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Strategies for formulation of effervescent granules of an herbal product for the management of typhoid fever
Herbal medicines are currently being adopted as alternatives to orthodox medicines for the management of drug-resistant and emerging multidrug-resistant microbial strains of various diseases, including typhoid fever. A herbal decoction, MA 001, manufactured by the Centre for Plant Medicine Research...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551464/ https://www.ncbi.nlm.nih.gov/pubmed/34746457 http://dx.doi.org/10.1016/j.heliyon.2021.e08147 |
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author | Adi-Dako, Ofosua Kumadoh, Doris Egbi, Godfred Okyem, Samuel Addo, Papa Yaw Nyarko, Alexander Osei-Asare, Christina Oppong, Esther Eshun Adase, Emmanuel |
author_facet | Adi-Dako, Ofosua Kumadoh, Doris Egbi, Godfred Okyem, Samuel Addo, Papa Yaw Nyarko, Alexander Osei-Asare, Christina Oppong, Esther Eshun Adase, Emmanuel |
author_sort | Adi-Dako, Ofosua |
collection | PubMed |
description | Herbal medicines are currently being adopted as alternatives to orthodox medicines for the management of drug-resistant and emerging multidrug-resistant microbial strains of various diseases, including typhoid fever. A herbal decoction, MA 001, manufactured by the Centre for Plant Medicine Research (CPMR), has been used for the treatment of typhoid fever for at least two decades in Ghana with desirable outcomes. MA 001 is formulated from Citrus aurantifolia, Spondias mombin, Latana camara, Bidens pilosa, Trema occidentalis, Psidium guajava, Morinda lucida, Vernonia amygdalina, Persea americana, Paulina pinnatta, Momordia charantia and Cnestis ferruguinea medicinal plants. The low palatability and compliance to treatment due to the bulky nature of the decoction poses challenges in its optimum use. This study sought to design and formulate the therapeutic components of the aqueous herbal decoction of MA 001 into an optimal solid dosage form of effervescent granules to improve the delivery of MA 001 as well as increase patient compliance and convenience of product handling. The methods involved pre-formulation studies on the suitability of effervescent vehicles, formulation and evaluation of effervescent granules for drug excipient interactions using high performance liquid chromatography analysis. The findings indicate that the effervescent granules were suitable for use in the delivery of the therapeutic constituents for the treatment of typhoid fever as done with the decoction due to minimal herbal extract-excipient interaction. |
format | Online Article Text |
id | pubmed-8551464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-85514642021-11-04 Strategies for formulation of effervescent granules of an herbal product for the management of typhoid fever Adi-Dako, Ofosua Kumadoh, Doris Egbi, Godfred Okyem, Samuel Addo, Papa Yaw Nyarko, Alexander Osei-Asare, Christina Oppong, Esther Eshun Adase, Emmanuel Heliyon Research Article Herbal medicines are currently being adopted as alternatives to orthodox medicines for the management of drug-resistant and emerging multidrug-resistant microbial strains of various diseases, including typhoid fever. A herbal decoction, MA 001, manufactured by the Centre for Plant Medicine Research (CPMR), has been used for the treatment of typhoid fever for at least two decades in Ghana with desirable outcomes. MA 001 is formulated from Citrus aurantifolia, Spondias mombin, Latana camara, Bidens pilosa, Trema occidentalis, Psidium guajava, Morinda lucida, Vernonia amygdalina, Persea americana, Paulina pinnatta, Momordia charantia and Cnestis ferruguinea medicinal plants. The low palatability and compliance to treatment due to the bulky nature of the decoction poses challenges in its optimum use. This study sought to design and formulate the therapeutic components of the aqueous herbal decoction of MA 001 into an optimal solid dosage form of effervescent granules to improve the delivery of MA 001 as well as increase patient compliance and convenience of product handling. The methods involved pre-formulation studies on the suitability of effervescent vehicles, formulation and evaluation of effervescent granules for drug excipient interactions using high performance liquid chromatography analysis. The findings indicate that the effervescent granules were suitable for use in the delivery of the therapeutic constituents for the treatment of typhoid fever as done with the decoction due to minimal herbal extract-excipient interaction. Elsevier 2021-10-09 /pmc/articles/PMC8551464/ /pubmed/34746457 http://dx.doi.org/10.1016/j.heliyon.2021.e08147 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Adi-Dako, Ofosua Kumadoh, Doris Egbi, Godfred Okyem, Samuel Addo, Papa Yaw Nyarko, Alexander Osei-Asare, Christina Oppong, Esther Eshun Adase, Emmanuel Strategies for formulation of effervescent granules of an herbal product for the management of typhoid fever |
title | Strategies for formulation of effervescent granules of an herbal product for the management of typhoid fever |
title_full | Strategies for formulation of effervescent granules of an herbal product for the management of typhoid fever |
title_fullStr | Strategies for formulation of effervescent granules of an herbal product for the management of typhoid fever |
title_full_unstemmed | Strategies for formulation of effervescent granules of an herbal product for the management of typhoid fever |
title_short | Strategies for formulation of effervescent granules of an herbal product for the management of typhoid fever |
title_sort | strategies for formulation of effervescent granules of an herbal product for the management of typhoid fever |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551464/ https://www.ncbi.nlm.nih.gov/pubmed/34746457 http://dx.doi.org/10.1016/j.heliyon.2021.e08147 |
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