Comparative Study on Fast Dissolving Tablets of Piroxicam Prepared by Direct Compression and Sublimation Methods

Fast dissolving tablets (FDTs) are designed to disintegrate rapidly in the oral cavity without the need for water, enhancing patient compliance. Piroxicam, a non-steroidal anti-inflammatory drug (NSAID) with poor solubility, can be formulated as FDTs to improve its bioavailability and therapeutic efficacy. In this study, FDTs of piroxicam were prepared using direct compression and sublimation techniques. Various sublimating agents, such as camphor, was employed to create a porous structure, enhancing the dissolution rate. The prepared tablets were evaluated for post-compression parameters, including weight variation, friability, hardness, wetting time, disintegration time, and in vitro drug release. The results demonstrated that tablets formulated using sublimation exhibited faster disintegration and improved dissolution compared to those prepared by direct compression alone.

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Publication Details

Journal
International Journal of Pharmaceutical Quality Assurance
Published
2024-12-30
DOI
https://doi.org/10.25258/ijpqa.15.4.44
Primary Topic
Drug Solubulity and Delivery Systems
Type
article
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article

Comparative Study on Fast Dissolving Tablets of Piroxicam Prepared by Direct Compression and Sublimation Methods

Abhay Gupta, R. K. Yadav
International Journal of Pharmaceutical Quality Assurance
Drug Solubulity and Delivery Systems
article

Comparative Study on Fast Dissolving Tablets of Piroxicam Prepared by Direct Compression and Sublimation Methods

Abhay Gupta, R. K. Yadav
article en

Abstract

Fast dissolving tablets (FDTs) are designed to disintegrate rapidly in the oral cavity without the need for water, enhancing patient compliance. Piroxicam, a non-steroidal anti-inflammatory drug (NSAID) with poor solubility, can be formulated as FDTs to improve its bioavailability and therapeutic efficacy. In this study, FDTs of piroxicam were prepared using direct compression and sublimation techniques. Various sublimating agents, such as camphor, was employed to create a porous structure, enhancing the dissolution rate. The prepared tablets were evaluated for post-compression parameters, including weight variation, friability, hardness, wetting time, disintegration time, and in vitro drug release. The results demonstrated that tablets formulated using sublimation exhibited faster disintegration and improved dissolution compared to those prepared by direct compression alone.

International Journal of Pharmaceutical Quality AssuranceVol. 15(04)
Sunrise University (IN), Alwar Pharmacy College (IN)
Openalex Percentile: Top 79%
Drug Solubulity and Delivery Systems
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