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[健康受试者中阿噻米德和螺内酯固定复方两剂的药代动力学]

[Pharmacokinetics in healthy subjects of althiazide and spironolactone in a fixed combination for 2 doses].

作者信息

Doignon J L, Grognet J M, Thébault J J, Caplain M, Capron M H, Pelletier B, Wehrlen M, Istin M

机构信息

Laboratoire d'Etudes du Métabolisme des Médicaments, Département de Biologie CEN-Saclay, Gif-sur-Yvette.

出版信息

Therapie. 1990 Nov-Dec;45(6):475-81.

PMID:2080486
Abstract

Pharmacokinetic plasma curves of altizide (ALT), spironolactone (SPI) and two of the main metabolites of spironolactone, 7 alpha-thiomethyl-spirolactone (7TM) and canrenone (CAN) have been established in 12 healthy human volunteers (6 men and 6 women) after unique oral administration of 1 or 2 tablets of a combination of the two diuretic compounds: altizide (15 mg per tablet) and spironolactone (25 mg per tablets). Main pharmacokinetic parameters have been calculated using a biexponential (ALT and SPI) or a triexponential model (7TM and CAN). Spironolactone is rapidly absorbed. Plasma curves show Tmax respectively equal to 1.19 +/- 0.47 hours (1 tablet) or 1.21 +/- 0.46 (2 tablets). Spironolactone is rapidly metabolized as it is shown by the mean Tmax of metabolites: 7TM and CAN Tmax are respectively 1.56 +/- 0.45 hours and 2.54 +/- 1.06 hours after administration of 1 tablet, or 1.58 +/- 0.42 hours and 2.67 +/- 1.13 hours after administration of 2 tablets. The mean residence time (MRT) of ALT [4.94 +/- 1.14 hours (1 tablet) or 5.31 +/- 1.06 hours (2 tablets)] and SPI [1.81 +/- 0.45 hours (1 tablet) or 1.88 +/- 0.50 hours (2 tablets)] shows a rapid elimination of both drugs. SPI metabolites present higher MRT than the unchanged drug. 7TM MRT after administration of 1 or 2 tablets, are 24.51 +/- 15.35 hours and 18.11 +/- 11.87 hours, respectively. CAN MRT are 39.65 +/- 23.58 hours (1 tablet) and 38.93 +/- 24.58 (2 tablets). Statistical analysis shows no significant administration order effect on the different parametres. Student' t test shows a significant sex effect on CAN AUC, for both formulations.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在12名健康人类志愿者(6名男性和6名女性)单次口服1片或2片两种利尿化合物(阿尔噻嗪(ALT),每片15毫克;螺内酯(SPI),每片25毫克)的组合制剂后,建立了阿尔噻嗪、螺内酯及其两种主要代谢物7α-硫甲基螺内酯(7TM)和坎利酮(CAN)的药代动力学血浆曲线。主要药代动力学参数使用双指数模型(ALT和SPI)或三指数模型(7TM和CAN)进行计算。螺内酯吸收迅速。血浆曲线显示达峰时间(Tmax)分别为1.19±0.47小时(1片)或1.21±0.46小时(2片)。螺内酯迅速代谢,代谢物的平均Tmax表明了这一点:服用1片后,7TM和CAN的Tmax分别为1.56±0.45小时和2.54±1.06小时;服用2片后,分别为1.58±0.42小时和2.67±1.13小时。ALT的平均驻留时间(MRT)[4.94±1.14小时(1片)或5.31±1.06小时(2片)]和SPI的平均驻留时间[1.81±0.45小时(1片)或1.88±0.50小时(2片)]表明两种药物消除迅速。SPI代谢物的MRT高于未代谢药物。服用1片或2片后,7TM的MRT分别为24.51±15.35小时和18.11±11.87小时。CAN的MRT分别为39.65±23.58小时(1片)和38.93±24.58小时(2片)。统计分析表明给药顺序对不同参数无显著影响。学生t检验表明,两种制剂中,性别对CAN的曲线下面积(AUC)有显著影响。(摘要截断于250字)

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