Department of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN, USA.
Department of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, TN, USA.
Eur J Pharm Sci. 2019 Jan 15;127:233-239. doi: 10.1016/j.ejps.2018.11.006. Epub 2018 Nov 9.
Spectinamides are a novel class of antibiotics under development for the treatment of MDR- and XDR-tuberculosis, with 1599 and 1445 as early lead candidates within this group. In order to evaluate and differentiate the pharmacological properties of these compounds and assist in candidate selection and design of optimal dosing regimens in animal models of Mtb infection, time kill curve assessments were performed in a previously established in vitro PK/PD model system. The performed studies and subsequent pharmacometric analysis indicate that the anti-mycobacterial activity of 1599 exhibits concentration-dependent killing whereas 1445 shows time-dependent killing. These findings are supported by the fact that the PKPD index that best describes bacterial killing is T > MIC for 1445, but fC/AUC for 1599. The differential killing behavior among the lead candidates can be rationalized by the differences in post-antibiotic effect: 15.7 h for 1445 compared the 133 h for 1599. Overall, the PK/PD based analysis of the in vitro pharmacologic killing profile of spectinamides 1599 and 1445 on mycobacteria provided valuable insights that contributed to lead candidate selection and preclinical development of these compounds.
spectinamides 是一类新型抗生素,正在开发用于治疗耐多药和广泛耐药结核病,其中 1599 和 1445 是该类别的早期先导候选物。为了评估和区分这些化合物的药理学特性,并协助在 Mtb 感染的动物模型中选择候选物和设计最佳剂量方案,在先前建立的体外 PK/PD 模型系统中进行了时间杀伤曲线评估。进行的研究和随后的药代动力学分析表明,1599 的抗分枝杆菌活性表现出浓度依赖性杀伤,而 1445 则表现出时间依赖性杀伤。这一发现得到了以下事实的支持:最佳描述细菌杀伤的 PKPD 指数是 T > MIC 用于 1445,但 fC/AUC 用于 1599。候选物之间的差异杀伤行为可以通过抗生素后效应的差异来合理化:1445 为 15.7 小时,而 1599 为 133 小时。总的来说,基于 PK/PD 的 spectinamides 1599 和 1445 对分枝杆菌体外药效杀伤谱的分析提供了有价值的见解,有助于候选物的选择和这些化合物的临床前开发。