Verderosa Anthony D, Mansour Sarah C, de la Fuente-Núñez César, Hancock Robert E W, Fairfull-Smith Kathryn E
ARC Centre of Excellence for Free Radical Chemistry and Biotechnology, Faculty of Science and Engineering, Queensland University of Technology, Queensland 4001, Australia.
Centre for Microbial Diseases and Immunity Research, Department of Microbiology and Immunology, University of British Columbia, Vancouver, BC V6T 1Z4, Canada.
Molecules. 2016 Jun 27;21(7):841. doi: 10.3390/molecules21070841.
As bacterial biofilms are often refractory to conventional antimicrobials, the need for alternative and/or novel strategies for the treatment of biofilm related infections has become of paramount importance. Herein, we report the synthesis of novel hybrid molecules comprised of two different hindered nitroxides linked to the piperazinyl secondary amine of ciprofloxacin via a tertiary amine linker achieved utilising reductive amination. The corresponding methoxyamine derivatives were prepared alongside their radical-containing counterparts as controls. Subsequent biological evaluation of the hybrid compounds on preformed P. aeruginosa flow cell biofilms divulged significant dispersal and eradication abilities for ciprofloxacin-nitroxide hybrid compound 10 (up to 95% eradication of mature biofilms at 40 μM). Importantly, these hybrids represent the first dual-action antimicrobial-nitroxide agents, which harness the dispersal properties of the nitroxide moiety to circumvent the well-known resistance of biofilms to treatment with antimicrobial agents.
由于细菌生物膜通常对传统抗菌药物具有耐药性,因此开发用于治疗生物膜相关感染的替代和/或新策略变得至关重要。在此,我们报告了通过还原胺化反应合成的新型杂化分子,该分子由两种不同的受阻氮氧化物组成,通过叔胺连接基与环丙沙星的哌嗪基仲胺相连。同时制备了相应的甲氧基胺衍生物及其含自由基的对应物作为对照。随后对杂化化合物在预先形成的铜绿假单胞菌流动细胞生物膜上进行生物学评估,结果表明环丙沙星-氮氧化物杂化化合物10具有显著的分散和根除能力(在40 μM时可根除高达95%的成熟生物膜)。重要的是,这些杂化物代表了首批双作用抗菌-氮氧化物药物,它们利用氮氧化物部分的分散特性来规避生物膜对抗菌药物治疗的众所周知的耐药性。