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清醒志愿者体内芬太尼的药代动力学

Fentanyl pharmacokinetics in awake volunteers.

作者信息

Fung D L, Eisele J H

出版信息

J Clin Pharmacol. 1980 Nov-Dec;20(11):652-8. doi: 10.1002/j.1552-4604.1980.tb01682.x.

DOI:10.1002/j.1552-4604.1980.tb01682.x
PMID:7229112
Abstract

A single intravenous dose of fentanyl (either 2 or 4 micrograms/kg body weight) was given to 13 healthy, young volunteer subjects. Serum fentanyl concentration decreased in a triexponential pattern. The terminal half-times were 750 and 853 minutes, respectively. A three-compartment, open, mammillary model is proposed for fentanyl kinetics.

摘要

给13名健康的年轻志愿者单次静脉注射芬太尼(2或4微克/千克体重)。血清芬太尼浓度呈三室指数下降模式。终末半衰期分别为750分钟和853分钟。提出了一个三室开放乳头模型用于芬太尼动力学研究。

相似文献

1
Fentanyl pharmacokinetics in awake volunteers.清醒志愿者体内芬太尼的药代动力学
J Clin Pharmacol. 1980 Nov-Dec;20(11):652-8. doi: 10.1002/j.1552-4604.1980.tb01682.x.
2
Intravenous fentanyl kinetics.静脉注射芬太尼的动力学
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Pharmacokinetics of fentanyl in neonates.芬太尼在新生儿中的药代动力学。
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Dose-independent pharmacokinetics of fentanyl.芬太尼的非剂量依赖性药代动力学。
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Pharmacokinetics of fentanyl in patients undergoing abdominal aortic surgery.
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Pharmacokinetics of fentanyl as determined by radioimmunoassay.通过放射免疫测定法测定的芬太尼药代动力学。
Clin Pharmacol Ther. 1978 Feb;23(2):188-94. doi: 10.1002/cpt1978232188.
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Pharmacokinetic properties of fentanyl effervescent buccal tablets: a phase I, open-label, crossover study of single-dose 100, 200, 400, and 800 microg in healthy adult volunteers.芬太尼泡腾颊含片的药代动力学特性:一项在健康成年志愿者中进行的单剂量100、200、400和800微克的I期开放标签交叉研究。
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[Development of continuous monitoring of spontaneous respiration in the postoperative phase. 2. Cutaneous oxygen and carbon dioxide partial pressures following i.v. bolus application of fentanyl, buprenorphine, naloxone and amiphenazole in healthy adult subjects].[术后阶段自主呼吸持续监测的发展。2. 健康成年受试者静脉推注芬太尼、丁丙诺啡、纳洛酮和阿米苯唑后的皮肤氧分压和二氧化碳分压]
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