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Influence of Solvent Composition on the Performance of Spray-Dried Co-Amorphous Formulations
Ball-milling is usually used to prepare co-amorphous drug–amino acid (AA) mixtures. In this study, co-amorphous drug–AA mixtures were produced using spray-drying, a scalable industrially preferred preparation method. The influence of the solvent type and solvent composition was investigated. Mixture...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027151/ https://www.ncbi.nlm.nih.gov/pubmed/29649124 http://dx.doi.org/10.3390/pharmaceutics10020047 |
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author | Mishra, Jaya Rades, Thomas Löbmann, Korbinian Grohganz, Holger |
author_facet | Mishra, Jaya Rades, Thomas Löbmann, Korbinian Grohganz, Holger |
author_sort | Mishra, Jaya |
collection | PubMed |
description | Ball-milling is usually used to prepare co-amorphous drug–amino acid (AA) mixtures. In this study, co-amorphous drug–AA mixtures were produced using spray-drying, a scalable industrially preferred preparation method. The influence of the solvent type and solvent composition was investigated. Mixtures of indomethacin (IND) and each of the three AAs arginine, histidine, and lysine were ball-milled and spray-dried at a 1:1 molar ratio, respectively. Spray-drying was performed at different solvent ratios in (a) ethanol and water mixtures and (b) acetone and water mixtures. Different ratios of these solvents were chosen to study the effect of solvent mixtures on co-amorphous formulation. Residual crystallinity, thermal properties, salt/partial salt formation, and powder dissolution profiles of the IND–AA mixtures were investigated and compared to pure crystalline and amorphous IND. It was found that using spray-drying as a preparation method, all IND–AA mixtures could be successfully converted into the respective co-amorphous forms, irrespective of the type of solvent used, but depending on the solvent mixture ratios. Both ball-milled and spray-dried co-amorphous samples showed an enhanced dissolution rate and maintained supersaturation compared to the crystalline and amorphous IND itself. The spray-dried samples resulting in co-amorphous samples were stable for at least seven months of storage. |
format | Online Article Text |
id | pubmed-6027151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60271512018-07-13 Influence of Solvent Composition on the Performance of Spray-Dried Co-Amorphous Formulations Mishra, Jaya Rades, Thomas Löbmann, Korbinian Grohganz, Holger Pharmaceutics Article Ball-milling is usually used to prepare co-amorphous drug–amino acid (AA) mixtures. In this study, co-amorphous drug–AA mixtures were produced using spray-drying, a scalable industrially preferred preparation method. The influence of the solvent type and solvent composition was investigated. Mixtures of indomethacin (IND) and each of the three AAs arginine, histidine, and lysine were ball-milled and spray-dried at a 1:1 molar ratio, respectively. Spray-drying was performed at different solvent ratios in (a) ethanol and water mixtures and (b) acetone and water mixtures. Different ratios of these solvents were chosen to study the effect of solvent mixtures on co-amorphous formulation. Residual crystallinity, thermal properties, salt/partial salt formation, and powder dissolution profiles of the IND–AA mixtures were investigated and compared to pure crystalline and amorphous IND. It was found that using spray-drying as a preparation method, all IND–AA mixtures could be successfully converted into the respective co-amorphous forms, irrespective of the type of solvent used, but depending on the solvent mixture ratios. Both ball-milled and spray-dried co-amorphous samples showed an enhanced dissolution rate and maintained supersaturation compared to the crystalline and amorphous IND itself. The spray-dried samples resulting in co-amorphous samples were stable for at least seven months of storage. MDPI 2018-04-12 /pmc/articles/PMC6027151/ /pubmed/29649124 http://dx.doi.org/10.3390/pharmaceutics10020047 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mishra, Jaya Rades, Thomas Löbmann, Korbinian Grohganz, Holger Influence of Solvent Composition on the Performance of Spray-Dried Co-Amorphous Formulations |
title | Influence of Solvent Composition on the Performance of Spray-Dried Co-Amorphous Formulations |
title_full | Influence of Solvent Composition on the Performance of Spray-Dried Co-Amorphous Formulations |
title_fullStr | Influence of Solvent Composition on the Performance of Spray-Dried Co-Amorphous Formulations |
title_full_unstemmed | Influence of Solvent Composition on the Performance of Spray-Dried Co-Amorphous Formulations |
title_short | Influence of Solvent Composition on the Performance of Spray-Dried Co-Amorphous Formulations |
title_sort | influence of solvent composition on the performance of spray-dried co-amorphous formulations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027151/ https://www.ncbi.nlm.nih.gov/pubmed/29649124 http://dx.doi.org/10.3390/pharmaceutics10020047 |
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