Infection‐responsive nano‐assembly for dual‐modal treatment against drug‐resistant bacterial lung infection

Abstract

The escalating issue of lung infections induced by multi‐drug resistant(MDR) bacteria is threatening human health. Thus, the development of efficient drug delivery systems is essential to eliminate MDR bacterial lung infections effectively. Herein, we designed inhalable drug‐loaded nano‐assemblies by the electrostatic interaction between negatively charged sodium alginate and a positively charged antibacterial polymer, quaternized polyethyleneimine (QPEI‐C6),aswellasakindoftypicalantibioticfortherapyoflunginfection, azithromycin(AZT). By adjusting the feed ratios, we optimized the size of the nano‐assembly to approximately 200 nm (STQ12), which was beneficial for penetration through the mucus layer and biofilm. In the slightly acidic envi-ronment of the infected site, the nano‐assembly could dissemble responsively and release AZT and QPEI‐C6. Because of the combined bactericidal effect, STQ12 exhibited high bactericidal efficiency against MDR bacteria. In animal experiments, STQ12 showed notable efficacy against MDR bacterial lung infection. Gene transcriptomic results showed that the main effects of STQ12 against bacteria were through influencing the bacterial cell components and metabolic processes, and affecting their growth and reproduction. This work provides a promising strategy to treat MDR bacterium‐induced lower respi-ratory tract infections.