Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/7553
Title: Formulation and Evaluation of in Situ Ocular Gel of Ketorolac Tromethamine
Authors: Sharma, Jitendra Radhey Shyam
Keywords: Dissertation Report
Pharmaceutical Technology
Biopharmaceutics
13MPH
13MPH107
Issue Date: May-2015
Publisher: Institute of Pharmacy, Nirma University, A'bad
Series/Report no.: PDR00324;
Abstract: The poor bioavailability and therapeutic response exhibited by conventional ophthalmic solutions due to rapid precorneal elimination of the drug may be overcome by the use of in situ gel-forming systems that are instilled as drops into the eye and undergo a sol–gel transition in the cul-de-sac. Hence, the purpose of the present studies was to formulation and evaluation of an ophthalmic delivery system for a nonsteroidal anti-inflammatory drug, ketorolac tromethamine, based on the concept of thermo-sensitive, pH-sensitive, ion sensitive, in situ gelation. These gelling systems involve the use of poloxamer 407 and poloxamer 188, (thermo-sensitive polymer), carbopol 934 and carbopol 980 (pH-sensitive polymer), gelrite (ion sensitive polymer) was used as gelling agent and HPMC K4M was used as viscosity-enhancing agent. It was found that the optimum concentration of poloxamer 407 solution for the thermo-sensitive in situ gel forming delivery systems was 20% (w/w), carbopol 980 solution for the pH-sensitive in situ gel forming delivery systems was 0.3% (w/w) and gelrite solution for the ion-sensitive in situ gel forming delivery systems was 0.50% (w/w). In vitro drug release studies showed that the formulation released drug over a period of 8 hours with formulation KT-T71 (gelrite 0.50% w/v/HPMC K4M 0.2% w/v) showing the highest drug release of 95.29% of ketorolac tromethamine. Formulation (KT-T71) showed zero order drug release. Formulations (KT-T23, KT-T57, and KT-T71) used to determine the in vivo eye irritation studies (as per draize test) using six male rabbits. The formulations were found to be non-irritating with no ocular damage. The results demonstrated that the gelrite /HPMC K4M mixture can be used as an in situ gelling vehicle to enhance the ocular bioavailability and patient compliance. The prepared formulation was stable, non-irritant and provided sustained release of the drug over an 8-h period. The developed system is thus a viable alternative to conventional eye drops.
URI: http://hdl.handle.net/123456789/7553
Appears in Collections:M.Pharm. Research Reports, Department of Pharmaceutical Technology and Biopharmaceutics

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