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Natural gums as sustained release carriers: development of gastroretentive drug delivery system of ziprasidone HCl
BACKGROUND: Objective of this study is to show the potential use of natural gums in the development of drug delivery systems. Therefore in this work gastro retentive tablet formulations of ziprasidone HCl were developed using simplex lattice design considering concentration of okra gum, locust bean...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3556007/ https://www.ncbi.nlm.nih.gov/pubmed/23352292 http://dx.doi.org/10.1186/2008-2231-20-58 |
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author | AJ, Rajamma HN, Yogesha SB, Sateesha |
author_facet | AJ, Rajamma HN, Yogesha SB, Sateesha |
author_sort | AJ, Rajamma |
collection | PubMed |
description | BACKGROUND: Objective of this study is to show the potential use of natural gums in the development of drug delivery systems. Therefore in this work gastro retentive tablet formulations of ziprasidone HCl were developed using simplex lattice design considering concentration of okra gum, locust bean gum and HPMC K4M as independent variables. A response surface plot and multiple regression equations were used to evaluate the effect of independent variables on hardness, f(lag) time, floating time and drug release for 1 h, 2 h, and 8 h and for 24 h. A checkpoint batch was also prepared by considering the constraints and desirability of optimized formulation to improve its in vitro performance. Significance of result was analyzed using ANOVA and p < 0.05 was considered statistically significant. RESULTS: Formulation chiefly contains locust bean gum found to be favorable for hardness and floatability but combined effect of three variables was responsible for the sustained release of drug. The in vitro drug release data of check point batch (F8) was found to be sustained well compared to the most satisfactory formulation (F7) of 7 runs. The ‘n’ value was found to be between 0.5 and 1 suggesting that release of drug follows anomalous (non-fickian) diffusion mechanism indicating both diffusion and erosion mechanism from these natural gums. Predicted results were almost similar to the observed experimental values indicating the accuracy of the design. In vivo floatability test indicated non adherence to the gastric mucosa and tablets remain buoyant for more than 24 h. CONCLUSIONS: Study showed these eco-friendly natural gums can be considered as promising SR polymers. |
format | Online Article Text |
id | pubmed-3556007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35560072013-01-31 Natural gums as sustained release carriers: development of gastroretentive drug delivery system of ziprasidone HCl AJ, Rajamma HN, Yogesha SB, Sateesha Daru Research Article BACKGROUND: Objective of this study is to show the potential use of natural gums in the development of drug delivery systems. Therefore in this work gastro retentive tablet formulations of ziprasidone HCl were developed using simplex lattice design considering concentration of okra gum, locust bean gum and HPMC K4M as independent variables. A response surface plot and multiple regression equations were used to evaluate the effect of independent variables on hardness, f(lag) time, floating time and drug release for 1 h, 2 h, and 8 h and for 24 h. A checkpoint batch was also prepared by considering the constraints and desirability of optimized formulation to improve its in vitro performance. Significance of result was analyzed using ANOVA and p < 0.05 was considered statistically significant. RESULTS: Formulation chiefly contains locust bean gum found to be favorable for hardness and floatability but combined effect of three variables was responsible for the sustained release of drug. The in vitro drug release data of check point batch (F8) was found to be sustained well compared to the most satisfactory formulation (F7) of 7 runs. The ‘n’ value was found to be between 0.5 and 1 suggesting that release of drug follows anomalous (non-fickian) diffusion mechanism indicating both diffusion and erosion mechanism from these natural gums. Predicted results were almost similar to the observed experimental values indicating the accuracy of the design. In vivo floatability test indicated non adherence to the gastric mucosa and tablets remain buoyant for more than 24 h. CONCLUSIONS: Study showed these eco-friendly natural gums can be considered as promising SR polymers. BioMed Central 2012-10-17 /pmc/articles/PMC3556007/ /pubmed/23352292 http://dx.doi.org/10.1186/2008-2231-20-58 Text en Copyright ©2012 AJ et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 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 | Research Article AJ, Rajamma HN, Yogesha SB, Sateesha Natural gums as sustained release carriers: development of gastroretentive drug delivery system of ziprasidone HCl |
title | Natural gums as sustained release carriers: development of gastroretentive drug delivery system of ziprasidone HCl |
title_full | Natural gums as sustained release carriers: development of gastroretentive drug delivery system of ziprasidone HCl |
title_fullStr | Natural gums as sustained release carriers: development of gastroretentive drug delivery system of ziprasidone HCl |
title_full_unstemmed | Natural gums as sustained release carriers: development of gastroretentive drug delivery system of ziprasidone HCl |
title_short | Natural gums as sustained release carriers: development of gastroretentive drug delivery system of ziprasidone HCl |
title_sort | natural gums as sustained release carriers: development of gastroretentive drug delivery system of ziprasidone hcl |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3556007/ https://www.ncbi.nlm.nih.gov/pubmed/23352292 http://dx.doi.org/10.1186/2008-2231-20-58 |
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