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Authors
Affiliations
1 Parul Institute of Pharmacy, Limda, Vadodara-
391760, Gujarat, IN
2 Parul Institute of Pharmacy, Limda, Vadodara-391760, Gujarat, IN
3 Indo Soviet Friendship College of Pharmacy, Ghalkalan, Moga, Punjab, IN
Source
Research Journal of Pharmaceutical Dosage Form and Technology, Vol 2, No 2 (2010), Pagination: 198-203
Abstract
In the present work, Orodispersible tablet of Aceclofenac were designed with a view to Enhance patient compliance. A combination of superdisintegrants i.e.Ac-di-sol (Croscarmellose sodium), Polyplasdone XL-10, Microcrystalline Cellulose pH 102 was Used along with directly compressible dextrose to enhance mouth feel. The prepared Batches of tablet were evaluated for hardness, friability, drug content uniformity, wetting time, water absorption ratio and in vitro dispersion time. Based on in vitro dispersion time, two formulation were tested for in vitro drug release pattern (in pH7. 4phosphatebuffer), short - term stability at 25°C ± 2°C/60% RH, 30°C ± 2°C/65% RH, 40°C ± 2°C/75% RH for 3 month and drug -excipient interaction (IR Spectroscopy) among the two formulation, the formulation prepared by direct Compression method using Ac-di-sol (croscarmellose sodium) 50mg, Polyplasdone XL- 10 -25mg, Microcrystalline Cellulose pH 102- 25mg was found tobe better formulation T80% = 5 min. based on in- vitro drug release characteristics. Short term stability studies on the formulation indicated that there is no significant change in drug content and in vitro dispersion time.
Keywords
Orodispersible Tablet, Aceclofenac, Direct Compression, 23 Factorial Design.
