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新型口服青霉烯类药物FCE 22891的药代动力学

Pharmacokinetics of FCE 22891, a new oral penem.

作者信息

Saathoff A, Lode H, Hampel B, Deppermann K M, Borner K, Koeppe P

机构信息

Medical Department, Klinikum Steglitz, Freie Universität Berlin, Federal Republic of Germany.

出版信息

Antimicrob Agents Chemother. 1990 Jun;34(6):1001-6. doi: 10.1128/AAC.34.6.1001.

Abstract

FCE 22891 is the oral prodrug of FCE 22101, a new broad-spectrum penem. The pharmacokinetics of FCE 22891 after single-dose administration, its absolute bioavailability, and the effect of food intake on its absorption were investigated in three different randomized crossover studies in healthy volunteers. Drug levels in blood and urine were measured by high-pressure liquid chromatography and bioassay. For optimal comparison of the results of all studies, and since there was good agreement of both methods, only the high-pressure liquid chromatography results are included. The pharmacokinetics of the penem were linear, and its bioavailability after oral administration was 42 +/- 11%. Food intake increased the total area under the curve from 0 h to infinity from 11.9 +/- 3.5 to 14.1 +/- 2.4 mg.h/liter. A specific side effect, i.e., bladder complaints, was registered in some volunteers taking FCE 22891 at doses greater than or equal to 1.0 g.

摘要

FCE 22891是新型广谱青霉烯类药物FCE 22101的口服前体药物。在三项针对健康志愿者的不同随机交叉研究中,对FCE 22891单次给药后的药代动力学、其绝对生物利用度以及食物摄入对其吸收的影响进行了研究。通过高压液相色谱法和生物测定法测量血液和尿液中的药物水平。为了对所有研究结果进行最佳比较,并且由于两种方法的结果一致性良好,仅纳入了高压液相色谱法的结果。该青霉烯类药物的药代动力学呈线性,口服给药后的生物利用度为42±11%。食物摄入使0小时至无穷大的曲线下总面积从11.9±3.5增加至14.1±2.4mg·h/升。一些服用剂量大于或等于1.0g的FCE 22891的志愿者出现了一种特定的副作用,即膀胱不适。

相似文献

1
Pharmacokinetics of FCE 22891, a new oral penem.新型口服青霉烯类药物FCE 22891的药代动力学
Antimicrob Agents Chemother. 1990 Jun;34(6):1001-6. doi: 10.1128/AAC.34.6.1001.

本文引用的文献

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Pharmacokinetics of imipenem in healthy volunteers.健康志愿者中亚胺培南的药代动力学。
J Antimicrob Chemother. 1983 Dec;12 Suppl D:109-24. doi: 10.1093/jac/12.suppl_d.109.

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