Cheng Ana V, Wuest William M
Department of Chemistry , Emory University , 1515 Dickey Drive , Atlanta , Georgia 30322 , United States.
Emory Antibiotic Resistance Center , Emory School of Medicine , 201 Dowman Drive , Atlanta , Georgia 30322 , United States.
ACS Infect Dis. 2019 Jun 14;5(6):816-828. doi: 10.1021/acsinfecdis.9b00019. Epub 2019 Apr 10.
Innate and developed resistance mechanisms of bacteria to antibiotics are obstacles in the design of novel drugs. However, antibacterial prodrugs and conjugates have shown promise in circumventing resistance and tolerance mechanisms via directed delivery of antibiotics to the site of infection or to specific species or strains of bacteria. The selective targeting and increased permeability and accumulation of these prodrugs not only improves efficacy over unmodified drugs but also reduces off-target effects, toxicity, and development of resistance. Herein, we discuss some of these methods, including sideromycins, antibody-directed prodrugs, cell penetrating peptide conjugates, and codrugs.
细菌对抗生素的固有和后天抗性机制是新型药物设计中的障碍。然而,抗菌前体药物和偶联物在规避抗性和耐受机制方面已显示出前景,它们可通过将抗生素定向递送至感染部位或特定种类或菌株的细菌。这些前体药物的选择性靶向以及更高的渗透性和蓄积性不仅提高了相对于未修饰药物的疗效,还减少了脱靶效应、毒性和抗性的产生。在此,我们讨论其中一些方法,包括铁载体霉素、抗体导向前体药物、细胞穿透肽偶联物和协同药物。