Roberts J, Waller D G, O'Shea N, Macklin B S, Renwick A G
Clinical Pharmacology Group, University of Southampton, UK.
Br J Clin Pharmacol. 1995 Oct;40(4):404-6. doi: 10.1111/j.1365-2125.1995.tb04564.x.
The plasma pharmacokinetics of levodopa were studied in eight healthy young subjects following an i.v. infusion of 50 mg over 5 min. Subjects were studied on two occasions in random order following treatment with carbidopa; on one occasion they were pretreated with selegiline (four doses of 10 mg over the preceding 3 days) and on the other with a placebo. The mean plasma concentration-time curves on each occasion were essentially superimposable and there were no significant differences in any calculated pharmacokinetic parameter. Selegiline does not significantly alter the distribution or elimination of levodopa from plasma.
在8名健康年轻受试者中,静脉输注50毫克左旋多巴,历时5分钟,研究其血浆药代动力学。受试者在接受卡比多巴治疗后分两次随机接受研究;一次是在接受司来吉兰预处理(在前3天服用4剂,每剂10毫克)后,另一次是在接受安慰剂治疗后。每次的平均血浆浓度-时间曲线基本可叠加,任何计算得出的药代动力学参数均无显著差异。司来吉兰不会显著改变左旋多巴在血浆中的分布或消除。