{"title":"Establishing Population Pharmacokinetic Model for Ethambutol on Pulmonary Tuberculosis Patients","authors":"Ta Viet Ha, Bui Son Nhat, Le Thi Luyen","doi":"10.25073/2588-1132/vnumps.4500","DOIUrl":null,"url":null,"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.","PeriodicalId":23520,"journal":{"name":"VNU Journal of Science: Medical and Pharmaceutical Sciences","volume":"30 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"VNU Journal of Science: Medical and Pharmaceutical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.25073/2588-1132/vnumps.4500","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
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.