Chapuis Ronan J J, Smith Joe S, French Hilari M, Toka Felix Ngosa, Peterson Erik W, Little Erika L
Department of Clinical Sciences, Ross University School of Veterinary Medicine, Basseterre, Saint Kitts and Nevis.
Large Animal Clinical Sciences, College of Veterinary Medicine, University of Tennessee, Knoxville, TN 37996, USA.
Animals (Basel). 2021 Jul 9;11(7):2047. doi: 10.3390/ani11072047.
Doxycycline (DXC) is a broad-spectrum antibacterial antimicrobial administered to horses for the treatment of bacterial infections which may also affect donkeys. Donkeys have a different metabolism than horses, leading to differences in the pharmacokinetics of drugs compared to horses. This study aimed to describe the population pharmacokinetics of DXC in donkeys. Five doses of DXC hyclate (10 mg/kg) were administered via a nasogastric tube, q12 h, to eight non-fasted, healthy, adult jennies. Serum, urine, synovial fluid and endometrium were collected for 72 h following the first administration. Doxycycline concentration was measured by competitive enzyme immunoassay. Serum concentrations versus time data were fitted simultaneously using the stochastic approximation expectation-maximization algorithm for nonlinear mixed effects. A one-compartment model with linear elimination and first-order absorption after intragastric administration, best described the available pharmacokinetic data. Final parameter estimates indicate that DXC has a high volume of distribution (108 L/kg) as well as high absorption (10.3 h) in donkeys. However, results suggest that oral DXC at 10 mg/kg q12 h in donkeys would not result in a therapeutic concentration in serum, urine, synovial fluid or endometrium by comparison to the minimum inhibitory concentration of common equine pathogens. Further studies are recommended to identify appropriate dosage and dosing intervals of oral DXC in donkeys.
强力霉素(DXC)是一种广谱抗菌药物,用于治疗马匹的细菌感染,这些感染也可能影响驴子。驴子的新陈代谢与马不同,导致与马相比药物的药代动力学存在差异。本研究旨在描述强力霉素在驴子体内的群体药代动力学。通过鼻胃管向8头非禁食、健康的成年母驴每12小时给予5剂盐酸强力霉素(10mg/kg)。首次给药后72小时收集血清、尿液、滑液和子宫内膜。通过竞争性酶免疫测定法测量强力霉素浓度。使用随机近似期望最大化算法对血清浓度与时间数据进行非线性混合效应拟合。胃内给药后具有线性消除和一级吸收的一室模型最能描述现有的药代动力学数据。最终参数估计表明,强力霉素在驴子体内具有高分布容积(108L/kg)以及高吸收(10.3小时)。然而,结果表明,与常见马病原体的最低抑菌浓度相比,驴子每12小时口服10mg/kg强力霉素不会在血清、尿液、滑液或子宫内膜中产生治疗浓度。建议进一步研究以确定驴子口服强力霉素的合适剂量和给药间隔。