Lauven P M, Stoeckel H, Schwilden H, Schüttler J
Anasth Intensivther Notfallmed. 1981 Jun;16(3):135-42.
Diazepam, flunitrazepam and midazolam have different pharmacokinetic properties, their biological halflives for instance, being 24 to 48 hours, 4,5 hours and 2,5 hours respectively. Moreover, the total plasma clearances calculated for these drugs resulted in 30 ml/min for diazepam, 250 ml/min for flunitrazepam and 450 ml/min for midazolam. On the other hand, all three drugs were found to have nearly the same volumes of distribution (V1: 25 l, VdSS: 80-100 l). A tissue binding of over 90% of the drugs applied can further be computed from their high plasmaprotein binding action and their volumes of distribution. Of the 3 benzodiazepines investigated, diazepam reveals extremely complex pharmacokinetic effects which vary the duration of pharmacological responses very widely; besides drug interaction, enzyme induction and -inhibition it gives rise to the active metabolite N-desmethyl-diazepam (biological halflife 50 to 120 hours). In this respect however, the metabolic products of flunitrazepam and midazolam seem to be of minor clinical importance only. The pharmacokinetics of flunitrazepam will be presented as an example to discuss several modes of dosage.
地西泮、氟硝西泮和咪达唑仑具有不同的药代动力学特性,例如它们的生物半衰期分别为24至48小时、4.5小时和2.5小时。此外,计算得出这些药物的血浆总清除率分别为:地西泮30毫升/分钟、氟硝西泮250毫升/分钟、咪达唑仑450毫升/分钟。另一方面,发现这三种药物的分布容积几乎相同(V1:25升,VdSS:80 - 100升)。根据它们较高的血浆蛋白结合作用和分布容积,还可进一步推算出所应用药物超过90%与组织结合。在所研究的3种苯二氮䓬类药物中,地西泮显示出极其复杂的药代动力学效应,这使得药理反应的持续时间差异很大;除了药物相互作用、酶诱导和抑制作用外,它还会产生活性代谢产物N - 去甲基地西泮(生物半衰期50至120小时)。然而,在这方面,氟硝西泮和咪达唑仑的代谢产物似乎仅具有较小的临床意义。将以氟硝西泮的药代动力学为例来讨论几种给药方式。