Laczay P, Semjén G, Lehel J, Nagy G
Department of Pharmacology and Toxicology, Faculty of Veterinary Science, Szent István University, H-1400 Budapest, P.O. Box 2, Hungary.
Acta Vet Hung. 2001;49(1):31-7. doi: 10.1556/004.49.2001.1.5.
The pharmacokinetics and the influence of food on the kinetic profile and bioavailability of doxycycline was studied after a single intravenous (i.v.) and oral dose of 10.0 mg/kg body weight in 7-week-old broiler chickens. Following i.v. administration the drug was rapidly distributed in the body with a distribution half-life of 0.21 +/- 0.01 h. The elimination half-life of 6.78 +/- 0.06 h was relatively long and resulted from both a low total body clearance of 0.139 +/- 0.007 L/h.kg and a large volume of distribution of 1.36 +/- 0.06 L/kg. After oral administration to fasted chickens, the absorption of doxycycline was quite fast and substantial as shown by the absorption half-life of 0.39 +/- 0.03 h, the maximal plasma concentration of 4.47 +/- 0.16 micrograms/mL and the time to reach the Cmax of 1.73 +/- 0.06 h. The distribution and the final elimination of the drug were slower than after i.v. administration. The absolute bioavailability was 73.4 +/- 2.5%. The presence of food in the intestinal tract reduced and extended the absorption (t1/2a = 1.23 +/- 0.21 h; Cmax = 3.07 +/- 0.23 micrograms/mL; tmax = 3.34 +/- 0.21 h). The absolute bioavailability was reduced to 61.1% +/- 4.4%.
在7周龄的肉鸡中,静脉注射(i.v.)和口服10.0mg/kg体重的单次剂量后,研究了强力霉素的药代动力学以及食物对其动力学特征和生物利用度的影响。静脉给药后,药物在体内迅速分布,分布半衰期为0.21±0.01小时。消除半衰期为6.78±0.06小时,相对较长,这是由于全身清除率较低,为0.139±0.007L/h.kg,以及分布容积较大,为1.36±0.06L/kg。在禁食的鸡口服给药后,强力霉素的吸收相当快且充分,吸收半衰期为0.39±0.03小时,最大血浆浓度为4.47±0.16μg/mL,达到Cmax的时间为1.73±0.06小时。药物的分布和最终消除比静脉给药后慢。绝对生物利用度为73.4±2.5%。肠道中食物的存在会减少并延长吸收(t1/2a = 1.23±0.21小时;Cmax = 3.07±0.23μg/mL;tmax = 3.34±0.21小时)。绝对生物利用度降至61.1%±4.4%。