Barnes Kay B, Hamblin Karleigh A, Richards Mark I, Laws Thomas R, Vente Andreas, Atkins Helen S, Harding Sarah V
Defence Science and Technology Laboratory, Salisbury, United Kingdom.
MerLion Pharmaceuticals, Berlin, Germany.
Front Microbiol. 2019 May 1;10:904. doi: 10.3389/fmicb.2019.00904. eCollection 2019.
The efficacy of the novel fluoroquinolone finafloxacin was evaluated as a potential therapeutic and , following an intranasal infection of strain SchuS4 in BALB/c mice. We demonstrated that short treatment courses of finafloxacin provide high levels of protection, with a single dose resulting in a significant increase in time to death when compared to ciprofloxacin. In addition, following investigation into the window of opportunity for treatment, we have shown that finafloxacin can provided protection when administered up to 96 h post-challenge. This is particularly encouraging since mice displayed severe signs of disease at this time point. In summary, finafloxacin may be a promising therapy for use in the event of exposure to , perhaps enabling the treatment regimen to be shortened or if therapy is delayed. The efficacy of finafloxacin against other biological threat agents also warrants investigation.
新型氟喹诺酮类药物非那沙星作为一种潜在的治疗药物进行了疗效评估,实验采用SchuS4菌株经鼻感染BALB/c小鼠。我们证明,与环丙沙星相比,短疗程的非那沙星能提供高水平的保护,单剂量给药就能显著延长死亡时间。此外,在研究治疗的机会窗口后,我们发现非那沙星在感染后96小时内给药仍可提供保护。这尤其令人鼓舞,因为此时小鼠已表现出严重的疾病症状。总之,非那沙星可能是暴露于[病原体名称未给出]时一种有前景的治疗药物,或许能缩短治疗方案或在治疗延迟时发挥作用。非那沙星对其他生物威胁因子的疗效也值得研究。