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The load and release characteristics on a strong cationic ion-exchange fiber: kinetics, thermodynamics, and influences
Ion-exchange fibers were different from conventional ion-exchange resins in their non-cross-linked structure. The exchange was located on the surface of the framework, and the transport resistance reduced significantly, which might mean that the exchange is controlled by an ionic reaction instead of...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4109635/ https://www.ncbi.nlm.nih.gov/pubmed/25114504 http://dx.doi.org/10.2147/DDDT.S64604 |
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author | Yuan, Jing Gao, Yanan Wang, Xinyu Liu, Hongzhuo Che, Xin Xu, Lu Yang, Yang Wang, Qifang Wang, Yan Li, Sanming |
author_facet | Yuan, Jing Gao, Yanan Wang, Xinyu Liu, Hongzhuo Che, Xin Xu, Lu Yang, Yang Wang, Qifang Wang, Yan Li, Sanming |
author_sort | Yuan, Jing |
collection | PubMed |
description | Ion-exchange fibers were different from conventional ion-exchange resins in their non-cross-linked structure. The exchange was located on the surface of the framework, and the transport resistance reduced significantly, which might mean that the exchange is controlled by an ionic reaction instead of diffusion. Therefore, this work aimed to investigate the load and release characteristics of five model drugs with the strong cationic ion-exchange fiber ZB-1. Drugs were loaded using a batch process and released in United States Pharmacopoeia (USP) dissolution apparatus 2. Opposing exchange kinetics, suitable for the special structure of the fiber, were developed for describing the exchange process with the help of thermodynamics, which illustrated that the load was controlled by an ionic reaction. The molecular weight was the most important factor to influence the drug load and release rate. Strong alkalinity and rings in the molecular structures made the affinity between the drug and fiber strong, while logP did not cause any profound differences. The drug–fiber complexes exhibited sustained release. Different kinds and concentrations of counter ions or different amounts of drug–fiber complexes in the release medium affected the release behavior, while the pH value was independent of it. The groundwork for in-depth exploration and further application of ion-exchange fibers has been laid. |
format | Online Article Text |
id | pubmed-4109635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-41096352014-08-11 The load and release characteristics on a strong cationic ion-exchange fiber: kinetics, thermodynamics, and influences Yuan, Jing Gao, Yanan Wang, Xinyu Liu, Hongzhuo Che, Xin Xu, Lu Yang, Yang Wang, Qifang Wang, Yan Li, Sanming Drug Des Devel Ther Original Research Ion-exchange fibers were different from conventional ion-exchange resins in their non-cross-linked structure. The exchange was located on the surface of the framework, and the transport resistance reduced significantly, which might mean that the exchange is controlled by an ionic reaction instead of diffusion. Therefore, this work aimed to investigate the load and release characteristics of five model drugs with the strong cationic ion-exchange fiber ZB-1. Drugs were loaded using a batch process and released in United States Pharmacopoeia (USP) dissolution apparatus 2. Opposing exchange kinetics, suitable for the special structure of the fiber, were developed for describing the exchange process with the help of thermodynamics, which illustrated that the load was controlled by an ionic reaction. The molecular weight was the most important factor to influence the drug load and release rate. Strong alkalinity and rings in the molecular structures made the affinity between the drug and fiber strong, while logP did not cause any profound differences. The drug–fiber complexes exhibited sustained release. Different kinds and concentrations of counter ions or different amounts of drug–fiber complexes in the release medium affected the release behavior, while the pH value was independent of it. The groundwork for in-depth exploration and further application of ion-exchange fibers has been laid. Dove Medical Press 2014-07-16 /pmc/articles/PMC4109635/ /pubmed/25114504 http://dx.doi.org/10.2147/DDDT.S64604 Text en © 2014 Yuan et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Yuan, Jing Gao, Yanan Wang, Xinyu Liu, Hongzhuo Che, Xin Xu, Lu Yang, Yang Wang, Qifang Wang, Yan Li, Sanming The load and release characteristics on a strong cationic ion-exchange fiber: kinetics, thermodynamics, and influences |
title | The load and release characteristics on a strong cationic ion-exchange fiber: kinetics, thermodynamics, and influences |
title_full | The load and release characteristics on a strong cationic ion-exchange fiber: kinetics, thermodynamics, and influences |
title_fullStr | The load and release characteristics on a strong cationic ion-exchange fiber: kinetics, thermodynamics, and influences |
title_full_unstemmed | The load and release characteristics on a strong cationic ion-exchange fiber: kinetics, thermodynamics, and influences |
title_short | The load and release characteristics on a strong cationic ion-exchange fiber: kinetics, thermodynamics, and influences |
title_sort | load and release characteristics on a strong cationic ion-exchange fiber: kinetics, thermodynamics, and influences |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4109635/ https://www.ncbi.nlm.nih.gov/pubmed/25114504 http://dx.doi.org/10.2147/DDDT.S64604 |
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