Hishikawa T, Kusunoki T, Tsuchiya K, Uzuka Y, Sakamoto T, Nagatake T, Matsumoto K
New Product Planning and Development Division, Takeda Chemical Industries, Ltd., Osaka, Japan.
Antimicrob Agents Chemother. 1990 Feb;34(2):326-31. doi: 10.1128/AAC.34.2.326.
Two beta-lactam antibiotics, cefazolin and cefmenoxime, were administered in an experimental model of murine pneumonia caused by Klebsiella pneumoniae in a way which enabled us to approximate the serum antibiotic concentration time course in humans. Bacterial counts during the experiments were subjected to nonlinear least-squares analyses by using a mathematical model that explained the bacterial killing by the antibiotic concentration time course and other factors associated with antimicrobial potency and bacterial growth. Cefazolin gave a killing curve that changed synchronously with the drug levels in serum; in contrast, cefmenoxime gave a curve that was prolonged as compared with the change in the drug levels in serum. Multiple correlation coefficients were about 0.9, and the model worked well for bacterial count data. Parameters relating to antimicrobial potency of the drugs, bacterial growth rate, and drug distribution into the tissue were estimated numerically.
在由肺炎克雷伯菌引起的小鼠肺炎实验模型中,以能够使我们近似人类血清抗生素浓度随时间变化过程的方式,给予了两种β-内酰胺类抗生素,头孢唑林和头孢甲肟。实验期间的细菌计数通过使用一种数学模型进行非线性最小二乘法分析,该模型解释了抗生素浓度随时间变化过程以及与抗菌效力和细菌生长相关的其他因素对细菌的杀灭作用。头孢唑林给出的杀灭曲线与血清中的药物水平同步变化;相比之下,头孢甲肟给出的曲线与血清中药物水平的变化相比有所延长。多重相关系数约为0.9,该模型对细菌计数数据效果良好。通过数值估计了与药物抗菌效力、细菌生长速率以及药物在组织中的分布相关的参数。