左旋多巴
生物利用度
恩他卡彭
卡比多巴
药理学
药代动力学
交叉研究
最大值
苄丝肼
就寝时间
医学
生物等效性
化学
帕金森病
内科学
安慰剂
替代医学
病理
疾病
作者
Mikko Kuoppamäki,A Sauramo,K Korpela,Mikko Vahteristo,Marita Kailajärvi,Tessa Lehtinen,Juha Ellmén
摘要
Controlled-release levodopa/carbidopa (CR-LC) is often used to provide prolonged control of night-time motor symptoms in patients with Parkinson's disease (PD). Levodopa/carbidopa/entacapone (LCE) provides higher bioavailability of levodopa compared with levodopa/carbidopa formulations and has been shown to be effective in PD patients with wearing-off symptoms. The aim of this study was to compare the bioavailability of levodopa after a single evening dose (administered at 10 p.m.) of LCE 200 or CR-LC 200.This was an open-label, randomized, crossover study in healthy subjects. The main pharmacokinetic (PK) parameters were AUC, Cmax, C6h and t1/2 of levodopa.A single evening dose of LCE 200 was associated with significantly better bioavailability compared with CR-LC 200. In line with increased bioavailability of levodopa, LCE 200 induced more nausea.The results of this study demonstrate that a single bedtime dose of LCE 200 provides higher bioavailability of levodopa compared to CR-LC 200.
科研通智能强力驱动
Strongly Powered by AbleSci AI