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Screening of Several Anti-Infectives for in Vitro Activity against Mycobacterium smegmatis

机译:筛选抗耻垢分枝杆菌体外活性的几种抗感染药

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Aim: To evaluate in vitro the effectiveness of several anti-infective agents alone or in combination against Mycobacterium smegmatis. Method: A convenient stratified sampling method was used to obtain selected anti-infective agents. For individual drug samples, Minimum Inhibitory Concentrations (MIC) were obtained using the agar-well plate diffusion technique. Fractional Inhibitory Concentration Indices (FICI) were calculated for drug combinations using their MIC as obtained from the broth dilution method. Results: Of the thirty (30) anti-infective agents analyzed, ten (10) had MIC equivalent to or better than rifampicin (reference TB drug). Seven (7) drugs had MIC higher than rifampicin, while twelve (12) showed no growth inhibition of M. smegmatis. Analysis of the effect of drug combinations on M. smegmatis indicated that four (4) combinations, including rifampicin/ethambutol showed synergism. One (1) was additive, two (2) were indifferent and one (1) combination showed antagonism. Conclusion: Notable in the results obtained was the high effectiveness of the carbapenems in inhibiting the growth of M. smegmatis. Carbapenems, though not indicated for TB treatment, has a potential of playing a significant role in the treatment of tuberculosis. Also the drug combinations which showed synergism, especially those that involved the macrolide antibiotics, should further be investigated. These results have to be confirmed by in vivo clinical studies to define their roles in tuberculosis treatment.
机译:目的:在体外评估几种抗感染剂单独或联合使用对耻垢分枝杆菌的有效性。方法:采用方便的分层抽样方法获得所选的抗感染药。对于单个药物样品,使用琼脂孔板扩散技术获得最小抑菌浓度(MIC)。使用从肉汤稀释法获得的MIC来计算药物组合的分数抑制浓度指数(FICI)。结果:在分析的三十(30)种抗感染药中,十(10)种的MIC等于或优于利福平(参考TB药物)。七(7)种药物的MIC高于利福平,而十二(12)种药物对耻垢分枝杆菌没有生长抑制作用。对药物组合物对耻垢分枝杆菌的作用的分析表明,包括利福平/乙胺丁醇在内的四(4)种组合物表现出协同作用。一(1)是加性的,两(2)漠不关心,一(1)的组合表现出拮抗作用。结论:获得的结果值得注意的是碳青霉烯类具有抑制耻垢分枝杆菌生长的高效性。碳青霉烯类尽管未指明可用于结核病治疗,但在结核病的治疗中具有重要作用。还应进一步研究显示协同作用的药物组合,尤其是涉及大环内酯类抗生素的药物组合。这些结果必须通过体内临床研究来证实,以定义其在结核病治疗中的作用。

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