Formulation And Evaluation Of Fast Dissolving Tablets By Addition Of Different Concentra-tions Of Superdisintegrant And By Effervescent Technology.
Keywords:
Ketoprofen, Solid dispersion, Fast dissolving Tablets, Superdisintigrant, Effervescence TechnologyAbstract
Ketoprofen is NSAID drug used for osteoarthritis and rheumatoid arthritis. The major problem with this drug is very low solubility in biological fluids. Therefore solid dispersion of Ketoprofen with PVP K30 in different weight ratios were prepared to increase its water solubility. The solid dispersions were evaluated by solubility study, drug content, in-vitro drug release, dissolution efficiency and characterized by FT-IR. The Ketoprofen SD with PVP K30 (1:4) ratio showed maximum amount of drug release it was selected for Fast Dissolving Tablet formulation. The Tablets were prepared by by addition of different concentrations of superdisintigrant and By Effervescence Technology, The tablets were evaluated for Pre-Compression and Post-Compression Studies, among all the formulations F5 showed least disintegration time and 99.60% of drug release in 20 minutes. Stability study of F5 was carried out at 400c and 75% RH for three months. it confirms there is no significant change in the formulation.
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References
Fu Y, Yang S, Jeong SH, et al. Orally Fast-disintegrating tablets: Development, technologies, taste-masking and clinical studies Crit. Rev. Ther.Drug Carr. Syst. 2004; 21: 433-475.
Bogner RH, Wilkosz MF. Fast-dissolving tablets: new dosage convenience for patients. U.S. Pharm. 2002; 27; 34-43.
Chang RK, Guo X, Burnside BA, et al. Fast dissolving tablets. Pharm. Technol. N. Am. 2000; 24; 52-58.
Dobetti L. Fast-melting tablets: developments and technologies. Pharm. Technol. N. Am. Suppl. 2001; 44-50.
Goodman, Gilman C, The pharmacological basis of therapeutic. 10th Edn, The McGraw-Hill Companies Inc.: 710-712, (1996).
Indian pharmacopoeia, Vol 2, Government of India, Ministry of Health and Family welfare. The controller of publications, Delhi; 424, (1996).
http://www.rxlist.com/cgi/generic/ketoprofen.htm29/07/09
https://www.medicinescomplete.com/ahfs/ketoprofen.htm29/07/09
Satoskar R.S, Bhandarkar S.D, Ainapure S.S. Pharmacology and pharmacotherapeutics. 17th Edn. Mumbai: Popular prakashan publishers: 209-218,2001.
Martin.A, Physical pharmacy, 4th Edn, Philadelphia LippinCott Williams and Wilkins, 324-362, (1993).
Sethi S, Squllante E, Solid Dispersions of Carbamazepine in PVPK-30 by conventional solvent evaporation and supercritical methods. Int. J. Pharma. 2004; 19: 1-10.
Raymond C. Rowe, Paul J. Sheskey and Paul J. Weller, Handbook of Pharmaceutical Excipients, 4th ed, The pharmaceutical press, London:184-185 (2003).
BankarG.S, Anderson N.R, IN: lachman.L, Lieberman.H.A And Kanig.J.L, The Theory And Practice of Industrial Pharmacy, 3rdEdn, 4th Ineian Reprint, Verghese Publishing House, Bombay; 297, (1991).
Pharmacopoeia of India, 4th, Edn, controller publications, New Delhi: A-80, (1996).
Pharmacopoeia of India, 2nd, Edn, controller publications, New Delhi: 740, (1996).
Pharmacopoeia of India, 4 th, Edn, controller publications, New Delhi: A-82, (1996).
USP-24, NF-19, US Pharmacopoeial Convention Inc. Rockville: 1941, (2000).
19. Khan K.A, The concept of dissolution efficiency J. Pharmacol,1975; 27: 48-49.
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