FORMULATION AND EVALUATION OF GASTRORETENTIVE FLOATING TABLETS OF LAFUTIDINE
Abstract
The purpose of this research was to develop a novel gastroretentive drug delivery system based on wet granulation technique for sustained delivery of active agent. Quick GI transit could result in incomplete drug release from the drug delivery system above the absorption zone leading to decreased efficacy of the administered dose and thus less patient compliance. Gastroretentive floating tablets, which was designed to provide the desired sustained and complete release of drug for prolonged period of time. Gastroretentive floating tablets of lafutidine were prepared by wet granulation technique using different concentrations of Gum Kondagagu, Gum olibanum and Locust bean Gum. The optimized formulation (LF14) exhibited 99.54% drug release in 12 hrs, while the buoyancy lag time was 33 sec. In-vitro drug release kinetics was found to follow both the Zero order and the possible mechanism of lafutidine release from the optimized formulation might be attributed to super case II transport mechanism. The Optimized formulation (LF14) showed no significant change in physical appearance, drug content, floating lag time, in vitro dissolution studies after 75%±5% RH at 40±20C relative humidity for 6 months.
Keyword: Wet granulation, Floating lag Time, Gastroretentive, Lafutidine
DOI
https://doi.org/10.22270/jddt.v8i5.1898References
Nayak AK, Maji R, Das B, Gastroretentive drug delivery systems: a review. Asian J Pharm Clin Res 2010; 3:2-10.
Khan FN, Dehghan MHG, Gastroretentive drug delivery systems: a patent perspective. Int J Health Res 2009; 2:23-44.
Ikawa K, Shimatani T, Hayato S, Morikawa N, Tazuma S. Pharmacokinetic and Pharmacodynamic Properties of Lafutidine after Postprandial Oral Administration in Healthy Subjects: Comparison with Famotidine Biol. Pharm. Bull. May 2007; 30(5):1003-1006.
Patrick J. Sinko. Micrometrics. In: Martin’s Physical Pharmacy and Pharmaceutical Sciences. 5th ed., Lippincott Williams and Wilkins – Indian Edition. 2006: pp.553 – 559.
Loyd V. Allen. Jr, Nicholos G, Popvich Howard C. Ansels. Powders and Granules. In: Ansel’s Pharmaceutical Dosage Forms and Drug Delivery System. 9th ed., Wolters Kluwer Health and Lippincott Williams and Wilkins. 2009; 225-226.
Glibert S. Banker and Neil R. Anderson. Tablets. In: The theory and Pratice of Industrial Pharmacy. 3rd ed., Varghese Publishing House. 1987; 293-345.
United States Pharmacopoeial Convention, United States Pharmacopoeia and National Formulary, Asian ed., United States Pharmacopoeial Convention, Inc., Rockville, MD, 2007; 1: 819-820.
Government of India Ministry of Health and Family Welfare. Reagents and Solutions-Buffer Solutions. In: The Pharmacopoeia of India. Delhi, India: Controller of Publication. 2010; 1:194-196
Nagaraju R, Kaza R. Stability Evaluation of Amoxicilliin and Potassium Clavulanate Tablets USP by Accelerated Studies. Turk J. Pharm. Sci. 2008; 5(3):201-214.
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