Wretlind M, Pilbrant A, Sundwall A, Vessman J
Acta Pharmacol Toxicol (Copenh). 1977 Jan;40 Suppl 1(1):28-39.
Three benzodiazepines in equipotent doses: oxazepam 15 mg, dipotassium chlorazepate 10 mg and diazepam 5 mg, were administered in single, oral doses to seven healthy volunteers in a three-way cross-over study. The serum concentrations of oxazepam, N-desmethyldiazepam and diazepam were followed for 72 hours by gas chromatography and electron capture detection. The absorption of diazepam was most rapid and the mean time required to reach peak serum concentration was 45 minutes, followed by N-desmethyldiazepam 80 minutes and oxazepam 114 minutes. The serum concentration decay curves were biphasic with terminal mean half-lives of 48, 62 and 11 hours for diazepam, N-desmethyldiazepam and oxazepam, respectively. The mean and individual serum concentration time data were fitted to a two-compartment open model with first order absorption using a non linear least square program. The mean serum data fitted the model well. The same rank order was obtained with mean absorption half-lives as when comparing mean peak times while slightly shorter terminal half-lives were obtained in the curve fitting of mean serum data. Due to irregularities in the serum concentration time curves only five out of the 21 sets of individual data could satisfy the convergence criterion. The obtained parameters in the curve fitting were also accompanied with very large asymptotic standard deviations.
在一项三交叉研究中,给7名健康志愿者单次口服给予三种等效剂量的苯二氮䓬类药物:奥沙西泮15毫克、氯氮䓬二钾10毫克和地西泮5毫克。通过气相色谱法和电子捕获检测法对奥沙西泮、N-去甲基地西泮和地西泮的血清浓度进行了72小时的跟踪监测。地西泮的吸收最快,达到血清峰值浓度所需的平均时间为45分钟,其次是N-去甲基地西泮80分钟和奥沙西泮114分钟。血清浓度衰减曲线呈双相,地西泮、N-去甲基地西泮和奥沙西泮的终末平均半衰期分别为48、62和11小时。使用非线性最小二乘法程序将平均和个体血清浓度时间数据拟合为具有一级吸收的二室开放模型。平均血清数据与模型拟合良好。平均吸收半衰期的排序与比较平均峰值时间时相同,而在平均血清数据的曲线拟合中获得的终末半衰期略短。由于血清浓度时间曲线不规则,21组个体数据中只有5组能满足收敛标准。曲线拟合中获得的参数还伴随着非常大的渐近标准差。