Population pharmacokinetics of biapenem in patients and healthy subjects

Population pharmacokinetic parameters of biapenem (BIPM), a carbapenem antibiotic, were generated by a nonlinear mixed effects model using the NONMEM program based on plasma concentrations in patients and healthy subjects. A total of 384 plasma samples were collected from 66 subjects, and their demo...

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Bibliographic Details
Published inJapanese Journal of Chemotherapy Vol. 54; no. 1; pp. 7 - 17
Main Authors Shibasaki, Shigeki, Sato, Nobuo, Tanaka, Yukari, Shibutani, Sachiyo
Format Journal Article
LanguageJapanese
Published Japanese Society of Chemotherapy 01.01.2006
公益社団法人 日本化学療法学会
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ISSN1340-7007
1884-5886
DOI10.11250/chemotherapy1995.54.7

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Summary:Population pharmacokinetic parameters of biapenem (BIPM), a carbapenem antibiotic, were generated by a nonlinear mixed effects model using the NONMEM program based on plasma concentrations in patients and healthy subjects. A total of 384 plasma samples were collected from 66 subjects, and their demographic background data were recorded. The data obtained were analyzed using the two-compartment model. The covariates (age, weight [Wt], creatinine clearance [Ccr]) and one factor (the effect of disease) were tested for an effect on the pharmacokinetics of BIPM. Population pharmacokinetic parameters were not related to the effect of disease. Total clearance (CL) was found to be associated with Ccr, and the volume of distribution of the central compartment (V1) was associated with Wt. The volume of distributionof the peripheral compartment (V2) was not associated with Wt. The final formulae for the population mean parameters were: CL=0.0720×Ccr+3.04 (L/h), V1=0.0990×Wt (L), inter-compartmental clearance (Q)=13.5 (L/h), V2=7.00 (L).The validity of the model has been evaluated by the bootstrapping method. The time above the MIC's (T>MIC) were estimated from the plasma concentration profiles calculated based on population mean parameters and MICe s in order to create tables for establishment of dosing regimens for BIPM.
ISSN:1340-7007
1884-5886
DOI:10.11250/chemotherapy1995.54.7