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佐芬普利与依那普利在健康志愿者中的药代动力学和药效学对比研究。

Pharmacokinetic and pharmacodynamic comparative study of zofenopril and enalapril in healthy volunteers.

作者信息

Marzo Antonio, Dal Bo Lorenzo, Mazzucchelli Paolo, Monti Nunzia Ceppi, Crivelli Fabrizio, Ismaili Shevqet, Giusti Andrea, Uhr Mario Richard

机构信息

I.P.A.S. Institute for Pharmacokinetic and Analytical Studies S.A., Ligornetto, Switzerland.

出版信息

Arzneimittelforschung. 2002;52(4):233-42. doi: 10.1055/s-0031-1299886.

Abstract

Zofenopril calcium (CAS 81938-43-4) is a new angiotensin converting enzyme (ACE) inhibitor, which in addition to the typical activity of the class, proved to possess a specific cardioprotective effect due also to the presence of the sulfhydryl group. In this trial zofenopril calcium and enalapril maleate (CAS 76095-16-4) were given to 20 healthy volunteers of both sexes in repeated dose regiment at two dose levels: 30 mg and 60 mg zofenopril calcium and 10 mg and 20 mg enalapril maleate. The study was conducted according to a two-period, two-sequence, crossover design, with washout. ACE activity in serum and zofenopril, zofenoprilat, enalapril and enalaprilat plasma concentrations were determined during and on the last day of the two study periods. Both zofenopril and enalapril were extensively converted through hydrolysis to their active metabolites zofenoprilat and enalaprilat, respectively. Zofenopril exhibited a complete and a more rapid hydrolysis rate compared to enalapril, which is reflected by the higher metabolite to parent drug ratio of Cmax and AUCss, tau showed by this compound. Even though only two dose levels were investigated in this trial, the pharmacokinetics of both drugs seem to be linear. In line with previous trials, both compounds at both dose levels investigated produced complete or almost complete inhibition of ACE activity in serum, for a period lasting 6-8 h after administration, the inhibition being still relevant 24 h thereafter. The tolerability of the two drugs at both dose levels proved to be very good as demonstrated by subjective and objective symptoms, by the absence of relevant adverse events, and by laboratory biochemical parameters and vital signs evaluated before and after the trial. Blood pressure showed a fairly decreasing trend with both the drugs, systolic and diastolic blood pressure values being however within normal range in all the subjects. In no case symptoms of hypotension were experienced. In conclusion, zofenopril calcium and enalapril maleate show very good tolerability and appear to exert similar activity on serum ACE. The main difference in the pharmacokinetics of the two compounds is the conversion from pro-drug to the active metabolite which is faster with zofenopril.

摘要

佐芬普利钙(CAS 81938-43-4)是一种新型血管紧张素转换酶(ACE)抑制剂,除了具有该类药物的典型活性外,还因含有巯基而具有特定的心脏保护作用。在本试验中,将佐芬普利钙和马来酸依那普利(CAS 76095-16-4)以重复给药方案给予20名健康志愿者,分两个剂量水平:30mg和60mg佐芬普利钙以及10mg和20mg马来酸依那普利。该研究按照两期、两序列、交叉设计进行,并设有洗脱期。在两个研究期内及最后一天测定血清中的ACE活性以及佐芬普利、佐芬普利拉、依那普利和依那普利拉的血浆浓度。佐芬普利和依那普利均通过水解广泛转化为其活性代谢产物佐芬普利拉和依那普利拉。与依那普利相比,佐芬普利表现出完全且更快的水解速率,这体现在该化合物的Cmax和AUCss的代谢物与母体药物比率更高,tau也更高。尽管本试验仅研究了两个剂量水平,但两种药物的药代动力学似乎都是线性的。与先前的试验一致,所研究的两个剂量水平的两种化合物在给药后6-8小时内均产生了对血清ACE活性的完全或几乎完全抑制,此后24小时仍有相关抑制作用。从主观和客观症状、无相关不良事件以及试验前后评估的实验室生化参数和生命体征来看,两个剂量水平的两种药物耐受性都非常好。两种药物均使血压呈现相当的下降趋势,但所有受试者的收缩压和舒张压值均在正常范围内。无一例出现低血压症状。总之,佐芬普利钙和马来酸依那普利耐受性良好,且对血清ACE似乎具有相似的活性。两种化合物药代动力学的主要差异在于前体药物向活性代谢产物的转化,佐芬普利的转化更快。

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