McGuirk S M, Muir W W, Sams R A
Am J Vet Res. 1981 Jun;42(6):938-42.
A pharmacokinetic study was made, using 7 healthy adult horses (weighing between 400 and 560 kg) given quinidine gluconate IV and quinidine sulfate orally. The apparent volume of distribution of quinidine base was 3.10 +/- 0.79 L/kg, total body clearance was 5.49 +/- 2.40 ml/minute/kg, and plasma half-life was 6.65 +/- 3.00 hours. The systemic availability of quinidine sulfate after oral administration of a 10 mg/kg dose was 48.5 +/- 20.4%. Oral administrations of quinidine sulfate in doses of 10 mg/kg and 10 g produced peak plasma concentrations of 0.79 microgram/ml at 146 minutes and 1.47 microgram/ml at 131 minutes, respectively. In 4 horses given 4 oral doses of 10 mg of quinidine sulfate/kg, each dose separated by 2 hours, maximal plasma concentrations of quinidine averaged 13% higher than the preceding minimal plasma concentration. The application of these pharmacokinetic determinations to the clinical use of quinidine in the horse is discussed.
进行了一项药代动力学研究,使用7匹健康成年马(体重在400至560千克之间),静脉注射葡萄糖酸奎尼丁并口服硫酸奎尼丁。奎尼丁碱的表观分布容积为3.10±0.79升/千克,全身清除率为5.49±2.40毫升/分钟/千克,血浆半衰期为6.65±3.00小时。口服10毫克/千克剂量的硫酸奎尼丁后的系统利用率为48.5±20.4%。口服10毫克/千克和10克剂量的硫酸奎尼丁分别在146分钟和131分钟时产生的血浆峰值浓度为0.79微克/毫升和1.47微克/毫升。在4匹马中,每2小时口服4次10毫克/千克的硫酸奎尼丁,奎尼丁的最大血浆浓度平均比前一个最小血浆浓度高13%。讨论了这些药代动力学测定在马临床使用奎尼丁中的应用。