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Composite alginate hydrogel microparticulate delivery system of zidovudine hydrochloride based on counter ion induced aggregation
AIM: The present study deals with preparation of zidovudine loaded microparticle by counter ion induced aggregation method. During this study effect of polyacrylates and hypromellose polymers on release study were investigated. MATERIALS AND METHODS: The ion induced aggregated alginate based micropa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4181129/ https://www.ncbi.nlm.nih.gov/pubmed/25298940 http://dx.doi.org/10.4103/2229-516X.140728 |
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author | Roy, Harekrishna Rao, P. Venkateswar Panda, Sanjay Kumar Biswal, Asim Kumar Parida, Kirti Ranjan Dash, Jharana |
author_facet | Roy, Harekrishna Rao, P. Venkateswar Panda, Sanjay Kumar Biswal, Asim Kumar Parida, Kirti Ranjan Dash, Jharana |
author_sort | Roy, Harekrishna |
collection | PubMed |
description | AIM: The present study deals with preparation of zidovudine loaded microparticle by counter ion induced aggregation method. During this study effect of polyacrylates and hypromellose polymers on release study were investigated. MATERIALS AND METHODS: The ion induced aggregated alginate based microparticles were characterized for surface morphology, particle size analysis, drug entrapment study, in-vitro study, Fourier-transform infrared (FTIR) spectroscopy, and differential scanning calorimetry (DSC) study. RESULTS AND DISCUSSION: The result showed Eudragit RL-100 (ERL) based formulations had smoother surface as well as their mean particle sizes were found greater compared with Eudragit RS-100 (ERS) microparticles. Furthermore, drug entrapments were found to be more in ERL formulae as compared with ERS. RL3 released 101.05% drug over a period of 8(th) h and followed Higuchi profile and Fickian diffusion. Moreover, data obtained illustrated that, higher amount of quaternary ammonium group, alkali value, and glass transition temperature may be possible reason for improving permeability of ERL based formulations. It was also noticed, hyroxypropyl methylcellulose (HPMC) K4M premium grade polymer sustained drug release more than HPMC K15M. In addition, drug-excipient interaction study was carried out by FTIR and DSC study. |
format | Online Article Text |
id | pubmed-4181129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41811292014-10-08 Composite alginate hydrogel microparticulate delivery system of zidovudine hydrochloride based on counter ion induced aggregation Roy, Harekrishna Rao, P. Venkateswar Panda, Sanjay Kumar Biswal, Asim Kumar Parida, Kirti Ranjan Dash, Jharana Int J Appl Basic Med Res Original Article AIM: The present study deals with preparation of zidovudine loaded microparticle by counter ion induced aggregation method. During this study effect of polyacrylates and hypromellose polymers on release study were investigated. MATERIALS AND METHODS: The ion induced aggregated alginate based microparticles were characterized for surface morphology, particle size analysis, drug entrapment study, in-vitro study, Fourier-transform infrared (FTIR) spectroscopy, and differential scanning calorimetry (DSC) study. RESULTS AND DISCUSSION: The result showed Eudragit RL-100 (ERL) based formulations had smoother surface as well as their mean particle sizes were found greater compared with Eudragit RS-100 (ERS) microparticles. Furthermore, drug entrapments were found to be more in ERL formulae as compared with ERS. RL3 released 101.05% drug over a period of 8(th) h and followed Higuchi profile and Fickian diffusion. Moreover, data obtained illustrated that, higher amount of quaternary ammonium group, alkali value, and glass transition temperature may be possible reason for improving permeability of ERL based formulations. It was also noticed, hyroxypropyl methylcellulose (HPMC) K4M premium grade polymer sustained drug release more than HPMC K15M. In addition, drug-excipient interaction study was carried out by FTIR and DSC study. Medknow Publications & Media Pvt Ltd 2014-09 /pmc/articles/PMC4181129/ /pubmed/25298940 http://dx.doi.org/10.4103/2229-516X.140728 Text en Copyright: © International Journal of Applied and Basic Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Roy, Harekrishna Rao, P. Venkateswar Panda, Sanjay Kumar Biswal, Asim Kumar Parida, Kirti Ranjan Dash, Jharana Composite alginate hydrogel microparticulate delivery system of zidovudine hydrochloride based on counter ion induced aggregation |
title | Composite alginate hydrogel microparticulate delivery system of zidovudine hydrochloride based on counter ion induced aggregation |
title_full | Composite alginate hydrogel microparticulate delivery system of zidovudine hydrochloride based on counter ion induced aggregation |
title_fullStr | Composite alginate hydrogel microparticulate delivery system of zidovudine hydrochloride based on counter ion induced aggregation |
title_full_unstemmed | Composite alginate hydrogel microparticulate delivery system of zidovudine hydrochloride based on counter ion induced aggregation |
title_short | Composite alginate hydrogel microparticulate delivery system of zidovudine hydrochloride based on counter ion induced aggregation |
title_sort | composite alginate hydrogel microparticulate delivery system of zidovudine hydrochloride based on counter ion induced aggregation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4181129/ https://www.ncbi.nlm.nih.gov/pubmed/25298940 http://dx.doi.org/10.4103/2229-516X.140728 |
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