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依那普利单次及长期口服给药后的药代动力学及血管紧张素转换酶抑制作用

Enalapril pharmacokinetics and ACE inhibition, following single and chronic oral dosing.

作者信息

Edeki T, Johnston A, Li Kam Wa E, Turner P

机构信息

Department of Pharmacology, Meharry Medical College, Nashville, Tennessee 37208.

出版信息

Int J Clin Pharmacol Ther. 1994 Mar;32(3):142-6.

PMID:8205376
Abstract

Twelve normal volunteers were given 10 mg enalapril maleate by single and 2 weeks multiple dose administration, and blood samples were collected for the determination of enalaprilat concentration and angiotensin converting enzyme (ACE) activity. The mean terminal elimination half-life following a single administration of 10 mg enalapril, was 27 hours. The inhibition of ACE activity paralleled enalaprilat concentrations following both single and multiple dosing and the time of maximum inhibition of ACE activity was associated on both occasions with maximum concentration of enalaprilat. Emax modelling of enalaprilat concentration and ACE activity gave comparable values of Emax for both methods of administration. An accumulation factor of 1.7 was calculated from the area under the concentration time curve (AUC) of enalaprilat within a dosing interval at steady-state and the total AUC following single administration of enalapril. There were no significant differences between males and females in the accumulation factor, half-life and AUCinf.

摘要

12名正常志愿者接受了单次10毫克马来酸依那普利给药以及为期2周的多次给药,随后采集血样以测定依那普利拉浓度和血管紧张素转换酶(ACE)活性。单次给予10毫克依那普利后的平均终末消除半衰期为27小时。单次和多次给药后,ACE活性的抑制与依那普利拉浓度平行,且两种情况下ACE活性最大抑制时间均与依那普利拉的最大浓度相关。依那普利拉浓度和ACE活性的Emax模型在两种给药方法下得出了相当的Emax值。根据稳态给药间隔内依那普利拉的浓度-时间曲线(AUC)以及依那普利单次给药后的总AUC计算出蓄积因子为1.7。在蓄积因子、半衰期和AUCinf方面,男性和女性之间无显著差异。

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