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Ficin–Cyclodextrin-Based Docking Nanoarchitectonics of Self-Propelled Nanomotors for Bacterial Biofilm Eradication
[Image: see text] Development of bioinspired nanomotors showing effective propulsion and cargo delivery capabilities has attracted much attention in the last few years due to their potential use in biomedical applications. However, implementation of this technology in realistic settings is still a b...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10269336/ https://www.ncbi.nlm.nih.gov/pubmed/37332683 http://dx.doi.org/10.1021/acs.chemmater.3c00587 |
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author | Žiemytė, Miglė Escudero, Andrea Díez, Paula Ferrer, María D. Murguía, Jose R. Martí-Centelles, Vicente Mira, Alex Martínez-Máñez, Ramón |
author_facet | Žiemytė, Miglė Escudero, Andrea Díez, Paula Ferrer, María D. Murguía, Jose R. Martí-Centelles, Vicente Mira, Alex Martínez-Máñez, Ramón |
author_sort | Žiemytė, Miglė |
collection | PubMed |
description | [Image: see text] Development of bioinspired nanomotors showing effective propulsion and cargo delivery capabilities has attracted much attention in the last few years due to their potential use in biomedical applications. However, implementation of this technology in realistic settings is still a barely explored field. Herein, we report the design and application of a multifunctional gated Janus platinum–mesoporous silica nanomotor constituted of a propelling element (platinum nanodendrites) and a drug-loaded nanocontainer (mesoporous silica nanoparticle) capped with ficin enzyme modified with β-cyclodextrins (β-CD). The engineered nanomotor is designed to effectively disrupt bacterial biofilms via H(2)O(2)-induced self-propelled motion, ficin hydrolysis of the extracellular polymeric matrix (EPS) of the biofilm, and controlled pH-triggered cargo (vancomycin) delivery. The effective synergic antimicrobial activity of the nanomotor is demonstrated in the elimination of Staphylococcus aureus biofilms. The nanomotor achieves 82% of EPS biomass disruption and a 96% reduction in cell viability, which contrasts with a remarkably lower reduction in biofilm elimination when the components of the nanomotors are used separately at the same concentrations. Such a large reduction in biofilm biomass in S. aureus has never been achieved previously by any conventional therapy. The strategy proposed suggests that engineered nanomotors have great potential for the elimination of biofilms. |
format | Online Article Text |
id | pubmed-10269336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-102693362023-06-16 Ficin–Cyclodextrin-Based Docking Nanoarchitectonics of Self-Propelled Nanomotors for Bacterial Biofilm Eradication Žiemytė, Miglė Escudero, Andrea Díez, Paula Ferrer, María D. Murguía, Jose R. Martí-Centelles, Vicente Mira, Alex Martínez-Máñez, Ramón Chem Mater [Image: see text] Development of bioinspired nanomotors showing effective propulsion and cargo delivery capabilities has attracted much attention in the last few years due to their potential use in biomedical applications. However, implementation of this technology in realistic settings is still a barely explored field. Herein, we report the design and application of a multifunctional gated Janus platinum–mesoporous silica nanomotor constituted of a propelling element (platinum nanodendrites) and a drug-loaded nanocontainer (mesoporous silica nanoparticle) capped with ficin enzyme modified with β-cyclodextrins (β-CD). The engineered nanomotor is designed to effectively disrupt bacterial biofilms via H(2)O(2)-induced self-propelled motion, ficin hydrolysis of the extracellular polymeric matrix (EPS) of the biofilm, and controlled pH-triggered cargo (vancomycin) delivery. The effective synergic antimicrobial activity of the nanomotor is demonstrated in the elimination of Staphylococcus aureus biofilms. The nanomotor achieves 82% of EPS biomass disruption and a 96% reduction in cell viability, which contrasts with a remarkably lower reduction in biofilm elimination when the components of the nanomotors are used separately at the same concentrations. Such a large reduction in biofilm biomass in S. aureus has never been achieved previously by any conventional therapy. The strategy proposed suggests that engineered nanomotors have great potential for the elimination of biofilms. American Chemical Society 2023-05-09 /pmc/articles/PMC10269336/ /pubmed/37332683 http://dx.doi.org/10.1021/acs.chemmater.3c00587 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Žiemytė, Miglė Escudero, Andrea Díez, Paula Ferrer, María D. Murguía, Jose R. Martí-Centelles, Vicente Mira, Alex Martínez-Máñez, Ramón Ficin–Cyclodextrin-Based Docking Nanoarchitectonics of Self-Propelled Nanomotors for Bacterial Biofilm Eradication |
title | Ficin–Cyclodextrin-Based Docking Nanoarchitectonics
of Self-Propelled Nanomotors for Bacterial Biofilm Eradication |
title_full | Ficin–Cyclodextrin-Based Docking Nanoarchitectonics
of Self-Propelled Nanomotors for Bacterial Biofilm Eradication |
title_fullStr | Ficin–Cyclodextrin-Based Docking Nanoarchitectonics
of Self-Propelled Nanomotors for Bacterial Biofilm Eradication |
title_full_unstemmed | Ficin–Cyclodextrin-Based Docking Nanoarchitectonics
of Self-Propelled Nanomotors for Bacterial Biofilm Eradication |
title_short | Ficin–Cyclodextrin-Based Docking Nanoarchitectonics
of Self-Propelled Nanomotors for Bacterial Biofilm Eradication |
title_sort | ficin–cyclodextrin-based docking nanoarchitectonics
of self-propelled nanomotors for bacterial biofilm eradication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10269336/ https://www.ncbi.nlm.nih.gov/pubmed/37332683 http://dx.doi.org/10.1021/acs.chemmater.3c00587 |
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