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Formulation and Evaluation of Liquisolid Compacts for Olmesartan Medoxomil
Olmesartan medoxomil is an angiotensin type II receptor blocker, antihypertensive agent, administered orally. It is highly lipophilic (log P 5.5) and a poorly water-soluble drug with absolute bioavailability of 26%. The poor dissolution rate of water-insoluble drugs is still a major problem confront...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3818897/ https://www.ncbi.nlm.nih.gov/pubmed/24232077 http://dx.doi.org/10.1155/2013/870579 |
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author | Prajapati, Shailesh T. Bulchandani, Hitesh H. Patel, Dashrath M. Dumaniya, Suresh K. Patel, Chhaganbhai N. |
author_facet | Prajapati, Shailesh T. Bulchandani, Hitesh H. Patel, Dashrath M. Dumaniya, Suresh K. Patel, Chhaganbhai N. |
author_sort | Prajapati, Shailesh T. |
collection | PubMed |
description | Olmesartan medoxomil is an angiotensin type II receptor blocker, antihypertensive agent, administered orally. It is highly lipophilic (log P 5.5) and a poorly water-soluble drug with absolute bioavailability of 26%. The poor dissolution rate of water-insoluble drugs is still a major problem confronting the pharmaceutical industry. The objective of the present investigation was to develop liquisolid compacts for olmesartan medoxomil to improve the dissolution rate. Liquisolid compacts were prepared using Acrysol El 135 as a solvent, Avicel PH 102, Fujicalin and Neusilin as carrier materials, and Aerosil as coating material in different ratios. The interaction between drug and excipients was characterized by DSC and FT-IR studies, which showed that there is no interaction between drug and excipients. The powder characteristics were evaluated by different flow parameters to comply with pharmacopoeial limits. The dissolution studies for liquisolid compacts and conventional formulations were carried out, and it was found that liquisolid compacts with 80% w/w of Acrysol EL 135 to the drug showed significant higher drug release rates than conventional tablets. Amongst carriers used Fujicalin and Neusilin were found to be more effective carrier materials for liquid adsorption. |
format | Online Article Text |
id | pubmed-3818897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-38188972013-11-14 Formulation and Evaluation of Liquisolid Compacts for Olmesartan Medoxomil Prajapati, Shailesh T. Bulchandani, Hitesh H. Patel, Dashrath M. Dumaniya, Suresh K. Patel, Chhaganbhai N. J Drug Deliv Research Article Olmesartan medoxomil is an angiotensin type II receptor blocker, antihypertensive agent, administered orally. It is highly lipophilic (log P 5.5) and a poorly water-soluble drug with absolute bioavailability of 26%. The poor dissolution rate of water-insoluble drugs is still a major problem confronting the pharmaceutical industry. The objective of the present investigation was to develop liquisolid compacts for olmesartan medoxomil to improve the dissolution rate. Liquisolid compacts were prepared using Acrysol El 135 as a solvent, Avicel PH 102, Fujicalin and Neusilin as carrier materials, and Aerosil as coating material in different ratios. The interaction between drug and excipients was characterized by DSC and FT-IR studies, which showed that there is no interaction between drug and excipients. The powder characteristics were evaluated by different flow parameters to comply with pharmacopoeial limits. The dissolution studies for liquisolid compacts and conventional formulations were carried out, and it was found that liquisolid compacts with 80% w/w of Acrysol EL 135 to the drug showed significant higher drug release rates than conventional tablets. Amongst carriers used Fujicalin and Neusilin were found to be more effective carrier materials for liquid adsorption. Hindawi Publishing Corporation 2013 2013-10-21 /pmc/articles/PMC3818897/ /pubmed/24232077 http://dx.doi.org/10.1155/2013/870579 Text en Copyright © 2013 Shailesh T. Prajapati et al. https://creativecommons.org/licenses/by/3.0/ 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 Prajapati, Shailesh T. Bulchandani, Hitesh H. Patel, Dashrath M. Dumaniya, Suresh K. Patel, Chhaganbhai N. Formulation and Evaluation of Liquisolid Compacts for Olmesartan Medoxomil |
title | Formulation and Evaluation of Liquisolid Compacts for Olmesartan Medoxomil |
title_full | Formulation and Evaluation of Liquisolid Compacts for Olmesartan Medoxomil |
title_fullStr | Formulation and Evaluation of Liquisolid Compacts for Olmesartan Medoxomil |
title_full_unstemmed | Formulation and Evaluation of Liquisolid Compacts for Olmesartan Medoxomil |
title_short | Formulation and Evaluation of Liquisolid Compacts for Olmesartan Medoxomil |
title_sort | formulation and evaluation of liquisolid compacts for olmesartan medoxomil |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3818897/ https://www.ncbi.nlm.nih.gov/pubmed/24232077 http://dx.doi.org/10.1155/2013/870579 |
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