Evaluation of Anti-GERD Activity of Gastro Retentive Drug Delivery System of Itopride Hydrochloride

REFERENCES

• Goyal, R.K. (1998). Diseases of the esophagus. Fauci, A.S., Braunwald, E., Isselbacher, K.J.. Harrison's Principles of Internal Medicine 14th, McGraw Hill, New York, 1592–93.
   Google Scholar
• Kim, Y.S., Kim, T.H., Choi, C.S., Shon, Y.W., Kim, S.W., Seo, G.S., . (2005). Effect of itopride, a new prokinetic, in patients with mild GERD: A pilot study. World J. Gastroenterol 11(27): 4210–14.
   PubMed Web of Science ®Google Scholar
• Sethu, B. (2003). Drug therapy of Gastroesophageal reflux disease (GERD): Focus on itopride hydrochloride. The Indian Pract. 56(12): 827–30.
   Google Scholar
• Kakrani, A.L., Madraki, R. (2002). Clinical evaluation of itopride hydrochloride in patients with non-ulcer dyspepsia and chronic gastritis. The Indian Pract. 55(7): 441–44.
   Google Scholar
• Klausner, E.A., Lavy, E., Stepensky, D., Friedman, M., Hoffman, A. (2002). Novel gastroretentive dosage forms: Evaluation of gastroretentivity and its effect on riboflavin absorption in dogs. Pharm Res. 19(10): 1516–23.
   PubMed Web of Science ®Google Scholar
• Hoffman, A., Stepensky, D. (1999). Pharmacodynamic aspects of modes of drug administration for optimization of drug therapy. Crit Rev Ther Drug Carrier Syst 16(6): 571–639.
   PubMed Web of Science ®Google Scholar
• Dave, B.S., Amin, A.F., Patel, M.M. (2004). Gastroretentive drug delivery system of ranitidine hydrochloride: Formulation and in-vitro evaluation. AAPS Pharm Sci Tech. 5(2): 1–6.
   Web of Science ®Google Scholar
• Struszczyk, H., Wawro, D., Niekraszewicz, A. (1991). Biodegradability of chitosan fibres. Brine, C.J., Sandford, P.A., Zikakis, J.P., Advances in Chitin and Chitosan, Elsevier Applied Science, London, 580–585.
   Google Scholar
• Chandy, T., Sharma, C. (1990). Chitosan–as a biomaterial. Biomat Art Cells Art Org. 18: 1–24.
   PubMed Web of Science ®Google Scholar
• Hirano, S., Seino, H., Akiyama, Y., Nonaka Y. (1990). Chitosan: a biocompatible material for oral and intravenous administrations. Gebelein, C.G., Dunn, R.L., Progress in Biomedical Polymers, Plenum, New York, 283–290.
   Google Scholar
• Choi, B.Y., Park, H.J., Hwang, S.J., Park, J.B. (2002). Preparation of alginate beads for floating drug delivery system: Effects of CO2 gas-forming agents. Int. J. Pharm. 239: 81–91.
   PubMed Web of Science ®Google Scholar
• Johnson, F.A., Craig, D.Q.M., Mercer, A.D., Chauhan, S. (1997). The effects of alginate molecular structure and formulation variables on the physical characteristics of alginate raft systems. Int J Pharm 159: 35–42.
   Web of Science ®Google Scholar
• Garg, S., Sharma, S. (2003). Gastroretentive drug delivery systems. Pharmatech, 160–66.
   Google Scholar
• Kulkarni, A.R., Soppimath, K.S., Aminabhavi, T.M. (2001). Chemically modified polyacrylamide-g-guargum based crosslinked anionic microgels as pH sensitive drug delivery systems. J Controlled Release 75: 331–45.
   PubMed Web of Science ®Google Scholar
• Singh, B.N., Kim, K.H. (2000). Floating drug delivery systems: an approach to oral controlled drug delivery via gastric retention. J Control Release 63: 235–59.
   PubMed Web of Science ®Google Scholar
• Joffe, S.N., Roberts, M.B., Taylor, W.H. (1980). Exogenous and endogenous acid and pepsin in the pathogenesis of duodenal ulcers in rat. Dig Dis Sci, 825–37.
   Web of Science ®Google Scholar
• Maity, S., Chaudhari, T. (2003). Cytoprotection mediated anti-ulcer effect of tea root extract. Indian J Pharmacol 35: 213–19.
   Google Scholar
• Akhtar, H.A., Ahmed, U.K. (1995). Anti-ulcerogenic evaluation of methanolic extract of some indigenous medicinal plants of Pakistan in aspirin-ulcerated rats. J Ethnopharmacol. 46: 1–6.
   PubMed Web of Science ®Google Scholar
• Mittelstadt, S.W., Hemenway, C.L., Spruell, R.D. (2005). Effects of fasting on evaluation of gastrointestinal transit with charcoal meal. J Pharmacol Toxicol Methods 52: 154–58.
   PubMedGoogle Scholar
• Lee, H.T., Seo, E.K., Chung, S.J., Shim, C.K. (2005). Prokinetic activity of an aqueous extract from dried immature fruit of Poncirus trifoliate (L.) Raf. J Ethnopharmacol 102: 131–36.
   PubMed Web of Science ®Google Scholar
• Kulkarni, S.K. (1999). Handbook of Experimental Pharmacology, 2nd, Vallabh Prakashan, Delhi, 148–50.
   Google Scholar