Cargando…

Synthesis, characterization and evaluation of deacetylated xanthan derivatives as new excipients in the formulation of chitosan-based polyelectrolytes for the sustained release of tramadol

This paper addressed the application of deacetylated xanthan (XGDS) and chitosan (CTS) as a mixture blend forming hydrophilic matrices for Tramadol (TD) sustained release tablets. XGDSs derivatives were obtained by alkaline treatment of xanthan gum (XG) with various degrees of deacetylation (DD). Th...

Descripción completa

Detalles Bibliográficos
Autores principales: Boudoukhani, Meriem, Yahoum, Madiha M., Lefnaoui, Sonia, Moulai-Mostefa, Nadji, Banhobre, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921171/
https://www.ncbi.nlm.nih.gov/pubmed/31885472
http://dx.doi.org/10.1016/j.jsps.2019.09.009
_version_ 1783481101346406400
author Boudoukhani, Meriem
Yahoum, Madiha M.
Lefnaoui, Sonia
Moulai-Mostefa, Nadji
Banhobre, Manuel
author_facet Boudoukhani, Meriem
Yahoum, Madiha M.
Lefnaoui, Sonia
Moulai-Mostefa, Nadji
Banhobre, Manuel
author_sort Boudoukhani, Meriem
collection PubMed
description This paper addressed the application of deacetylated xanthan (XGDS) and chitosan (CTS) as a mixture blend forming hydrophilic matrices for Tramadol (TD) sustained release tablets. XGDSs derivatives were obtained by alkaline treatment of xanthan gum (XG) with various degrees of deacetylation (DD). The obtained products were characterized in terms of structural, thermal and physicochemical properties. Different tablet formulations containing CTS/XGDSs were prepared by direct compression method and compared to CTS/XG tablets. Flow properties of powder mixtures and pharmaceutical characteristics were evaluated. The dissolution test of TD was realized under simulated gastric and intestinal conditions to achieve drug release more than 24 h. All developed tablets were found conforming to standard evaluation tests. It was shown that CTS/XGDSs matrices ensure a slower release of TD in comparison with CTS/XG based formulations. Meanwhile, increasing DD resulted in a decrease of drug release. In addition, TD release from XGDS matrices was faster at pH (6.8) than at acidic pH (1.2). The matrix tablets based on CTS/XGDS4 (DD = 98.08%) were selected as the best candidates compared to the other systems in prolonging drug release. The optimal formulation was found to release 99.99% of TD after 24 h following a non-Fickian type.
format Online
Article
Text
id pubmed-6921171
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-69211712019-12-27 Synthesis, characterization and evaluation of deacetylated xanthan derivatives as new excipients in the formulation of chitosan-based polyelectrolytes for the sustained release of tramadol Boudoukhani, Meriem Yahoum, Madiha M. Lefnaoui, Sonia Moulai-Mostefa, Nadji Banhobre, Manuel Saudi Pharm J Original Article This paper addressed the application of deacetylated xanthan (XGDS) and chitosan (CTS) as a mixture blend forming hydrophilic matrices for Tramadol (TD) sustained release tablets. XGDSs derivatives were obtained by alkaline treatment of xanthan gum (XG) with various degrees of deacetylation (DD). The obtained products were characterized in terms of structural, thermal and physicochemical properties. Different tablet formulations containing CTS/XGDSs were prepared by direct compression method and compared to CTS/XG tablets. Flow properties of powder mixtures and pharmaceutical characteristics were evaluated. The dissolution test of TD was realized under simulated gastric and intestinal conditions to achieve drug release more than 24 h. All developed tablets were found conforming to standard evaluation tests. It was shown that CTS/XGDSs matrices ensure a slower release of TD in comparison with CTS/XG based formulations. Meanwhile, increasing DD resulted in a decrease of drug release. In addition, TD release from XGDS matrices was faster at pH (6.8) than at acidic pH (1.2). The matrix tablets based on CTS/XGDS4 (DD = 98.08%) were selected as the best candidates compared to the other systems in prolonging drug release. The optimal formulation was found to release 99.99% of TD after 24 h following a non-Fickian type. Elsevier 2019-12 2019-09-25 /pmc/articles/PMC6921171/ /pubmed/31885472 http://dx.doi.org/10.1016/j.jsps.2019.09.009 Text en © 2019 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Boudoukhani, Meriem
Yahoum, Madiha M.
Lefnaoui, Sonia
Moulai-Mostefa, Nadji
Banhobre, Manuel
Synthesis, characterization and evaluation of deacetylated xanthan derivatives as new excipients in the formulation of chitosan-based polyelectrolytes for the sustained release of tramadol
title Synthesis, characterization and evaluation of deacetylated xanthan derivatives as new excipients in the formulation of chitosan-based polyelectrolytes for the sustained release of tramadol
title_full Synthesis, characterization and evaluation of deacetylated xanthan derivatives as new excipients in the formulation of chitosan-based polyelectrolytes for the sustained release of tramadol
title_fullStr Synthesis, characterization and evaluation of deacetylated xanthan derivatives as new excipients in the formulation of chitosan-based polyelectrolytes for the sustained release of tramadol
title_full_unstemmed Synthesis, characterization and evaluation of deacetylated xanthan derivatives as new excipients in the formulation of chitosan-based polyelectrolytes for the sustained release of tramadol
title_short Synthesis, characterization and evaluation of deacetylated xanthan derivatives as new excipients in the formulation of chitosan-based polyelectrolytes for the sustained release of tramadol
title_sort synthesis, characterization and evaluation of deacetylated xanthan derivatives as new excipients in the formulation of chitosan-based polyelectrolytes for the sustained release of tramadol
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921171/
https://www.ncbi.nlm.nih.gov/pubmed/31885472
http://dx.doi.org/10.1016/j.jsps.2019.09.009
work_keys_str_mv AT boudoukhanimeriem synthesischaracterizationandevaluationofdeacetylatedxanthanderivativesasnewexcipientsintheformulationofchitosanbasedpolyelectrolytesforthesustainedreleaseoftramadol
AT yahoummadiham synthesischaracterizationandevaluationofdeacetylatedxanthanderivativesasnewexcipientsintheformulationofchitosanbasedpolyelectrolytesforthesustainedreleaseoftramadol
AT lefnaouisonia synthesischaracterizationandevaluationofdeacetylatedxanthanderivativesasnewexcipientsintheformulationofchitosanbasedpolyelectrolytesforthesustainedreleaseoftramadol
AT moulaimostefanadji synthesischaracterizationandevaluationofdeacetylatedxanthanderivativesasnewexcipientsintheformulationofchitosanbasedpolyelectrolytesforthesustainedreleaseoftramadol
AT banhobremanuel synthesischaracterizationandevaluationofdeacetylatedxanthanderivativesasnewexcipientsintheformulationofchitosanbasedpolyelectrolytesforthesustainedreleaseoftramadol