Mevius D J, Vellenga L, Breukink H J, Nouws J F, Vree T B, Driessens F
Vet Q. 1986 Oct;8(4):274-84. doi: 10.1080/01652176.1986.9694056.
The pharmacokinetics of oxytetracycline (OTC) in three weaned piglets was studied following three routes of administration: intravenously, orally as drench, both at a dose of 20 mg/kg, and orally as medicated (400 ppm OTC) pelleted feed administered during 3 consecutive days. Analysis of the intravenous data according to the three compartment pharmacokinetic model revealed that OTC was well distributed in the body (Vf: 1.62 l/kg), had an overall body clearance of 0.25 litre/kg/h, and the elimination half-lives were in the range between 11.6 and 17.2 hrs. The mean OTC binding to plasma proteins was 75.5 +/- 4%. Following the drench route of administration the maximum plasma OTC concentration was achieved between 1 and 5 h post application and ranged between 1.18 and 1.41 micrograms/ml. The mean maximum plasma OTC concentration during medicated feed administration was 0.20 +/- 0.06 microgram/ml, which was achieved approximately 30 hours after the onset of the administration. A steady state OTC plasma level (approximately 0.2 microgram/ml) was maintained till the end of the trial. Within 48 hours after cessation of medicated feed administration the plasma OTC levels were beneath 0.06 microgram/ml. The mean OTC bioavailabilities of the oral routes were low: after the drench route of administration 9.0 +/- 0.67%, and after medicated pelleted feed administration 3.69 +/- 0.8%. The mean OTC renal clearances of each piglet ranged between 10.1 and 13.9 ml/min/kg (based on free OTC plasma fractions). The renal OTC clearance values were urine flow dependent in all piglets and significantly correlated with the renal creatinine clearance (P less than 0.005), being 3-5 times higher than the latter. It is concluded that in piglets OTC is excreted mainly by glomerular filtration and partly by tubular secretion. The potential clinical efficacy of 400 ppm OTC as medicated feed with respect to treatment, e.g. atrophic rhinitis, is discussed.
研究了土霉素(OTC)在三只断奶仔猪体内的药代动力学,给药途径有三种:静脉注射、口服灌服(均为20mg/kg剂量)以及连续3天口服含药(400ppm OTC)颗粒饲料。根据三室药代动力学模型对静脉注射数据进行分析,结果显示OTC在体内分布良好(分布容积:1.62l/kg),总体清除率为0.25升/千克/小时,消除半衰期在11.6至17.2小时之间。OTC与血浆蛋白的平均结合率为75.5±4%。口服灌服给药后,在给药后1至5小时达到最大血浆OTC浓度,范围在1.18至1.41微克/毫升之间。含药饲料给药期间的平均最大血浆OTC浓度为0.20±0.06微克/毫升,大约在给药开始后30小时达到。直至试验结束,维持了稳定的OTC血浆水平(约0.2微克/毫升)。停止含药饲料给药后48小时内,血浆OTC水平低于0.06微克/毫升。口服给药途径的平均OTC生物利用度较低:口服灌服后为9.0±0.67%,含药颗粒饲料给药后为3.69±0.8%。每只仔猪的平均OTC肾清除率在10.1至13.9毫升/分钟/千克之间(基于游离OTC血浆分数)。所有仔猪的肾OTC清除率值均依赖于尿流,且与肾肌酐清除率显著相关(P<0.005),比后者高3至5倍。得出的结论是,在仔猪中,OTC主要通过肾小球滤过排泄,部分通过肾小管分泌排泄。讨论了400ppm OTC作为含药饲料在治疗(如萎缩性鼻炎)方面的潜在临床疗效。