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Factorial analysis of the binding properties of acetylated ginger starch in metronidazole tablet formulations
INTRODUCTION: The delivery of drug is often affected by formulation processes and the excipients used in the formulation. MATERIALS AND METHODS: A 2(3) factorial analysis was used in this study to evaluate the effect of acetylated ginger starch (AGS) (Zingiber officinale) as a binder in metronidazol...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370345/ https://www.ncbi.nlm.nih.gov/pubmed/28405575 http://dx.doi.org/10.4103/jphi.JPHI_31_16 |
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author | Bamiro, Oluyemisi Adebowale Duro-Emanuel, Abioye Josephina |
author_facet | Bamiro, Oluyemisi Adebowale Duro-Emanuel, Abioye Josephina |
author_sort | Bamiro, Oluyemisi Adebowale |
collection | PubMed |
description | INTRODUCTION: The delivery of drug is often affected by formulation processes and the excipients used in the formulation. MATERIALS AND METHODS: A 2(3) factorial analysis was used in this study to evaluate the effect of acetylated ginger starch (AGS) (Zingiber officinale) as a binder in metronidazole tablets, in comparison to corn starch (CS) BP. The individual and interacting effects of variables (binder type X(1), binder concentration X(2), and compression pressure X(3)) used on tablet properties such as friability, crushing strength, crushing strength friability ratio (CSFR), disintegration and crushing strength friability/disintegration time ratio (CSFR/DT) were determined. The effect of these binders on the granule properties using Hausner's ratio, Carr's index (CI), angle of repose, and densities as response parameters was also determined. RESULTS: Granules prepared with AGS had high densities and small granule sizes when compared with those containing CS. Granules containing CS have better flow properties. X(1) (binder type) has a significant effect on the crushing strength of the tablet. It also had the highest effects on CSFR and CSFR/DT. The combination of X(I)X(3) had the highest effect on crushing strength and DT. CONCLUSION: This study shows that, in formulations, care must be taken in choosing the excipients and the process parameters required for the formulation since these can affect the delivery of the drug individually or in combination. AGS could be useful as a binder when a tablet with low crushing strength and fast disintegration is desired. |
format | Online Article Text |
id | pubmed-5370345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53703452017-04-12 Factorial analysis of the binding properties of acetylated ginger starch in metronidazole tablet formulations Bamiro, Oluyemisi Adebowale Duro-Emanuel, Abioye Josephina Int J Pharm Investig Original Research Article INTRODUCTION: The delivery of drug is often affected by formulation processes and the excipients used in the formulation. MATERIALS AND METHODS: A 2(3) factorial analysis was used in this study to evaluate the effect of acetylated ginger starch (AGS) (Zingiber officinale) as a binder in metronidazole tablets, in comparison to corn starch (CS) BP. The individual and interacting effects of variables (binder type X(1), binder concentration X(2), and compression pressure X(3)) used on tablet properties such as friability, crushing strength, crushing strength friability ratio (CSFR), disintegration and crushing strength friability/disintegration time ratio (CSFR/DT) were determined. The effect of these binders on the granule properties using Hausner's ratio, Carr's index (CI), angle of repose, and densities as response parameters was also determined. RESULTS: Granules prepared with AGS had high densities and small granule sizes when compared with those containing CS. Granules containing CS have better flow properties. X(1) (binder type) has a significant effect on the crushing strength of the tablet. It also had the highest effects on CSFR and CSFR/DT. The combination of X(I)X(3) had the highest effect on crushing strength and DT. CONCLUSION: This study shows that, in formulations, care must be taken in choosing the excipients and the process parameters required for the formulation since these can affect the delivery of the drug individually or in combination. AGS could be useful as a binder when a tablet with low crushing strength and fast disintegration is desired. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5370345/ /pubmed/28405575 http://dx.doi.org/10.4103/jphi.JPHI_31_16 Text en Copyright: © 2017 International Journal of Pharmaceutical Investigation http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Research Article Bamiro, Oluyemisi Adebowale Duro-Emanuel, Abioye Josephina Factorial analysis of the binding properties of acetylated ginger starch in metronidazole tablet formulations |
title | Factorial analysis of the binding properties of acetylated ginger starch in metronidazole tablet formulations |
title_full | Factorial analysis of the binding properties of acetylated ginger starch in metronidazole tablet formulations |
title_fullStr | Factorial analysis of the binding properties of acetylated ginger starch in metronidazole tablet formulations |
title_full_unstemmed | Factorial analysis of the binding properties of acetylated ginger starch in metronidazole tablet formulations |
title_short | Factorial analysis of the binding properties of acetylated ginger starch in metronidazole tablet formulations |
title_sort | factorial analysis of the binding properties of acetylated ginger starch in metronidazole tablet formulations |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370345/ https://www.ncbi.nlm.nih.gov/pubmed/28405575 http://dx.doi.org/10.4103/jphi.JPHI_31_16 |
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