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巴卡西林与高口服剂量氨苄西林的比较临床药理学

Comparative clinical pharmacology of bacampicillin and high oral doses of ampicillin.

作者信息

Magni L, Sjövall J, Syvälahti E

出版信息

Infection. 1978;6(6):283-9. doi: 10.1007/BF01641988.

Abstract

Ampicillin is often used in high oral doses due to its incomplete absorption. The objective of this study was to compare the bioavailability of bacampicillin, a new prodrug of ampicillin which is nearly completely absorbed, to that of high doses of oral ampicillin. Single oral doses of bacampicillin 400 mg or 800 mg and ampicillin 500 mg, 1 g, or 2 g were given to 12 male subjects according to a cross-over design after overnight fasting. The median time after administration till the peak serum level was 0.75 and 1.0 hour with bacampicillin 400 mg and 800 mg respectively, as compared to 1.5, 2.0 and 1.5 hours for the ampicillin doses. The mean of the individual peak serum level after bacampicillin 400 mg, was 7.7 mg/l, which is higher than that after ampicillin 500 mg, 5.2 mg/l, and about the same as that after ampicillin 1 g, 7.6 mg/l. A slightly higher mean peak level was seen after bacampicillin 800 mg, 12.2 mg/l, as compared to ampicillin 2 g, 10.5 mg/l. The absorption rate was highest with bacampicillin, for which 90% of the absorption had occurred 1 hour after administration as compared to 2.5 hours after administration of ampicillin. The relative bioavailability was about 2--3 times higher after bacampicillin as compared to ampicillin. The data imply dose-dependent absorption of oral ampicillin in high doses as there seems to be a less than proportional increase in AUC. The urinary recovery after bacampicillin was 68--75% as compared to 25--41% after ampicillin. Higher doses gave a lower percentage recovery and this phenomenon was more pronounced with ampicillin.

摘要

由于氨苄西林吸收不完全,常采用高口服剂量。本研究的目的是比较氨苄西林的一种新前体药物巴氨西林(其吸收几乎完全)与高剂量口服氨苄西林的生物利用度。根据交叉设计,在12名男性受试者过夜禁食后,分别给予单次口服剂量的400mg或800mg巴氨西林以及500mg、1g或2g氨苄西林。服用巴氨西林400mg和800mg后,达到血清峰值水平的中位时间分别为0.75小时和1.0小时,而服用上述剂量氨苄西林后的时间分别为1.5小时、2.0小时和1.5小时。服用400mg巴氨西林后个体血清峰值水平的平均值为7.7mg/l,高于服用500mg氨苄西林后的5.2mg/l,与服用1g氨苄西林后的7.6mg/l大致相同。服用800mg巴氨西林后的平均峰值水平略高于服用2g氨苄西林后的,分别为12.2mg/l和10.5mg/l。巴氨西林的吸收速率最高,给药1小时后90%的药物已被吸收,而氨苄西林给药后2.5小时才达到这一吸收比例。与氨苄西林相比,巴氨西林后的相对生物利用度约高2 - 3倍。数据表明高剂量口服氨苄西林存在剂量依赖性吸收,因为曲线下面积(AUC)的增加似乎并非成比例。巴氨西林后的尿回收率为68 - 75%,而氨苄西林后的为25 - 41%。较高剂量的回收率较低,且这种现象在氨苄西林中更为明显。

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