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用于量化阿洛西林和妥布霉素对铜绿假单胞菌作用的时间-存活研究。

Time-survival studies for quantifying effects of azlocillin and tobramycin on Pseudomonas aeruginosa.

作者信息

McFarland M M, Scott E M, Li Wan Po A

机构信息

School of Pharmacy, Queen's University of Belfast, Northern Ireland, United Kingdom.

出版信息

Antimicrob Agents Chemother. 1994 Jun;38(6):1271-6. doi: 10.1128/AAC.38.6.1271.

Abstract

Time-survival studies were conducted to estimate the effects of azlocillin and tobramycin on Pseudomonas aeruginosa NCIMB 8295 (in the exponential phase of growth) at concentrations ranging from one-quarter to twice the MIC. The effects of the individual agents and their combinations were determined by measuring the viable counts (CFU per milliliter) over a 24-h period. The typical pattern observed from the plot of the logarithm of the CFU per milliliter against time was an initial rapid killing; this was followed by a period of stasis and regrowth. Initial rates of killing by tobramycin were concentration dependent, whereas this was not the case with azlocillin. From the time-survivor plots, the area under the curve for viable bacteria was also calculated. It offered a useful method of interpreting the results of time-kill studies, taking the overall pattern of killing and regrowth into consideration. The area under the curve for viable bacteria was concentration dependent for both antibiotics. A 2(2) factorial experimental design was used to analyze the joint effects of azlocillin and tobramycin. In such a factorial experiment, an interaction between two factors, in this case, azlocillin and tobramycin concentrations, is shown by a change in the slope of the plot when the concentration of the interactant is changed. Analysis of variance showed that the combination was synergistic at low concentrations, but this was not significant when the concentration of either interactant was increased.

摘要

进行了时间-存活研究,以评估阿洛西林和妥布霉素在浓度范围为最低抑菌浓度(MIC)的四分之一至两倍时,对处于生长指数期的铜绿假单胞菌NCIMB 8295的影响。通过在24小时内测量活菌计数(每毫升菌落形成单位)来确定单一药物及其组合的效果。从每毫升菌落形成单位的对数与时间的关系图中观察到的典型模式是初期快速杀灭;随后是一段停滞和再生长时期。妥布霉素的初期杀灭速率与浓度有关,而阿洛西林并非如此。从时间-存活关系图中,还计算了活菌的曲线下面积。它提供了一种有用的方法来解释时间杀灭研究的结果,同时考虑到杀灭和再生长的总体模式。两种抗生素的活菌曲线下面积均与浓度有关。采用2(2)析因实验设计来分析阿洛西林和妥布霉素的联合效应。在这样的析因实验中,当相互作用因子的浓度改变时,两个因子(在这种情况下为阿洛西林和妥布霉素浓度)之间的相互作用通过关系图斜率的变化来显示。方差分析表明,该组合在低浓度时具有协同作用,但当任何一个相互作用因子的浓度增加时,这种协同作用并不显著。

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