Department of Hospital and Clinical Pharmacy, University Medical Center Groningen, University of Groningen, P.O. Box 30.001, 9700 RB Groningen, Netherlands.
Antimicrob Agents Chemother. 2011 Mar;55(3):1287-9. doi: 10.1128/AAC.01297-10. Epub 2011 Jan 3.
Susceptibility of clinical Mycobacterium tuberculosis isolates to PNU-100480 and linezolid was evaluated by the MGIT 960 system. The isolates had various susceptibilities to isoniazid (INH), rifampin, ethambutol, and streptomycin. The mean MIC for PNU-100480 was 3.2 times lower than that for linezolid. Therefore, PNU-100480 is a promising candidate to be developed further as an adjunct in the treatment of multidrug- and extensively drug-resistant tuberculosis (MDR/XDR-TB).
采用 MGIT960 系统评估了临床分离结核分枝杆菌对 PNU-100480 和利奈唑胺的敏感性。这些分离株对异烟肼(INH)、利福平、乙胺丁醇和链霉素的敏感性各不相同。PNU-100480 的平均 MIC 比利奈唑胺低 3.2 倍。因此,PNU-100480 是一种很有前途的候选药物,可进一步开发作为治疗耐多药和广泛耐药结核病(MDR/XDR-TB)的辅助药物。