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The effect of polymer and CaCl(2) concentrations on the sulfasalazine release from alginate-N,O-carboxymethyl chitosan beads
In this study, pH-sensitive blended polymeric beads were prepared by ionic gelation of mixed alginate and N,O-carboxymethyl chitosan (NOCC) solutions in aqueous media containing calcium chloride. To prepare drug-loaded beads, sulfasalazine (SA) as a model drug was added to the initial aqueous polyme...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5151116/ https://www.ncbi.nlm.nih.gov/pubmed/29470666 http://dx.doi.org/10.1186/2194-0517-2-10 |
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author | Tavakol, Moslem Vasheghani-Farahani, Ebrahim Hashemi-Najafabadi, Sameereh |
author_facet | Tavakol, Moslem Vasheghani-Farahani, Ebrahim Hashemi-Najafabadi, Sameereh |
author_sort | Tavakol, Moslem |
collection | PubMed |
description | In this study, pH-sensitive blended polymeric beads were prepared by ionic gelation of mixed alginate and N,O-carboxymethyl chitosan (NOCC) solutions in aqueous media containing calcium chloride. To prepare drug-loaded beads, sulfasalazine (SA) as a model drug was added to the initial aqueous polymer solution. These beads were characterized and evaluated in vitro as potential carriers for colon-specific drug delivery. A 3(2) full factorial experimental design was employed to evaluate the effect of polymer and CaCl(2) concentrations on swelling and drug release behavior of the beads in simulated gastrointestinal tract fluid. It was found that the rate of swelling and drug release decreased significantly with increasing polymer and CaCl(2) concentrations, but polymer concentration was more effective than CaCl(2) concentration. The beads prepared using 4.5% polymer concentration and 4% CaCl(2) concentration retained approximately 60% of the loaded drug before approaching the simulated colonic fluid. Based on the results, the alginate-NOCC beads prepared with high polymer concentration could be potentially suitable polymeric carriers for colon-specific delivery of SA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2194-0517-2-10) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5151116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-51511162016-12-27 The effect of polymer and CaCl(2) concentrations on the sulfasalazine release from alginate-N,O-carboxymethyl chitosan beads Tavakol, Moslem Vasheghani-Farahani, Ebrahim Hashemi-Najafabadi, Sameereh Prog Biomater Original Research In this study, pH-sensitive blended polymeric beads were prepared by ionic gelation of mixed alginate and N,O-carboxymethyl chitosan (NOCC) solutions in aqueous media containing calcium chloride. To prepare drug-loaded beads, sulfasalazine (SA) as a model drug was added to the initial aqueous polymer solution. These beads were characterized and evaluated in vitro as potential carriers for colon-specific drug delivery. A 3(2) full factorial experimental design was employed to evaluate the effect of polymer and CaCl(2) concentrations on swelling and drug release behavior of the beads in simulated gastrointestinal tract fluid. It was found that the rate of swelling and drug release decreased significantly with increasing polymer and CaCl(2) concentrations, but polymer concentration was more effective than CaCl(2) concentration. The beads prepared using 4.5% polymer concentration and 4% CaCl(2) concentration retained approximately 60% of the loaded drug before approaching the simulated colonic fluid. Based on the results, the alginate-NOCC beads prepared with high polymer concentration could be potentially suitable polymeric carriers for colon-specific delivery of SA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2194-0517-2-10) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2013-04-04 /pmc/articles/PMC5151116/ /pubmed/29470666 http://dx.doi.org/10.1186/2194-0517-2-10 Text en © Tavakol et al.; licensee Springer. 2013 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Tavakol, Moslem Vasheghani-Farahani, Ebrahim Hashemi-Najafabadi, Sameereh The effect of polymer and CaCl(2) concentrations on the sulfasalazine release from alginate-N,O-carboxymethyl chitosan beads |
title | The effect of polymer and CaCl(2) concentrations on the sulfasalazine release from alginate-N,O-carboxymethyl chitosan beads |
title_full | The effect of polymer and CaCl(2) concentrations on the sulfasalazine release from alginate-N,O-carboxymethyl chitosan beads |
title_fullStr | The effect of polymer and CaCl(2) concentrations on the sulfasalazine release from alginate-N,O-carboxymethyl chitosan beads |
title_full_unstemmed | The effect of polymer and CaCl(2) concentrations on the sulfasalazine release from alginate-N,O-carboxymethyl chitosan beads |
title_short | The effect of polymer and CaCl(2) concentrations on the sulfasalazine release from alginate-N,O-carboxymethyl chitosan beads |
title_sort | effect of polymer and cacl(2) concentrations on the sulfasalazine release from alginate-n,o-carboxymethyl chitosan beads |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5151116/ https://www.ncbi.nlm.nih.gov/pubmed/29470666 http://dx.doi.org/10.1186/2194-0517-2-10 |
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