Formulation and Evaluation of Atenolol Orodispersible Tablets

The main objective of this study was to prepare and evaluate fast dissolving tablets of Atenolol using three different types of superdisintegrants. Various formulations were prepared by direct compression using different concentrations of superdisintegrant i.e. namely Kyron T-104, Kyron T-154 and Kyron T-314. The compatibility studies between drug and excipients were carried out using FTIR spectroscopy. The blend was evaluated for additive properties. The tablets were evaluated for physical properties and in vitro drug release. From this study formulation containing Kyron T-154 was found to possess better disintegration time of 15 secs, water absorption ratio (77.5 %), and wetting time (22.7 sec) with taste masking property at low concentration. An accelerated stability study on optimized formulation was performed as per ICH guidelines. It was found to be stable, with insignificant changes in the hardness, disintegration time, and in-vitro drug release pattern.

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Publication Details

Journal
Asian Journal of Pharmaceutical Research and Development
Published
2024-12-15
DOI
https://doi.org/10.22270/ajprd.v12i6.1454
Primary Topic
Drug Solubulity and Delivery Systems
Type
article
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article

Formulation and Evaluation of Atenolol Orodispersible Tablets

D Prasanthi, Ruhi Anjum, Mohammed M. Shareef
Asian Journal of Pharmaceutical Research and Development
Drug Solubulity and Delivery Systems
article

Formulation and Evaluation of Atenolol Orodispersible Tablets

D Prasanthi, Ruhi Anjum, Mohammed M. Shareef
article en

Abstract

The main objective of this study was to prepare and evaluate fast dissolving tablets of Atenolol using three different types of superdisintegrants. Various formulations were prepared by direct compression using different concentrations of superdisintegrant i.e. namely Kyron T-104, Kyron T-154 and Kyron T-314. The compatibility studies between drug and excipients were carried out using FTIR spectroscopy. The blend was evaluated for additive properties. The tablets were evaluated for physical properties and in vitro drug release. From this study formulation containing Kyron T-154 was found to possess better disintegration time of 15 secs, water absorption ratio (77.5 %), and wetting time (22.7 sec) with taste masking property at low concentration. An accelerated stability study on optimized formulation was performed as per ICH guidelines. It was found to be stable, with insignificant changes in the hardness, disintegration time, and in-vitro drug release pattern.

Asian Journal of Pharmaceutical Research and DevelopmentVol. 12(6)
Osmania University (IN)
Openalex Percentile: Top 80%
Drug Solubulity and Delivery Systems
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