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口服给药后匹莫林在血浆、唾液和尿液中的药代动力学。

Pharmacokinetics of pemoline in plasma, saliva and urine following oral administration.

作者信息

Vermeulen N P, Teunissen M W, Breimer D D

出版信息

Br J Clin Pharmacol. 1979 Nov;8(5):459-63. doi: 10.1111/j.1365-2125.1979.tb01026.x.

Abstract

1 Pemoline concentrations were measured in plasma and saliva following a single oral dose (37.5 or 50.0 mg) to healthy volunteers. In addition urinary excretion rates and cumulative urinary excretion of the parent compound and its oxazolidinedione metabolite were determined. 2 The plasma curves exhibited a mean elimination half-live of 11.0 +/- 1.2 h (n=4). Peak levels were reached at 2.7 +/- 0.6 h (n=4). The saliva concentrations were about 50% lower than the corresponding plasma concentrations during the elimination phase. During the absorption phase irregularities in the saliva to plasma concentration ratios were observed. 3 In urine 47.0 +/- 8.4% of the dose (n=6) administered was excreted as unchanged drug and only 3.7 +/- 0.8% (n=3) as the oxazolidinedione metabolite. Urinary half-lives were slightly shorter than the corresponding plasma half-lives.

摘要
  1. 给健康志愿者单次口服一剂(37.5或50.0毫克)匹莫林后,测量其血浆和唾液中的匹莫林浓度。此外,还测定了母体化合物及其恶唑烷二酮代谢物的尿排泄率和累积尿排泄量。2. 血浆曲线显示平均消除半衰期为11.0±1.2小时(n = 4)。在2.7±0.6小时(n = 4)达到峰值水平。在消除阶段,唾液浓度比相应的血浆浓度低约50%。在吸收阶段,观察到唾液与血浆浓度比存在不规则情况。3. 在尿液中,给药剂量的47.0±8.4%(n = 6)以原形药物排泄,只有3.7±0.8%(n = 3)以恶唑烷二酮代谢物排泄。尿半衰期略短于相应的血浆半衰期。

相似文献

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Oral pemoline kinetics in hyperactive children.多动儿童口服匹莫林的药代动力学
Clin Pharmacol Ther. 1985 Jun;37(6):606-9. doi: 10.1038/clpt.1985.96.

本文引用的文献

2
Tests of learning and memory with Cylert.
Psychopharmacologia. 1967;10(5):445-51. doi: 10.1007/BF00403986.
6
Effects of pemoline on hyperactive boys.匹莫林对多动男孩的影响。
Pharmacol Biochem Behav. 1975 Nov-Dec;3(6):1107-14. doi: 10.1016/0091-3057(75)90024-6.
8
Therapeutic drug monitoring in saliva.唾液中的治疗药物监测。
Clin Pharmacokinet. 1978 Jan-Feb;3(1):39-57. doi: 10.2165/00003088-197803010-00003.

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