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福辛普利与氢氯噻嗪联合用药对比单一成分用药:不存在药代动力学相互作用。

Fosinopril and hydrochlorothiazide combination versus individual components: lack of a pharmacokinetic interaction.

作者信息

Uderman H D, Much D R, Brennan J, Delaney C L, Morgenthien E A, Weaver J, Stouffer B C, Chang S Y, VanHarken D, Liao W

机构信息

Bristol-Myers Squibb Clinical Research Unit, Hamilton, NJ 08690, USA.

出版信息

Ann Pharmacother. 1999 May;33(5):525-30. doi: 10.1345/aph.18228.

Abstract

OBJECTIVE

To evaluate the pharmacokinetic interaction and bioequivalence of a combination formulation of the angiotensin-converting enzyme inhibitor fosinopril and the diuretic hydrochlorothiazide (HCTZ).

METHODS

In an open-label, balanced, randomized incomplete block, three-way crossover fashion, healthy men received single doses of three of four regimens in one of two independent studies. Regimens for study A (36 subjects): (1) fosinopril 10-mg tablet, (2) HCTZ 12.5-mg tablet, (3) a combination tablet of fosinopril 10 mg plus HCTZ 12.5 mg, or (4) coadministered tablets of fosinopril 10 mg and HCTZ 12.5 mg. Study B (40 subjects) received: (1) fosinopril 20-mg tablet, (2) HCTZ 12.5-mg tablet, (3) a combination tablet of fosinopril 20 mg plus HCTZ 12.5 mg, or (4) coadministered tablets of fosinopril 20 mg and HCTZ 12.5 mg.

RESULTS

There was no evidence of any significant effect of HCTZ on the pharmacokinetics of fosinoprilat, based on maximum concentration value, AUC, or cumulative urinary recovery over 24 hours. Fosinoprilat had no clinically important effect on the pharmacokinetics of HCTZ only slightly decreasing its AUC by 14% in study A. Coadministration was well tolerated; no new adverse events were reported with the combination tablet.

CONCLUSIONS

Fosinopril and HCTZ in a combination tablet display pharmacokinetic profiles similar to those achieved when either drug is administered alone or when coadministered in separate tablets. When used with HCTZ, the favorable pharmacokinetic feature of fosinopril, dual and compensatory pathways of renal and hepatic elimination, is preserved.

摘要

目的

评估血管紧张素转换酶抑制剂福辛普利与利尿剂氢氯噻嗪(HCTZ)联合制剂的药代动力学相互作用及生物等效性。

方法

在一项开放标签、平衡、随机不完全区组、三向交叉试验中,健康男性在两项独立研究之一中接受四种给药方案中三种的单剂量给药。研究A(36名受试者)的给药方案:(1)福辛普利10毫克片剂,(2)氢氯噻嗪12.5毫克片剂,(3)福辛普利10毫克加氢氯噻嗪12.5毫克的复方片剂,或(4)福辛普利10毫克与氢氯噻嗪12.5毫克的联用片剂。研究B(40名受试者)接受:(1)福辛普利20毫克片剂,(2)氢氯噻嗪12.5毫克片剂,(3)福辛普利20毫克加氢氯噻嗪12.5毫克的复方片剂,或(4)福辛普利20毫克与氢氯噻嗪12.5毫克的联用片剂。

结果

基于最大浓度值、曲线下面积(AUC)或24小时累积尿回收率,没有证据表明氢氯噻嗪对福辛普利拉的药代动力学有任何显著影响。福辛普利拉对氢氯噻嗪的药代动力学没有临床重要影响,仅在研究A中使其AUC略有降低14%。联合给药耐受性良好;复方片剂未报告新的不良事件。

结论

福辛普利和氢氯噻嗪复方片剂的药代动力学特征与单独给药或分开片剂联用给药时相似。与氢氯噻嗪合用时福辛普利有利的药代动力学特征,即肾和肝消除的双重和代偿途径得以保留。

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