4.3 Article

Multifunctional fluorescent gold nanoclusters with enhanced aggregation-induced emissions (AIEs) and excellent antibacterial effect for bacterial imaging and wound healing

Journal

BIOMATERIALS ADVANCES
Volume 137, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.bioadv.2022.212841

Keywords

Gold nanoclusters; Antimicrobial peptide; Aggregation-induced emissions (AIEs); Antibacterial effect; Imaging; Wound healing

Funding

  1. National Natural Science Foundation of China [31922070]
  2. Natural Science Foundation of Jiangsu Province [BK20180038]
  3. Jiangsu Synergetic Innovation Center for Advanced Bio-Manufacture [XTC2205]
  4. Cultivation Program for the Excellent Doctoral Dissertation of Nanjing Tech University
  5. Postgraduate Research & Practice Innovation Program of Jiangsu Province [KYCX20_1033]

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This study presents the construction of ultra-small gold nanoclusters protected by a cationic antimicrobial peptide and glutathione co-ligand. The nanoclusters exhibited enhanced luminescent properties and antibacterial activities, with the potential for imaging-guided antibacterial applications and excellent therapeutic outcomes for wound healing in vivo.
To explore new alternatives to combat increasing risk of bacterial infection, in this work, a cationic antimicrobial peptide (HHC10) and glutathione (GSH) co-ligand protected ultra-small gold nanoclusters (Au NCs) was constructed by a simple one-pot method. The intrinsic luminescent property of GSH-protected Au NCs (Au(x)GSF) endowed enhanced aggregation-induced emissions (AIEs) of co-ligand-protected Au NCs (Au(x)GSH-HHC10), which exhibited a very strong orange luminescence. Based on the AIE effect, for one thing, Au(x)GSH could be applied to rapidly and selectively detect Gram-positive bacteria. For another, Au(x)GSH-HHC10 exhibited potential for multicolor imaging of both Gram-negative and Gram-positive bacteria. Besides, as-synthesized Au(x)GSH-HHC10 could act as potent nanoantibiotics against both Gram-negative and Gram-positive bacteria, which could not only avoid drug tolerance but also be effective toward drug-resistance bacteria. The antibacterial mechanism indicated that the synergetic effect of the generation of reactive oxygen species (ROS), binding with DNA, and broad-spectrum antibacterial activity of HHC10 led to the membrane damage, depolarization, and interference of biological function, thus enhancing the antibacterial effect. More importantly, such an Au NCs could realize excellent therapeutic outcomes for wound healing in vivo, and showed good biocompatibility and biosafety toward health tissues. The results will provide a great potential for the application of Au NCs for imaging-guided antibacterial platform.

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