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Solvent Vapor Annealing of Amorphous Carbamazepine Films for Fast Polymorph Screening and Dissolution Alteration
[Image: see text] Solubility enhancement and thus higher bioavailability are of great importance and a constant challenge in pharmaceutical research whereby polymorph screening and selection is one of the most important tasks. A very promising approach for polymorph screening is solvent vapor anneal...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5623942/ https://www.ncbi.nlm.nih.gov/pubmed/28983522 http://dx.doi.org/10.1021/acsomega.7b00783 |
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author | Schrode, Benedikt Bodak, Brigitta Riegler, Hans Zimmer, Andreas Christian, Paul Werzer, Oliver |
author_facet | Schrode, Benedikt Bodak, Brigitta Riegler, Hans Zimmer, Andreas Christian, Paul Werzer, Oliver |
author_sort | Schrode, Benedikt |
collection | PubMed |
description | [Image: see text] Solubility enhancement and thus higher bioavailability are of great importance and a constant challenge in pharmaceutical research whereby polymorph screening and selection is one of the most important tasks. A very promising approach for polymorph screening is solvent vapor annealing where a sample is exposed to an atmosphere saturated with molecules of a specific chemical/solvent. In this work, amorphous carbamazepine thin films were prepared by spin coating, and the transformation into crystalline forms under exposure to solvent vapors was investigated. Employing grazing incidence X-ray diffraction, four distinct carbamazepine polymorphs, a solvate, and hydrates could be identified, while optical microscopy showed mainly spherulitic morphologies. In vitro dissolution experiments revealed different carbamazepine release from the various thin-film samples containing distinct polymorphic compositions: heat treatment of amorphous samples at 80 °C results in an immediate release; samples exposed to EtOH vapors show a drug release about 5 times slower than this immediate one; and all the others had intermediate release profiles. Noteworthy, even the sample of slowest release has a manifold faster release compared to a standard powder sample demonstrating the capabilities of thin-film preparation for faster drug release in general. Despite the small number of samples in this screening experiment, the results clearly show how solvent vapor annealing can assist in identifying potential polymorphs and allows for estimating their impact on properties like bioavailability. |
format | Online Article Text |
id | pubmed-5623942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-56239422017-10-03 Solvent Vapor Annealing of Amorphous Carbamazepine Films for Fast Polymorph Screening and Dissolution Alteration Schrode, Benedikt Bodak, Brigitta Riegler, Hans Zimmer, Andreas Christian, Paul Werzer, Oliver ACS Omega [Image: see text] Solubility enhancement and thus higher bioavailability are of great importance and a constant challenge in pharmaceutical research whereby polymorph screening and selection is one of the most important tasks. A very promising approach for polymorph screening is solvent vapor annealing where a sample is exposed to an atmosphere saturated with molecules of a specific chemical/solvent. In this work, amorphous carbamazepine thin films were prepared by spin coating, and the transformation into crystalline forms under exposure to solvent vapors was investigated. Employing grazing incidence X-ray diffraction, four distinct carbamazepine polymorphs, a solvate, and hydrates could be identified, while optical microscopy showed mainly spherulitic morphologies. In vitro dissolution experiments revealed different carbamazepine release from the various thin-film samples containing distinct polymorphic compositions: heat treatment of amorphous samples at 80 °C results in an immediate release; samples exposed to EtOH vapors show a drug release about 5 times slower than this immediate one; and all the others had intermediate release profiles. Noteworthy, even the sample of slowest release has a manifold faster release compared to a standard powder sample demonstrating the capabilities of thin-film preparation for faster drug release in general. Despite the small number of samples in this screening experiment, the results clearly show how solvent vapor annealing can assist in identifying potential polymorphs and allows for estimating their impact on properties like bioavailability. American Chemical Society 2017-09-07 /pmc/articles/PMC5623942/ /pubmed/28983522 http://dx.doi.org/10.1021/acsomega.7b00783 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Schrode, Benedikt Bodak, Brigitta Riegler, Hans Zimmer, Andreas Christian, Paul Werzer, Oliver Solvent Vapor Annealing of Amorphous Carbamazepine Films for Fast Polymorph Screening and Dissolution Alteration |
title | Solvent Vapor Annealing of Amorphous Carbamazepine
Films for Fast Polymorph Screening and Dissolution Alteration |
title_full | Solvent Vapor Annealing of Amorphous Carbamazepine
Films for Fast Polymorph Screening and Dissolution Alteration |
title_fullStr | Solvent Vapor Annealing of Amorphous Carbamazepine
Films for Fast Polymorph Screening and Dissolution Alteration |
title_full_unstemmed | Solvent Vapor Annealing of Amorphous Carbamazepine
Films for Fast Polymorph Screening and Dissolution Alteration |
title_short | Solvent Vapor Annealing of Amorphous Carbamazepine
Films for Fast Polymorph Screening and Dissolution Alteration |
title_sort | solvent vapor annealing of amorphous carbamazepine
films for fast polymorph screening and dissolution alteration |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5623942/ https://www.ncbi.nlm.nih.gov/pubmed/28983522 http://dx.doi.org/10.1021/acsomega.7b00783 |
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