Alves Izabel Almeida, Staudt Keli Jaqueline, Silva Carolina de Miranda, Lock Graziela de Araujo, Dalla Costa Teresa, de Araujo Bibiana Verlindo
Pharmaceutical Sciences Graduate Program of Federal University of Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil.
Medical Sciences Graduate Program of Federal University of Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil.
Antimicrob Agents Chemother. 2017 Jun 27;61(7). doi: 10.1128/AAC.00321-17. Print 2017 Jul.
To make advances in the treatment of cryptococcal meningitis, it is crucial to know a given drug's free fraction that reaches the biophase. In the present study, we applied microdialysis (μD) as a tool to determine the free levels reached by voriconazole (VRC) in the brains of healthy and -infected rats. The infection was induced by the intravenous (i.v.) administration of 1 × 10 CFU of yeast. The dose administered was 5 mg/kg (of body weight) of VRC, given i.v. Plasma and microdialysate samples were analyzed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) and LC-UV methods. The free brain/free plasma ratio (T) and population pharmacokinetic (popPK) analyses were performed to evaluate the impact of infection on PK parameters of the drug. The brain penetration ratio showed an increase on brain exposure in infected animals (T = 0.85 versus T = 1.86). The structural PK model with two compartments and Michaelis-Menten (MM) elimination describes the VRC concentration-time profile in plasma and tissue simultaneously. The covariate infection was included in volume of distribution in the peripheral compartment in healthy animals () and maximum rate of metabolism ( ). The levels reached in infected tissues were higher than the values described for MIC of VRC for (0.03 to 0.5 μg ml), indicating its great potential to treat meningitis associated with .
要在隐球菌性脑膜炎的治疗方面取得进展,了解某种药物到达生物相的游离分数至关重要。在本研究中,我们应用微透析(μD)作为一种工具,来测定伏立康唑(VRC)在健康大鼠和感染大鼠脑中所达到的游离水平。通过静脉注射1×10 CFU酵母诱导感染。给药剂量为5 mg/kg(体重)的VRC,静脉注射。血浆和微透析液样本通过液相色谱 - 串联质谱(LC-MS/MS)和LC-UV方法进行分析。进行了脑游离/血浆游离比率(T)和群体药代动力学(popPK)分析,以评估感染对药物药代动力学参数的影响。脑渗透比率显示感染动物的脑暴露增加(T = 0.85对T = 1.86)。具有两个隔室和米氏(MM)消除的结构药代动力学模型同时描述了血浆和组织中VRC的浓度 - 时间曲线。协变量感染包含在健康动物外周隔室的分布容积()和最大代谢速率()中。感染组织中达到的水平高于VRC对(0.03至0.5μg/ml)的最低抑菌浓度(MIC)所描述的值,表明其治疗与相关的脑膜炎的巨大潜力。