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Comparative pharmacokinetics of spectinamide 1599 after subcutaneous and intrapulmonary aerosol administration in mice

机译:小鼠皮下和颅内气溶胶施用后露西酰胺的比较药代动力学

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摘要

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 8h 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.
机译:SpectInamides是一种用于治疗结核病的新型一系列侧霉素类似物。颅内气溶胶(IPA)授予铅赤酰胺1599的施用,先前已被证明比在可比较剂量下皮下(SC)给药更有效。目前研究的目的是在小鼠中表征血浆和肺部的血浆和肺部的配置,以便为观察到的疗效差异提供潜在的理由。通过SC注射或通过IPA递送给予健康BALB / C小鼠200mg / kg 1599。在指定时间点收集血浆和主要器官直至给药后8小时。通过LC-MS / MS测量药物浓度并通过非组分药代动力学分析分析。 1599在IPA和SC给药后表现出快速吸收血浆,导致两条途径非常相似的等离子体暴露。相反,与SC给药相比,IPA的肺中的药物暴露是48倍,这是由于肺部是肺结核中感染的主要部位。与SC授权相比,肺中肺部局部暴露可能是在IPA后提高疗效的基础。总体而言,本研究支持肺部路线作为治疗结核病的潜在途径,1599年。

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