Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Formulation and Evaluation of Ondansetron Floating Tablet


Affiliations
1 Department of Pharmaceutics, Sardar Patel College of Technology (B. Pharmacy), Balaghat, M.P., India
     

   Subscribe/Renew Journal


Some drugs are absorbed in a particular portion of the GIT only or are absorbed to a different extent in various segments of the GIT. Such drugs are said to have an absorption window, which identifies the drug’s primary region of absorption in the GIT. Gastroretentive tablets of Ondansetron hcl were successfully prepared by effervescent technique using different gel forming polymers- HPMC (K15M, K4M, 15cps, 3cps), and carbopol 934. Formulation was optimized on basis of floating time and in vitro release. The prepared gastroretentive test formulation was found to exhibit satisfactory physico-chemical characteristics at the end of 30 days, during the stability studies. The optimized formulation was found to be stable at 400C/ 75% RH.

Keywords

Absorption Window, Effervescent Technique, HPMC, Carbopol 934, Floating Time, Stability Studies.
Subscription Login to verify subscription
User
Notifications
Font Size


  • Hirtz J. The git absorption of drugs in man: a review of current concepts and methods of investigation. Br. J. Clin. Pharmacol. 1985; 19:77-83.
  • Harder S, Furh U, and Bergmann D. Ciprofloxacin Absorption in Different Regions of the Human GIT, Investigation with the Hf Capsule. Br. J. Clin. Pharmacol. 1990; 30(1):35–39.
  • Rouge N, Buri P, and Doelker E. Drug Absorption Site in the Gastrointestinal Tract and Dosage Forms for Site-Specific Delivery. Int. J. Pharm.1996; 136(1): 117–139.
  • Drewe J, Beglinger C, and Kissel T. The Absorption Site of Cyclosporin in Human GIT. Br. J. Clin. Pharmacol.1992; 33(1):39–43.
  • Streubel A, Siepmann J and Bodmeier R. Gastroretentive drug delivery system, Ex Ponchel G and Irache JM. Specific and non-specific bioadhesive particulate system for oral delivery to the gastrointestinal tract. Adv. Drug. Del. 1998; 34:191-219.
  • Ponchel G and Irache JM. Specific and non-specific bioadhesive particulate system for oral delivery to the gastrointestinal tract. Adv. Drug. Del. 1998; 34:191-219.
  • Lenaerts VM and Gurny R. Gastrointestinal Tract- Physiological variables affecting the performance of oral sustained release dosage forms Bioadhesive Drug Delivery System. CRC Press; 1990
  • Deshpande AA, Shah NH, Rhodes and CT, Malick W. Development of a novel controlled-release system for gastric retention. Pharm. Res. 1997; 14:815-819.
  • Rednick AB and Tucker SJ. Sustained release bolus for animal husbandry. US patent 3 507 952. April 22, 1970.
  • Davis SS, Stockwell AF, Taylor MJ, et al. The effect of density on the gastric emptying of single and multiple unit dosage forms. Pharm Res. 1986; 3:208-213.
  • Mamajek RC, Moyer ES, inventors. Drug dispensing device and method. US Patent 4 207 890. June 17, 1980.
  • Fix JA, Cargill R and Engle K. Controlled gastric emptying. III. Gastric residence time of a non-disintegrating geometric shape in human volunteers. Pharm. Res. 1993; 10:1087-1089.

Abstract Views: 198

PDF Views: 0




  • Formulation and Evaluation of Ondansetron Floating Tablet

Abstract Views: 198  |  PDF Views: 0

Authors

Lokesh Patle
Department of Pharmaceutics, Sardar Patel College of Technology (B. Pharmacy), Balaghat, M.P., India

Abstract


Some drugs are absorbed in a particular portion of the GIT only or are absorbed to a different extent in various segments of the GIT. Such drugs are said to have an absorption window, which identifies the drug’s primary region of absorption in the GIT. Gastroretentive tablets of Ondansetron hcl were successfully prepared by effervescent technique using different gel forming polymers- HPMC (K15M, K4M, 15cps, 3cps), and carbopol 934. Formulation was optimized on basis of floating time and in vitro release. The prepared gastroretentive test formulation was found to exhibit satisfactory physico-chemical characteristics at the end of 30 days, during the stability studies. The optimized formulation was found to be stable at 400C/ 75% RH.

Keywords


Absorption Window, Effervescent Technique, HPMC, Carbopol 934, Floating Time, Stability Studies.

References