Pharmacokinetics of caffeic acid phenethyl ester and its catechol-ring fluorinated derivative following intravenous administration to rats
Document Type
Article
Publication Date
2009
Abstract
The pharmacokinetic profiles of caffeic acid phenethyl ester (CAPE) and its catechol-ring fluorinated derivative (FCAPE) were determined in rats after intravenous administration of 5, 10 or 20 mg/kg for CAPE and 20 mg/kg for FCAPE, respectively. The plasma concentrations of CAPE and FCAPE were measured using a validated liquid chromatography tandem mass spectrometric method. The pharmacokinetic parameters were estimated using non compartmental analysis (NCA) and biexponential fit. The results showed that the area under the plasma concentration-time curve for CAPE treatment increased in a proportion greater than the increase in dose from 5 to 20 mg/kg of CAPE. Total body clearance values for CAPE ranged from 42.1 to 172 ml/min/kg (NCA) and decreased with the increasing dose of CAPE. Similarly, the volume of distribution values for CAPE ranged from 1555 to 5209 ml/kg, decreasing with increasing dose. The elimination half-life for CAPE ranged from 21.2 to 26.7 min and was independent of dose. That FCAPE was distributed extensively into rat tissues and eliminated rapidly was indicated by a high value of volume of distribution and similar short elimination half-life as that of CAPE.
Publication Title
Biopharmaceutics & drug disposition
Volume
30
Issue
5
First Page
221
Last Page
228
Recommended Citation
Wang, Xinyu; Pang, Jihai; Maffucci, Jacqueline A.; Patel, Devandra S.; Newman, Robert A.; Kerwin, Sean M.; Bowman, Phillip D.; and Stavchansky, Salomon, "Pharmacokinetics of caffeic acid phenethyl ester and its catechol-ring fluorinated derivative following intravenous administration to rats" (2009). PCOM Scholarly Works. 439.
https://digitalcommons.pcom.edu/scholarly_papers/439
Comments
This article was published in Biopharmaceutics & drug disposition, Volume 30, Issue 5, Pages 221-228.
The published version is available at http://dx.doi.org/10.1002/bdd.657 [doi].Copyright © 2009 Wiley.