|
KMID : 0369820150450050441
|
|
Jorunal of Korean Pharmaceutical Sciences
2015 Volume.45 No. 5 p.441 ~ p.448
|
|
|
Pharmacokinetic scaling of epirubicin using allometric and species-invariant time methods
|
|
Shin Dae-Hwan
Park Seung-Hyeok
Jeong Sung-Woo
Kwon Oh-Seung
Park Chun-Woong
Han Kun
Chung Youn-Bok
|
|
|
Abstract
|
|
|
|
The pharmacokinetics of epirubicin, an anthracycline, were investigated after intravenous bolus administration (5 mg/kg) in mice, rats, rabbits and dogs. Based on animal data, we predicted the following human pharmacokinetic parameters using allometric scaling: 120 and 35.2 L/h for total body clearance (CLt) using simple and maximum life-span potential (MLP)-corrected allometry, respectively; 702 L for steady-state volume of distribution (Vdss). The scaled Vdss value was twofold lower than the corresponding values in humans. However, the scaled CLt values were consistent with those clinically observed in humans (35.6?133.4 L/h). We also predicted human parameters using species-invariant time transformations (equivalent time, kallynochrons, apolysichrons and dienetichrons). The mean Vdss (854 L) obtained using kallynochrons and that derived from simple allometry were comparable. The lowest CLt (121 L/h) derived using kallynochrons was comparable to that obtained using simple allometry. The results of this study also indicated that the predicted human CLt generated using MLP-corrected allometry can be used for the selection of a safe dose for studies in healthy adult human volunteers. These results suggest that such approaches may be useful in designing pharmacokinetic studies for novel anthracyclines.
|
|
|
KEYWORD
|
|
|
Epirubicin, Allometric scaling, Species-invariant time methods, Clearance, Pharmacokinetics
|
|
|
FullTexts / Linksout information
|
|
|
|
|
|
Listed journal information
|
|
|