Mevius D J, Breukink H J, Guelen P J, Jansen T, De Grève B
Department of Large Animal Medicine and Nutrition, Veterinary Faculty, State University of Utrecht, The Netherlands.
J Vet Pharmacol Ther. 1990 Jun;13(2):159-69. doi: 10.1111/j.1365-2885.1990.tb00764.x.
The pharmacokinetics of flumequine was studied in 1-, 5- and 18-week-old veal calves. A two-compartment model was used to fit the plasma concentration-time curve of flumequine after the intravenous injection of 10 mg/kg of a 10% solution. The elimination half-life (t1/2 beta) of the drug ranged from 6 to 7 h. The Vd beta and ClB of 1-week-old calves (1.07 l/kg, 1.78 ml/min/kg) were significantly lower than those of 5-week-old (1.89 l/kg, 3.23 ml/min/kg) and 18-week-old calves (1.57 l/kg, 3.10 ml/min/kg). After the oral administration of 10 mg/kg of a 2% flumequine formulation mixed with milk replacer, the Cmax was highest in 1-week-old (9.27 micrograms/ml) and lowest in 18-week-old calves (4.47 micrograms/ml). The absorption was rapid (Tmax of approximately 3 h) and complete. When flumequine itself and a formulation containing 2% flumequine and 20 X 10(6) iu of colistin sulphate were mixed with milk replacer and administered at the same dose rate, absorption was incomplete and Cmax was lower. The main urinary metabolite of flumequine was the glucuronide conjugate (approximately 40% recovery within 48 h of intravenous injection) and the second most important metabolite was 7-hydroxy-flumequine (approximately 3% recovery within 12 h of intravenous injection). Only 3.2-6.5% was excreted in the urine unchanged. After oral administration a 'first-pass' effect was observed, with a significant increase in the excretion of conjugated drug. For 1-week-old calves it is recommended that the 2% formulation should be administered at a dose rate of 8 mg/kg every 24 h or 4 mg/kg every 12 h; for calves over 6 weeks old, the dose should be increased to 15 mg/kg every 24 h or 7.5 mg/kg every 12 h. The formulation containing colistin sulphate should be administered to 1-week-old calves at a flumequine dose of 12 mg/kg every 24 h or 6 mg/kg every 12 h.
在1周龄、5周龄和18周龄的犊牛中研究了氟甲喹的药代动力学。静脉注射10%溶液10mg/kg后,采用二室模型拟合氟甲喹的血药浓度-时间曲线。该药的消除半衰期(t1/2β)为6至7小时。1周龄犊牛的Vdβ和ClB(分别为1.07l/kg、1.78ml/min/kg)显著低于5周龄(分别为1.89l/kg、3.23ml/min/kg)和18周龄犊牛(分别为1.57l/kg、3.10ml/min/kg)。口服与代乳粉混合的2%氟甲喹制剂10mg/kg后,1周龄犊牛的Cmax最高(9.27μg/ml),18周龄犊牛最低(4.47μg/ml)。吸收迅速(Tmax约为3小时)且完全。当将氟甲喹本身以及含有2%氟甲喹和20×10⁶iu硫酸黏菌素的制剂与代乳粉混合并以相同剂量率给药时,吸收不完全且Cmax较低。氟甲喹的主要尿液代谢物是葡糖醛酸缀合物(静脉注射后48小时内回收率约为40%),第二重要的代谢物是7-羟基氟甲喹(静脉注射后12小时内回收率约为3%)。仅3.2 - 6.5%以原形经尿液排泄。口服给药后观察到“首过”效应,结合型药物的排泄显著增加。对于1周龄犊牛,建议以8mg/kg的剂量率每24小时给药一次2%制剂,或以4mg/kg的剂量率每12小时给药一次;对于6周龄以上的犊牛,剂量应增加至每24小时15mg/kg或每12小时7.5mg/kg。含硫酸黏菌素的制剂应以每24小时12mg/kg氟甲喹的剂量或每12小时6mg/kg的剂量给予1周龄犊牛。