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Novel Concentration-Killing Curve Method for Estimation of Bactericidal Potency of Antibiotics in an In Vitro Dynamic Model

机译:新的浓度-杀死曲线法估算体外动态模型中抗生素的杀菌力

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摘要

The bactericidal pharmacodynamics of antibiotics against Escherichia coli were analyzed by a concentration-killing curve (CKC) approach, and the novel parameters median bactericidal concentration (BC50) and bactericidal intensity (r) for bactericidal potency were proposed. By using the agar plate method, about 500 E. coli cells were inoculated onto Luria-Bertani plates containing a series of antibiotic concentrations, and after 24 h of incubation at 37°C, all the viable colonies were enumerated. This resulted in a sigmoidal CKC that could be perfectly fitted (R2 > 0.9) with the function N = N0/[1 + er(x − BC50)], where N is number of colonies surviving on each plate with an x series of concentrations of an antibiotic, and N0 represents the meaningful inoculum size. Construction of the CKC method was based on the bactericidal effect of each antibiotic against the bacterial strain versus the concentration in two dimensions and may be a more valid, accurate, and reproducible method for estimating the bactericidal effect than the endpoint minimum bactericidal concentration (MBC) method. Mathematically, the CKC approach was point symmetrical toward its inflexion (BC50, N0/2); thus, 2BC50 could replace MBC. The parameter BC1 can be defined as BC50 + [ln(N0 − 1)/r], which is the drug concentration at which only one colony survived and which is the least critical value of MBC in the CKC. The variate r, which determined the tangent slope on inflexion when N0 was limited, could estimate the bactericidal intensity of an antibiotic. This verified that the CKC approach may be useful in studies with other classes of antibiotics and has considerable value as a tool for the accurate and proper administration of antibiotics.
机译:通过浓度杀灭曲线(CKC)方法分析了抗生素对大肠杆菌的杀菌药效,并提出了杀菌力中值浓度(BC50)和杀菌强度(r)的新参数。通过琼脂平板法,将约500株大肠杆菌细胞接种到含有一系列抗生素浓度的Luria-Bertani平板上,并在37°C孵育24小时后,计数所有活菌落。这样就产生了一个S形CKC,可以完美地拟合(R 2 r(x-BC50)],其中N是在x浓度的一系列x浓度的抗生素上在每个平板上存活的菌落数,而N0表示有意义的接种量。 CKC方法的构建是基于每种抗生素对细菌菌株的杀菌效果与二维浓度的关系,它可能是比终点最低杀菌浓度(MBC)更有效,准确且可重现的估算杀菌效果的方法。方法。在数学上,CKC方法是针对其弯曲点对称的(BC50,N0 / 2);因此,2BC50可以代替MBC。可以将参数BC1定义为BC50 + [ln(N0-1-)/ r],这是仅一个菌落存活的药物浓度,并且是CKC中MBC的最低临界值。变量r决定了N0受限制时弯曲的切线斜率,它可以估算抗生素的杀菌强度。这证明了CKC方法可能在研究其他类别的抗生素中有用,并且作为准确正确地使用抗生素的工具具有相当大的价值。

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