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Pharmacokinetics and bioavailability of azithromycin following intramuscular and oral administrations in broiler chickens

机译:肉鸡肌肉和口服给药后阿奇霉素的药代动力学和生物利用度

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The pharmacokinetics azithromycin were investigated in broiler chickens after intravenous (i.v.), intramuscular (i.m.) and oral (p.o.) administrations to estimate an appropriate dosage regimen of azithromycin. Moreover, to determine the bioavailability after the extravascular routes and the serum protein binding capacity with azithromycin's molecules. Three equal groups of 5 chickens each were given a single dose of 20 mg/kg body weight (bw) of azithromycin via i.v., i.m. and p.o. administrations. Serum concentrations of azithromycin were determined by a modified agar diffusion bioas-say using Bacillus subtilis ATCC 6633 as the test organism. Following compartmental analysis, a three-compartment open model best described the concentration-time dataof azithromycin after i.v. administration. The total body clearance (CI ) was 0.77 L/kg/h the volume of distribution at steady-state (V ) was 47.75 L/kg and the value of the elimination half-life (t_(1/213)) was 31.91 h. After i.m. administration, the elimination half-life (t_(1/2e)) and mean residence time (MRT) were significantly higher (38.95 h and 47.16) than after p.o. route (31.50 h and 39.93 h), respectively. Azithromycin was bound to the extent of 24.42 % to serum protein of chickens. The absolute bioavailabilities were 95.17 and 83.52 % after i.m. and p.o. administrations, respectively. Based on the fortunate pharmacokinetic characteristics, a single dose of azithromycin at 20 mg/kg (bw) via i.m. and p.o. administrations every 72 h for susceptible bacterial infections in chickens is greatly recommended.
机译:静脉(i.v.),肌内(i.m.)和口服(p.o.)给药后,在肉鸡中研究了阿奇霉素的药代动力学,以估算阿奇霉素的合适剂量方案。此外,确定血管外途径后的生物利用度以及血清蛋白与阿奇霉素分子的结合能力。通过静脉内,静脉内注射,每组三只相等的5只鸡,分别给予阿奇霉素20 mg / kg体重(bw)的单剂量。和p.o.行政部门。通过改良的琼脂扩散生物测定法,使用枯草芽孢杆菌ATCC 6633作为测试生物,测定阿奇霉素的血清浓度。隔室分析后,一个三室开放模型最好地描述了静脉注射后阿奇霉素的浓度-时间数据。行政。总体清除率(CI)为0.77 L / kg / h,稳态时的分布体积(V)为47.75 L / kg,消除半衰期的值(t_(1/213))为31.91 h 。在我之后给药后,消除半衰期(t_(1 / 2e))和平均停留时间(MRT)明显高于口服后(38.95 h和47.16)。路线(分别为31.50小时和39.93小时)。阿奇霉素对鸡血清蛋白的结合率为24.42%。 i.m.后绝对生物利用度为95.17和83.52%。和p.o.主管部门。根据幸运的药代动力学特征,通过i.m.一次单剂量阿奇霉素的剂量为20 mg / kg(bw)。和p.o.强烈建议每72小时一次对鸡进行易感细菌感染。

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