Development and release kinetics of a novel formulation of nimesulide prepared by microencapsulation using synthetic polymers
The synthetic polymers and their combinations were employed to retard the release of nimesulide from microcapsules. Microcapsules were prepared in different ratios of Eudragit RL 100 and hydroxy propyl methyl cellulose (HPMC) separately and in combination. All formulations of microcapsules were comp...
Guardado en:
Autores principales: | , , , , , |
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Formato: | Articulo |
Lenguaje: | Inglés |
Publicado: |
2011
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Materias: | |
Acceso en línea: | http://sedici.unlp.edu.ar/handle/10915/8263 http://www.latamjpharm.org/resumenes/30/6/LAJOP_30_6_1_5.pdf |
Aporte de: |
id |
I19-R120-10915-8263 |
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record_format |
dspace |
institution |
Universidad Nacional de La Plata |
institution_str |
I-19 |
repository_str |
R-120 |
collection |
SEDICI (UNLP) |
language |
Inglés |
topic |
Farmacia eudragit; HPMC; microencapsulation; nimesulide; release kinetics Agentes Antiinflamatorios no Esteroides Sistemas de Liberación de Medicamentos |
spellingShingle |
Farmacia eudragit; HPMC; microencapsulation; nimesulide; release kinetics Agentes Antiinflamatorios no Esteroides Sistemas de Liberación de Medicamentos Ranjha, Nazar M. Iqbal, Furqan Madni, Asadullah Usman, Muhammad Ahmad, Mahmood Aamir, Muhammad N. Development and release kinetics of a novel formulation of nimesulide prepared by microencapsulation using synthetic polymers |
topic_facet |
Farmacia eudragit; HPMC; microencapsulation; nimesulide; release kinetics Agentes Antiinflamatorios no Esteroides Sistemas de Liberación de Medicamentos |
description |
The synthetic polymers and their combinations were employed to retard the release of nimesulide from microcapsules. Microcapsules were prepared in different ratios of Eudragit RL 100 and hydroxy propyl methyl cellulose (HPMC) separately and in combination. All formulations of microcapsules were compressed to tablets. Dissolution of microcapsules and their tablets was performed by USP-apparatus-II in 900 mL borate buffer of pH 8.4 at 37.0 ± 0.5 ºC, at 50 rpm. In vitro kinetics was determined by various models including Zero order, First Order, Higuchi, Korsmeyer-Peppas and Hixson-Crowell. Eudragit showed higher retarding effect over extended period of time on release of drug than HPMC alone or its combination with Eudragit. |
format |
Articulo Articulo |
author |
Ranjha, Nazar M. Iqbal, Furqan Madni, Asadullah Usman, Muhammad Ahmad, Mahmood Aamir, Muhammad N. |
author_facet |
Ranjha, Nazar M. Iqbal, Furqan Madni, Asadullah Usman, Muhammad Ahmad, Mahmood Aamir, Muhammad N. |
author_sort |
Ranjha, Nazar M. |
title |
Development and release kinetics of a novel formulation of nimesulide prepared by microencapsulation using synthetic polymers |
title_short |
Development and release kinetics of a novel formulation of nimesulide prepared by microencapsulation using synthetic polymers |
title_full |
Development and release kinetics of a novel formulation of nimesulide prepared by microencapsulation using synthetic polymers |
title_fullStr |
Development and release kinetics of a novel formulation of nimesulide prepared by microencapsulation using synthetic polymers |
title_full_unstemmed |
Development and release kinetics of a novel formulation of nimesulide prepared by microencapsulation using synthetic polymers |
title_sort |
development and release kinetics of a novel formulation of nimesulide prepared by microencapsulation using synthetic polymers |
publishDate |
2011 |
url |
http://sedici.unlp.edu.ar/handle/10915/8263 http://www.latamjpharm.org/resumenes/30/6/LAJOP_30_6_1_5.pdf |
work_keys_str_mv |
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bdutipo_str |
Repositorios |
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1764820488463319041 |