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In vitro-in vivo evaluation of xanthan gum and eudragit inter polyelectrolyte complex based sustained release tablets

INTRODUCTION: Polyelectrolyte complexes (PECs) are the association complexes formed between oppositely charged particles (e.g., polymer-polymer, polymer-drug and polymer-drug-polymer). These are formed due to electrostatic interaction between oppositely charged polyions. Diclofenac is a nonsteroidal...

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Autores principales: Deb, Tamal Krishna, Ramireddy, B., Moin, Afrasim, Shivakumar, H.G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4286837/
https://www.ncbi.nlm.nih.gov/pubmed/25599035
http://dx.doi.org/10.4103/2230-973X.147236
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author Deb, Tamal Krishna
Ramireddy, B.
Moin, Afrasim
Shivakumar, H.G.
author_facet Deb, Tamal Krishna
Ramireddy, B.
Moin, Afrasim
Shivakumar, H.G.
author_sort Deb, Tamal Krishna
collection PubMed
description INTRODUCTION: Polyelectrolyte complexes (PECs) are the association complexes formed between oppositely charged particles (e.g., polymer-polymer, polymer-drug and polymer-drug-polymer). These are formed due to electrostatic interaction between oppositely charged polyions. Diclofenac is a nonsteroidal anti-inflammatory drug (NSAID) advocated in use of painful and inflammatory rheumatic and certain non-rheumatic conditions. The drug has a relatively short elimination half-life, which limits the potential for drug accumulation. As an analgesic, it has a fast onset and long duration of action. AIM: invitro-invivo evaluation of Xanthan gum and Eudragit E100 inter polyelectrolyte complex based sustained release tablet. MATERIALS AND METHOD: Xanthan gum and Eudragit E100 were used as PEC and were prepared using different proportions i.e. in 1:1 to 1:6 ratio. The optimum ratio of E100 and XG was 1:6 used to characterize the IPC and the formulation of tablet. The tablets were prepared by wet granulation using PVP K30 as binder. RESULTS AND DISCUSSION: FT-IR and DSC studies confirmed the formation of IPC. Scanning Electron Microscopy (SEM) studies showed highly porous tablet surface. The tablets were evaluated for hardness, weight variation, and drug content, found to be within limits. In vitro and in vivo studies concluded that tablets showed sustained release profile. The short term stability study of the optimized formulation indicated that the formulation was stable. CONCLUSION: Since the Poly Electrolyte Complex delay the release of the drug, it can be employed in formulating sustained release matrix tablets.
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spelling pubmed-42868372015-01-16 In vitro-in vivo evaluation of xanthan gum and eudragit inter polyelectrolyte complex based sustained release tablets Deb, Tamal Krishna Ramireddy, B. Moin, Afrasim Shivakumar, H.G. Int J Pharm Investig Original Research Article INTRODUCTION: Polyelectrolyte complexes (PECs) are the association complexes formed between oppositely charged particles (e.g., polymer-polymer, polymer-drug and polymer-drug-polymer). These are formed due to electrostatic interaction between oppositely charged polyions. Diclofenac is a nonsteroidal anti-inflammatory drug (NSAID) advocated in use of painful and inflammatory rheumatic and certain non-rheumatic conditions. The drug has a relatively short elimination half-life, which limits the potential for drug accumulation. As an analgesic, it has a fast onset and long duration of action. AIM: invitro-invivo evaluation of Xanthan gum and Eudragit E100 inter polyelectrolyte complex based sustained release tablet. MATERIALS AND METHOD: Xanthan gum and Eudragit E100 were used as PEC and were prepared using different proportions i.e. in 1:1 to 1:6 ratio. The optimum ratio of E100 and XG was 1:6 used to characterize the IPC and the formulation of tablet. The tablets were prepared by wet granulation using PVP K30 as binder. RESULTS AND DISCUSSION: FT-IR and DSC studies confirmed the formation of IPC. Scanning Electron Microscopy (SEM) studies showed highly porous tablet surface. The tablets were evaluated for hardness, weight variation, and drug content, found to be within limits. In vitro and in vivo studies concluded that tablets showed sustained release profile. The short term stability study of the optimized formulation indicated that the formulation was stable. CONCLUSION: Since the Poly Electrolyte Complex delay the release of the drug, it can be employed in formulating sustained release matrix tablets. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4286837/ /pubmed/25599035 http://dx.doi.org/10.4103/2230-973X.147236 Text en Copyright: © International Journal of Pharmaceutical Investigation 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 Research Article
Deb, Tamal Krishna
Ramireddy, B.
Moin, Afrasim
Shivakumar, H.G.
In vitro-in vivo evaluation of xanthan gum and eudragit inter polyelectrolyte complex based sustained release tablets
title In vitro-in vivo evaluation of xanthan gum and eudragit inter polyelectrolyte complex based sustained release tablets
title_full In vitro-in vivo evaluation of xanthan gum and eudragit inter polyelectrolyte complex based sustained release tablets
title_fullStr In vitro-in vivo evaluation of xanthan gum and eudragit inter polyelectrolyte complex based sustained release tablets
title_full_unstemmed In vitro-in vivo evaluation of xanthan gum and eudragit inter polyelectrolyte complex based sustained release tablets
title_short In vitro-in vivo evaluation of xanthan gum and eudragit inter polyelectrolyte complex based sustained release tablets
title_sort in vitro-in vivo evaluation of xanthan gum and eudragit inter polyelectrolyte complex based sustained release tablets
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4286837/
https://www.ncbi.nlm.nih.gov/pubmed/25599035
http://dx.doi.org/10.4103/2230-973X.147236
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