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The Combined Use of Imaging Approaches to Assess Drug Release from Multicomponent Solid Dispersions

PURPOSE: Imaging methods were used as tools to provide an understanding of phenomena that occur during dissolution experiments, and ultimately to select the best ratio of two polymers in a matrix in terms of enhancement of the dissolution rate and prevention of crystallization during dissolution. ME...

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Autores principales: Punčochová, Kateřina, Ewing, Andrew V., Gajdošová, Michaela, Pekárek, Tomáš, Beránek, Josef, Kazarian, Sergei G., Štěpánek, František
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382183/
https://www.ncbi.nlm.nih.gov/pubmed/27573574
http://dx.doi.org/10.1007/s11095-016-2018-x
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author Punčochová, Kateřina
Ewing, Andrew V.
Gajdošová, Michaela
Pekárek, Tomáš
Beránek, Josef
Kazarian, Sergei G.
Štěpánek, František
author_facet Punčochová, Kateřina
Ewing, Andrew V.
Gajdošová, Michaela
Pekárek, Tomáš
Beránek, Josef
Kazarian, Sergei G.
Štěpánek, František
author_sort Punčochová, Kateřina
collection PubMed
description PURPOSE: Imaging methods were used as tools to provide an understanding of phenomena that occur during dissolution experiments, and ultimately to select the best ratio of two polymers in a matrix in terms of enhancement of the dissolution rate and prevention of crystallization during dissolution. METHODS: Magnetic resonance imaging, ATR-FTIR spectroscopic imaging and Raman mapping have been used to study the release mechanism of a poorly water soluble drug, aprepitant, from multicomponent amorphous solid dispersions. Solid dispersions were prepared based on the combination of two selected polymers - Soluplus, as a solubilizer, and PVP, as a dissolution enhancer. Formulations were prepared in a ratio of Soluplus:PVP 1:10, 1:5, 1:3, and 1:1, in order to obtain favorable properties of the polymer carrier. RESULTS: The crystallization of aprepitant during dissolution has occurred to a varying degree in the polymer ratios 1:10, 1:5, and 1:3, but the increasing presence of Soluplus in the formulation delayed the onset of crystallization. The Soluplus:PVP 1:1 solid dispersion proved to be the best matrix studied, combining the abilities of both polymers in a synergistic manner. CONCLUSIONS: Aprepitant dissolution rate has been significantly enhanced. This study highlights the benefits of combining imaging methods in order to understand the release process. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11095-016-2018-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-53821832017-04-20 The Combined Use of Imaging Approaches to Assess Drug Release from Multicomponent Solid Dispersions Punčochová, Kateřina Ewing, Andrew V. Gajdošová, Michaela Pekárek, Tomáš Beránek, Josef Kazarian, Sergei G. Štěpánek, František Pharm Res Research Paper PURPOSE: Imaging methods were used as tools to provide an understanding of phenomena that occur during dissolution experiments, and ultimately to select the best ratio of two polymers in a matrix in terms of enhancement of the dissolution rate and prevention of crystallization during dissolution. METHODS: Magnetic resonance imaging, ATR-FTIR spectroscopic imaging and Raman mapping have been used to study the release mechanism of a poorly water soluble drug, aprepitant, from multicomponent amorphous solid dispersions. Solid dispersions were prepared based on the combination of two selected polymers - Soluplus, as a solubilizer, and PVP, as a dissolution enhancer. Formulations were prepared in a ratio of Soluplus:PVP 1:10, 1:5, 1:3, and 1:1, in order to obtain favorable properties of the polymer carrier. RESULTS: The crystallization of aprepitant during dissolution has occurred to a varying degree in the polymer ratios 1:10, 1:5, and 1:3, but the increasing presence of Soluplus in the formulation delayed the onset of crystallization. The Soluplus:PVP 1:1 solid dispersion proved to be the best matrix studied, combining the abilities of both polymers in a synergistic manner. CONCLUSIONS: Aprepitant dissolution rate has been significantly enhanced. This study highlights the benefits of combining imaging methods in order to understand the release process. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11095-016-2018-x) contains supplementary material, which is available to authorized users. Springer US 2016-08-29 2017 /pmc/articles/PMC5382183/ /pubmed/27573574 http://dx.doi.org/10.1007/s11095-016-2018-x Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research Paper
Punčochová, Kateřina
Ewing, Andrew V.
Gajdošová, Michaela
Pekárek, Tomáš
Beránek, Josef
Kazarian, Sergei G.
Štěpánek, František
The Combined Use of Imaging Approaches to Assess Drug Release from Multicomponent Solid Dispersions
title The Combined Use of Imaging Approaches to Assess Drug Release from Multicomponent Solid Dispersions
title_full The Combined Use of Imaging Approaches to Assess Drug Release from Multicomponent Solid Dispersions
title_fullStr The Combined Use of Imaging Approaches to Assess Drug Release from Multicomponent Solid Dispersions
title_full_unstemmed The Combined Use of Imaging Approaches to Assess Drug Release from Multicomponent Solid Dispersions
title_short The Combined Use of Imaging Approaches to Assess Drug Release from Multicomponent Solid Dispersions
title_sort combined use of imaging approaches to assess drug release from multicomponent solid dispersions
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382183/
https://www.ncbi.nlm.nih.gov/pubmed/27573574
http://dx.doi.org/10.1007/s11095-016-2018-x
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