Single dose pharmacokinetics of pleconaril in neonates

被引:24
作者
Kearns, GL
Bradley, JS
Jacobs, RF
Capparelli, EV
James, LP
Johnson, KM
Abdel-Rahman, SM
机构
[1] Childrens Mercy Hosp, Sect Pediat Clin Pharmacol & Expt Therapeut, Kansas City, MO 64108 USA
[2] Univ Missouri, Dept Pediat, Kansas City, MO 64110 USA
[3] Univ Missouri, Dept Pharmacol, Kansas City, MO 64110 USA
[4] Univ Missouri, Dept Pharm Practice, Kansas City, MO 64110 USA
[5] Univ Calif San Diego, Childrens Hosp & Hlth Ctr, Div Infect Dis, La Jolla, CA 92093 USA
[6] Univ Calif San Diego, Dept Pediat, La Jolla, CA 92093 USA
[7] Univ Arkansas Med Sci, Dept Pediat, Little Rock, AR 72205 USA
[8] Arkansas Childrens Hosp, Div Pediat Infect Dis, Little Rock, AR 72202 USA
[9] Arkansas Childrens Hosp, Div Clin Pharmacol & Toxicol, Little Rock, AR 72202 USA
[10] NICHHD, Pediat Pharmacol Res Unit Network, Bethesda, MD 20892 USA
关键词
pleconaril; neonates; pharmacokinetics; enterovirus;
D O I
10.1097/00006454-200009000-00005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Pleconaril is an orally active, broad spectrum antipicornaviral agent with activity against nonpolio enteroviruses. Pleconaril phamacokinetics was evaluated in 16 neonates (16.4 +/- 8.7 days postnatal age) with suspected enteroviral infection, Methods, Pleconaril (5 or 7.5 mg/kg) was administered orally to study subjects and plasma pleconaril concentrations quantified from serial blood samples obtained during 24 h after a single oral dose by gas chromatography with electrochemical detection. Pharmacokinetic parameter estimates were determined by noncompartmental methods and compared between doses and with similar data obtained from a previous study of pleconaril disposition in children (n = 18, 2 to 12 years). Results. Pleconaril was well-tolerated in all neonates without discernible adverse events. Comparison between the 5.0- and 7.5-mg/kg doses revealed no significant differences in peak plasma concentration (C-max 686.7 vs. 617.1 ng/ml), elimination half-life (t(1/2); 4.6 us. 6.6 h), area under the plasma concentration vs. time curve (AUC; 5162.6 vs. 5523.9 ng/ml/h), apparent steady state volume of distribution (V-dss/F; 9.3 vs. 17.1 liters/ kg) and apparent oral clearance (Cl/F; 1.3 vs. 1.7 liters/h/kg), In addition, no correlation was observed between postconceptional age and AUG, V-dss/F, t(1/2) or Cl/F for pleconaril, Comparison of pleconaril pharmacokinetics between neonates and children suggested a significant difference in V-dss/F (9.3 vs, 4.7 liters/kg), dose-normalized C-max (686.7 vs. 1272.5 ng/ml) and AUC (5125.6 vs. 8131.2 ng/ml/h). In contrast, the mean elimination t(1/2) between neonates and children was not appreciably different. Conclusions. The apparent age-dependent differences in the pharmacokinetics of pleconaril may in part be related to increased bioavailability of the drug in older children and adults than in neonates, Our data appear to support the use of a 5.0-mg/kg dose given every 8 to 12 h in future studies of pleconaril in neonatal patients with enteroviral infection.
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页码:833 / 839
页数:7
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