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The Effect of Humidity on the Dissolution Kinetics and Tablet Properties of Immediate-Release Tablet Formulation Containing Lamotrigine

This study aims to find the effects of high (75%) and low (30%) humidity conditions and its correlation with formulation composition on dissolution kinetics of lamotrigine (LMT) from prepared immediate-release tablets during one- and four-week periods. Two types of fillers microcrystalline cellulose...

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Autores principales: Lalić-Popović, Mladena, Švonja Parezanović, Gordana, Todorović, Nemanja, Zeković, Zoran, Pavlić, Branimir, Milošević, Nataša, Čanji Panić, Jelena, Stjepanović, Ana, Andrijević, Ljiljana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9608154/
https://www.ncbi.nlm.nih.gov/pubmed/36297531
http://dx.doi.org/10.3390/pharmaceutics14102096
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author Lalić-Popović, Mladena
Švonja Parezanović, Gordana
Todorović, Nemanja
Zeković, Zoran
Pavlić, Branimir
Milošević, Nataša
Čanji Panić, Jelena
Stjepanović, Ana
Andrijević, Ljiljana
author_facet Lalić-Popović, Mladena
Švonja Parezanović, Gordana
Todorović, Nemanja
Zeković, Zoran
Pavlić, Branimir
Milošević, Nataša
Čanji Panić, Jelena
Stjepanović, Ana
Andrijević, Ljiljana
author_sort Lalić-Popović, Mladena
collection PubMed
description This study aims to find the effects of high (75%) and low (30%) humidity conditions and its correlation with formulation composition on dissolution kinetics of lamotrigine (LMT) from prepared immediate-release tablets during one- and four-week periods. Two types of fillers microcrystalline cellulose (MCC) or anhydrous lactose (LAC), disintegrant sodium starch glycolate (NaSG, 0.5% or 4%), and lubricant magnesium stearate (MgST, 0.25% or 5%) were used. A three-factor two-stage complete factorial design (2(3)) was used to assess the influence of the composition of the tested formulations. The tablets were produced by direct compression and characterized using a disintegration test, a resistance to crushing test, and dissolution tests (pH 1.2 and pH 6.8). Using Design Expert software, it was concluded that in addition to the effect of fillers on pH 6.8, NaSG has a significant impact after exposure to high and low humidity, as well as its interaction with LAC and MCC. In the dissolution medium pH 1.2, under conditions of high humidity, the content of MgST and NaSG and their interaction show a significant influence. The release rate of LMT was affected by humidity as well as type of excipients and their interactions.
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spelling pubmed-96081542022-10-28 The Effect of Humidity on the Dissolution Kinetics and Tablet Properties of Immediate-Release Tablet Formulation Containing Lamotrigine Lalić-Popović, Mladena Švonja Parezanović, Gordana Todorović, Nemanja Zeković, Zoran Pavlić, Branimir Milošević, Nataša Čanji Panić, Jelena Stjepanović, Ana Andrijević, Ljiljana Pharmaceutics Article This study aims to find the effects of high (75%) and low (30%) humidity conditions and its correlation with formulation composition on dissolution kinetics of lamotrigine (LMT) from prepared immediate-release tablets during one- and four-week periods. Two types of fillers microcrystalline cellulose (MCC) or anhydrous lactose (LAC), disintegrant sodium starch glycolate (NaSG, 0.5% or 4%), and lubricant magnesium stearate (MgST, 0.25% or 5%) were used. A three-factor two-stage complete factorial design (2(3)) was used to assess the influence of the composition of the tested formulations. The tablets were produced by direct compression and characterized using a disintegration test, a resistance to crushing test, and dissolution tests (pH 1.2 and pH 6.8). Using Design Expert software, it was concluded that in addition to the effect of fillers on pH 6.8, NaSG has a significant impact after exposure to high and low humidity, as well as its interaction with LAC and MCC. In the dissolution medium pH 1.2, under conditions of high humidity, the content of MgST and NaSG and their interaction show a significant influence. The release rate of LMT was affected by humidity as well as type of excipients and their interactions. MDPI 2022-09-30 /pmc/articles/PMC9608154/ /pubmed/36297531 http://dx.doi.org/10.3390/pharmaceutics14102096 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lalić-Popović, Mladena
Švonja Parezanović, Gordana
Todorović, Nemanja
Zeković, Zoran
Pavlić, Branimir
Milošević, Nataša
Čanji Panić, Jelena
Stjepanović, Ana
Andrijević, Ljiljana
The Effect of Humidity on the Dissolution Kinetics and Tablet Properties of Immediate-Release Tablet Formulation Containing Lamotrigine
title The Effect of Humidity on the Dissolution Kinetics and Tablet Properties of Immediate-Release Tablet Formulation Containing Lamotrigine
title_full The Effect of Humidity on the Dissolution Kinetics and Tablet Properties of Immediate-Release Tablet Formulation Containing Lamotrigine
title_fullStr The Effect of Humidity on the Dissolution Kinetics and Tablet Properties of Immediate-Release Tablet Formulation Containing Lamotrigine
title_full_unstemmed The Effect of Humidity on the Dissolution Kinetics and Tablet Properties of Immediate-Release Tablet Formulation Containing Lamotrigine
title_short The Effect of Humidity on the Dissolution Kinetics and Tablet Properties of Immediate-Release Tablet Formulation Containing Lamotrigine
title_sort effect of humidity on the dissolution kinetics and tablet properties of immediate-release tablet formulation containing lamotrigine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9608154/
https://www.ncbi.nlm.nih.gov/pubmed/36297531
http://dx.doi.org/10.3390/pharmaceutics14102096
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