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Formulation and evaluation of taste-masked oral disintegrating tablet containing tolterodine-loaded montmorillonite

BACKGROUND AND PURPOSE: The present study aimed to obtain a taste-masked oral disintegrating tablet (ODT) containing tolterodine tartrate (TT) intercalated into montmorillonite (MMT) EXPERIMENTAL APPROACH: The TT-MMT hybrid was prepared by ion exchange reaction. The effect of the initial concentrati...

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Autores principales: Taymouri, Somayeh, Mostafavi, Abolfazl, Talabaki, Homa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568959/
https://www.ncbi.nlm.nih.gov/pubmed/37842521
http://dx.doi.org/10.4103/1735-5362.383708
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author Taymouri, Somayeh
Mostafavi, Abolfazl
Talabaki, Homa
author_facet Taymouri, Somayeh
Mostafavi, Abolfazl
Talabaki, Homa
author_sort Taymouri, Somayeh
collection PubMed
description BACKGROUND AND PURPOSE: The present study aimed to obtain a taste-masked oral disintegrating tablet (ODT) containing tolterodine tartrate (TT) intercalated into montmorillonite (MMT) EXPERIMENTAL APPROACH: The TT-MMT hybrid was prepared by ion exchange reaction. The effect of the initial concentration of TT, MMT, temperature, and pH on the encapsulation efficiency (EE) % of the drug in MMT was evaluated. The selected TT-MMT hybrid was characterized by X-ray diffraction (XRD), Fourier transforms infrared (FTIR), differential scanning calorimetry (DSC), and scanning electron microscopy (SEM). Then, the optimized TT-MMT hybrid was incorporated in the ODT prepared by direct compression method and taste-masking assessment performed by a human test panel. FINDINGS/RESULTS: The EE% of TT was in the range of 22.67 to 71.06% in different formulations. It was found that increases in MMT concentration significantly increased EE%. DSC and XRD studies indicated that the TT was intercalated in the MMT interlayer space in an amorphous or molecular state. In-vitro release studies at pH 6.8 showed that the amount of the drug released from the TT-MMT hybrid was negligible for the first 3 min. The post-compression of ODT also showed satisfactory results in terms of friability, hardness, disintegration time, and taste. CONCLUSION AND IMPLICATIONS: MMT-ODT could be a suitable vehicle for the taste masking of TT, with the potential for use in patients with swallowing problems.
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spelling pubmed-105689592023-10-13 Formulation and evaluation of taste-masked oral disintegrating tablet containing tolterodine-loaded montmorillonite Taymouri, Somayeh Mostafavi, Abolfazl Talabaki, Homa Res Pharm Sci Original Article BACKGROUND AND PURPOSE: The present study aimed to obtain a taste-masked oral disintegrating tablet (ODT) containing tolterodine tartrate (TT) intercalated into montmorillonite (MMT) EXPERIMENTAL APPROACH: The TT-MMT hybrid was prepared by ion exchange reaction. The effect of the initial concentration of TT, MMT, temperature, and pH on the encapsulation efficiency (EE) % of the drug in MMT was evaluated. The selected TT-MMT hybrid was characterized by X-ray diffraction (XRD), Fourier transforms infrared (FTIR), differential scanning calorimetry (DSC), and scanning electron microscopy (SEM). Then, the optimized TT-MMT hybrid was incorporated in the ODT prepared by direct compression method and taste-masking assessment performed by a human test panel. FINDINGS/RESULTS: The EE% of TT was in the range of 22.67 to 71.06% in different formulations. It was found that increases in MMT concentration significantly increased EE%. DSC and XRD studies indicated that the TT was intercalated in the MMT interlayer space in an amorphous or molecular state. In-vitro release studies at pH 6.8 showed that the amount of the drug released from the TT-MMT hybrid was negligible for the first 3 min. The post-compression of ODT also showed satisfactory results in terms of friability, hardness, disintegration time, and taste. CONCLUSION AND IMPLICATIONS: MMT-ODT could be a suitable vehicle for the taste masking of TT, with the potential for use in patients with swallowing problems. Medknow Publications & Media Pvt Ltd 2023-08-20 /pmc/articles/PMC10568959/ /pubmed/37842521 http://dx.doi.org/10.4103/1735-5362.383708 Text en Copyright: © 2023 Research in Pharmaceutical Sciences https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Taymouri, Somayeh
Mostafavi, Abolfazl
Talabaki, Homa
Formulation and evaluation of taste-masked oral disintegrating tablet containing tolterodine-loaded montmorillonite
title Formulation and evaluation of taste-masked oral disintegrating tablet containing tolterodine-loaded montmorillonite
title_full Formulation and evaluation of taste-masked oral disintegrating tablet containing tolterodine-loaded montmorillonite
title_fullStr Formulation and evaluation of taste-masked oral disintegrating tablet containing tolterodine-loaded montmorillonite
title_full_unstemmed Formulation and evaluation of taste-masked oral disintegrating tablet containing tolterodine-loaded montmorillonite
title_short Formulation and evaluation of taste-masked oral disintegrating tablet containing tolterodine-loaded montmorillonite
title_sort formulation and evaluation of taste-masked oral disintegrating tablet containing tolterodine-loaded montmorillonite
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568959/
https://www.ncbi.nlm.nih.gov/pubmed/37842521
http://dx.doi.org/10.4103/1735-5362.383708
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