V. Gayrard et al., Comparison of pharmacokinetic profiles of doramectin and ivermectin pour-on formulations in cattle, VET PARASIT, 81(1), 1999, pp. 47-55
The plasma pharmacokinetics of doramectin and invermectin after topical adm
inistration (500 mu g kg(-1)) were compared over a 50-day period in 24 youn
g beef cattle. Observed maximum concentration (C-max) and time to maximum c
oncentration (T-max) were determined directly from plasma concentrations fo
r each animal. The area under the plasma concentration-time curve (AUC) and
mean residence time (MRT) were calculated as indices of drug exposure and
persistence. The C-max of doramectin (12.2 +/- 4.8 ng ml(-1)) and ivermecti
n (12.2 +/- 6.0 ng ml(-1)) and T-max of doramectin (4.3 +/- 1.6 days) and i
vermectin (3.4 +/- 0.8 days) were not significantly different (p > 0.05). I
n contrast, the AUC of doramectin (168.0 +/- 41.7 ng day ml(-1)) was signif
icantly greater than that of ivermectin (115.5 +/- 43.0 ng day ml(-1)). Fur
thermore, the range of AUC values calculated for ivermectin was wider than
that obtained for doramectin, extending from 51.3 to 182.3 ng day ml(-1) fo
r ivermectin versus 104.3-228.7 ng day ml(-1) for doramectin. The MRT was s
ignificantly greater for doramectin (12.8 +/- 1.9 days) than for ivermectin
(8.4 +/- 1.5 days). It was concluded that a 500 mu g kg(-1) pour-on admini
stration of doramectin and ivermectin led to an overall exposure as reflect
ed by the mean AUG, that was 45% higher for doramectin compared to ivermect
in and that the relative inter-individual variability was less for doramect
in than for ivermectin. Possible therapeutic consequences of these differen
ces between doramectin and ivermectin pour-on formulations are discussed. (
C) 1999 Elsevier Science B.V. All rights reserved.