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Development of ε-poly(L-lysine) carbon dots-modified magnetic nanoparticles and their applications as novel antibacterial agents

Magnetic nanoparticles (MNPs) are widely applied in antibacterial therapy owing to their distinct nanoscale structure, intrinsic peroxidase-like activities, and magnetic behavior. However, some deficiencies, such as the tendency to aggregate in water, unsatisfactory biocompatibility, and limited ant...

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Autores principales: Jiang, Yuying, Xu, Xinkai, Lu, Jinglin, Yin, Chuqiang, Li, Guotai, Bai, Longjian, Zhang, Tiantian, Mo, Jianning, Wang, Xiaoyu, Shi, Qiang, Wang, Ting, Zhou, Qihui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10119404/
https://www.ncbi.nlm.nih.gov/pubmed/37090244
http://dx.doi.org/10.3389/fchem.2023.1184592
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author Jiang, Yuying
Xu, Xinkai
Lu, Jinglin
Yin, Chuqiang
Li, Guotai
Bai, Longjian
Zhang, Tiantian
Mo, Jianning
Wang, Xiaoyu
Shi, Qiang
Wang, Ting
Zhou, Qihui
author_facet Jiang, Yuying
Xu, Xinkai
Lu, Jinglin
Yin, Chuqiang
Li, Guotai
Bai, Longjian
Zhang, Tiantian
Mo, Jianning
Wang, Xiaoyu
Shi, Qiang
Wang, Ting
Zhou, Qihui
author_sort Jiang, Yuying
collection PubMed
description Magnetic nanoparticles (MNPs) are widely applied in antibacterial therapy owing to their distinct nanoscale structure, intrinsic peroxidase-like activities, and magnetic behavior. However, some deficiencies, such as the tendency to aggregate in water, unsatisfactory biocompatibility, and limited antibacterial effect, hindered their further clinical applications. Surface modification of MNPs is one of the main strategies to improve their (bio)physicochemical properties and enhance biological functions. Herein, antibacterial ε-poly (L-lysine) carbon dots (PL-CDs) modified MNPs (CMNPs) were synthesized to investigate their performance in eliminating pathogenic bacteria. It was found that the PL-CDs were successfully loaded on the surface of MNPs by detecting their morphology, surface charges, functional groups, and other physicochemical properties. The positively charged CMNPs show superparamagnetic properties and are well dispersed in water. Furthermore, bacterial experiments indicate that the CMNPs exhibited highly effective antimicrobial properties against Staphylococcus aureus. Notably, the in vitro cellular assays show that CMNPs have favorable cytocompatibility. Thus, CMNPs acting as novel smart nanomaterials could offer great potential for the clinical treatment of bacterial infections.
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spelling pubmed-101194042023-04-22 Development of ε-poly(L-lysine) carbon dots-modified magnetic nanoparticles and their applications as novel antibacterial agents Jiang, Yuying Xu, Xinkai Lu, Jinglin Yin, Chuqiang Li, Guotai Bai, Longjian Zhang, Tiantian Mo, Jianning Wang, Xiaoyu Shi, Qiang Wang, Ting Zhou, Qihui Front Chem Chemistry Magnetic nanoparticles (MNPs) are widely applied in antibacterial therapy owing to their distinct nanoscale structure, intrinsic peroxidase-like activities, and magnetic behavior. However, some deficiencies, such as the tendency to aggregate in water, unsatisfactory biocompatibility, and limited antibacterial effect, hindered their further clinical applications. Surface modification of MNPs is one of the main strategies to improve their (bio)physicochemical properties and enhance biological functions. Herein, antibacterial ε-poly (L-lysine) carbon dots (PL-CDs) modified MNPs (CMNPs) were synthesized to investigate their performance in eliminating pathogenic bacteria. It was found that the PL-CDs were successfully loaded on the surface of MNPs by detecting their morphology, surface charges, functional groups, and other physicochemical properties. The positively charged CMNPs show superparamagnetic properties and are well dispersed in water. Furthermore, bacterial experiments indicate that the CMNPs exhibited highly effective antimicrobial properties against Staphylococcus aureus. Notably, the in vitro cellular assays show that CMNPs have favorable cytocompatibility. Thus, CMNPs acting as novel smart nanomaterials could offer great potential for the clinical treatment of bacterial infections. Frontiers Media S.A. 2023-04-07 /pmc/articles/PMC10119404/ /pubmed/37090244 http://dx.doi.org/10.3389/fchem.2023.1184592 Text en Copyright © 2023 Jiang, Xu, Lu, Yin, Li, Bai, Zhang, Mo, Wang, Shi, Wang and Zhou. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Jiang, Yuying
Xu, Xinkai
Lu, Jinglin
Yin, Chuqiang
Li, Guotai
Bai, Longjian
Zhang, Tiantian
Mo, Jianning
Wang, Xiaoyu
Shi, Qiang
Wang, Ting
Zhou, Qihui
Development of ε-poly(L-lysine) carbon dots-modified magnetic nanoparticles and their applications as novel antibacterial agents
title Development of ε-poly(L-lysine) carbon dots-modified magnetic nanoparticles and their applications as novel antibacterial agents
title_full Development of ε-poly(L-lysine) carbon dots-modified magnetic nanoparticles and their applications as novel antibacterial agents
title_fullStr Development of ε-poly(L-lysine) carbon dots-modified magnetic nanoparticles and their applications as novel antibacterial agents
title_full_unstemmed Development of ε-poly(L-lysine) carbon dots-modified magnetic nanoparticles and their applications as novel antibacterial agents
title_short Development of ε-poly(L-lysine) carbon dots-modified magnetic nanoparticles and their applications as novel antibacterial agents
title_sort development of ε-poly(l-lysine) carbon dots-modified magnetic nanoparticles and their applications as novel antibacterial agents
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10119404/
https://www.ncbi.nlm.nih.gov/pubmed/37090244
http://dx.doi.org/10.3389/fchem.2023.1184592
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