Saini S P, Srivastava A K
Department of Pharmacology and Toxicology, College of Veterinary Science, Punjab Agricultural University, Ludhiana, India.
Vet Res Commun. 1998 Jan;22(1):59-65. doi: 10.1023/a:1005987212046.
The disposition kinetics, urinary excretion and dosage regimen of amikacin after a single intravenous administration of 10 mg/kg was investigated in six cross-bred bovine calves. At 1 min, the concentration of amikacin in the plasma was 116.9 +/- 3.16 micrograms/ml and the minimum therapeutic concentration was maintained for 8 h. The elimination half-life and volume of distribution were 3.09 +/- 0.27 h and 0.4 +/- 0.03 L/kg, respectively. The total body clearance (ClB) and T/P ratio were 0.09 +/- 0.002 L/kg/h and 4.98 +/- 0.41, respectively. Approximately 50% of the total dose of amikacin was recovered in the urine within 24 h after administration. Amikacin in concentrations ranging from 5 to 150 micrograms/ml bound to plasma proteins to the extent of 6.32% +/- 0.42%. A satisfactory intravenous dosage regimen of amikacin in bovine calves would be 13 mg/kg followed by 12 mg/kg at 12 h intervals.
在6头杂交牛犊中研究了单次静脉注射10mg/kg阿米卡星后的处置动力学、尿排泄及给药方案。给药1分钟时,血浆中阿米卡星浓度为116.9±3.16μg/ml,最低治疗浓度维持8小时。消除半衰期和分布容积分别为3.09±0.27小时和0.4±0.03L/kg。总体清除率(ClB)和T/P比值分别为0.09±0.002L/kg/h和4.98±0.41。给药后24小时内,尿中回收了约50%的阿米卡星总剂量。浓度为5至150μg/ml的阿米卡星与血浆蛋白结合程度为6.32%±0.42%。牛犊中令人满意的阿米卡星静脉给药方案为13mg/kg,随后每隔12小时给药12mg/kg。