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Particular Film Formation of Phenytoin at Silica Surfaces

[Image: see text] Given the increasing number of poorly soluble and thus poorly bioavailable active pharmaceutical materials, there is a demand for innovative formulation platforms for such molecules. Thus a focus on enhancing dissolution properties of poorly soluble drugs exists. Within this study,...

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Autores principales: Werzer, Oliver, Baumgartner, Ramona, Zawodzki, Michael, Roblegg, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3915752/
https://www.ncbi.nlm.nih.gov/pubmed/24417472
http://dx.doi.org/10.1021/mp4006479
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author Werzer, Oliver
Baumgartner, Ramona
Zawodzki, Michael
Roblegg, Eva
author_facet Werzer, Oliver
Baumgartner, Ramona
Zawodzki, Michael
Roblegg, Eva
author_sort Werzer, Oliver
collection PubMed
description [Image: see text] Given the increasing number of poorly soluble and thus poorly bioavailable active pharmaceutical materials, there is a demand for innovative formulation platforms for such molecules. Thus a focus on enhancing dissolution properties of poorly soluble drugs exists. Within this study, the spin coating of acetone solutions containing 5,5-diphenyl-2,4-imidazolidinedione (phenytoin) in various concentrations is evaluated. The results reveal strong variations of the morphology of deposited phenytoin crystals at silica surfaces. Individual separated particles are obtained on low phenytoin concentrations, and closely packed particular films form when the concentration is increased. As the material is isomorphic, these various morphologies have the same crystalline structure. Dissolution experiments reveal that both the apparent maximum solubility and as the dissolution rate are strongly enhanced compared to bulk powder, suggesting that formulation based on this preparative technique will allow overcoming the low solubility problematic for a variety of drugs.
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spelling pubmed-39157522014-02-06 Particular Film Formation of Phenytoin at Silica Surfaces Werzer, Oliver Baumgartner, Ramona Zawodzki, Michael Roblegg, Eva Mol Pharm [Image: see text] Given the increasing number of poorly soluble and thus poorly bioavailable active pharmaceutical materials, there is a demand for innovative formulation platforms for such molecules. Thus a focus on enhancing dissolution properties of poorly soluble drugs exists. Within this study, the spin coating of acetone solutions containing 5,5-diphenyl-2,4-imidazolidinedione (phenytoin) in various concentrations is evaluated. The results reveal strong variations of the morphology of deposited phenytoin crystals at silica surfaces. Individual separated particles are obtained on low phenytoin concentrations, and closely packed particular films form when the concentration is increased. As the material is isomorphic, these various morphologies have the same crystalline structure. Dissolution experiments reveal that both the apparent maximum solubility and as the dissolution rate are strongly enhanced compared to bulk powder, suggesting that formulation based on this preparative technique will allow overcoming the low solubility problematic for a variety of drugs. American Chemical Society 2014-01-13 2014-02-03 /pmc/articles/PMC3915752/ /pubmed/24417472 http://dx.doi.org/10.1021/mp4006479 Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Werzer, Oliver
Baumgartner, Ramona
Zawodzki, Michael
Roblegg, Eva
Particular Film Formation of Phenytoin at Silica Surfaces
title Particular Film Formation of Phenytoin at Silica Surfaces
title_full Particular Film Formation of Phenytoin at Silica Surfaces
title_fullStr Particular Film Formation of Phenytoin at Silica Surfaces
title_full_unstemmed Particular Film Formation of Phenytoin at Silica Surfaces
title_short Particular Film Formation of Phenytoin at Silica Surfaces
title_sort particular film formation of phenytoin at silica surfaces
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3915752/
https://www.ncbi.nlm.nih.gov/pubmed/24417472
http://dx.doi.org/10.1021/mp4006479
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