Advanced drug delivery and targeting technologies for the ocular diseases

被引:104
作者
Barar, Jaleh [1 ]
Aghanejad, Ayuob [1 ]
Fathi, Marziyeh [1 ]
Omidi, Yadollah [1 ]
机构
[1] Tabriz Univ Med Sci, Res Ctr Pharmaceut Nanotechnol, Fac Pharm, Tabriz, Iran
关键词
Eye diseases; Intraocular drug delivery; Ocular barriers; Ocular pharmacotherapy; Ophthalmic implants; Ocular drug targeting; Ophthalmology; Targeted therapy;
D O I
10.15171/bi.2016.07
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Introduction: Ocular targeted therapy has enormously been advanced by implementation of new methods of drug delivery and targeting using implantable drug delivery systems (DDSs) or devices (DDDs), stimuli-responsive advanced biomaterials, multimodal nanomedicines, cell therapy modalities and medical bioMEMs. These technologies tackle several ocular diseases such as inflammation-based diseases (e.g., scleritis, keratitis, uveitis, iritis, conjunctivitis, chorioretinitis, choroiditis, retinitis, retinochoroiditis), ocular hypertension and neuropathy, age-related macular degeneration and mucopolysaccharidosis (MPS) due to accumulation of glycosaminoglycans (GAGs). Such therapies appear to provide ultimate treatments, even though much more effective, yet biocompatible, noninvasive therapies are needed to control some disabling ocular diseases/disorders. Methods: In the current study, we have reviewed and discussed recent advancements on ocular targeted therapies. Results: On the ground that the pharmacokinetic and pharmacodynamic analyses of ophthalmic drugs need special techniques, most of ocular DDSs/devices developments have been designed to localized therapy within the eye. Application of advanced DDSs such as Subconjunctival insert/implants (e.g., latanoprost implant, Gamunex-C), episcleral implant (e.g., LX201), cationic emulsions (e.g., Cationorm (TM), Vekacia (TM), Cyclokat (TM)), intac/punctal plug DDSs (latanoprost punctal plug delivery system, L-PPDS), and intravitreal implants (I-vitaion (TM), NT-501, NT-503, MicroPump, Thethadur, IB-20089 Verisome (TM), Cortiject, DE-102, Retisert (TM), Iluvein (TM) and Ozurdex (TM)) have significantly improved the treatment of ocular diseases. However, most of these DDSs/devices are applied invasively and even need surgical procedures. Of these, use of de novo technologies such as advanced stimuli-responsive nanomaterials, multimodal nanosystems (NSs)/nanoconjugates (NCs), biomacromolecualr scaffolds, and bioengineered cell therapies need to be further advanced to get better compliance and higher clinical impacts. Conclusion: Despite mankind successful battle on ocular diseases, our challenge will continue to battle the ocular disease that happen with aging. Yet, we need to understand the molecular aspects of eye diseases in a holistic way and develop ultimate treatment protocols preferably as non-invasive systems.
引用
收藏
页码:49 / 67
页数:19
相关论文
共 144 条
[1]
Ocular ciprofloxacin hydrochloride mucoadhesive chitosan-coated liposomes [J].
Abdelbary, Ghada .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2011, 16 (01) :44-56
[2]
Biopharmaceutical profile of pranoprofen-loaded PLGA nanoparticles containing hydrogels for ocular administration [J].
Abrego, Guadalupe ;
Alvarado, Helen ;
Souto, Eliana B. ;
Guevara, Bessy ;
Halbaut Bellowa, Lyda ;
Parra, Alexander ;
Calpena, Ana ;
Luisa Garcia, Maria .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2015, 95 :261-270
[3]
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
[4]
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
[5]
Improved pharmacodynamics of timolol maleate from a mucoadhesive niosomal ophthalmic drug delivery system [J].
Aggarwal, D ;
Kaur, IP .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 290 (1-2) :155-159
[6]
In situ gel systems as 'smart' carriers for sustained ocular drug delivery [J].
Agrawal, Ashish Kumar ;
Das, Manasmita ;
Jain, Sanyog .
EXPERT OPINION ON DRUG DELIVERY, 2012, 9 (04) :383-402
[7]
Hydrogel: Preparation, characterization, and applications: A review [J].
Ahmed, Enas M. .
JOURNAL OF ADVANCED RESEARCH, 2015, 6 (02) :105-121
[8]
Assessment of Ocular Pharmacokinetics and Safety of Ganciclovir Loaded Nanoformulations [J].
Akhter, Sohail ;
Talegaonkar, Sushama ;
Khan, Zeenat I. ;
Jain, Gaurav K. ;
Khar, Roop K. ;
Ahmed, Farhan J. .
JOURNAL OF BIOMEDICAL NANOTECHNOLOGY, 2011, 7 (01) :144-145
[9]
Shall we use Avastin® or Lucentis® for ocular neovascularization? [J].
Algvere, Peep V. ;
Kvanta, Anders ;
Seregard, Stefan .
ACTA OPHTHALMOLOGICA, 2008, 86 (04) :352-355
[10]
In situ gelling systems: a strategy to improve the bioavailability of ophthalmic pharmaceutical formulations [J].
Almeida, Hugo ;
Amaral, Maria Helena ;
Lobao, Paulo ;
Sousa Lobo, Jose Manuel .
DRUG DISCOVERY TODAY, 2014, 19 (04) :400-412