Suppr超能文献

硝苯地平与β-肾上腺素受体阻滞剂美托洛尔和阿替洛尔之间不存在药代动力学相互作用。

Lack of a pharmacokinetic interaction between nifedipine and the beta-adrenoceptor blockers metoprolol and atenolol.

作者信息

Kendall M J, Jack D B, Laugher S J, Lobo J, Rolf Smith S

出版信息

Br J Clin Pharmacol. 1984 Sep;18(3):331-5. doi: 10.1111/j.1365-2125.1984.tb02472.x.

Abstract

Nifedipine, metoprolol and atenolol were administered orally to young, healthy volunteers. Each drug was given alone and nifedipine was also given with both beta-adrenoceptor blockers. Each drug was given for 3 days immediately before the study days. Plasma and urine drug concentrations were measured and the relevant pharmacokinetic parameters calculated. No pharmacokinetic interaction between nifedipine and the beta-adrenoceptor blockers was revealed.

摘要

对年轻健康志愿者口服硝苯地平、美托洛尔和阿替洛尔。每种药物单独给药,硝苯地平也与两种β肾上腺素受体阻滞剂联合给药。每种药物在研究日前连续3天给药。测量血浆和尿液中的药物浓度,并计算相关的药代动力学参数。未发现硝苯地平和β肾上腺素受体阻滞剂之间存在药代动力学相互作用。

相似文献

引用本文的文献

2
Pharmacokinetic interactions between felodipine and metoprolol.
Eur J Clin Pharmacol. 1987;31(5):575-8. doi: 10.1007/BF00606633.

本文引用的文献

1
Bioavailability of atenolol formulations.阿替洛尔制剂的生物利用度。
Biopharm Drug Dispos. 1980 Oct-Dec;1(6):323-32. doi: 10.1002/bdd.2510010604.
3
5
Identification of nifedipine metabolites and their determination by gas chromatography.
Chem Pharm Bull (Tokyo). 1980 Jan;28(1):1-7. doi: 10.1248/cpb.28.1.
6
Effects of treatment with nifedipine and metoprolol in essential hypertension.
Eur J Clin Pharmacol. 1982;21(5):389-90. doi: 10.1007/BF00542324.
7
Nifedipine and propranolol: a beneficial drug interaction.
Am J Med. 1981 Oct;71(4):676-82. doi: 10.1016/0002-9343(81)90238-2.
8
Clinical pharmacokinetics of metoprolol.美托洛尔的临床药代动力学
Clin Pharmacokinet. 1980 Nov-Dec;5(6):557-69. doi: 10.2165/00003088-198005060-00004.
10
Lack of evidence for polymorphism in metoprolol metabolism.美托洛尔代谢中缺乏多态性的证据。
Br J Clin Pharmacol. 1983 Aug;16(2):188-90. doi: 10.1111/j.1365-2125.1983.tb04984.x.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验