Rathi Chetan, Lukka Pradeep B, Wagh Santosh, Lee Richard E, Lenaerts Anne J, Braunstein Miriam, Hickey Anthony, Gonzalez-Juarrero Mercedes, Meibohm Bernd
Department of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Department of Chemical Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Tuberculosis (Edinb). 2019 Jan;114:119-122. doi: 10.1016/j.tube.2018.12.006. Epub 2018 Dec 31.
Spectinamides are a novel series of spectinomycin analogs being developed for the treatment of tuberculosis. Intrapulmonary aerosol (IPA) administration of lead spectinamide 1599 has previously been shown to be more efficacious than subcutaneous (SC) administration at comparable doses. The objective of the current study was to characterize the disposition of 1599 in plasma and lungs in mice in order to provide a potential rationale for the observed efficacy differences. 200 mg/kg of 1599 was administered to healthy BALB/c mice by SC injection or by IPA delivery. Plasma and major organs were collected at specified time points until 8 h after dosing. Drug concentrations were measured by LC-MS/MS and analyzed by noncompartmental pharmacokinetic analysis. 1599 demonstrated rapid absorption into plasma after IPA and SC administration, resulting in very similar plasma exposure for both routes. In contrast, drug exposure in the lungs was 48 times higher following IPA as compared to SC administration, which is highly desirable as the lungs are the main site of infection in pulmonary TB. The higher local exposure in the lungs is likely the basis for the increased efficacy after IPA compared to SC administration. Overall, this study supports the pulmonary route as a potential pathway for the treatment of tuberculosis with 1599.
氨甲环酸酰胺是正在开发用于治疗结核病的一系列新型大观霉素类似物。先前已表明,在可比剂量下,肺部气溶胶(IPA)给药铅氨甲环酸酰胺1599比皮下(SC)给药更有效。本研究的目的是表征1599在小鼠血浆和肺中的处置情况,以便为观察到的疗效差异提供潜在的理论依据。通过皮下注射或IPA给药,将200mg/kg的1599给予健康的BALB/c小鼠。在给药后8小时内的特定时间点收集血浆和主要器官。通过LC-MS/MS测量药物浓度,并通过非房室药代动力学分析进行分析。IPA和SC给药后,1599均迅速吸收进入血浆,导致两种给药途径的血浆暴露非常相似。相比之下,与SC给药相比,IPA给药后肺中的药物暴露高48倍,这是非常理想的,因为肺是肺结核的主要感染部位。与SC给药相比,IPA给药后肺中更高的局部暴露可能是疗效增加的基础。总体而言,本研究支持肺部给药途径作为用1599治疗结核病的潜在途径。