Population pharmacokinetics of levodopa/carbidopa microtablets in healthy subjects and Parkinson’s disease patients

被引:0
作者
Marina Senek
Dag Nyholm
Elisabet I. Nielsen
机构
[1] Uppsala University,Department of Neuroscience, Neurology
[2] Akademiska Sjukhuset/Uppsala University Hospital,Department of Pharmaceutical Biosciences
[3] Uppsala University,undefined
来源
European Journal of Clinical Pharmacology | 2018年 / 74卷
关键词
Parkinson’s disease; Population modeling; Levodopa; Microtablets; Pharmacokinetics;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:1299 / 1307
页数:8
相关论文
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  • [1] Senek M(2014)Continuous drug delivery in Parkinson’s disease CNS Drugs 28 19-27
  • [2] Nyholm D(2012)Pharmacokinetics of levodopa/carbidopa microtablets versus levodopa/benserazide and levodopa/carbidopa in healthy volunteers Clin Neuropharmacol 35 111-117
  • [3] Nyholm D(2013)Frequent administration of levodopa/carbidopa microtablets vs levodopa/carbidopa/entacapone in healthy volunteers Acta Neurol Scand 127 124-132
  • [4] Lewander T(2003)An automatic dose dispenser for microtablets—a new concept for individual dosage of drugs in tablet form Int J Pharm 261 137-146
  • [5] Gomes-Trolin C(2017)First clinical experience with levodopa/carbidopa microtablets in Parkinson’s disease Acta Neurol Scand 136 727-731
  • [6] Bäckström T(1997)Pharmacodynamics of benserazide assessed by its effects on endogenous and exogenous levodopa pharmacokinetics Br J Clin Pharmacol 44 41-48
  • [7] Panagiotidis G(1981)A specific radioenzymatic assay for dihydroxyphenylalanine (DOPA). Plasma dopa may be the precursor of urine free dopamine Br J Clin Pharmacol 11 79-83
  • [8] Ehrnebo M(2017)Elucidation of factor VIII activity pharmacokinetics: a pooled population analysis in patients with hemophilia a treated with moroctocog alfa Clin Pharmacol Ther 102 977-988
  • [9] Nyström C(2017)Population pharmacokinetic analysis of vaginally and intravenously administered oxytocin in postmenopausal women J Clin Pharmacol 57 1573-1581
  • [10] Aquilonius SM(2007)Implementation of a transit compartment model for describing drug absorption in pharmacokinetic studies J Pharmacokinet Pharmacodyn 34 711-726