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Highly Soluble Drugs Directly Granulated by Water Dispersions of Insoluble Eudragit® Polymers as a Part of Hypromellose K100M Matrix Systems

The aim of the present study was to investigate the suitability of insoluble Eudragit® water dispersions (NE, NM, RL, and RS) for direct high-shear granulation of very soluble levetiracetam in order to decrease its burst effect from HPMC K100M matrices. The process characteristics, ss-NMR analysis,...

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Autores principales: Mašková, Eliška, Naiserová, Martina, Kubová, Kateřina, Mašek, Josef, Pavloková, Sylvie, Urbanová, Martina, Brus, Jiří, Vysloužil, Jakub, Vetchý, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6425467/
https://www.ncbi.nlm.nih.gov/pubmed/30949510
http://dx.doi.org/10.1155/2019/8043415
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author Mašková, Eliška
Naiserová, Martina
Kubová, Kateřina
Mašek, Josef
Pavloková, Sylvie
Urbanová, Martina
Brus, Jiří
Vysloužil, Jakub
Vetchý, David
author_facet Mašková, Eliška
Naiserová, Martina
Kubová, Kateřina
Mašek, Josef
Pavloková, Sylvie
Urbanová, Martina
Brus, Jiří
Vysloužil, Jakub
Vetchý, David
author_sort Mašková, Eliška
collection PubMed
description The aim of the present study was to investigate the suitability of insoluble Eudragit® water dispersions (NE, NM, RL, and RS) for direct high-shear granulation of very soluble levetiracetam in order to decrease its burst effect from HPMC K100M matrices. The process characteristics, ss-NMR analysis, in vitro dissolution behavior, drug release mechanism and kinetics, texture profile analysis of the gel layer, and PCA analysis were explored. An application of water dispersions directly on levetiracetam was feasible only in a multistep process. All prepared formulations exhibited a 12-hour sustained release profile characterized by a reduced burst effect in a concentration-dependent manner. No effect on swelling extent of HPMC K100M was observed in the presence of Eudragit®. Contrary, higher rigidity of formed gel layer was observed using combination of HPMC and Eudragit®. Not only the type and concentration of Eudragit®, but also the presence of the surfactant in water dispersions played a key role in the dissolution characteristics. The dissolution profile close to zero-order kinetic was achieved from the sample containing levetiracetam directly granulated by the water dispersion of Eudragit® NE (5% of solid polymer per tablet) with a relatively high amount of surfactant nonoxynol 100 (1.5%). The initial burst release of drug was reduced to 8.04% in 30 min (a 64.2% decrease) while the total amount of the released drug was retained (97.02%).
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spelling pubmed-64254672019-04-04 Highly Soluble Drugs Directly Granulated by Water Dispersions of Insoluble Eudragit® Polymers as a Part of Hypromellose K100M Matrix Systems Mašková, Eliška Naiserová, Martina Kubová, Kateřina Mašek, Josef Pavloková, Sylvie Urbanová, Martina Brus, Jiří Vysloužil, Jakub Vetchý, David Biomed Res Int Research Article The aim of the present study was to investigate the suitability of insoluble Eudragit® water dispersions (NE, NM, RL, and RS) for direct high-shear granulation of very soluble levetiracetam in order to decrease its burst effect from HPMC K100M matrices. The process characteristics, ss-NMR analysis, in vitro dissolution behavior, drug release mechanism and kinetics, texture profile analysis of the gel layer, and PCA analysis were explored. An application of water dispersions directly on levetiracetam was feasible only in a multistep process. All prepared formulations exhibited a 12-hour sustained release profile characterized by a reduced burst effect in a concentration-dependent manner. No effect on swelling extent of HPMC K100M was observed in the presence of Eudragit®. Contrary, higher rigidity of formed gel layer was observed using combination of HPMC and Eudragit®. Not only the type and concentration of Eudragit®, but also the presence of the surfactant in water dispersions played a key role in the dissolution characteristics. The dissolution profile close to zero-order kinetic was achieved from the sample containing levetiracetam directly granulated by the water dispersion of Eudragit® NE (5% of solid polymer per tablet) with a relatively high amount of surfactant nonoxynol 100 (1.5%). The initial burst release of drug was reduced to 8.04% in 30 min (a 64.2% decrease) while the total amount of the released drug was retained (97.02%). Hindawi 2019-03-05 /pmc/articles/PMC6425467/ /pubmed/30949510 http://dx.doi.org/10.1155/2019/8043415 Text en Copyright © 2019 Eliška Mašková et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mašková, Eliška
Naiserová, Martina
Kubová, Kateřina
Mašek, Josef
Pavloková, Sylvie
Urbanová, Martina
Brus, Jiří
Vysloužil, Jakub
Vetchý, David
Highly Soluble Drugs Directly Granulated by Water Dispersions of Insoluble Eudragit® Polymers as a Part of Hypromellose K100M Matrix Systems
title Highly Soluble Drugs Directly Granulated by Water Dispersions of Insoluble Eudragit® Polymers as a Part of Hypromellose K100M Matrix Systems
title_full Highly Soluble Drugs Directly Granulated by Water Dispersions of Insoluble Eudragit® Polymers as a Part of Hypromellose K100M Matrix Systems
title_fullStr Highly Soluble Drugs Directly Granulated by Water Dispersions of Insoluble Eudragit® Polymers as a Part of Hypromellose K100M Matrix Systems
title_full_unstemmed Highly Soluble Drugs Directly Granulated by Water Dispersions of Insoluble Eudragit® Polymers as a Part of Hypromellose K100M Matrix Systems
title_short Highly Soluble Drugs Directly Granulated by Water Dispersions of Insoluble Eudragit® Polymers as a Part of Hypromellose K100M Matrix Systems
title_sort highly soluble drugs directly granulated by water dispersions of insoluble eudragit® polymers as a part of hypromellose k100m matrix systems
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6425467/
https://www.ncbi.nlm.nih.gov/pubmed/30949510
http://dx.doi.org/10.1155/2019/8043415
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