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1.
Colloids Surf B Biointerfaces ; 213: 112425, 2022 May.
Article in English | MEDLINE | ID: mdl-35231687

ABSTRACT

Antibiotics, being critical antimicrobial agents, have been widely used for treating bacterial infections. However, prolonged use of antibiotics can induce drug resistance resulting in "superbug" that threatens human health. Therefore, developing antibiotic-free materials with intrinsic antibacterial properties is the key to the "superbug" challenge. In this study, two highly efficient metal-organic frameworks (MOFs) were successfully assembled through synergistic use of the antibacterial properties of reactive organic radicals and silver (Ag) cations. These hybrid Ag-based materials possessed radical-doped characteristics, continuously releasing Ag+, which significantly inhibited the growth of four common Gram-negative and Gram-positive human pathogens (Escherichia coli, Pseudomonas aeruginosa, Bacillus subtilis, and Staphylococcus aureus), and particularly two multi-drug-resistance bacteria (MRSA and MDR-PA). Furthermore, in vivo assays indicated that the synergistic antibacterial effect of these compounds could significantly accelerate the healing rate of infected wounds in mice. Blood biochemistry and histological analyses of main organs in treated mice also exhibited negligible cytotoxicity. This study unveiled the promising potential of Ag-MOFs for anti-infective therapies and future clinical applications.


Subject(s)
Metal Nanoparticles , Metal-Organic Frameworks , Staphylococcal Infections , Animals , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacology , Escherichia coli , Metal Nanoparticles/chemistry , Metal-Organic Frameworks/chemistry , Metal-Organic Frameworks/pharmacology , Mice , Microbial Sensitivity Tests , Silver/chemistry , Silver/pharmacology , Staphylococcus aureus
2.
Chem Commun (Camb) ; 56(92): 14353-14356, 2020 Nov 19.
Article in English | MEDLINE | ID: mdl-33169746

ABSTRACT

In the present work, we have introduced a series of stable radical-doped coordination compounds composed of donor-acceptor structures and shown to produce organic radicals in situ as a result of unconventional lone pair-π interactions in ambient conditions. Inconspicuous lone pair-π and C-Hπ interactions were shown to play a key role in self-assembly as well as the charge transfer process, resulting in a long-lived charge-separated state able to generate organic radicals. The resultant species displayed broad-spectrum antimicrobial activity, including against multi-drug-resistant bacteria. This study unveiled the promise of reactive organic radical-doped materials as a new platform for developing antimicrobial agents that can overcome antibiotic resistance.


Subject(s)
Anti-Bacterial Agents/chemistry , Free Radicals/chemistry , Metal-Organic Frameworks/chemistry , Naphthalimides/chemistry , Anti-Bacterial Agents/pharmacology , Bacillus subtilis , Drug Resistance, Multiple, Bacterial , Escherichia coli , Metal-Organic Frameworks/pharmacology , Microbial Sensitivity Tests , Pseudomonas aeruginosa , Semiconductors , Staphylococcus aureus , Structure-Activity Relationship
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