Establishing Population Pharmacokinetic Model for Ethambutol on Pulmonary Tuberculosis Patients

Ta Viet Ha, Bui Son Nhat, Le Thi Luyen
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Abstract

The population pharmacokinetic model of ethambutol with covariates was built from data from 136 pulmonary tuberculosis patients recruited from 3 hospitals: Hanoi Lung Hospital, Central Hospital 74, and Central Lung Hospital. Blood samples were obtained on the 10-14th day after initiation of treatment for plasma drug analysis by LC-MS/MS method. Time - concentration data were processed by the method of non-linear mixed effect modeling on MONOLIX 2021R1 software. The final population pharmacokinetic model is a two-compartment model, sequential zero (with prior lag time Tk01) followed by first-order absorption, and linear elimination. The volumes of distribution of the central and peripheral compartments were respectively 6.73 L and 1250 L; the clearance value Cl was 45.8 L/h. Janmahasatian’s Fat-free mass and age were found to be influential to the inter-individual variability of clearance.
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乙胺丁醇在肺结核患者体内的人群药动学模型的建立
从河内肺科医院、中心肺科医院74号和中心肺科医院3家医院招募136例肺结核患者,建立了乙胺丁醇人群药代动力学协变量模型。治疗开始后10 ~ 14天采血,采用LC-MS/MS法进行血浆药物分析。在MONOLIX 2021R1软件上对时间-浓度数据进行非线性混合效应建模。最终的群体药代动力学模型是一个双室模型,顺序零(先验滞后时间Tk01),然后是一阶吸收,线性消除。中央室和外周室分布容积分别为6.73 L和1250 L;清除率Cl为45.8 L/h。发现Janmahasatian的无脂量和年龄对清除率的个体间变异性有影响。
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