Sulochana S, Rahman F, Paramasivan C N
Tuberculosis Research Centre, Chennai, India.
J Chemother. 2005 Apr;17(2):169-73. doi: 10.1179/joc.2005.17.2.169.
The in vitro activity of fluoroquinolones, including lomefloxacin, ofloxacin, ciprofloxacin, sparfloxacin, moxifloxacin and gatifloxacin, was evaluated against 55 clinical isolates of Mycobacterium tuberculosis by absolute concentration method on Lowenstein-Jensen (L-J) and Middlebrook's 7H11 media. Both ofloxacin susceptible and ofloxacin resistant strains of M. tuberculosis isolates were tested. The in vitro activities of these fluoroquinolones on the M. tuberculosis isolates were in the order: lomefloxacin < ciprofloxacin < or = ofloxacin < sparfloxacin < moxifloxacin = gatifloxacin. Gatifloxacin and moxifloxacin showed low minimal inhibitory concentrations (MIC) for both ofloxacin resistant and ofloxacin susceptible strains even though some cross resistances were observed.
采用绝对浓度法,在罗-琴(L-J)培养基和Middlebrook 7H11培养基上,对55株临床分离的结核分枝杆菌,评估了包括洛美沙星、氧氟沙星、环丙沙星、司帕沙星、莫西沙星和加替沙星在内的氟喹诺酮类药物的体外活性。测试了结核分枝杆菌分离株中的氧氟沙星敏感株和氧氟沙星耐药株。这些氟喹诺酮类药物对结核分枝杆菌分离株的体外活性顺序为:洛美沙星<环丙沙星<或=氧氟沙星<司帕沙星<莫西沙星=加替沙星。尽管观察到一些交叉耐药性,但加替沙星和莫西沙星对氧氟沙星耐药株和氧氟沙星敏感株均显示出较低的最低抑菌浓度(MIC)。