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Development and Evaluation of Oral Controlled Release Chlorpheniramine-Ion Exchange Resinate Suspension

An oral controlled release suspension of chlorpheniramine maleate was prepared using ion-exchange resin technology. A strong cation exchange resin Indion 244 was utilized for the sorption of the drug and the drug resinates was evaluated for various physical and chemical parameters. The drug-resinate...

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Detalles Bibliográficos
Autores principales: Kadam, A. U., Sakarkar, D. M., Kawtikwar, P. S.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2792540/
https://www.ncbi.nlm.nih.gov/pubmed/20046790
http://dx.doi.org/10.4103/0250-474X.44613
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author Kadam, A. U.
Sakarkar, D. M.
Kawtikwar, P. S.
author_facet Kadam, A. U.
Sakarkar, D. M.
Kawtikwar, P. S.
author_sort Kadam, A. U.
collection PubMed
description An oral controlled release suspension of chlorpheniramine maleate was prepared using ion-exchange resin technology. A strong cation exchange resin Indion 244 was utilized for the sorption of the drug and the drug resinates was evaluated for various physical and chemical parameters. The drug-resinate complex was microencapsulated with a polymer Eudragit RS 100 to further retard the release characteristics. Both the drug-resinate complex and microencapsulated drug resinate were suspended in a palatable aqueous suspension base and were evaluated for controlled release characteristic. Stability study indicated that elevated temperature did not alter the sustained release nature of the dosage form indicating that polymer membrane surrounding the core material remained intact throughout the storage period.
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spelling pubmed-27925402009-12-14 Development and Evaluation of Oral Controlled Release Chlorpheniramine-Ion Exchange Resinate Suspension Kadam, A. U. Sakarkar, D. M. Kawtikwar, P. S. Indian J Pharm Sci Short Communications An oral controlled release suspension of chlorpheniramine maleate was prepared using ion-exchange resin technology. A strong cation exchange resin Indion 244 was utilized for the sorption of the drug and the drug resinates was evaluated for various physical and chemical parameters. The drug-resinate complex was microencapsulated with a polymer Eudragit RS 100 to further retard the release characteristics. Both the drug-resinate complex and microencapsulated drug resinate were suspended in a palatable aqueous suspension base and were evaluated for controlled release characteristic. Stability study indicated that elevated temperature did not alter the sustained release nature of the dosage form indicating that polymer membrane surrounding the core material remained intact throughout the storage period. Medknow Publications 2008 /pmc/articles/PMC2792540/ /pubmed/20046790 http://dx.doi.org/10.4103/0250-474X.44613 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 Short Communications
Kadam, A. U.
Sakarkar, D. M.
Kawtikwar, P. S.
Development and Evaluation of Oral Controlled Release Chlorpheniramine-Ion Exchange Resinate Suspension
title Development and Evaluation of Oral Controlled Release Chlorpheniramine-Ion Exchange Resinate Suspension
title_full Development and Evaluation of Oral Controlled Release Chlorpheniramine-Ion Exchange Resinate Suspension
title_fullStr Development and Evaluation of Oral Controlled Release Chlorpheniramine-Ion Exchange Resinate Suspension
title_full_unstemmed Development and Evaluation of Oral Controlled Release Chlorpheniramine-Ion Exchange Resinate Suspension
title_short Development and Evaluation of Oral Controlled Release Chlorpheniramine-Ion Exchange Resinate Suspension
title_sort development and evaluation of oral controlled release chlorpheniramine-ion exchange resinate suspension
topic Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2792540/
https://www.ncbi.nlm.nih.gov/pubmed/20046790
http://dx.doi.org/10.4103/0250-474X.44613
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