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氟硝西泮不同药剂配方的生物利用度。

Bioavailability from various galenic formulations of flunitrazepam.

作者信息

Cano J P, Soliva M, Hartmann D, Ziegler W H, Amrein R

出版信息

Arzneimittelforschung. 1977;27(12):2383-8.

PMID:23801
Abstract

The absolute and relative bioavailability of flunitrazepam (Rohypnol) tablet, oral solution and suppository formulations was determined in a cross-over study on 6 healthy volunteers. The tablet and the oral solution were shown to be bioequivalent, absorption being at least 80%. For flunitrazepam suppositories the bioavailability was found to be about 50%. The plasma concentrations are described on the basis of a three-compartment model, the adjustment of the curves from the same subject being made simultaneously. The central compartment and the second compartment are about equal in size and rapid exchange takes place between them. The third compartment is about four times as large as the central one. The slow reflux of the compound from the third to the first compartment is the rate determining factor for the overall elimination in the beta-phase.

摘要

在一项针对6名健康志愿者的交叉研究中,测定了氟硝西泮(“迷奸药”)片剂、口服溶液剂和栓剂剂型的绝对生物利用度和相对生物利用度。结果表明,片剂和口服溶液剂具有生物等效性,吸收至少达80%。氟硝西泮栓剂的生物利用度约为50%。血浆浓度基于三室模型进行描述,同时对同一受试者的曲线进行校正。中央室和第二室大小相近,二者之间有快速交换。第三室大小约为中央室的四倍。化合物从第三室向第一室的缓慢回流是β期总体消除的速率决定因素。

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