Orally disintegrating tablet: formulation design and optimisation using Response Surface Methodology
The objective of this study was to develop diazepam orally disintegrating tablets and to optimize tablets characteristics using response surface methodology (RSM). Tablets were prepared by direct compression of mixture containing mannitol, copovidone, crosspovidone flavor and lubricant. A full fac...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
University Ss Cyril and Methodius in Skopje, Faculty of Pharmacy and Macedonian Pharmaceutical Association
2005-12-01
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| Series: | Makedonsko Farmacevtski Bilten |
| Online Access: | http://bulletin.mfd.org.mk/volumes/Volume%2051/51_003.pdf |
| Summary: | The objective of this study was to develop diazepam orally disintegrating tablets and to optimize tablets characteristics using
response surface methodology (RSM). Tablets were prepared by direct compression of mixture containing mannitol, copovidone,
crosspovidone flavor and lubricant. A full factorial design for 2 factors at 3 levels each was applied to investigate the influence of 2
formulation variables on the mechanical strength/hardness, the percent of friability, disintegration time and dissolution of the poorly
soluble active ingredient. The amounts of copovidone and crosspovidone were taken as independent variables. All data were analyzed by using statistical program.
The results of multiple linear regression analysis revealed that for obtaining a rapidly disintegrating dosage form, tablets should be
prepared using an optimum concentration of crospovidone and copovidone. A contour plot is also presented to graphically represent the effect of the independent variables on the tablet hardness, disintegration time, percentage friability and dissolution. A checkpoint batch was also prepared to prove the validity of the evolved mathematical model. 3 level factorial design allowed us to obtain ODT with rapid disintegration and dissolution of the active ingredient with desirable properties of low tablet friability and appropriate mechanical strength (hardness) of the tablet. |
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| ISSN: | 1409-8695 1857-8969 |