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Journal ArticleDOI

Development and Performance of a Highly Sensitive Model Formulation Based on Torasemide to Enhance Hot-Melt Extrusion Process Understanding and Process Development

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TLDR
It is found that 10% w/w PEG 1500 as plasticizer resulted in the widest operating space with the widest range of measurable residual crystallinity and degradant levels, and it was found that torasemide first dissolved into the matrix and then degraded.
Abstract
The aim of this work was to investigate the use of torasemide as a highly sensitive indicator substance and to develop a formulation thereof for establishing quantitative relationships between hot-melt extrusion process conditions and critical quality attributes (CQAs). Using solid-state characterization techniques and a 10 mm lab-scale co-rotating twin-screw extruder, we studied torasemide in a Soluplus® (SOL)-polyethylene glycol 1500 (PEG 1500) matrix, and developed and characterized a formulation which was used as a process indicator to study thermal- and hydrolysis-induced degradation, as well as residual crystallinity. We found that torasemide first dissolved into the matrix and then degraded. Based on this mechanism, extrudates with measurable levels of degradation and residual crystallinity were produced, depending strongly on the main barrel and die temperature and residence time applied. In addition, we found that 10% w/w PEG 1500 as plasticizer resulted in the widest operating space with the widest range of measurable residual crystallinity and degradant levels. Torasemide as an indicator substance behaves like a challenging-to-process API, only with higher sensitivity and more pronounced effects, e.g., degradation and residual crystallinity. Application of a model formulation containing torasemide will enhance the understanding of the dynamic environment inside an extruder and elucidate the cumulative thermal and hydrolysis effects of the extrusion process. The use of such a formulation will also facilitate rational process development and scaling by establishing clear links between process conditions and CQAs.

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Journal ArticleDOI

Hot-melt extrusion in the pharmaceutical industry: toward filing a new drug application.

TL;DR: A systematic step-by-step approach is presented, where thermodynamics, polymer screening, multivariate statistics and process optimization are combined, to increase the success of HME-based drug product development.
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The application of temperature-composition phase diagrams for hot melt extrusion processing of amorphous solid dispersions to prevent residual crystallinity

TL;DR: In this article, the authors apply the temperature-composition phase diagram to the HME process, correlating process conditions to ASD residual crystallinity, and identifying the formulation critical temperature, which defines the theoretical minimum processing temperature.
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Innovations in Thermal Processing: Hot-Melt Extrusion and KinetiSol® Dispersing

TL;DR: An update on recent innovations reported for using hot-melt extrusion and KinetiSol Dispersing technologies to formulate poorly water-soluble APIs in amorphous solid dispersions is provided.
Journal ArticleDOI

Scale-Up of pharmaceutical Hot-Melt-Extrusion: Process optimization and transfer.

TL;DR: The focus of the investigations was on the impact of the different approaches on the residence tme distribution and the comparison, which revealed a change of the most sufficient approach for the two different extruder sizes.
Journal ArticleDOI

Application and limitations of thermogravimetric analysis to delineate the hot melt extrusion chemical stability processing window

TL;DR: TGA mass loss of volatiles should be considered only as an approximate indicator of degradation, as actual potency loss is likely to be significantly higher; this was confirmed by high performance liquid chromatographic analysis of samples.
References
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Journal ArticleDOI

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TL;DR: The pharmaceutical applications of hot-melt extrusion, including equipment, principles of operation, and process technology, are reviewed and the physicochemical properties of the resultant dosage forms are described.
Journal ArticleDOI

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