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Pharmacokinetics of FCE 22891, a new oral penem.

机译:FCE 22891(一种新的口服Penem)的药代动力学。

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摘要

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.
机译:FCE 22891是FCE 22101(一种新型广谱青霉素)的口服前药。在健康志愿者中进行了三项不同的随机交叉研究,研究了单剂量给药后FCE 22891的药代动力学,绝对生物利用度以及食物摄入对其吸收的影响。通过高压液相色谱和生物测定法测量血液和尿液中的药物水平。为了对所有研究的结果进行最佳比较,并且由于两种方法的一致性很高,因此只包括了高压液相色谱法的结果。 Penem的药代动力学是线性的,口服后的生物利用度为42 +/- 11%。食物摄入量使曲线下的总面积从0 h增加到无穷大,从11.9 +/- 3.5增加到14.1 +/- 2.4 mg.h /升。在一些以大于或等于1.0 g的剂量服用FCE 22891的志愿者中,出现了特定的副作用,即膀胱不适。

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