Premium
Pharmacokinetic modelling of serum and bronchial concentrations for clarithromycin and telithromycin, and site‐specific pharmacodynamic simulation for their dosages
Author(s) -
Ikawa K.,
Kikuchi E.,
Kikuchi J.,
Nishimura M.,
Derendorf H.,
Morikawa N.
Publication year - 2014
Publication title -
journal of clinical pharmacy and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.622
H-Index - 73
eISSN - 1365-2710
pISSN - 0269-4727
DOI - 10.1111/jcpt.12157
Subject(s) - telithromycin , pharmacokinetics , nonmem , clarithromycin , pharmacodynamics , pharmacology , area under the curve , antibacterial agent , population , chemistry , elimination rate constant , minimum inhibitory concentration , volume of distribution , medicine , antibiotics , biochemistry , environmental health
Summary What is known and objective Clinical pharmacokinetic profiles of clarithromycin and telithromycin in bronchopulmonary sites have not been fully characterized. This study aimed to describe in more detail the pharmacokinetics of the two macrolides in epithelial lining fluid ( ELF ) of human bronchi and to evaluate their pharmacodynamic target attainment at this site. Methods Previously reported drug concentration data for serum and ELF were simultaneously fitted to a three‐compartment pharmacokinetic model using nonmem program. The model parameter estimates were used for site‐specific pharmacodynamic simulation. Results and discussion Population mean parameters for clarithromycin were as follows: distribution volumes of central, peripheral and ELF compartments ( V 1 / F , V 2 / F and V 3 / F ) = 204·7, 168·9 and 67·1 L; clearance ( CL / F ) = 34·4 L/h; absorption rate constant ( K a ) = 0·680 1/h; transfer rate constants connecting compartments ( K 12 , K 21 , K 13 and K 31 = 0·0193, 0·434, 0·667 and 0·260 1/h, respectively). Mean parameters for telithromycin were as follows: V 1 / F , V 2 / F and V 3 / F = 370·3, 290·3 and 213·8 L; CL / F = 89·5 L/h; K a = 0·740 1/h; K 12 , K 21 , K 13 and K 31 = 0·0026, 1·044, 0·758 and 0·158 1/h, respectively. Using these parameters, the mean ELF /serum ratio in the area under drug concentration–time curve ( AUC ) was 7·80 for clarithromycin and 8·05 for telithromycin. Clarithromycin achieved a ≥ 90% probability of attaining a pharmacodynamic target [ AUC /minimum inhibitory concentration ( MIC ) = 100] in ELF against bacterial isolates for which MIC s were ≤0·5 and ≤1 mg/L for twice‐daily doses of 250 and 500 mg, respectively. For telithromycin, once‐daily doses of 600 and 800 mg achieved a ≥90% probability in ELF against Streptococcus pneumoniae , Staphylococcus aureus and Moraxella catarrhalis isolates but not Haemophilus influenzae isolates. What is new and conclusion These results should provide a better understanding of the bronchial pharmacokinetics of clarithromycin and telithromycin, while also providing useful information about their dosages for respiratory tract infections based on site‐specific pharmacodynamic evaluation. Further studies in a large number of patients are needed to confirm our findings and clarify their therapeutic implications.