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两种抗酸剂对扑热息痛生物利用度的影响。

Effect of two antacids on the bioavailability of paracetamol.

作者信息

Albin H, Demotes-Mainard F, Vinçon G, Bedjaoui A, Begaud B

出版信息

Eur J Clin Pharmacol. 1985;29(2):251-3. doi: 10.1007/BF00547432.

Abstract

The effect of two antacids on the bioavailability of paracetamol has been investigated in 12 young healthy volunteers. Following a random cross over design, each subject swallowed, on three separate occasions, one weak apart, 500 mg paracetamol alone, or together with two different aluminium hydroxide, magnesium hydroxide preparations (Dimalan and Maalox). Plasma paracetamol levels were measured by HPLC. The bioavailability of paracetamol was not altered by either antacid, but they both delayed the time to peak plasma concentration (0.85 h; 1.43 h; 1.25 h, without antacid, with Dimalan and with Maalox respectively). The peak plasma concentration was not affected by concurrent antacid administration.

摘要

在12名年轻健康志愿者中研究了两种抗酸剂对扑热息痛生物利用度的影响。按照随机交叉设计,每位受试者在三个不同场合分别吞服500毫克单独的扑热息痛,或与两种不同的氢氧化铝、氢氧化镁制剂(迪马兰和氢氧化铝镁)一起服用。通过高效液相色谱法测定血浆扑热息痛水平。两种抗酸剂均未改变扑热息痛的生物利用度,但它们都延迟了达到血浆浓度峰值的时间(分别为0.85小时、1.43小时、1.25小时,无抗酸剂、与迪马兰和与氢氧化铝镁一起服用时)。同时服用抗酸剂对血浆浓度峰值没有影响。

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