Formulation and evaluation of amoxicillin Oro-dispersible tablets

The purpose of the project was to prepare amoxicillin orodispersible tablets specially for enhanced pediatrics compliance. The amoxicillin drug belongs to BCS class II with poor solubility and high permeability property. It has a very good bioavailability over 90%, which is available in tablet and parenteral formulation. The orodispersible tablets of amoxicillin prepared with sodium starch glycollate as superdisintegrant in varying amount by wet granulation technique. The prepared tablets were tested for preformulation compatibility studies by FTIR for the drug and excipient and post compression studies of the tablet formulation and all the parameters were found in acceptable limits. The invitro dissolution studies of five formulations were done and the optimized formulation was found to be F5 with 97%.

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Publication Details

Journal
International Journal of Pharmacy and Pharmaceutical Science
Published
2025-01-01
DOI
https://doi.org/10.33545/26647222.2025.v7.i1b.159
Primary Topic
Analytical Methods in Pharmaceuticals
Type
article
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article

Formulation and evaluation of amoxicillin Oro-dispersible tablets

Chandrasekhara Rao Baru, Darupally Madhuri, Sushma Desai, Naik Arkprabha et al.
International Journal of Pharmacy and Pharmaceutical Science
Analytical Methods in Pharmaceuticals
article

Formulation and evaluation of amoxicillin Oro-dispersible tablets

Chandrasekhara Rao Baru, Darupally Madhuri, Sushma Desai, Naik Arkprabha, Tene Akhil Kumar, Khan Sufiyan Zahiruddin, Raihan Aftab
article en

Abstract

The purpose of the project was to prepare amoxicillin orodispersible tablets specially for enhanced pediatrics compliance. The amoxicillin drug belongs to BCS class II with poor solubility and high permeability property. It has a very good bioavailability over 90%, which is available in tablet and parenteral formulation. The orodispersible tablets of amoxicillin prepared with sodium starch glycollate as superdisintegrant in varying amount by wet granulation technique. The prepared tablets were tested for preformulation compatibility studies by FTIR for the drug and excipient and post compression studies of the tablet formulation and all the parameters were found in acceptable limits. The invitro dissolution studies of five formulations were done and the optimized formulation was found to be F5 with 97%.

International Journal of Pharmacy and Pharmaceutical ScienceVol. 7(1)
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Openalex Percentile: Top 94%
Analytical Methods in Pharmaceuticals
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