Zhao H-Y, Zhang G-H, Bai L, Zhu S, Shan Q, Zeng D-P, Sun Y-X
Laboratory of Veterinary Pharmacology, College of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
J Vet Pharmacol Ther. 2011 Oct;34(5):460-3. doi: 10.1111/j.1365-2885.2011.01273.x. Epub 2011 Mar 28.
The pharmacokinetics of florfenicol (FF) was studied in plasma after a single dose (40 mg/kg) of intramuscular (i.m.) or oral gavage (p.o.) administration to crucian carp (Carassius auratus cuvieri) in freshwater at 25 °C. Ten fish per sampling point were examined after treatment. The data were fitted to two-compartment open models follow both routes of administration. The estimates of total body clearance (CL(b) ), volume of distribution (V(d) /F), and absorption half-life (T(1/2(ka)) ) were 0.067 L/h/kg and 0.145 L/h/kg, 2.21 L/kg and 1.04 L/kg, 2.75 and 1.54/h following i.m. and p.o. administration, respectively. After i.m. injection, the elimination half-life (T(1/2(β)) ) was calculated to be 38.2h, the maximum plasma concentration (C(max) ) to be 16.82 μg/mL, the time to peak plasma FF concentration (T(max) ) to be 1.50 h, and the area under the plasma concentration-time curve (AUC) to be 597.4 μg/mL·h. Following p.o. administration, the corresponding estimates were 2.17 h, 29.32 μg/mL, 1.61 h, and 276.1 μg/mL·h.
在25℃的淡水中,对鲫鱼(Carassius auratus cuvieri)单次肌内注射(i.m.)或口服灌胃(p.o.)40mg/kg氟苯尼考(FF)后,研究了其在血浆中的药代动力学。处理后,每个采样点检查10条鱼。两种给药途径的数据均拟合为二室开放模型。肌内注射和口服给药后,总体清除率(CL(b))、分布容积(V(d)/F)和吸收半衰期(T(1/2(ka)))的估计值分别为0.067L/h/kg和0.145L/h/kg、2.21L/kg和1.04L/kg、2.75和1.54/h。肌内注射后,消除半衰期(T(1/2(β)))计算为38.2h,血浆最大浓度(C(max))为16.82μg/mL,血浆FF浓度达峰时间(T(max))为1.50h,血浆浓度-时间曲线下面积(AUC)为597.4μg/mL·h。口服给药后,相应的估计值分别为2.17h、29.32μg/mL、1.61h和276.1μg/mL·h。