensively researched in recent years. Mucoadhesive
compositions extend precorneal residence time while reducing precorneal clearance.
They increase the likelihood of adhesion to corneal and conjunctival surfaces and, as a result, allow
for enhanced delivery to the posterior eye segment. Due to its remarkable mucoadhesive
characteristics, chitosan (CS) has undergone the most extensive research of any mucoadhesive
polymer. Drug delivery to the front and back of the eye is still difficult. The pharmaceutical industry
has shown greater interest in drug delivery systems (DDSs) based on nanotechnology (NT)
in recent years, particularly those made from natural polymers like chitosan, alginate, etc. Because
of their incredible adaptability, higher biological effects, and favourable physicochemical
properties, CS-oriented nanomaterials (NMs) are explored by researchers as prospective nanocarriers.
CS are the right substrates to develop pharmaceutical products, such as hydrogels, nanoparticles
(NP), microparticles, and nanofibers, whether used alone or in composite form. CS-based
nanocarriers deliver medicine, such as peptides, growth factors, vaccines, and genetic materials in
regulated and targeted form. This review highlights current developments and challenges in chitosan-
mediated nano therapies associated with AMD.
Graphical Abstract
[11]
Flores R, Carneiro Â, Vieira M, Tenreiro S, Seabra MC. Age-Related macular degeneration: Pathophysiology, management, and future perspectives. IntJ ophthal 2021; 244(6): 495-511.
[27]
Iwase T, Fu J, Yoshida T, Muramatsu D, Miki A, Hashida N, et al. Sustained delivery of a HIF-1 antagonist for ocular neovascularization. J control rel offJ Control Rel Soc 2013; 172(3): 625-33.
[38]
Karati D. A concise review on bio-responsive polymers in targeted drug delivery system. Polym Bull 2022; 1-23.
[62]
Borchert M, Liu GT, Pineles S, Waldman AT. Pediatric optic neuritis: What is new. J neuro-ophthal offic J North Am Neuro-Ophthalmol Soc 2017; 37(Suppl 1): S14-22.
[106]
Chang E. Relevance of nanotechnology to retinal disease. Retin Physician 2017; 14: 44-6.
[110]
Kiernan DF, Lim JI. Topical drug delivery for posterior segment disease. Retina Today 2010; 5(4): 48-51.
[112]
Sahoo S, Sahoo R, Nayak P. Mucoadhesive nanopolymers for posterior segment drug delivery. Retina Today 2011; 3: 60-3.
[115]
Arroyo CM, Quinteros D, Cózar-Bernal MJ, Palma SD, Rabasco AM, González-Rodríguez ML. Ophthalmic administration of a 10-fold-lower dose of conventional nanoliposome formulations caused levels of intraocular pressure similar to those induced by marketed eye drops. Europ J pharmac sci 2018; 111: 186-94.
[137]
Mateescu MA, Ispas-Szabo P, Assaad E. Chitosan and its derivatives as self-assembled systems for drug deliveryControlled Drug Delivery 1st. Cambridge: Woodhead Publishing Limited 2015; pp. 86-119.
[138]
Supper S, Anton N, Boisclair J, Seidel N, Riemenschnitter M, Curdy C, et al. Chitosan/glucose 1-phosphate as new stable in situ forming depot system for controlled drug delivery. Eur J Pharm Biopharm 2014; 88(2): 361-73.
[140]
Varshosaz J, Tabbakhian M, Salmani Z. Designing of a thermosensitive chitosan/poloxamer in situ gel for ocular delivery of ciprofloxacin. The Open Drug Deliv J 2008; 2(1)
[175]
Fernandez MJA, Rey MBS, De la Fuente Freire M, Pena AIV. Nanoparticles of chitosan and hyaluronan for the administration of active molecules. US20110142890A1, 2011.
[176]
Desai Tejal A, Chirra Hariharasudhan D. Univ california, assignee. bioactive agent delivery devices and methods of making and using the same. EP2856259B1, 2013.
[177]
Hebert R. Water-soluble indole-3-propionic acid. US20040029830 A1, 2004.