Floating In Situ Gel based on Alginate as Carrier for Stomach-Specific Drug Delivery of Famotidine
DOI:
https://doi.org/10.37285/ijpsn.2010.3.3.7Abstract
Alginate based floating in situ gelling systems of famotidine (FIGF) were prepared by dissolving varying concentrations of alginate in deionized water containing sodium citrate, to which varying concentrations of drug and calcium chloride was added and dissolved by stirring. Results of preliminary trials indicate that concentrations of sodium alginate, calcium chloride and sodium citrate affected the characteristics of in situ gel. A 32 full factorial design was employed to study the effect of independent variables, concentration of sodium alginate (X1) and concentration of calcium chloride (X2) on dependent variables, i.e. viscosity, drug content, drug release at 4 hrs (Q50) and drug release at 8 hrs (Q80). A sustained drug release was obtained for more than 8 hrs. In vivo testing of FIGF to albino Wistar rats demonstrated significant anti-ulcer effect of famotidine.
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Alginate, floating, in situ gel, famotidine, ulcer indexDownloads
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Arora S, Ali J, Ahuja A, Khar R and Baboota S. Floating Drug Delivery Systems: A Review. AAPS Pharm Sci Tech. 6: E372-390 (2005).
Bardonnet PL, Faivre V and Pugh WJ. Gastroretentive dosage forms: overview and special case of Helicobacter pylori. J Control Rel. 111: 1-18 (2006).
Cao SL., Zhang QZ and Jiang XG. Preparation of ion-activated in situ gel systems of scopolamine hydrobromide and evaluation of its antimotion sickness efficacy. Acta. Pharmacol. Sin. 28: 584–590 (2007).
Chawla G and Bansal A. A means to address regional variability in intestinal drug absorption. Pharm Tech. 27: 50-68 (2003).
Coffin M and Parr A. Ranitidine solid dosage form. US Patent 5 407 687, 1995.
Davis SS, Stockwell AF, Taylor MJ, Hardy JG, Whalley DR, Wilson CG, Bechgaard H and Christensen FN. The effect of density on the gastric emptying of single and multiple-unit dosage forms. Pharm. Res. 3: 208–213 (1986).
Doi Y, Mori Y, Urata N, Miziro M, Syoji M and Marubuchi S. Histological study on healing of cryocautery induced rat gastric ulcer treated with T-593. Nippon Yakurigaku Zasshi. 113: 167–176 (1999).
Elmowafy EM, Gehanne AS, Mansour S, Abd El-Hamid A and El-Shamy. Ionotropically emulsion gelled polysaccharides beads: Preparation, in vitro and in vivo evaluation. Carbohydrate Polymers. 75: 135-142 (2009).
Gajbhiye VP, Vijayaraj K, Tekade RK and Jain NK. PEGylated PPI dendritic architectures for sustained delivery of H2 receptor antagonist. European J. of Medicinal Chemistry. 44: 1155-1166 (2009).
Ganguly AK. A method for quantitative assement of experimentally produced ulcers in stomach of rats. Experientia. 25: 1124-1127 (1969).
Groning R and Heun G. Dosage forms with controlled gastrointestinal passage-studies on the absorption of nitrofurantoin. Int. J. Pharm. 56: 111–116 (1989).
Higuchi WI. Mechanism of sustained action medication. J. Pharm Sci. 51: 802-804 (1962).
Jaimini M, Rana AC and Tanwar YS. Formulation and Evaluation of Famotidine Floating Tablets. Current Drug Delivery. 4: 51-55 (2007).
Karasulu E, Karasuslu HY, Ertan G, Kirilmaz L and Guneri T. Extended release lipophillic indomethacin microspheres: formulation factors and mathematical equations fitted drug release rates. Eur J Pharm Sci. 19: 99–104 (2003).
Kedzierewicz F, Thouvenot P, Lemut J, Etienne A, Hoffman M and Maincent P. Evaluation of per oral silicone dosage forms in humans by gamma-scintigraphy. J. Control. Rel. 58: 195–105 (1999).
Korsmeyer RW, Gurney R, Doelker E, Buri P and Peppas NA. Mechanisms of solute release from porous hydrophilic polymers. J. Pharm. Sci. 15: 25-35 (1983).
Kubo W, Miyazaki S and Attwood D. Oral sustained delivery of paracetamol from in situ-gelling gellan and sodium alginate formulations. Int J Pharm. 258: 55-64 (2003).
Kulkarni SK. Hand book of experimental pharmacology, Vallabh Prakashan, New Delhi, 1999.
Li S, Lin S, Chein YW, Daggy BP and Mirchandani HL. Effect of HPMC and carbopol on the release and the floating properties of gastric floating drug delivery system using factorial design. Int. J. Pharm. 253: 13–22 (2003).
Li S, Lin S, Chein YW, Daggy BP and Mirchandani HL. Statistical optimization of gastric floating system for oral controlled delivery of calcium. AAPS Pharm. Sci. Tech. 2: (2001).
Miyazaki S, Kubo W and Attwood D. Oral sustained delivery of theophylline using in-situ gelation of sodium alginate. J. Control. Rel. 67: 275-280 (2000).
Müller W and Anders E. Floating system for oral therapy. WO Patent 89/06956, 1989.
Narayan S., Devi RS, Jainu M, Sabitha KE and Devi CSS. Protective effect of a polyherbal drug, ambrex in ethanol-induced gastric mucosal lesions in experimental rats. Indian J. Pharmacol. 36: 34-37 (2004).
Paulo Costa, Jose Manuel and Sousa Labo, Modeling and comparison of dissolution profiles, European Journal of Pharm. Sci. 13: 123-133 (2001).
Reynolds J.E.F. Martindale the Extra Pharmacopoeia, The Royal Pharmaceutical Society, London, 1996.
Shay H, Komarov SA, Fele SS, Meranze D, Gruenstein H and Siplet H. A simple method for uniform production of gastric ulceration in rat. Gastroenterology. 5: 43-61 (1945).
Shi-lei C, Xiao-wei R, Qi-zhi Z, En C, Feng X, Jun C, Li-Chun L and Xin-guo J. In situ gel based on gellan gum as new carrier for nasal administration of mometasone furoate. Int J Pharm. 365: 109–115 (2009).
Singh BN and Kim KH. Floating drug delivery systems: an approach to oral controlled drug delivery via gastric retention. J. Control. Release. 63: 235-259 (2000).
Streubel A, Siepmann J and Bodmeier R. Floating matrix tablets based on low density foam powder: effects of formulation and processing parameters on drug release, European J. of Pharma. Sci. 18: 37–45 (2003).
Streubel A, Siepmann J and Bodmeier R. Floating microparticles based on low density foam powder. Int J Pharm. 241: 279–292 (2002).
Wagner JG. Interpretation of percent dissolved-time plots derided from in vitro testing of conventional tablets and capsules. J. Pharm. Sci. 58: 1253-1257 (1969).
Zatz JL and Woodford DW. Prolonged release of theophylline from aqueous suspension. Drug.Dev.Ind.Pharm. 13: 2159-2178 (1987).