Jangaran Nejad Abdolhossein, Peyghan Rahim, Najafzadeh Varzi Hossein, Shahriyari Ali
Department of Clinical Sciences, Faculty of Veterinary Medicine, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Department of Basic Sciences, Faculty of Veterinary Medicine, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Vet Res Forum. 2017;8(4):327-331. Epub 2017 Dec 15.
The aim of this study was to evaluate pharmacokinetic profiles of florfenicol after a single dose of intravenous (5.00 mg kg body weight) and oral (40.00 mg kg body weight) administrations in common carp (). The residue depletion of florfenicol was also investigated after oral administration (10.00 mg kg body weight) and bath treatment (5.00 mg L) for 10 consecutive days. Pharmacokinetics of florfenicol in plasma after a single dose administration, at 10 time points (0.50, 1, 2, 4, 8, 12, 24, 72, 120 and 168 hr) and florfenicol concentrations in tissues (plasma, liver and muscle) at three time points (1, 7 and 14 days) after 10 consecutive days, were analyzed by high performance liquid chromatography. The peak concentration of florfenicol was 137.02 ng mL and the time to reach peak concentration in plasma was two hr. The elimination half-lives, the volume of distribution at steady state and total body clearance were estimated as 21.40 hr, 0.30 and 0.03 L hr, respectively. After drug administration for 10 days, it's concentration in plasma and muscle in oral treatment was significantly more than bath treatment in all days. Drug concentrations in the liver after bath treatment were significantly higher for a shorter period than the concentration in the oral treatment, indicating that higher levels of florfenicol for a longer period can be achieved in the tissues after oral drug administration. According to pharmacokinetic results, florfenicol may be a suitable candidate for the treatment of common bacterial infections in common carp farming.
本研究的目的是评估单剂量静脉注射(5.00毫克/千克体重)和口服(40.00毫克/千克体重)氟苯尼考后在鲤鱼体内的药代动力学特征。还研究了连续10天口服给药(10.00毫克/千克体重)和药浴处理(5.00毫克/升)后氟苯尼考的残留消除情况。通过高效液相色谱法分析单剂量给药后10个时间点(0.50、1、2、4、8、12、24、72、120和168小时)血浆中氟苯尼考的药代动力学以及连续10天后三个时间点(1、7和14天)组织(血浆、肝脏和肌肉)中氟苯尼考的浓度。氟苯尼考的峰值浓度为137.02纳克/毫升,血浆中达到峰值浓度的时间为2小时。消除半衰期、稳态分布容积和全身清除率分别估计为21.40小时、0.30和0.03升/小时。给药10天后,口服处理组血浆和肌肉中的浓度在所有天数均显著高于药浴处理组。药浴处理后肝脏中的药物浓度在较短时间内显著高于口服处理组,表明口服给药后组织中可在较长时间内达到较高水平的氟苯尼考。根据药代动力学结果,氟苯尼考可能是鲤鱼养殖中治疗常见细菌感染的合适候选药物。