THE EFFECTS ON THE PHARMACOKINETICS OF INTRAVENOUS CEFTIOFUR SODIUM IN DAIRY-CATTLE OF SIMULTANEOUS INTRAVENOUS ACETYL SALICYLATE (ASPIRIN)OR PROBENECID
T. Whittem et al., THE EFFECTS ON THE PHARMACOKINETICS OF INTRAVENOUS CEFTIOFUR SODIUM IN DAIRY-CATTLE OF SIMULTANEOUS INTRAVENOUS ACETYL SALICYLATE (ASPIRIN)OR PROBENECID, Journal of veterinary pharmacology and therapeutics, 18(1), 1995, pp. 61-67
Ceftiofur sodium is a third-generation cephalosporin antibiotic. It is
possible that non-steroidal anti-inflammatory drugs such as acetyl sa
licylate (aspirin) may be used concomitantly with ceftiofur sodium in
dairy cattle. Therefore this study evaluated potential pharmacokinetic
interactions between ceftiofur sodium and aspirin. In addition, this
study evaluated the potential for interaction between ceftiofur and it
s active metabolites and the organic anion transporter. The organic an
ion transporter substrate used in this evaluation was probenecid. Ten
healthy, non-pregnant, non-lactating dairy cows were used in a randomi
zed complete three-way crossover design. In repeated experiments all c
ows were administered: (1) 2 mg of ceftiofur sodium per kg body weight
by intravenous bolus or (2) 10 mg of probenecid per kg body weight by
intravenous bolus, followed immediately by 2 mg of ceftiofur sodium p
er kg body weight by intravenous bolus or (3) 26 mg of aspirin per kg
body weight by intravenous bolus, followed immediately by 2 mg of ceft
iofur sodium per kg body weight by intravenous bolus. For treatment wi
th ceftiofur sodium alone, the mean volume of distribution at steady-s
tate V-d(ss) was 0.2 +/- 0.06 L/kg, the mean volume of distribution by
the area method V-d(area) was 0.38 +/- 0.22 L/kg, mean residence time
(MRT) was 6.5 +/- 1.8 h, mean residence time in peripheral tissues (M
RT(p)) was 2.6 +/- 1.0 h, total body clearance (Cl) was 0.032 +/- 0.01
3 L/kg/h and elimination rate constant (beta) was 0.097 +/- 0.044 h(-1
) (mean +/- standard deviation). No statistically significant changes
were detected as a result of preceding treatment with aspirin. Precedi
ng treatment with probenecid resulted in a decrease in both Cl (0.007
+/- 0.005 L/kg/h) and MRT(p) (0.89 +/- 0.45 h). These results suggest
that ceftiofur or its metabolites may interact with the organic anion
transporter, but that consideration of alterations to dose and dose in
terval may not be necessary when ceftiofur sodium is administered to t
he cow concomitantly with a single dose of aspirin.