Please use this identifier to cite or link to this item: http://13.232.72.61:8080/jspui/handle/123456789/6604
Title: Sustained Gastroretentive Delivery Of Cimetidine From An Ion activated In-Situ Gelling System For Peptic Ulcer Disease
Authors: Panda, Satish chandra
Goli, Divakar
Keywords: Cimetidine; In situ gelling systems; Viscosity; Gelrite; H.P.M.C;Peptic ulcer
Issue Date: May-2011
Publisher: Acharya & BM Reddy College of Pharmacy (ABMRCP)
Citation: Panda, Satish chandra; Goli, Divakar;Cimetidine; In situ gelling systems; Viscosity; Gelrite; H.P.M.C;Peptic ulcer;Sustained Gastroretentive Delivery Of Cimetidine From An Ion activated In-Situ Gelling System For Peptic Ulcer Disease
Abstract: Cimetidine is a histamine H2-receptor antagonist that inhibits the production of acid in the stomach. It is largely used in the treatment of heartburn and peptic ulcers. In the present research work, cimetidine in situ gelling systems were prepared using gelrite in combination with HPMC E50LV. The formulations prepared were evaluated for several parameters like drug-polymer interaction, gelling time, clarity, pH measurement, drug content, in vitro drug release, viscosity, sterility and in-vivo studies. The prepared formulations were in liquid state and exhibited low viscosity and by addition of simulated gastric fluid caused the solutions to transform into gel with high viscosity. Among the formulations, F4 was selected as the best formulation as it fulfilled all the criteria. The drug release of F4 extended upto 12 h period. Two months of stability study were carried out at 40 ± 2°C / 75 ± 5 % RH for the best selected formulations. The results showed that there were no significant changes in all the parameters evaluated for all the formulations Finally, based on the clarity and viscosity of the prepared formulation, F4was evaluated for anti-ulcer activity on Albino wistar rats. The results of the study showed that the scores scored were less than the marketed formulation of cimetidine and the control group indicating a better sustained anti ulcer therapy.
Description: Dissertation
URI: http://13.232.72.61:8080/jspui/handle/123456789/6604
Appears in Collections:Dissertations

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