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Tytuł pozycji:

A multifunctional platform with single-NIR-laser-triggered photothermal and NO release for synergistic therapy against multidrug-resistant Gram-negative bacteria and their biofilms

Tytuł:
A multifunctional platform with single-NIR-laser-triggered photothermal and NO release for synergistic therapy against multidrug-resistant Gram-negative bacteria and their biofilms
Autorzy:
Baohua Zhao
He Wang
Wenjing Dong
Shaowen Cheng
Haisheng Li
Jianglin Tan
Junyi Zhou
Weifeng He
Lanlan Li
Jianxiang Zhang
Gaoxing Luo
Wei Qian
Temat:
Graphene
Single-NIR-laser-triggered
Photothermal
NO release
Synergistic
Multidrug-resistant Gram-negative bacteria
Biotechnology
TP248.13-248.65
Medical technology
R855-855.5
Źródło:
Journal of Nanobiotechnology, Vol 18, Iss 1, Pp 1-25 (2020)
Wydawca:
BMC, 2020.
Rok publikacji:
2020
Kolekcja:
LCC:Biotechnology
LCC:Medical technology
Typ dokumentu:
article
Opis pliku:
electronic resource
Język:
English
ISSN:
1477-3155
Relacje:
http://link.springer.com/article/10.1186/s12951-020-00614-5; https://doaj.org/toc/1477-3155
DOI:
10.1186/s12951-020-00614-5
Dostęp URL:
https://doaj.org/article/312338be37f64559be054bfabcfbc63d  Link otwiera się w nowym oknie
Numer akcesji:
edsdoj.312338be37f64559be054bfabcfbc63d
Czasopismo naukowe
Abstract Background Infectious diseases caused by multidrug-resistant (MDR) bacteria, especially MDR Gram-negative strains, have become a global public health challenge. Multifunctional nanomaterials for controlling MDR bacterial infections via eradication of planktonic bacteria and their biofilms are of great interest. Results In this study, we developed a multifunctional platform (TG-NO-B) with single NIR laser-triggered PTT and NO release for synergistic therapy against MDR Gram-negative bacteria and their biofilms. When located at the infected sites, TG-NO-B was able to selectively bind to the surfaces of Gram-negative bacterial cells and their biofilm matrix through covalent coupling between the BA groups of TG-NO-B and the bacterial LPS units, which could greatly improve the antibacterial efficiency, and reduce side damages to ambient normal tissues. Upon single NIR laser irradiation, TG-NO-B could generate hyperthermia and simultaneously release NO, which would synergistically disrupt bacterial cell membrane, further cause leakage and damage of intracellular components, and finally induce bacteria death. On one hand, the combination of NO and PTT could largely improve the antibacterial efficiency. On the other hand, the bacterial cell membrane damage could improve the permeability and sensitivity to heat, decrease the photothermal temperature and avoid damages caused by high temperature. Moreover, TG-NO-B could be effectively utilized for synergistic therapy against the in vivo infections of MDR Gram-negative bacteria and their biofilms and accelerate wound healing as well as exhibit excellent biocompatibility both in vitro and in vivo. Conclusions Our study demonstrates that TG-NO-B can be considered as a promising alternative for treating infections caused by MDR Gram-negative bacteria and their biofilms.
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