Volume : 09, Issue : 06, June – 2022

Title:

24.FORMULATION DEVELOPMENT OF FAMOTIDINE GASTRORETENTIVE TABLETS BY MELT GRANULATION TECHNIQUE

Authors :

H. Padmalatha

Abstract :

The aim of the present study is to formulate and evaluate gastro retentive tablet of famotidine for the treatment of peptic ulcer, thus the action would be specifically in the stomach. Preformulation studies which include Organoleptic properties, Bulk and Tapped densities, Carr’s index, Hausner’s ratio, Melting point, PH , Solubility, were carried out are as per IP specifications. Drug-excipient compatibility studies were performed which shows that there is no interaction between drug and polymers. Evaluation studies have been performed for tablets include friability, hardness, weight variation, content uniformity, buoyancy studies are as per IP specifications. Drug release studies have been performed by using 0.1N Hcl for 12 hrs. These studies have shown that the formulation F4 gave better drug release upto 12 hrs. which is formulated with HPMC K100 M. Drugs that have poor bio-availability because of their limited absorption to the upper gastrointestinal tract can be delivered efficiently into FDDS. Thereby maximizing their absorption and improving their absolute bioavailability. The floating concept can also be utilized in the development to treating various diseases. Buoyant delivery system considered as a beneficial strategy for the treatment of gastric and duodenal cancers.
KEYWORDS: Famotidine, Gastroprotective Tablets, Melt Granulation Technique, Kinetic Study

Cite This Article:

Please cite this article in press H. Padmalatha, Formulation Development Of Famotidine Gastroretentive Tablets By Melt Granulation Technique.,Indo Am. J. P. Sci, 2022; 09(6).,

Number of Downloads : 10

References:

1. Gupta PK and Robinson JR. Oral controlled release delivery. Treatise on controlled drug delivery. 1992;93(2):545-555.
2. Jantzen GM and Robinson JR. Sustained and Controlled- Release Drug Delivery systems. Modern Pharmaceutics. 1995; 121(4): 501-502.
3. Altaf AS, Friend DR, MASRx and COSRx Sustained-Release Technology in Rathbone MJ, Hadgraft J, and Robert MS. Modified Release Drug Delivery Technology, Marcel Dekker Inc., New York, 2003; 126: 996.
4. Gwen MJ and Joseph RR, In Banker GS and Rhodes CT, Eds. Modern Pharmaceutics, Marcel Dekker Inc. New York, 1996; 72(3): 575.
5. Salsa T, Veiga F and Pina ME. Oral controlled release dosage form. I. cellulose ether polymers in hydrophilic matrices. Drug Develop. Ind. Pharm. 1997; 23: 929-938.
6. Wani MS et al. Controlled Release system-A Review. Pharmaceutical Reviews. 2008; 6(1): 41-46.
7. Altaf AS, Friend DR, MASRx and COSRx Sustained-Release Technology in Rathbone MJ, Hadgraft J, Robert MS, Modified Release Drug Delivery Technology, Marcell Dekker Inc., New York, 2003. JPSBR: Volume 1, Issue 3: Nov Dec 2011 (143-151) Patel H. 151
8. Vidyadhara S, Rao PR, Prasad JA. Formulation And Evaluation Of Propranolol Hydrochloride Oral Controlled Release Matrix Tablets. Indian J.Pharm Sci, 2004; 66: 188-192.
9. Reddy KR, Mutalik S, Reddy S. Once-daily sustained release matrix tablets of Nicorandil: Formulation and in vitro evaluation,AAPS Pharm. Sci. Tech.,2003; 4: 1-9.
10. Mohammed AD, James LF, Michael HR, John EH, Rajabi-Siahboomi AR. Release of Propranolol hydrochloride from matrix tablets containing sodium carboxy methylcellulose and Hydroxy propyl methyl cellulose. Phar. Dev. Tech.,1999; 4: 313-324.
11. Lee BJ, Ryu SG, Cui JH. Formulation and release characteristics of hydroxypropyl methylcellulose matrix tablet containing melatonin. Drug Dev. Ind.Pharm.,1999; 25: 493-501.
12. Chowdary KPR, Rao YS. Design and in vitro and in vivo evaluation of mucoadesive microcapsules of glipizide for oral controlled release. AAPS Pharm Sci Tech 2003; 4: 1-6.
13. Cooper J, Gunn C. Powder flow and compaction. In: Carter SJ, (editor). Tutorial pharmacy. New Delhi: CBS Publishers and distributors, 1986; pp. 211-33.
14. Lachman L, Lieberman HA, Kanig JL. The theory and practice of industrial pharmacy. Philadelphia: Lea & Febieger, 1970; pp. 68-9.
15. The Pharmacopoeia of India. New Delhi: Controller of Publication, 1996; pp.736.
16. Rawlins EA. Bentley’s text book of pharmaceutics. London: Cassell and Colloer Macmillian, 1977. [16] Hadjioannou TP, Christain GD, Koupparis MA. Quantitative calculations in pharmaceutical practice and research. New York: VCH Publishers Inc., 1993; pp. 345-8.
17. Bourne DW. Pharmacokinetics. In: Banker GS, Rhoides CT, (editors). Modern pharmaceutics. 4th ed. New York: Marcel Dekker Inc. 2002; 67-92.