4.8 Article

Self-organization of zinc ions with a photosensitizer in vivo for enhanced antibiofilm and infected wound healing

Journal

NANOSCALE
Volume 14, Issue 21, Pages 7837-7848

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2nr01404a

Keywords

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Funding

  1. National Natural Science Foundation of China [21773172]
  2. Research Center of Clinical Functional Materials and Diagnosis & Treatment Devices of Zhejiang Province [WIBEK181006]
  3. Zhejiang/Wenzhou Public Welfare Science and Technology Project [LGF19H140001, S20170015, WIUCASQD2019001]

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In this study, a self-combination strategy using zinc ions and clinically applied 5-aminolevulinic acid hydrochloride (ALA) was introduced to combat Staphylococcus epidermidis (S. epidermidis) infection and promote wound healing. The strategy significantly inhibited and eliminated biofilms through a synergistic mechanism, enhanced photodynamic inactivation, and aggravated cell wall/membrane disruption. Additionally, it accelerated wound repair and reduced inflammatory response without causing cytotoxicity.
Antimicrobial materials have been developed to combat bacteria more effectively and promote infected wound healing. However, it is widely recognized that the potential toxic effects and complexity of the synthesis process hinder their practical applications. In this work, we introduced a strategy for fighting bacteria and promoting wound healing caused by Staphylococcus epidermidis (S. epidermidis) infection by the self-combination of Zn2+ and clinically applied 5-aminolevulinic acid hydrochloride (ALA) in the microbes. The clinical ALA could target and accumulate in the biofilm as well as contribute to the low-dose Zn2+ penetrating the biofilm due to the self-organized formation of Zn protoporphyrin IX in situ. Upon exposing to a 635 nm laser, the self-combination of ALA and Zn2+ significantly inhibited and eliminated the S. epidermidis biofilm via a synergistic biofilm eradication mechanism that enhanced photodynamic inactivation and aggravated cell wall/membrane disruption. In addition, the combination of ALA and Zn2+ could accelerate wound repair and reduce inflammatory response without causing cytotoxicity. The proposed strategy in this study illustrates the clinical prospects of eradicating biofilms and repairing infected wounds and demonstrates good biocompatibility towards infectious diseases.

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