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PHMB modified photothermally triggered nitric oxide release nanoplatform for precise synergistic therapy of wound bacterial infections

Cationic antimicrobial polymer modified NIR-controllable nitric oxide generation nanoplatform (PB-NO@PDA-PHMB) for precise synergistic therapy of wound bacterial infections. [Display omitted] Bacterial infection has been considered as a significant obstacle for wound healing. Nitric oxide (NO), as a...

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Published in:International journal of pharmaceutics 2023-06, Vol.640, p.123014-123014, Article 123014
Main Authors: Qi, Chenyang, Chen, Jie, Zhuang, Ying, Zhang, Yipin, Zhang, Qinqin, Tu, Jing
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cited_by cdi_FETCH-LOGICAL-c365t-d66708ce0d40c811fdd7e9386bbf82c56e5a3843afc57f4b1d97c6c07d54b9f43
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container_title International journal of pharmaceutics
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creator Qi, Chenyang
Chen, Jie
Zhuang, Ying
Zhang, Yipin
Zhang, Qinqin
Tu, Jing
description Cationic antimicrobial polymer modified NIR-controllable nitric oxide generation nanoplatform (PB-NO@PDA-PHMB) for precise synergistic therapy of wound bacterial infections. [Display omitted] Bacterial infection has been considered as a significant obstacle for wound healing. Nitric oxide (NO), as a novel alternative for antibiotics, has emerged as a promising antibacterial agent. However, the precise spatiotemporal controlled release of NO still remains a major challenge. Herein, a near-infrared (NIR) light triggered NO release nanoplatform (designated as PB-NO@PDA-PHMB) with enhanced broad-spectrum antibacterial and anti-biofilm properties was constructed. Given that PB-NO@PDA-PHMB has strong absorption in the NIR region and exhibits excellent photothermal effect, it can rapidly trigger NO release by NIR irradiation. PB-NO@PDA-PHMB can effectively contact and capture bacteria, and then exhibit synergistic effect of photothermal and gas therapy. In vitro and in vivo experiments indicated that PB-NO@PDA-PHMB exhibited excellent biocompatibility, satisfactory synergistic antibacterial efficacy and the capability of accelerating wound healing. Under NIR irradiation (808 nm, 1 W cm−2, 7 min), PB-NO@PDA-PHMB (80 μg mL−1) achieved 100% bactericidal activity against both Gram-negative bacteria Escherichia coli (E. coli) and Gram-positive bacteria Staphyloccocus aureus (S. aureus), removed 58.94% of S. aureus biofilm. Therefore, this all-in-one antibacterial nanoplatform with high NIR responsiveness provides a promising antibiotic-free strategy for bacterial infection treatment.
doi_str_mv 10.1016/j.ijpharm.2023.123014
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[Display omitted] Bacterial infection has been considered as a significant obstacle for wound healing. Nitric oxide (NO), as a novel alternative for antibiotics, has emerged as a promising antibacterial agent. However, the precise spatiotemporal controlled release of NO still remains a major challenge. Herein, a near-infrared (NIR) light triggered NO release nanoplatform (designated as PB-NO@PDA-PHMB) with enhanced broad-spectrum antibacterial and anti-biofilm properties was constructed. Given that PB-NO@PDA-PHMB has strong absorption in the NIR region and exhibits excellent photothermal effect, it can rapidly trigger NO release by NIR irradiation. PB-NO@PDA-PHMB can effectively contact and capture bacteria, and then exhibit synergistic effect of photothermal and gas therapy. In vitro and in vivo experiments indicated that PB-NO@PDA-PHMB exhibited excellent biocompatibility, satisfactory synergistic antibacterial efficacy and the capability of accelerating wound healing. Under NIR irradiation (808 nm, 1 W cm−2, 7 min), PB-NO@PDA-PHMB (80 μg mL−1) achieved 100% bactericidal activity against both Gram-negative bacteria Escherichia coli (E. coli) and Gram-positive bacteria Staphyloccocus aureus (S. aureus), removed 58.94% of S. aureus biofilm. 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subjects Anti-Bacterial Agents - pharmacology
Antibacterial
Bacterial Infections
Escherichia coli
Humans
Nitric Oxide
Nitric oxide release
Photothermal therapy
Prussian blue
Staphylococcus aureus
Synergistic therapy
title PHMB modified photothermally triggered nitric oxide release nanoplatform for precise synergistic therapy of wound bacterial infections
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