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Development and Evaluation of pH-Dependent Micro Beads for Colon Targeting

The purpose of this research was to develop and evaluate multiparticulates of alginate and chitosan hydrogel beads exploiting pH sensitive property for colon-targeted delivery of theophylline. Alginate and chitosan beads were prepared by ionotropic gelation method followed by enteric coating with Eu...

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Detalles Bibliográficos
Autores principales: Khan, M. S., Sridhar, B. K., Srinatha, A.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883222/
https://www.ncbi.nlm.nih.gov/pubmed/20582185
http://dx.doi.org/10.4103/0250-474X.62230
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author Khan, M. S.
Sridhar, B. K.
Srinatha, A.
author_facet Khan, M. S.
Sridhar, B. K.
Srinatha, A.
author_sort Khan, M. S.
collection PubMed
description The purpose of this research was to develop and evaluate multiparticulates of alginate and chitosan hydrogel beads exploiting pH sensitive property for colon-targeted delivery of theophylline. Alginate and chitosan beads were prepared by ionotropic gelation method followed by enteric coating with Eudragit S100. All formulations were evaluated for particle size, encapsulation efficiency, swellability and in vitro drug release.In vitro dissolution studies performed following pH progression method demonstrated that the drug release from coated beads depends on coat weights applied and pH of dissolution media. Mechanism of drug release was found to be swelling and erosion-dependent. The studies showed that formulated alginate and chitosan beads can be used effectively for the delivery of drug to colon and a coat weight of 20% weight gain was sufficient to impart an excellent gastro resistant property to the beads for effective release of drug at higher pH values.
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spelling pubmed-28832222010-06-25 Development and Evaluation of pH-Dependent Micro Beads for Colon Targeting Khan, M. S. Sridhar, B. K. Srinatha, A. Indian J Pharm Sci Research Paper The purpose of this research was to develop and evaluate multiparticulates of alginate and chitosan hydrogel beads exploiting pH sensitive property for colon-targeted delivery of theophylline. Alginate and chitosan beads were prepared by ionotropic gelation method followed by enteric coating with Eudragit S100. All formulations were evaluated for particle size, encapsulation efficiency, swellability and in vitro drug release.In vitro dissolution studies performed following pH progression method demonstrated that the drug release from coated beads depends on coat weights applied and pH of dissolution media. Mechanism of drug release was found to be swelling and erosion-dependent. The studies showed that formulated alginate and chitosan beads can be used effectively for the delivery of drug to colon and a coat weight of 20% weight gain was sufficient to impart an excellent gastro resistant property to the beads for effective release of drug at higher pH values. Medknow Publications 2010 /pmc/articles/PMC2883222/ /pubmed/20582185 http://dx.doi.org/10.4103/0250-474X.62230 Text en © Indian Journal of Pharmaceutical Sciences http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Khan, M. S.
Sridhar, B. K.
Srinatha, A.
Development and Evaluation of pH-Dependent Micro Beads for Colon Targeting
title Development and Evaluation of pH-Dependent Micro Beads for Colon Targeting
title_full Development and Evaluation of pH-Dependent Micro Beads for Colon Targeting
title_fullStr Development and Evaluation of pH-Dependent Micro Beads for Colon Targeting
title_full_unstemmed Development and Evaluation of pH-Dependent Micro Beads for Colon Targeting
title_short Development and Evaluation of pH-Dependent Micro Beads for Colon Targeting
title_sort development and evaluation of ph-dependent micro beads for colon targeting
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883222/
https://www.ncbi.nlm.nih.gov/pubmed/20582185
http://dx.doi.org/10.4103/0250-474X.62230
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