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Multilayered membrane-controlled microcapsules for controlled delivery of isoniazid
BACKGROUND AND THE PURPOSE OF THE STUDY: Layer-by-layer (LbL) deposition of polyelectrolytes (PEs) has received a great attention in the area of drug delivery due to its simplicity and versatility. This research was aimed to develop multilayered microcapsules through LbL deposition of chitosan (CHI)...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3232072/ https://www.ncbi.nlm.nih.gov/pubmed/22615638 |
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author | Tiwari, S Mishra, B |
author_facet | Tiwari, S Mishra, B |
author_sort | Tiwari, S |
collection | PubMed |
description | BACKGROUND AND THE PURPOSE OF THE STUDY: Layer-by-layer (LbL) deposition of polyelectrolytes (PEs) has received a great attention in the area of drug delivery due to its simplicity and versatility. This research was aimed to develop multilayered microcapsules through LbL deposition of chitosan (CHI) and sodium alginate (NaALG) and utilize them as vehicle for controlled delivery of isoniazid (INH). METHODS: CaCO(3) particles, prepared by colloidal crystallization of CaCl(2) and Na(2)CO(3) solutions, were used as micro-templates for LbL deposition of CHI and NaALG. Subsequent to the deposition, templates were decomposed to obtain hollow microcapsules. Prepared microcapsules were subjected to physicochemical evaluations, drug release and stability studies. RESULTS AND MAJOR CONCLUSION: Though CaCO(3) particles possessed a rough and irregular surface, prepared hollow microcapsules were spherical in shape, having smooth surface and regular thickness. Following deposition of each layer, alternating values of zeta potential were observed, indicating the formation of multilayered films. Microcapsules with 5 bilayers, i.e. (CHI/NaALG)(5) provided 39% entrapment efficiency and exhibited a controlled release behavior, lasting up to 24 hrs. An improvement in drug release rate and stability profile of the formulation was observed by increasing the number of deposition steps and performing the crosslinking of polyelectrolytes. This study showed that the prepared formulation could promisingly be utilized as controlled delivery vehicle for INH. |
format | Online Article Text |
id | pubmed-3232072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Tehran University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-32320722012-05-21 Multilayered membrane-controlled microcapsules for controlled delivery of isoniazid Tiwari, S Mishra, B Daru Original Article BACKGROUND AND THE PURPOSE OF THE STUDY: Layer-by-layer (LbL) deposition of polyelectrolytes (PEs) has received a great attention in the area of drug delivery due to its simplicity and versatility. This research was aimed to develop multilayered microcapsules through LbL deposition of chitosan (CHI) and sodium alginate (NaALG) and utilize them as vehicle for controlled delivery of isoniazid (INH). METHODS: CaCO(3) particles, prepared by colloidal crystallization of CaCl(2) and Na(2)CO(3) solutions, were used as micro-templates for LbL deposition of CHI and NaALG. Subsequent to the deposition, templates were decomposed to obtain hollow microcapsules. Prepared microcapsules were subjected to physicochemical evaluations, drug release and stability studies. RESULTS AND MAJOR CONCLUSION: Though CaCO(3) particles possessed a rough and irregular surface, prepared hollow microcapsules were spherical in shape, having smooth surface and regular thickness. Following deposition of each layer, alternating values of zeta potential were observed, indicating the formation of multilayered films. Microcapsules with 5 bilayers, i.e. (CHI/NaALG)(5) provided 39% entrapment efficiency and exhibited a controlled release behavior, lasting up to 24 hrs. An improvement in drug release rate and stability profile of the formulation was observed by increasing the number of deposition steps and performing the crosslinking of polyelectrolytes. This study showed that the prepared formulation could promisingly be utilized as controlled delivery vehicle for INH. Tehran University of Medical Sciences 2011 /pmc/articles/PMC3232072/ /pubmed/22615638 Text en © 2011 Tehran University of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly. |
spellingShingle | Original Article Tiwari, S Mishra, B Multilayered membrane-controlled microcapsules for controlled delivery of isoniazid |
title | Multilayered membrane-controlled microcapsules for controlled delivery of isoniazid |
title_full | Multilayered membrane-controlled microcapsules for controlled delivery of isoniazid |
title_fullStr | Multilayered membrane-controlled microcapsules for controlled delivery of isoniazid |
title_full_unstemmed | Multilayered membrane-controlled microcapsules for controlled delivery of isoniazid |
title_short | Multilayered membrane-controlled microcapsules for controlled delivery of isoniazid |
title_sort | multilayered membrane-controlled microcapsules for controlled delivery of isoniazid |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3232072/ https://www.ncbi.nlm.nih.gov/pubmed/22615638 |
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