Horspool L J, Taylor D J, McKellar Q A
Department of Veterinary Pharmacology, University of Glasgow Veterinary School, UK.
J Vet Pharmacol Ther. 1994 Aug;17(4):291-8. doi: 10.1111/j.1365-2885.1994.tb00248.x.
Amikacin was detectable (> 0.02 micrograms/ml) in plasma for 12 h in horses and donkeys and for 8 h in ponies following intravenous (i.v.) administration at a dose rate of 6 mg/kg bodyweight. The elimination half-life (harmonic mean) of amikacin was 2.8, 1.6 and 1.9 h in horses, ponies and donkeys, respectively, and the mean body clearance was relatively slow (45.2, 82.4 and 58.0 ml/h.kg, respectively). A suitable dosage interval for the i.v. administration of amikacin sulphate to horses, ponies and donkeys, at a dose rate of 6 mg/kg, would be every 8 h in horses, and every 6 h in ponies and donkeys. Following i.v. administration there were no marked alterations in caecal liquor pH, the number of viable bacteria isolated, or the short chain fatty acid (SCFA) concentrations in caecal liquor and faeces. Amikacin was not detected (< 0.02 micrograms/ml) in plasma following administration by nasogastric tube to ponies with cannulated caecal fistulae; however, there were high concentrations of amikacin measured in caecal liquor (maximum 16.2-99.4 micrograms/ml). Despite the high drug concentrations in caecal liquor, there were only slight alterations in the number of viable bacteria isolated. However, there was a reduction in caecal liquor pH to < 6.6, but few changes in caecal liquor SCFA concentrations. Faecal SCFA concentrations, dry matter content and consistency did not alter markedly.
按6mg/kg体重的剂量静脉注射后,马和驴血浆中丁胺卡那霉素可检测到(>0.02微克/毫升)的时间为12小时,小马为8小时。丁胺卡那霉素在马、小马和驴体内的消除半衰期(调和均值)分别为2.8、1.6和1.9小时,平均全身清除率相对较慢(分别为45.2、82.4和58.0毫升/小时·千克)。以6mg/kg的剂量率对马、小马和驴静脉注射硫酸丁胺卡那霉素时,合适的给药间隔时间在马为每8小时一次,在小马和驴为每6小时一次。静脉注射后,盲肠液pH值、分离出的活菌数量以及盲肠液和粪便中短链脂肪酸(SCFA)浓度均无明显变化。对有盲肠造瘘插管的小马经鼻胃管给药后,血浆中未检测到丁胺卡那霉素(<0.02微克/毫升);然而,在盲肠液中测得丁胺卡那霉素的浓度很高(最高为16.2 - 99.4微克/毫升)。尽管盲肠液中药物浓度很高,但分离出的活菌数量仅有轻微变化。不过,盲肠液pH值降至<6.6,而盲肠液SCFA浓度变化不大。粪便SCFA浓度、干物质含量和稠度均无明显改变。