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Superior ion release properties and antibacterial efficacy of nanostructured zeolites ion-exchanged with zinc, copper, and iron
Antimicrobial zeolites ion-exchanged with inexpensive transition metal ions (such as zinc, copper, and iron) are critically important for a broader adoption of the materials for public health applications. Due to the high surface area and small particle sizes, nanozeolites are particularly promising...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244489/ https://www.ncbi.nlm.nih.gov/pubmed/30555688 http://dx.doi.org/10.1039/c8ra06556j |
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author | Chen, Shaojiang Popovich, John Zhang, Wenwen Ganser, Collin Haydel, Shelley E. Seo, Dong-Kyun |
author_facet | Chen, Shaojiang Popovich, John Zhang, Wenwen Ganser, Collin Haydel, Shelley E. Seo, Dong-Kyun |
author_sort | Chen, Shaojiang |
collection | PubMed |
description | Antimicrobial zeolites ion-exchanged with inexpensive transition metal ions (such as zinc, copper, and iron) are critically important for a broader adoption of the materials for public health applications. Due to the high surface area and small particle sizes, nanozeolites are particularly promising in enhancing the efficacy of the zeolite-based antimicrobial materials. By using highly-crystalline nanostructured zeolites (FAU) with textural mesoporosity, we report a comprehensive study on the materials characteristics of zinc-, copper-, and iron-ion exchanged nanozeolites, the ion release properties, and antibacterial efficacy against methicillin-resistant Staphylococcus aureus (MRSA), as well as a comparison of the properties to those obtained for the corresponding microsized zeolites. Superior ion release properties were observed for both zinc and copper ion-exchanged nanostructured zeolite X, with ion release up to 73% for zinc and 36% for copper of their initial loadings, as compared to 50% and 12%, respectively, for the corresponding microsized zeolites, validating the importance of nanostructuring for enhanced ion diffusion through zeolite pore channels. The 2 hours minimum bactericidal concentration (MBC) in saline for the copper ion-exchanged nanostructured zeolite X was 32 μg mL(−1), half the corresponding microsized zeolite X MBC of 64 μg mL(−1). Our results established nanostructured zeolite X as a superior host material for metal ion-based antimicrobials, with the aforementioned improvements for copper-exchanged nanozeolites compared to previous studies. |
format | Online Article Text |
id | pubmed-6244489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-62444892018-12-12 Superior ion release properties and antibacterial efficacy of nanostructured zeolites ion-exchanged with zinc, copper, and iron Chen, Shaojiang Popovich, John Zhang, Wenwen Ganser, Collin Haydel, Shelley E. Seo, Dong-Kyun RSC Adv Chemistry Antimicrobial zeolites ion-exchanged with inexpensive transition metal ions (such as zinc, copper, and iron) are critically important for a broader adoption of the materials for public health applications. Due to the high surface area and small particle sizes, nanozeolites are particularly promising in enhancing the efficacy of the zeolite-based antimicrobial materials. By using highly-crystalline nanostructured zeolites (FAU) with textural mesoporosity, we report a comprehensive study on the materials characteristics of zinc-, copper-, and iron-ion exchanged nanozeolites, the ion release properties, and antibacterial efficacy against methicillin-resistant Staphylococcus aureus (MRSA), as well as a comparison of the properties to those obtained for the corresponding microsized zeolites. Superior ion release properties were observed for both zinc and copper ion-exchanged nanostructured zeolite X, with ion release up to 73% for zinc and 36% for copper of their initial loadings, as compared to 50% and 12%, respectively, for the corresponding microsized zeolites, validating the importance of nanostructuring for enhanced ion diffusion through zeolite pore channels. The 2 hours minimum bactericidal concentration (MBC) in saline for the copper ion-exchanged nanostructured zeolite X was 32 μg mL(−1), half the corresponding microsized zeolite X MBC of 64 μg mL(−1). Our results established nanostructured zeolite X as a superior host material for metal ion-based antimicrobials, with the aforementioned improvements for copper-exchanged nanozeolites compared to previous studies. The Royal Society of Chemistry 2018-11-12 /pmc/articles/PMC6244489/ /pubmed/30555688 http://dx.doi.org/10.1039/c8ra06556j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Chen, Shaojiang Popovich, John Zhang, Wenwen Ganser, Collin Haydel, Shelley E. Seo, Dong-Kyun Superior ion release properties and antibacterial efficacy of nanostructured zeolites ion-exchanged with zinc, copper, and iron |
title | Superior ion release properties and antibacterial efficacy of nanostructured zeolites ion-exchanged with zinc, copper, and iron |
title_full | Superior ion release properties and antibacterial efficacy of nanostructured zeolites ion-exchanged with zinc, copper, and iron |
title_fullStr | Superior ion release properties and antibacterial efficacy of nanostructured zeolites ion-exchanged with zinc, copper, and iron |
title_full_unstemmed | Superior ion release properties and antibacterial efficacy of nanostructured zeolites ion-exchanged with zinc, copper, and iron |
title_short | Superior ion release properties and antibacterial efficacy of nanostructured zeolites ion-exchanged with zinc, copper, and iron |
title_sort | superior ion release properties and antibacterial efficacy of nanostructured zeolites ion-exchanged with zinc, copper, and iron |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244489/ https://www.ncbi.nlm.nih.gov/pubmed/30555688 http://dx.doi.org/10.1039/c8ra06556j |
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