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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...

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Autores principales: Zhang, Shichang, Xia, Liye, Ding, Chenchen, Wen, Lu, Wan, Weihua, Chen, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
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.
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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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