Guerillot F, Carret G, Flandrois J P
Laboratoire de Biométrie, Centre National de la Recherche Scientifique (CNRS) URA 243, Université Claude Bernard, Villeurbanne, France.
Antimicrob Agents Chemother. 1993 Aug;37(8):1685-9. doi: 10.1128/AAC.37.8.1685.
The relevance of mathematical modeling to investigations of the bactericidal effects of antimicrobial agents has been emphasized in many studies of killing kinetics. We propose here a descriptive model of general use, with four parameters which account for the lag phase, the initial number of bacteria, and the limit of effectiveness and bactericidal rate of antimicrobial agents. The model has been applied to several kinetic datum sets with amoxicillin, cephalothin, nalidixic acid, pefloxacin, and ofloxacin against two Escherichia coli strains. It is a useful tool to compare killing curves by taking into account model parameter confidence limits. This can be illustrated by studying drug effects, strain effects, and concentration effects. For the antibiotics used here, concentration effects had an influence mainly on the length of the lag phase and the minimum number of living cells observed. It is therefore clear that differences in the killing curves with changes in one or more parameters could occur.
数学建模在抗菌剂杀菌效果研究中的相关性在许多杀菌动力学研究中都得到了强调。我们在此提出一个通用的描述性模型,该模型有四个参数,分别用于说明延迟期、细菌初始数量、抗菌剂的有效性极限和杀菌速率。该模型已应用于阿莫西林、头孢噻吩、萘啶酸、培氟沙星和氧氟沙星针对两种大肠杆菌菌株的几个动力学数据集。通过考虑模型参数置信限来比较杀菌曲线,这是一个有用的工具。这可以通过研究药物效应、菌株效应和浓度效应来说明。对于此处使用的抗生素,浓度效应主要影响延迟期的长度和观察到的存活细胞的最小数量。因此很明显,随着一个或多个参数的变化,杀菌曲线可能会出现差异。