Author/Authors :
Mahboobian, Mohammad Mehdi Department of Pharmaceutics - School of Pharmacy & Protein Technology Research Center - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Seyfoddin, Ali School of Applied Sciences - Auckland University of Technology, New Zealand , Rupenthal, Ilva D Buchanan Ocular Therapeutics Unit - Department of Ophthalmology - New Zealand National Eye Centre - Faculty of Medical and Health Sciences - University of Auckland, New Zealand , Aboofazeli, Reza Department of Pharmaceutics - School of Pharmacy & Protein Technology Research Center - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Foroutan, Mohsen Department of Pharmaceutics - School of Pharmacy & Protein Technology Research Center - Shahid Beheshti University of Medical Sciences, Tehran, Iran
Abstract :
Brinzolamide (BZ) is an intraocular pressure reducing agent with low bioavailability. The
purpose of the present study was to overcome this issue by development of BZ containing
nanoemulsions (NEs) as an ocular drug delivery system with desirable therapeutic efficacy.
Brinzolamide NEs were prepared by the spontaneous emulsification method. Based on initial
release studies, twelve formulations with the slowest release characteristics were subjected to
further physicochemical investigations such as particle size, polydispersity index, pH, refractive
index, osmolality and viscosity. The therapeutic efficacy of these formulations was assessed by
measuring the intraocular pressure after instillation of the prepared NEs in normotensive albino
rabbit eyes. Nanoemulsions with suitable physicochemical properties exhibited high formulation
stability under different conditions. more over biological evaluations indicated that using lower
drug concentrations in NE formulations (0.4%) had a similar or even better pharmacodynamic
effect compared to the commercial suspension with a higher drug concentration (1%). Our
findings suggest that NEs could be effectively used as carriers for enhancing the bioavailability
of topically applied ophthalmic drugs.
Keywords :
Therapeutic efficacy , Ocular bioavailability , Physicochemical characterisation , Nanoemulsion , Brinzolamide , Ocular drug delivery