Recent Perspectives in Ocular Drug Delivery

被引:429
作者
Gaudana, Ripal [1 ]
Jwala, J. [1 ]
Boddu, Sai H. S. [1 ]
Mitra, Ashim K. [1 ]
机构
[1] Univ Missouri, Sch Pharm, Div Pharmaceut Sci, Kansas City, MO 64110 USA
关键词
nanotechnology; ocular drug delivery; transporter; AMINO-ACID TRANSPORTER; CILIARY NEUROTROPHIC FACTOR; MONOESTER GANCICLOVIR PRODRUGS; SUSTAINED OPHTHALMIC DELIVERY; ENDOTOXIN-INDUCED UVEITIS; PIGMENT EPITHELIAL-CELLS; IN-VITRO; P-GLYCOPROTEIN; CHOROIDAL NEOVASCULARIZATION; RABBIT EYE;
D O I
10.1007/s11095-008-9694-0
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Anatomy and physiology of the eye makes it a highly protected organ. Designing an effective therapy for ocular diseases, especially for the posterior segment, has been considered as a formidable task. Limitations of topical and intravitreal route of administration have challenged scientists to find alternative mode of administration like periocular routes. Transporter targeted drug delivery has generated a great deal of interest in the field because of its potential to overcome many barriers associated with current therapy. Application of nanotechnology has been very promising in the treatment of a gamut of diseases. In this review, we have briefly discussed several ocular drug delivery systems such as microemulsions, nanosuspensions, nanoparticles, liposomes, niosomes, dendrimers, implants, and hydrogels. Potential for ocular gene therapy has also been described in this article. In near future, a great deal of attention will be paid to develop non-invasive sustained drug release for both anterior and posterior segment eye disorders. A better understanding of nature of ocular diseases, barriers and factors affecting in vivo performance, would greatly drive the development of new delivery systems. Current momentum in the invention of new drug delivery systems hold a promise towards much improved therapies for the treatment of vision threatening disorders.
引用
收藏
页码:1197 / 1216
页数:20
相关论文
共 250 条
[1]   Renal assimilation of oligopeptides: Physiological mechanisms and metabolic importance [J].
Adibi, SA .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1997, 272 (05) :E723-E736
[2]   Inhibition of endotoxin-induced uveitis by methylprednisolone acetate nanosuspension in rabbits [J].
Adibkia, Khosro ;
Omidi, Yadollah ;
Siahi, Mohammad R. ;
Javadzadeh, Ali R. ;
Barzegar-Jalali, Mohammad ;
Barar, Jaleh ;
Maleki, Nasrin ;
Mohammadi, Ghobad ;
Nokhodchi, Ali .
JOURNAL OF OCULAR PHARMACOLOGY AND THERAPEUTICS, 2007, 23 (05) :421-432
[3]   Piroxicam nanoparticles for ocular delivery: Physicochemical characterization and implementation in endotoxin-induced uveitis [J].
Adibkia, Khosro ;
Shadbad, Mohammad Reza Siahi ;
Nokhodchi, Ali ;
Javadzedeh, Alireza ;
Barzegar-Jalali, Mohammad ;
Barar, Jaleh ;
Mohammadi, Ghobad ;
Omidi, Yadollah .
JOURNAL OF DRUG TARGETING, 2007, 15 (06) :407-416
[4]  
AHMED I, 1985, INVEST OPHTH VIS SCI, V26, P584
[5]   Influence of hydroxypropyl β-cyclodextrin on the corneal permeation of pilocarpine [J].
Aktas, Y ;
Ünlü, N ;
Orhan, M ;
Irkeç, M ;
Hincal, AA .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2003, 29 (02) :223-230
[6]   Phase I and phase II ocular metabolic activities and the role of metabolism in ophthalmic prodrug and codrug design and delivery [J].
Al-Ghananeem, Abeer M. ;
Crooks, Peter A. .
MOLECULES, 2007, 12 (03) :373-388
[7]  
Amrite AC, 2008, MOL VIS, V14, P150
[8]   Mechanism of corneal permeation of L-valyl ester of acyclovir: Targeting the oligopeptide transporter on the rabbit cornea [J].
Anand, BS ;
Mitra, AK .
PHARMACEUTICAL RESEARCH, 2002, 19 (08) :1194-1202
[9]   In vivo antiviral efficacy of a dipeptide acyclovir prodrug, val-val-acyclovir, against HSV-1 epithelial and stromal keratitis in the rabbit eye model [J].
Anand, BS ;
Hill, JM ;
Dey, S ;
Maruyama, K ;
Bhattacharjee, PS ;
Myles, ME ;
Nashed, YE ;
Mitra, AK .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 (06) :2529-2534
[10]   Inhibition of human cytomegalovirus immediate-early gene expression by an antisense oligonucleotide complementary to immediate-early RNA [J].
Anderson, KP ;
Fox, MC ;
BrownDriver, V ;
Martin, MJ ;
Azad, RF .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (09) :2004-2011