Cargando…
Co-Processed Chitin-Mannitol as a New Excipient for Oro-Dispersible Tablets
This study describes the preparation, characterization and performance of a novel excipient for use in oro-dispersible tablets (ODT). The excipient (Cop–CM) consists of chitin and mannitol. The excipient with optimal physicochemical properties was obtained at a chitin: mannitol ratio of 2:8 (w/w) an...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413185/ https://www.ncbi.nlm.nih.gov/pubmed/25830680 http://dx.doi.org/10.3390/md13041739 |
_version_ | 1782368753211670528 |
---|---|
author | Daraghmeh, Nidal Chowdhry, Babur Z. Leharne, Stephen A. Al Omari, Mahmoud M. H. Badwan, Adnan A. |
author_facet | Daraghmeh, Nidal Chowdhry, Babur Z. Leharne, Stephen A. Al Omari, Mahmoud M. H. Badwan, Adnan A. |
author_sort | Daraghmeh, Nidal |
collection | PubMed |
description | This study describes the preparation, characterization and performance of a novel excipient for use in oro-dispersible tablets (ODT). The excipient (Cop–CM) consists of chitin and mannitol. The excipient with optimal physicochemical properties was obtained at a chitin: mannitol ratio of 2:8 (w/w) and produced by roll compaction (RC). Differential scanning calorimetry (DSC), Fourier transform-Infrared (FT-IR), X-ray powder diffraction (XRPD) and scanning electron microscope (SEM) techniques were used to characterize Cop–CM, in addition to characterization of its powder and ODT dosage form. The effect of particle size distribution of Cop–CM was investigated and found to have no significant influence on the overall tablet physical properties. The compressibility parameter (a) for Cop–CM was calculated from a Kawakita plot and found to be higher (0.661) than that of mannitol (0.576) due to the presence of the highly compressible chitin (0.818). Montelukast sodium and domperidone ODTs produced, using Cop–CM, displayed excellent physicochemical properties. The exceptional binding, fast wetting and superdisintegration properties of Cop–CM, in comparison with commercially available co-processed ODT excipients, results in a unique multifunctional base which can successfully be used in the formulation of oro-dispersible and fast immediate release tablets. |
format | Online Article Text |
id | pubmed-4413185 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-44131852015-05-07 Co-Processed Chitin-Mannitol as a New Excipient for Oro-Dispersible Tablets Daraghmeh, Nidal Chowdhry, Babur Z. Leharne, Stephen A. Al Omari, Mahmoud M. H. Badwan, Adnan A. Mar Drugs Article This study describes the preparation, characterization and performance of a novel excipient for use in oro-dispersible tablets (ODT). The excipient (Cop–CM) consists of chitin and mannitol. The excipient with optimal physicochemical properties was obtained at a chitin: mannitol ratio of 2:8 (w/w) and produced by roll compaction (RC). Differential scanning calorimetry (DSC), Fourier transform-Infrared (FT-IR), X-ray powder diffraction (XRPD) and scanning electron microscope (SEM) techniques were used to characterize Cop–CM, in addition to characterization of its powder and ODT dosage form. The effect of particle size distribution of Cop–CM was investigated and found to have no significant influence on the overall tablet physical properties. The compressibility parameter (a) for Cop–CM was calculated from a Kawakita plot and found to be higher (0.661) than that of mannitol (0.576) due to the presence of the highly compressible chitin (0.818). Montelukast sodium and domperidone ODTs produced, using Cop–CM, displayed excellent physicochemical properties. The exceptional binding, fast wetting and superdisintegration properties of Cop–CM, in comparison with commercially available co-processed ODT excipients, results in a unique multifunctional base which can successfully be used in the formulation of oro-dispersible and fast immediate release tablets. MDPI 2015-03-30 /pmc/articles/PMC4413185/ /pubmed/25830680 http://dx.doi.org/10.3390/md13041739 Text en © 2015 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 license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Daraghmeh, Nidal Chowdhry, Babur Z. Leharne, Stephen A. Al Omari, Mahmoud M. H. Badwan, Adnan A. Co-Processed Chitin-Mannitol as a New Excipient for Oro-Dispersible Tablets |
title | Co-Processed Chitin-Mannitol as a New Excipient for Oro-Dispersible Tablets |
title_full | Co-Processed Chitin-Mannitol as a New Excipient for Oro-Dispersible Tablets |
title_fullStr | Co-Processed Chitin-Mannitol as a New Excipient for Oro-Dispersible Tablets |
title_full_unstemmed | Co-Processed Chitin-Mannitol as a New Excipient for Oro-Dispersible Tablets |
title_short | Co-Processed Chitin-Mannitol as a New Excipient for Oro-Dispersible Tablets |
title_sort | co-processed chitin-mannitol as a new excipient for oro-dispersible tablets |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413185/ https://www.ncbi.nlm.nih.gov/pubmed/25830680 http://dx.doi.org/10.3390/md13041739 |
work_keys_str_mv | AT daraghmehnidal coprocessedchitinmannitolasanewexcipientfororodispersibletablets AT chowdhrybaburz coprocessedchitinmannitolasanewexcipientfororodispersibletablets AT leharnestephena coprocessedchitinmannitolasanewexcipientfororodispersibletablets AT alomarimahmoudmh coprocessedchitinmannitolasanewexcipientfororodispersibletablets AT badwanadnana coprocessedchitinmannitolasanewexcipientfororodispersibletablets |