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Reduced incubation time for inhibition zone formation based on diffusion and growth mechanism elucidation

机译:基于扩散和生长机理的阐明减少了抑制区形成的孵育时间

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Microbiological agar diffusion methods are widely employed for clinical, pharmacological and industrial purposes. Usually, inhibition zone sizes are defined after a few hours of incubation; however, they can only be visualized after overnight microbial growth. Thus, the aim of this work was to determine the critical parameters and optimize them using the tool Solver (Microsoft Excel (R)), in order to elucidate the mechanism of inhibition zone formation and develop a microbiological assay for linezolid with a reduced incubation time. A Box-Behnken design was used to determine the critical parameters, such as the critical concentration (C'), critical population (N'), critical time (T'), diffusion coefficient (D), lag phase time (L), and generation time (G). Optimized critical parameters were coherent with the mean values of experimental parameters and were contained within the confidence interval 95%, validating the results obtained with the tool Solver. Furthermore the formation of inhibition zones was elucidated with 97.7% certainty. Increased inoculum sizes reduce critical time, which allow us to use TTC to visualize inhibition zones after 6 hours. The value of the critical concentration obtained with reduced incubation time (8.90 mg L-1) was consistent with the experimental value with standard incubation time (8.62 +/- 0.53 mg L-1; CI95% 7.77 to 9.45 mg L-1). Therefore our method was able to reduce incubation from 18 to 24 hours to approximately 6 hours.
机译:微生物琼脂扩散方法被广泛用于临床,药理学和工业目的。通常,孵育几个小时后即可确定抑制区的大小;但是,只有在过夜的微生物生长后才能看到它们。因此,这项工作的目的是确定关键参数,并使用Solver(Microsoft Excel(R))工具对其进行优化,以阐明抑制区形成的机理,并开发出减少孵化时间的利奈唑胺微生物检测方法。采用Box-Behnken设计确定关键参数,例如关键浓度(C'),关键种群(N'),关键时间(T'),扩散系数(D),滞后时间(L),和生成时间(G)。优化的关键参数与实验参数的平均值一致,并包含在95%的置信区间内,从而验证了使用工具求解器获得的结果。此外,以97.7%的确定性阐明了抑制区的形成。接种量的增加减少了关键时间,这使我们可以在6小时后使用TTC可视化抑制区。孵育时间减少的临界浓度值(8.90 mg L-1)与标准孵育时间的实验值(8.62 +/- 0.53 mg L-1; CI95%7.77至9.45 mg L-1)一致。因此,我们的方法能够将孵育时间从18到24小时减少到大约6小时。

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