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盐酸维洛沙嗪在人体中的药代动力学。

Pharmacokinetics of viloxazine hydrochloride in man.

作者信息

Vandel B, Vandel S, Jounet J M, Blum D

出版信息

Eur J Drug Metab Pharmacokinet. 1982 Jan-Mar;7(1):65-8. doi: 10.1007/BF03189545.

DOI:10.1007/BF03189545
PMID:7067726
Abstract

The pharmacokinetic characteristics of a new antidepressant, viloxazine hydrochloride, were investigated in five males and five females to study sex differences. Plasma levels were determined over a period of 9 h after a single dose of viloxazine of 100 mg (expressed as base). The half life of the drug was in the range of 2.19 - 4.21 for females and 2.61 - 4.31 h for males. The maximum plasma levels occurred in 29 - 171 min of the oral dose for females and 54 - 155 min for males. They reached 1382 - 1769 ng/ml-l for females and 1108 - 2932 ng/ml for males. Pharmacokinetic data were not statistically different between males and females.

摘要

为研究性别差异,对5名男性和5名女性进行了新型抗抑郁药盐酸维洛沙嗪的药代动力学特征研究。单次服用100毫克(以碱计)维洛沙嗪后9小时内测定血浆水平。该药物的半衰期女性为2.19 - 4.21小时,男性为2.61 - 4.31小时。女性口服给药后29 - 171分钟达到最大血浆水平,男性为54 - 155分钟。女性血浆水平达到1382 - 1769纳克/毫升,男性为1108 - 2932纳克/毫升。男性和女性的药代动力学数据无统计学差异。

相似文献

1
Pharmacokinetics of viloxazine hydrochloride in man.盐酸维洛沙嗪在人体中的药代动力学。
Eur J Drug Metab Pharmacokinet. 1982 Jan-Mar;7(1):65-8. doi: 10.1007/BF03189545.
2
Blood level studies with viloxazine hydrochloride in man.盐酸维洛沙嗪在人体中的血药浓度研究。
Br J Clin Pharmacol. 1975 Jun;2(3):209-14. doi: 10.1111/j.1365-2125.1975.tb01577.x.
3
Pharmacokinetics of the antidepressant drug viloxazine in normal subjects and in epileptic patients receiving chronic anticonvulsant treatment.
Psychopharmacology (Berl). 1986;90(3):295-8. doi: 10.1007/BF00179180.
4
Age-related differences in kinetics and side-effects of viloxazine in man and their clinical implications.维洛沙嗪在人体中的药代动力学及副作用的年龄相关差异及其临床意义。
Psychopharmacology (Berl). 1983;81(4):281-5. doi: 10.1007/BF00427563.
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Comparative pharmacokinetic study of conventional and sustained-release viloxazine in normal volunteers.正常志愿者中常规和缓释维洛沙嗪的比较药代动力学研究。
Neuropsychobiology. 1989;20(3):136-40. doi: 10.1159/000118487.
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Effects of administration route on pharmacokinetics of viloxazine in the rabbit.
Methods Find Exp Clin Pharmacol. 1992 Mar;14(2):125-9.
7
A sensitive gas chromatographic assay for the determination of serum viloxazine concentration using a nitrogen-phosphorus-selective detector.一种使用氮磷选择性检测器测定血清维洛沙嗪浓度的灵敏气相色谱分析法。
Ther Drug Monit. 1984;6(4):484-8. doi: 10.1097/00007691-198412000-00020.
8
Relationship between blood and cerebrospinal levels of the antidepressant agent viloxazine.
Eur J Clin Pharmacol. 1980;17(3):179-82. doi: 10.1007/BF00561897.
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Clinical pharmacology of viloxazine hydrochloride.盐酸维洛沙嗪的临床药理学
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[Synopsis of psychopathological, electroencephalographical, and pharmacokinetic variables during antidepressive treatment with viloxazine (author's transl)].
Arzneimittelforschung. 1978;28(8):1288-90.

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本文引用的文献

1
Some preliminary observations on ICI 58 834, a new psychotropic agent, in man.关于新型精神药物ICI 58 834在人体中的一些初步观察。
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Influence of neuroticism on oral absorption of diazepam.神经质对安定口腔吸收的影响。
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Clinical pharmacology of viloxazine hydrochloride.盐酸维洛沙嗪的临床药理学
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Pharmacokinetic optimisation of therapy with newer antidepressants.新型抗抑郁药治疗的药代动力学优化
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Pharmacokinetics of the antidepressant drug viloxazine in normal subjects and in epileptic patients receiving chronic anticonvulsant treatment.
Psychopharmacology (Berl). 1986;90(3):295-8. doi: 10.1007/BF00179180.
Pharmacopsychiatria. 1981 Mar;14(2):66-70. doi: 10.1055/s-2007-1019568.
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Gas-liquid chromatographic estimation in blood of ICI 58 834.血液中ICI 58 834的气液色谱法测定
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Blood level studies with viloxazine hydrochloride in man.盐酸维洛沙嗪在人体中的血药浓度研究。
Br J Clin Pharmacol. 1975 Jun;2(3):209-14. doi: 10.1111/j.1365-2125.1975.tb01577.x.
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The disposition and metabolism of I.C.I. 58,834 (viloxazine) in humans.I.C.I. 58,834(维洛沙嗪)在人体内的处置与代谢。
Xenobiotica. 1975 Feb;5(2):113-29. doi: 10.3109/00498257509056097.
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Clinical profile and serum concentration of viloxazine as compared to amitriptyline.与阿米替林相比,维洛沙嗪的临床特征和血清浓度
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