Nouws J F, Mevius D J, Vree T B, Baars A M, Laurensen J
Department for Large Animal Medicine, Faculty of Veterinary Medicine, Utrecht, The Netherlands.
Vet Q. 1988 Jul;10(3):156-63. doi: 10.1080/01652176.1988.9694165.
The pharmacokinetics of ciprofloxacin, a quinoline derivative with marked bactericidal activity against gram-negative bacteria, was studied in calves and pigs following intravenous and oral administration. Ciprofloxacin was rapidly and well distributed in the body, exhibited a short elimination half-life of 2.5 h in both species, and was rapidly absorbed after oral administration (Tmax:2 to 3 h). The oral bioavailability in calves was 53 +/- 14% and for 1 pig 37.3%. The renal clearance of the unbound ciprofloxacin for both species was of the same order, indicated a predominantly tubular secretion pattern, and accounted for about 46% of the total drug elimination. No complete drug mass balance could be demonstrated. Small amounts of two metabolites were detected in the urine of calves, but not in pig urine.
环丙沙星是一种对革兰氏阴性菌具有显著杀菌活性的喹啉衍生物,研究了其在犊牛和猪静脉注射及口服后的药代动力学。环丙沙星在体内分布迅速且良好,在两种动物中的消除半衰期均较短,为2.5小时,口服后吸收迅速(达峰时间:2至3小时)。犊牛的口服生物利用度为53±14%,一头猪为37.3%。两种动物中游离环丙沙星的肾清除率处于同一水平,表明主要为肾小管分泌模式,约占总药物消除的46%。未能证明完全的药物质量平衡。在犊牛尿液中检测到少量两种代谢物,但猪尿液中未检测到。