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Synthesis of Chitosan/Diatomite Composite as an Advanced Delivery System for Ibuprofen Drug; Equilibrium Studies and the Release Profile
[Image: see text] Chitosan/diatomite nanocomposite (CS/D) was synthesized as a low-cost and highly porous structure of enhanced physicochemical properties to be applied as advanced carriers for ibuprofen drug (IB). The loading properties of CS/D were studied in comparison to diatomite as a separated...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8158818/ https://www.ncbi.nlm.nih.gov/pubmed/34056488 http://dx.doi.org/10.1021/acsomega.1c01514 |
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author | Ibrahim, Sherouk M. Bin Jumah, May N. Othman, Sarah I. Alruhaimi, Reem Saleh Al-Khalawi, Nora Salama, Yasser F. Allam, Ahmed A. Abukhadra, Mostafa R. |
author_facet | Ibrahim, Sherouk M. Bin Jumah, May N. Othman, Sarah I. Alruhaimi, Reem Saleh Al-Khalawi, Nora Salama, Yasser F. Allam, Ahmed A. Abukhadra, Mostafa R. |
author_sort | Ibrahim, Sherouk M. |
collection | PubMed |
description | [Image: see text] Chitosan/diatomite nanocomposite (CS/D) was synthesized as a low-cost and highly porous structure of enhanced physicochemical properties to be applied as advanced carriers for ibuprofen drug (IB). The loading properties of CS/D were studied in comparison to diatomite as a separated phase and achieved a loading capacity of 562.6 mg/g. The loading reactions of IB into CS/D show pseudo-second-order kinetic behavior and Langmuir isotherm properties. This demonstrates homogeneous loading processes in monolayer forms and controlled essentially by physical mechanisms. This was confirmed by the calculated Gaussian energy (7.7 kJ/mol (D) and 7.9 kJ/mol (CS/D)) in addition to the thermodynamic parameters. The thermodynamic behavior for the IB loading process is related to spontaneous, favorable, and exothermic reactions. The CS/D composite is of promising IB release profile that extended to about 200 h with a maximum release of 91.5% at the gastric fluid (pH 1.2) and 97.3% in the intestinal fluid (pH 7.4). The IB release rate from CS/D can be controlled based on the ratio of the integrated chitosan in the composite. The IB release reactions from CS/D follow the assumption of Korsmeyer–Peppas kinetics with determined values for the diffusion exponent reflects complex diffusion and erosion as the affected mechanisms during the IB release process. |
format | Online Article Text |
id | pubmed-8158818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-81588182021-05-28 Synthesis of Chitosan/Diatomite Composite as an Advanced Delivery System for Ibuprofen Drug; Equilibrium Studies and the Release Profile Ibrahim, Sherouk M. Bin Jumah, May N. Othman, Sarah I. Alruhaimi, Reem Saleh Al-Khalawi, Nora Salama, Yasser F. Allam, Ahmed A. Abukhadra, Mostafa R. ACS Omega [Image: see text] Chitosan/diatomite nanocomposite (CS/D) was synthesized as a low-cost and highly porous structure of enhanced physicochemical properties to be applied as advanced carriers for ibuprofen drug (IB). The loading properties of CS/D were studied in comparison to diatomite as a separated phase and achieved a loading capacity of 562.6 mg/g. The loading reactions of IB into CS/D show pseudo-second-order kinetic behavior and Langmuir isotherm properties. This demonstrates homogeneous loading processes in monolayer forms and controlled essentially by physical mechanisms. This was confirmed by the calculated Gaussian energy (7.7 kJ/mol (D) and 7.9 kJ/mol (CS/D)) in addition to the thermodynamic parameters. The thermodynamic behavior for the IB loading process is related to spontaneous, favorable, and exothermic reactions. The CS/D composite is of promising IB release profile that extended to about 200 h with a maximum release of 91.5% at the gastric fluid (pH 1.2) and 97.3% in the intestinal fluid (pH 7.4). The IB release rate from CS/D can be controlled based on the ratio of the integrated chitosan in the composite. The IB release reactions from CS/D follow the assumption of Korsmeyer–Peppas kinetics with determined values for the diffusion exponent reflects complex diffusion and erosion as the affected mechanisms during the IB release process. American Chemical Society 2021-05-13 /pmc/articles/PMC8158818/ /pubmed/34056488 http://dx.doi.org/10.1021/acsomega.1c01514 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Ibrahim, Sherouk M. Bin Jumah, May N. Othman, Sarah I. Alruhaimi, Reem Saleh Al-Khalawi, Nora Salama, Yasser F. Allam, Ahmed A. Abukhadra, Mostafa R. Synthesis of Chitosan/Diatomite Composite as an Advanced Delivery System for Ibuprofen Drug; Equilibrium Studies and the Release Profile |
title | Synthesis of Chitosan/Diatomite Composite as an Advanced
Delivery System for Ibuprofen Drug; Equilibrium Studies and the Release
Profile |
title_full | Synthesis of Chitosan/Diatomite Composite as an Advanced
Delivery System for Ibuprofen Drug; Equilibrium Studies and the Release
Profile |
title_fullStr | Synthesis of Chitosan/Diatomite Composite as an Advanced
Delivery System for Ibuprofen Drug; Equilibrium Studies and the Release
Profile |
title_full_unstemmed | Synthesis of Chitosan/Diatomite Composite as an Advanced
Delivery System for Ibuprofen Drug; Equilibrium Studies and the Release
Profile |
title_short | Synthesis of Chitosan/Diatomite Composite as an Advanced
Delivery System for Ibuprofen Drug; Equilibrium Studies and the Release
Profile |
title_sort | synthesis of chitosan/diatomite composite as an advanced
delivery system for ibuprofen drug; equilibrium studies and the release
profile |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8158818/ https://www.ncbi.nlm.nih.gov/pubmed/34056488 http://dx.doi.org/10.1021/acsomega.1c01514 |
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