Corum Orhan, Durna Corum Duygu, Atik Orkun, Altan Feray, Er Ayse, Uney Kamil
Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, University of Kastamonu, Kastamonu, Turkey.
Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, University of Afyon Kocatepe, Afyonkarahisar, Turkey.
J Vet Pharmacol Ther. 2019 Nov;42(6):654-659. doi: 10.1111/jvp.12763. Epub 2019 Apr 1.
The pharmacokinetics and bioavailability of levamisole were determined in red-eared slider turtles after single intravenous (IV), intramuscular (IM), and subcutaneous (SC) administration. Nine turtles received levamisole (10 mg/kg) by each route in a three-way crossover design with a washout period of 30 days. Blood samples were collected at time 0 (pretreatment), and at 0.25, 0.5, 1, 1.5, 3, 6, 9, 12, 18, 24, 36, and 48 hr after drug administration. Plasma levamisole concentrations were determined by a high-performance liquid chromatography assay. Data were analyzed by noncompartmental methods. The mean elimination half-life was 5.00, 7.88, and 9.43 hr for IV, IM, and SC routes, respectively. The total clearance and volume of distribution at steady state for the IV route were 0.14 L hr kg and 0.81 L/kg, respectively. For the IM and SC routes, the peak plasma concentration was 9.63 and 10.51 μg/ml, respectively, with 0.5 hr of T . The bioavailability was 93.03 and 115.25% for the IM and SC routes, respectively. The IM and SC route of levamisole, which showed the high bioavailability and long t , can be recommended as an effective way for treating nematodes in turtles.
在红耳龟单次静脉注射(IV)、肌肉注射(IM)和皮下注射(SC)给药后,测定了左旋咪唑的药代动力学和生物利用度。采用三交叉设计,9只龟每种给药途径均接受10mg/kg左旋咪唑,洗脱期为30天。在给药前的0时以及给药后0.25、0.5、1、1.5、3、6、9、12、18、24、36和48小时采集血样。通过高效液相色谱法测定血浆左旋咪唑浓度。采用非房室方法分析数据。静脉注射、肌肉注射和皮下注射途径的平均消除半衰期分别为5.00、7.88和9.43小时。静脉注射途径的总清除率和稳态分布容积分别为0.14L·hr/kg和0.81L/kg。肌肉注射和皮下注射途径的血浆峰浓度分别为9.63和10.51μg/ml,达峰时间均为0.5小时。肌肉注射和皮下注射途径的生物利用度分别为93.03%和115.25%。左旋咪唑的肌肉注射和皮下注射途径生物利用度高、达峰时间长,可推荐作为治疗龟类线虫的有效给药方式。