Development, evaluation and optimization of baclofen oral floating tablet

The present investigation concerns the development of a floating matrix tablet, which after oral administration prolong the gastric residence time and increases bioavailability of drugs, which are predominantly absorbed from gastric region .With this aim, floating dosage form containing baclofen as...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Singh, Akhilesh V., Pandey, Rishabh D., Nath, Lila K., Das, Anudwipa
Formato: Articulo
Lenguaje:Inglés
Publicado: 2010
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/7948
http://www.latamjpharm.org/resumenes/29/4/LAJOP_29_4_1_11.pdf
Aporte de:
id I19-R120-10915-7948
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Farmacia
baclofen; floating tablets; optimization; sustained release
Farmacología
Medicamentos
Composición de medicamentos
spellingShingle Farmacia
baclofen; floating tablets; optimization; sustained release
Farmacología
Medicamentos
Composición de medicamentos
Singh, Akhilesh V.
Pandey, Rishabh D.
Nath, Lila K.
Das, Anudwipa
Development, evaluation and optimization of baclofen oral floating tablet
topic_facet Farmacia
baclofen; floating tablets; optimization; sustained release
Farmacología
Medicamentos
Composición de medicamentos
description The present investigation concerns the development of a floating matrix tablet, which after oral administration prolong the gastric residence time and increases bioavailability of drugs, which are predominantly absorbed from gastric region .With this aim, floating dosage form containing baclofen as drug, and different grades of HPMC as release retarding polymer was prepared. Sodium bicarbonate and citric acid were used as gas generating agents. Some factors were investigated concerning the effect of release retarding polymer on drug release behaviors like t50% and t90%. A 32 factorial design was applied to optimize the drug release profile. The amounts of HPMC K4M(X1) and HPMC K100M (X2) were selected as independent variables. The time required for 50% (t50%) and 90% (t90%) drug dissolution were selected as dependent variables. The results of full factorial design indicates that moderate amount of both the release retardant polymer, controlled the release behavior. It can be concluded from release kinetic models that the release followed Higuchi model, as the correlation coefficient (R2 value) was high in all the evaluated models. The release mechanism followed non-fickian diffusion as the release exponent (n-value) was >0.5 in all the optimized formulations.
format Articulo
Articulo
author Singh, Akhilesh V.
Pandey, Rishabh D.
Nath, Lila K.
Das, Anudwipa
author_facet Singh, Akhilesh V.
Pandey, Rishabh D.
Nath, Lila K.
Das, Anudwipa
author_sort Singh, Akhilesh V.
title Development, evaluation and optimization of baclofen oral floating tablet
title_short Development, evaluation and optimization of baclofen oral floating tablet
title_full Development, evaluation and optimization of baclofen oral floating tablet
title_fullStr Development, evaluation and optimization of baclofen oral floating tablet
title_full_unstemmed Development, evaluation and optimization of baclofen oral floating tablet
title_sort development, evaluation and optimization of baclofen oral floating tablet
publishDate 2010
url http://sedici.unlp.edu.ar/handle/10915/7948
http://www.latamjpharm.org/resumenes/29/4/LAJOP_29_4_1_11.pdf
work_keys_str_mv AT singhakhileshv developmentevaluationandoptimizationofbaclofenoralfloatingtablet
AT pandeyrishabhd developmentevaluationandoptimizationofbaclofenoralfloatingtablet
AT nathlilak developmentevaluationandoptimizationofbaclofenoralfloatingtablet
AT dasanudwipa developmentevaluationandoptimizationofbaclofenoralfloatingtablet
bdutipo_str Repositorios
_version_ 1764820486803423232