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Formulation, characterization and physicochemical evaluation of amoxicillin effervescent tablets

BACKGROUND: Amoxicillin is a semisynthetic antibiotic, which is used as an antimicrobial drug. This study was designed to formulate amoxicillin effervescent tablets, aimed at improved patient compliance and increased drug stability. MATERIALS AND METHODS: In this study, nine effervescent tablet form...

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Autores principales: Aslani, Abolfazl, Sharifian, Tahereh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219208/
https://www.ncbi.nlm.nih.gov/pubmed/25371866
http://dx.doi.org/10.4103/2277-9175.143252
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author Aslani, Abolfazl
Sharifian, Tahereh
author_facet Aslani, Abolfazl
Sharifian, Tahereh
author_sort Aslani, Abolfazl
collection PubMed
description BACKGROUND: Amoxicillin is a semisynthetic antibiotic, which is used as an antimicrobial drug. This study was designed to formulate amoxicillin effervescent tablets, aimed at improved patient compliance and increased drug stability. MATERIALS AND METHODS: In this study, nine effervescent tablet formulations were prepared from amoxicillin trihydrate. The effervescent base was comprised of various amounts of citric acid and sodium bicarbonate. Powders and granules were evaluated for their particle size, bulk density, tapped density, compressibility index, Hausner's ratio and angle of repose. The effervescent tablets were then prepared from powders and granules of acceptable quality by direct compression and fusion methods. The tablets were evaluated for weight variation, friability, pH of solution, carbon dioxide (CO(2)) content, hardness, effervescence time, thickness, assay, content uniformity, water content and equilibrium moisture content. RESULTS: The results indicated better flowability of granules prepared by fusion method as compared with the direct compression. The percent weight variations of tablets were within the acceptable limit of 0.5%. The friability was less than 1% in all formulations. The solution pH of tablets prepared by direct compression and fusion methods ranged from 4.55 to 5.74 and 4.74-5.84, respectively. The CO(2) amounts generated by of fusion method tablets were smaller as compared to the direct compression method. The hardness of tablets was 40.66-56 for direct compression method and 60.6-74.6 for fusion method. The tablets produced by the fusion method had a larger thickness and lower water content than tablets produced by direct compression method. CONCLUSION: Tablets prepared by the fusion method exhibited superior pre- and post-compression characteristics as compared to tablets prepared by direct compression method.
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spelling pubmed-42192082014-11-04 Formulation, characterization and physicochemical evaluation of amoxicillin effervescent tablets Aslani, Abolfazl Sharifian, Tahereh Adv Biomed Res Original Article BACKGROUND: Amoxicillin is a semisynthetic antibiotic, which is used as an antimicrobial drug. This study was designed to formulate amoxicillin effervescent tablets, aimed at improved patient compliance and increased drug stability. MATERIALS AND METHODS: In this study, nine effervescent tablet formulations were prepared from amoxicillin trihydrate. The effervescent base was comprised of various amounts of citric acid and sodium bicarbonate. Powders and granules were evaluated for their particle size, bulk density, tapped density, compressibility index, Hausner's ratio and angle of repose. The effervescent tablets were then prepared from powders and granules of acceptable quality by direct compression and fusion methods. The tablets were evaluated for weight variation, friability, pH of solution, carbon dioxide (CO(2)) content, hardness, effervescence time, thickness, assay, content uniformity, water content and equilibrium moisture content. RESULTS: The results indicated better flowability of granules prepared by fusion method as compared with the direct compression. The percent weight variations of tablets were within the acceptable limit of 0.5%. The friability was less than 1% in all formulations. The solution pH of tablets prepared by direct compression and fusion methods ranged from 4.55 to 5.74 and 4.74-5.84, respectively. The CO(2) amounts generated by of fusion method tablets were smaller as compared to the direct compression method. The hardness of tablets was 40.66-56 for direct compression method and 60.6-74.6 for fusion method. The tablets produced by the fusion method had a larger thickness and lower water content than tablets produced by direct compression method. CONCLUSION: Tablets prepared by the fusion method exhibited superior pre- and post-compression characteristics as compared to tablets prepared by direct compression method. Medknow Publications & Media Pvt Ltd 2014-10-20 /pmc/articles/PMC4219208/ /pubmed/25371866 http://dx.doi.org/10.4103/2277-9175.143252 Text en Copyright: © 2014 Aslani. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Original Article
Aslani, Abolfazl
Sharifian, Tahereh
Formulation, characterization and physicochemical evaluation of amoxicillin effervescent tablets
title Formulation, characterization and physicochemical evaluation of amoxicillin effervescent tablets
title_full Formulation, characterization and physicochemical evaluation of amoxicillin effervescent tablets
title_fullStr Formulation, characterization and physicochemical evaluation of amoxicillin effervescent tablets
title_full_unstemmed Formulation, characterization and physicochemical evaluation of amoxicillin effervescent tablets
title_short Formulation, characterization and physicochemical evaluation of amoxicillin effervescent tablets
title_sort formulation, characterization and physicochemical evaluation of amoxicillin effervescent tablets
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219208/
https://www.ncbi.nlm.nih.gov/pubmed/25371866
http://dx.doi.org/10.4103/2277-9175.143252
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