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首页> 外文期刊>Journal of chemotherapy >Serum bactericidal activity of gemifloxacin versus clarithromycin against Streptococcus pneumoniae with different susceptibility to quinolones.
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Serum bactericidal activity of gemifloxacin versus clarithromycin against Streptococcus pneumoniae with different susceptibility to quinolones.

机译:吉非沙星和克拉霉素对肺炎链球菌的血清杀菌活性对喹诺酮类药物的敏感性不同。

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The objective of this study was to determine serum bactericidal titers (SBT, the highest dilution of serum showing no growth) and the serum bactericidal activity (SBA, i.e. duration of SBT greater than 1:2) as well as the serum bactericidal rate of gemifloxacin and clarithromycin after single doses in healthy male volunteers against Streptococcus pneumoniae. Strains tested had various degrees of susceptibility to penicillin as well as different susceptibility to quinolones due to a different QRDR mutation pattern (parC, gyrA). Serum samples from volunteers (n = 12) who had received a single oral dose of either 320 mg gemifloxacin or 500 mg clarithromycin in an open-label crossover study were obtained over a 24-hour period. SBA was determined, using the microdilution method. SBA of wildtype strains for gemifloxacin ranged from 8.9 to 15.4 h (mean 12.6 h). For gemifloxacin, 2 strains with solitary gyrA mutation had an SBA from 4.5 to 4.7 h (median 4.5 h). One of the 2 strains with a single QRDR mutation in parC displayed an SBA of 4.5 h, comparable to the gyrA mutation strains, whereas the second strain had a nearly twice as long SBA of 8.9 h. Two strains with two mutations (parC and gyrA) did not display any SBA. For clarithromycin, the duration of SBA ranged from 11.3 to 15.5 h (mean 13.6 h) for 6 of the 12 strains with an MIC < or = 0.06 mg/L (no SBA was found for the remaining strains, with an MIC of 0.25 mg/L or higher). In conclusion, a correlation between individual serum concentrations and SBA was found for both antibiotics.
机译:这项研究的目的是确定血清杀菌滴度(SBT,最高稀释度的血清无生长)和血清杀菌活性(SBA,即SBT持续时间大于1:2)以及吉非沙星的血清杀菌率健康男性志愿者单剂量抗肺炎链球菌后,使用克拉霉素和克拉霉素。由于不同的QRDR突变模式(parC,gyrA),所测试菌株对青霉素的敏感性不同,对喹诺酮类的敏感性也不同。在开放标签交叉研究中,在24小时内从志愿者(n = 12)接受了一次口服剂量的320 mg吉非沙星或500 mg克拉霉素的血清样本。使用微量稀释法确定SBA。吉非沙星野生型菌株的SBA为8.9至15.4 h(平均12.6 h)。对于吉氟沙星,有两个具有单独的gyrA突变的菌株的SBA为4.5至4.7小时(中位数为4.5小时)。在parC中具有单个QRDR突变的2个菌株中的一个显示出4.5小时的SBA,与gyrA突变菌株相当,而第二个菌株具有8.9 h的几乎SBA两倍。具有两个突变的两个菌株(parC和gyrA)未显示任何SBA。对于克拉霉素,对于MIC <或= 0.06 mg / L的12株菌株中的6株,SBA的持续时间为11.3至15.5 h(平均13.6 h)(其余菌株均未发现SBA,MIC为0.25 mg / L或更高)。总之,两种抗生素的个体血清浓度和SBA之间均存在相关性。

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