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Biocompatible nanocarriers that respond to oxidative environments via interactions between chitosan and multiple metal ions
Hydrogen peroxide (H(2)O(2)) functions as an early damage signal contributing to the oxidative stress response and can act as a trigger in smart oxidation-responsive drug delivery systems that are currently in development. Current H(2)O(2)-triggered oxidation-responsive polymeric systems are usually...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4912346/ https://www.ncbi.nlm.nih.gov/pubmed/27358564 http://dx.doi.org/10.2147/IJN.S105339 |
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author | Zhang, Shichang Xia, Liye Ding, Chenchen Wen, Lu Wan, Weihua Chen, Gang |
author_facet | Zhang, Shichang Xia, Liye Ding, Chenchen Wen, Lu Wan, Weihua Chen, Gang |
author_sort | Zhang, Shichang |
collection | PubMed |
description | Hydrogen peroxide (H(2)O(2)) functions as an early damage signal contributing to the oxidative stress response and can act as a trigger in smart oxidation-responsive drug delivery systems that are currently in development. Current H(2)O(2)-triggered oxidation-responsive polymeric systems are usually derived from chemical synthesis and rarely include natural polymers. Herein, we report two series of nanoparticle (NP) complexes prepared with the biopolymer chitosan (CS) and four different metal ions (Cu(2+), Ca(2+), Zn(2+), and Fe(3+)), defined as CSNPs-metal complexes (Series 1) and CS-metal complexes NPs (Series 2), which responded to oxidation by dissolving upon H(2)O(2) exposure. Experiments examining Nile red release and H(2)O(2)-triggered degradation confirmed that both series of complexes showed better sensitivity to oxidation than the CSNPs alone. Furthermore, preliminary cytotoxicity and histological observations indicated that the two series exhibited little or no cytotoxicity and generated a mild inflammatory response. Our work provides a novel and promising strategy for developing NPs for use as intelligent oxidation-responsive systems. |
format | Online Article Text |
id | pubmed-4912346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49123462016-06-29 Biocompatible nanocarriers that respond to oxidative environments via interactions between chitosan and multiple metal ions Zhang, Shichang Xia, Liye Ding, Chenchen Wen, Lu Wan, Weihua Chen, Gang Int J Nanomedicine Original Research Hydrogen peroxide (H(2)O(2)) functions as an early damage signal contributing to the oxidative stress response and can act as a trigger in smart oxidation-responsive drug delivery systems that are currently in development. Current H(2)O(2)-triggered oxidation-responsive polymeric systems are usually derived from chemical synthesis and rarely include natural polymers. Herein, we report two series of nanoparticle (NP) complexes prepared with the biopolymer chitosan (CS) and four different metal ions (Cu(2+), Ca(2+), Zn(2+), and Fe(3+)), defined as CSNPs-metal complexes (Series 1) and CS-metal complexes NPs (Series 2), which responded to oxidation by dissolving upon H(2)O(2) exposure. Experiments examining Nile red release and H(2)O(2)-triggered degradation confirmed that both series of complexes showed better sensitivity to oxidation than the CSNPs alone. Furthermore, preliminary cytotoxicity and histological observations indicated that the two series exhibited little or no cytotoxicity and generated a mild inflammatory response. Our work provides a novel and promising strategy for developing NPs for use as intelligent oxidation-responsive systems. Dove Medical Press 2016-06-13 /pmc/articles/PMC4912346/ /pubmed/27358564 http://dx.doi.org/10.2147/IJN.S105339 Text en © 2016 Zhang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. 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 Zhang, Shichang Xia, Liye Ding, Chenchen Wen, Lu Wan, Weihua Chen, Gang Biocompatible nanocarriers that respond to oxidative environments via interactions between chitosan and multiple metal ions |
title | Biocompatible nanocarriers that respond to oxidative environments via interactions between chitosan and multiple metal ions |
title_full | Biocompatible nanocarriers that respond to oxidative environments via interactions between chitosan and multiple metal ions |
title_fullStr | Biocompatible nanocarriers that respond to oxidative environments via interactions between chitosan and multiple metal ions |
title_full_unstemmed | Biocompatible nanocarriers that respond to oxidative environments via interactions between chitosan and multiple metal ions |
title_short | Biocompatible nanocarriers that respond to oxidative environments via interactions between chitosan and multiple metal ions |
title_sort | biocompatible nanocarriers that respond to oxidative environments via interactions between chitosan and multiple metal ions |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4912346/ https://www.ncbi.nlm.nih.gov/pubmed/27358564 http://dx.doi.org/10.2147/IJN.S105339 |
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