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Evaluation of Aloe elegans Mucilage as a Suspending Agent in Paracetamol Suspension
BACKGROUND: There are various natural excipients which have been used as suspending agents in pharmaceutical suspensions due to the presence of mucilage in their specialized cells and their capacity to form a colloidal gel in an aqueous medium. OBJECTIVE: The purpose of this study was to evaluate th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8349256/ https://www.ncbi.nlm.nih.gov/pubmed/34373833 http://dx.doi.org/10.1155/2021/5058372 |
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author | Woldu, Gebremariam Baymot, Berhe Tesfay, Desta Demoz, Gebre Teklemariam |
author_facet | Woldu, Gebremariam Baymot, Berhe Tesfay, Desta Demoz, Gebre Teklemariam |
author_sort | Woldu, Gebremariam |
collection | PubMed |
description | BACKGROUND: There are various natural excipients which have been used as suspending agents in pharmaceutical suspensions due to the presence of mucilage in their specialized cells and their capacity to form a colloidal gel in an aqueous medium. OBJECTIVE: The purpose of this study was to evaluate the suspending capacity of Aloe elegans mucilage in suspension formulations. MATERIALS AND METHODS: Aloe elegans mucilage (AEM) was evaluated as a suspending agent in comparison with xanthan gum (XG) in paracetamol suspensions at 1, 2, 3, 4, and 5% (w/v) concentrations. The resulting suspensions were evaluated for their sedimentation volume, apparent viscosity, flow rate, rate of redispersibility, pH, assay, and dissolution profile. RESULTS: The volume of sedimentation, apparent viscosity, and redispersibility rate of the formulations were significantly increased (p < 0.05), with the concentration of the suspending agents. Meanwhile, the apparent viscosity for all formulations has significantly decreased (p < 0.05) with an increase in shear rates. Volume of sedimentation, apparent viscosity, and redispersibility degree of the formulations prepared with AEM were significantly (p < 0.05) lower than XG-containing formulations at the same concentration. Nevertheless, the sedimentation volume of all formulations with AEM was significantly (p < 0.05) higher than the suspension without any suspending agent. With regard to drug content and pH values, all formulations showed an acceptable result with the standards. All formulations showed a release of greater than 85% of drug content within 45 min. CONCLUSION: Aloe elegans mucilage could have a potential to be utilized as an alternative suspending agent in pharmaceutical suspensions. |
format | Online Article Text |
id | pubmed-8349256 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-83492562021-08-08 Evaluation of Aloe elegans Mucilage as a Suspending Agent in Paracetamol Suspension Woldu, Gebremariam Baymot, Berhe Tesfay, Desta Demoz, Gebre Teklemariam Biomed Res Int Research Article BACKGROUND: There are various natural excipients which have been used as suspending agents in pharmaceutical suspensions due to the presence of mucilage in their specialized cells and their capacity to form a colloidal gel in an aqueous medium. OBJECTIVE: The purpose of this study was to evaluate the suspending capacity of Aloe elegans mucilage in suspension formulations. MATERIALS AND METHODS: Aloe elegans mucilage (AEM) was evaluated as a suspending agent in comparison with xanthan gum (XG) in paracetamol suspensions at 1, 2, 3, 4, and 5% (w/v) concentrations. The resulting suspensions were evaluated for their sedimentation volume, apparent viscosity, flow rate, rate of redispersibility, pH, assay, and dissolution profile. RESULTS: The volume of sedimentation, apparent viscosity, and redispersibility rate of the formulations were significantly increased (p < 0.05), with the concentration of the suspending agents. Meanwhile, the apparent viscosity for all formulations has significantly decreased (p < 0.05) with an increase in shear rates. Volume of sedimentation, apparent viscosity, and redispersibility degree of the formulations prepared with AEM were significantly (p < 0.05) lower than XG-containing formulations at the same concentration. Nevertheless, the sedimentation volume of all formulations with AEM was significantly (p < 0.05) higher than the suspension without any suspending agent. With regard to drug content and pH values, all formulations showed an acceptable result with the standards. All formulations showed a release of greater than 85% of drug content within 45 min. CONCLUSION: Aloe elegans mucilage could have a potential to be utilized as an alternative suspending agent in pharmaceutical suspensions. Hindawi 2021-07-31 /pmc/articles/PMC8349256/ /pubmed/34373833 http://dx.doi.org/10.1155/2021/5058372 Text en Copyright © 2021 Gebremariam Woldu et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Woldu, Gebremariam Baymot, Berhe Tesfay, Desta Demoz, Gebre Teklemariam Evaluation of Aloe elegans Mucilage as a Suspending Agent in Paracetamol Suspension |
title | Evaluation of Aloe elegans Mucilage as a Suspending Agent in Paracetamol Suspension |
title_full | Evaluation of Aloe elegans Mucilage as a Suspending Agent in Paracetamol Suspension |
title_fullStr | Evaluation of Aloe elegans Mucilage as a Suspending Agent in Paracetamol Suspension |
title_full_unstemmed | Evaluation of Aloe elegans Mucilage as a Suspending Agent in Paracetamol Suspension |
title_short | Evaluation of Aloe elegans Mucilage as a Suspending Agent in Paracetamol Suspension |
title_sort | evaluation of aloe elegans mucilage as a suspending agent in paracetamol suspension |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8349256/ https://www.ncbi.nlm.nih.gov/pubmed/34373833 http://dx.doi.org/10.1155/2021/5058372 |
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