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抗惊厥药物左乙拉西坦在新生马驹体内的药代动力学

Pharmacokinetics of the anticonvulsant levetiracetam in neonatal foals.

作者信息

MacDonald K D, Hart K A, Davis J L, Berghaus L J, Giguère S

机构信息

Department of Large Animal Medicine, College of Veterinary Medicine, University of Georgia, Athens, Georgia, USA.

Department of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Blacksburg, Virginia, USA.

出版信息

Equine Vet J. 2018 Jul;50(4):532-536. doi: 10.1111/evj.12790. Epub 2017 Dec 30.

Abstract

BACKGROUND

Seizures are a common manifestation of neurological disease in the neonatal foal and are an important cause of morbidity and mortality in this population. Current antiepileptic options are effective, but often have undesirable adverse effects, short duration of action and high cost. Levetiracetam has an ideal safety and pharmacokinetic profile in multiple species, including the adult horse, and may be a safe and cost-effective alternative anticonvulsant in neonatal foals. Due to differences in drug disposition and clearance dosages in neonates, dosing recommendations in other species or adult horses cannot be extrapolated to foals.

OBJECTIVE

To establish the pharmacokinetic profile of single-dose i.v. and intragastric administration of levetiracetam in healthy neonatal foals.

STUDY DESIGN

Randomised crossover experimental study.

METHODS

Levetiracetam was administered as a single dose to six healthy foals (ages 1-10 days) at a dose of 32 mg/kg bwt i.v. or intragastrically. Plasma levetiracetam concentrations were measured using a validated HPLC protocol.

RESULTS

After i.v. administration to healthy foals, levetiracetam had a mean (±s.d.) elimination half-life of 7.76 ± 0.51 h, a mean systemic clearance of 61.67 ± 10.96 (mL/h/kg) and a mean apparent volume of distribution at steady state of 0.670 ± 0.124 (L/kg). Following intragastric administration, levetiracetam had a peak concentration of 38.34 ± 7.42 mg/L and time to achieve peak concentration was 0.875 (0.5-1.5) h. Mean bioavailability for IG administration was excellent (103.04 ± 14.51%). No significant differences in pharmacokinetic variables between routes and order of administration were observed.

MAIN LIMITATIONS

Small sample size and single-dose administration.

CONCLUSIONS

Levetiracetam has excellent intragastric bioavailability in foals and is predicted to maintain plasma concentrations at or above the proposed target concentration with twice daily i.v. or oral administration. Once-daily administration may be possible in some foals based on the therapeutic range recommended in other species.

摘要

背景

癫痫发作是新生马驹神经系统疾病的常见表现,也是该群体发病和死亡的重要原因。目前的抗癫痫药物有效,但往往有不良副作用、作用持续时间短且成本高。左乙拉西坦在包括成年马在内的多个物种中具有理想的安全性和药代动力学特征,可能是新生马驹安全且经济有效的替代抗惊厥药物。由于新生儿药物处置和清除剂量的差异,其他物种或成年马的给药建议不能外推至马驹。

目的

确定单剂量静脉注射和胃内给予左乙拉西坦在健康新生马驹中的药代动力学特征。

研究设计

随机交叉实验研究。

方法

以32mg/kg体重的剂量给6匹健康马驹(年龄1 - 10天)单剂量静脉注射或胃内给予左乙拉西坦。使用经过验证的高效液相色谱法测定血浆左乙拉西坦浓度。

结果

健康马驹静脉注射后,左乙拉西坦的平均(±标准差)消除半衰期为7.76±0.51小时,平均全身清除率为61.67±10.96(mL/h/kg),稳态时平均表观分布容积为0.670±0.124(L/kg)。胃内给药后,左乙拉西坦的峰值浓度为38.34±7.42mg/L,达到峰值浓度的时间为0.875(0.5 - 1.5)小时。胃内给药的平均生物利用度极佳(103.04±14.51%)。未观察到给药途径和给药顺序之间药代动力学变量的显著差异。

主要局限性

样本量小且为单剂量给药。

结论

左乙拉西坦在马驹中具有极佳的胃内生物利用度,预计通过每日两次静脉注射或口服给药可使血浆浓度维持在或高于建议的目标浓度。根据其他物种推荐的治疗范围,一些马驹可能可以每日给药一次。

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