Hilbert J M, Chung M, Radwanski E, Gural R, Symchowicz S, Zampaglione N
Clin Pharmacol Ther. 1984 Oct;36(4):566-9. doi: 10.1038/clpt.1984.220.
The kinetics of quazepam, a benzodiazepine hypnotic, was studied in 10 geriatric subjects. Each received one 15-mg tablet of quazepam. Blood samples were collected before and at specified times (up to 672 hr) after dosing. Plasma concentrations of quazepam and its two major active plasma metabolites, 2-oxoquazepam and N-desalkyl-2-oxoquazepam (N-desalkylflurazepam), were determined by specific GLC methods. Kinetics were best described by a two-compartment open model with first-order absorption/formation kinetics and standard equations. Quazepam was rapidly absorbed, with a t1/2 of 0.8 hr. The mean maximum plasma level (Cmax) was 29.3 ng/ml. The disposition t1/2s in the distribution (t1/2 alpha) and elimination (t1/2 beta) phases were 3.5 and 53.3 hr. 2-Oxoquazepam was rapidly formed with quazepam, with an apparent formation t1/2 of 0.8 hr. Mean Cmax was 14.5 ng/ml. The t1/2 alpha and t1/2 beta of 2-oxoquazepam were 4.2 and 43.1 hr, of the order of those of quazepam. The t1/2 beta of N-desalkyl-2-oxoquazepam, formed from 2-oxoquazepam, was 189.7 hr, much longer than that of its precursor. Comparison of these data with reported kinetic data in young subjects shows that t 1/2 betas of quazepam and 2-oxoquazepam increased only slightly or not at all with age, but that the t 1/2 beta of N-desalkyl-2-oxoquazepam in the elderly was more than twice that in young subjects.
在10名老年受试者中研究了苯二氮䓬类催眠药夸西泮的动力学。每人服用一片15毫克的夸西泮片剂。给药前及给药后特定时间(长达672小时)采集血样。采用特定的气相色谱法测定血浆中夸西泮及其两种主要活性代谢物2-氧代夸西泮和N-去烷基-2-氧代夸西泮(N-去烷基氟西泮)的浓度。动力学最好用具有一级吸收/形成动力学和标准方程的二室开放模型来描述。夸西泮吸收迅速,半衰期为0.8小时。平均最大血浆浓度(Cmax)为29.3纳克/毫升。分布相(t1/2α)和消除相(t1/2β)的处置半衰期分别为3.5小时和53.3小时。2-氧代夸西泮与夸西泮同时迅速形成,表观形成半衰期为0.8小时。平均Cmax为14.5纳克/毫升。2-氧代夸西泮的t1/2α和t1/2β分别为4.2小时和43.1小时,与夸西泮的相近。由2-氧代夸西泮形成的N-去烷基-2-氧代夸西泮的t1/2β为189.7小时,比其前体长得多。将这些数据与年轻受试者中报道的动力学数据进行比较表明,夸西泮和2-氧代夸西泮的t1/2β随年龄增长仅略有增加或根本没有增加,但老年人中N-去烷基-2-氧代夸西泮的t1/2β是年轻受试者的两倍多。