Antibiotic tolerance is implicated in difficult-to-treat infections and the development and spread of antibiotic resistance. The high storage capacities and excellent biocompatibilities of UiO-66-based metal-organic frameworks (MOFs) have made them emerging candidates as drug-delivery vectors. In view of hydrogen sulfide (HS) having been associated with the development of intrinsic resistance to antibacterial agents, we designed a strategy to potentiate existing antibiotics by eliminating bacterial endogenous HS. We efficiently fabricated an antibiotic enhancer Gm@UiO-66-MA to remove bacterial HS and sensitize an antibacterial by modifying UiO-66-NH with maleic anhydride (MA) and then loading it with gentamicin (Gm). UiO-66-MA achieved the removal of bacterial endogenous HS and the destruction of bacterial biofilm by selectively undergoing Michael addition with HS. Moreover, Gm@UiO-66-MA further enhanced the susceptibility of tolerant to Gm after reducing bacterial intracellular HS levels. An skin wound healing experiment confirmed that Gm@UiO-66-MA could greatly reduce the risk of bacterial reinfection and accelerate wound healing. Overall, Gm@UiO-66-MA offers a promising antibiotic sensitizer for minimizing bacterial resistance and a therapeutic strategy for tolerant bacteria-related refractory infections.
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http://dx.doi.org/10.1039/d3tb00552f | DOI Listing |
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